CNRS Nantes University US2B US2B
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***  ROMORO  ***

elNémo ID: 240415171241475139

Job options:

ID        	=	 240415171241475139
JOBID     	=	 ROMORO
USERID    	=	 unknown
PRIVAT    	=	 0

NMODES    	=	 5
DQMIN     	=	 -100
DQMAX     	=	 100
DQSTEP    	=	 20
DOGRAPHS  	=	 on

DOPROJMODS	=	 0
DORMSD    	=	 0

NRBL      	=	 0
CUTOFF    	=	 0
CAONLY    	=	 0


Input data for this run:

HEADER ROMORO

HEADER    NUCLEAR RECEPTOR                        30-MAR-99   3ERT              
TITLE     HUMAN ESTROGEN RECEPTOR ALPHA LIGAND-BINDING DOMAIN IN COMPLEX WITH 4-
TITLE    2 HYDROXYTAMOXIFEN                                                     
COMPND    MOL_ID: 1;                                                            
COMPND   2 MOLECULE: PROTEIN (ESTROGEN RECEPTOR ALPHA);                         
COMPND   3 CHAIN: A;                                                            
COMPND   4 FRAGMENT: LIGAND-BINDING DOMAIN;                                     
COMPND   5 SYNONYM: OESTROGEN RECEPTOR, ER LBD;                                 
COMPND   6 ENGINEERED: YES                                                      
SOURCE    MOL_ID: 1;                                                            
SOURCE   2 ORGANISM_SCIENTIFIC: HOMO SAPIENS;                                   
SOURCE   3 ORGANISM_COMMON: HUMAN;                                              
SOURCE   4 ORGANISM_TAXID: 9606;                                                
SOURCE   5 GENE: ESTROGEN RECEPTOR ALPHA;                                       
SOURCE   6 EXPRESSION_SYSTEM: ESCHERICHIA COLI;                                 
SOURCE   7 EXPRESSION_SYSTEM_TAXID: 562;                                        
SOURCE   8 EXPRESSION_SYSTEM_STRAIN: BL21(DE3)PLYSS;                            
SOURCE   9 EXPRESSION_SYSTEM_CELLULAR_LOCATION: CYTOPLASM;                      
SOURCE  10 EXPRESSION_SYSTEM_PLASMID: PET23D                                    
KEYWDS    NUCLEAR RECEPTOR, TRANSCRIPTION FACTOR, ESTROGEN, ANTAGONIST          
EXPDTA    X-RAY DIFFRACTION                                                     
AUTHOR    A.K.SHIAU,D.BARSTAD,P.M.LORIA,L.CHENG,P.J.KUSHNER,D.A.AGARD,          
AUTHOR   2 G.L.GREENE                                                           
REVDAT   4   06-SEP-23 3ERT    1       REMARK SEQADV                            
REVDAT   3   16-NOV-11 3ERT    1       VERSN  HETATM                            
REVDAT   2   24-FEB-09 3ERT    1       VERSN                                    
REVDAT   1   08-APR-99 3ERT    0                                                
SPRSDE     08-APR-99 3ERT      2ERT                                             
JRNL        AUTH   A.K.SHIAU,D.BARSTAD,P.M.LORIA,L.CHENG,P.J.KUSHNER,D.A.AGARD, 
JRNL        AUTH 2 G.L.GREENE                                                   
JRNL        TITL   THE STRUCTURAL BASIS OF ESTROGEN RECEPTOR/COACTIVATOR        
JRNL        TITL 2 RECOGNITION AND THE ANTAGONISM OF THIS INTERACTION BY        
JRNL        TITL 3 TAMOXIFEN.                                                   
JRNL        REF    CELL(CAMBRIDGE,MASS.)         V.  95   927 1998              
JRNL        REFN                   ISSN 0092-8674                               
JRNL        PMID   9875847                                                      
JRNL        DOI    10.1016/S0092-8674(00)81717-1                                
REMARK   2                                                                      
REMARK   2 RESOLUTION.    1.90 ANGSTROMS.                                       
REMARK   3                                                                      
REMARK   3 REFINEMENT.                                                          
REMARK   3   PROGRAM     : X-PLOR 3.854                                         
REMARK   3   AUTHORS     : BRUNGER                                              
REMARK   3                                                                      
REMARK   3  DATA USED IN REFINEMENT.                                            
REMARK   3   RESOLUTION RANGE HIGH (ANGSTROMS) : 1.90                           
REMARK   3   RESOLUTION RANGE LOW  (ANGSTROMS) : 41.00                          
REMARK   3   DATA CUTOFF            (SIGMA(F)) : 0.000                          
REMARK   3   DATA CUTOFF HIGH         (ABS(F)) : 10000000.000                   
REMARK   3   DATA CUTOFF LOW          (ABS(F)) : 0.0010                         
REMARK   3   COMPLETENESS (WORKING+TEST)   (%) : 99.1                           
REMARK   3   NUMBER OF REFLECTIONS             : 23009                          
REMARK   3                                                                      
REMARK   3  FIT TO DATA USED IN REFINEMENT.                                     
REMARK   3   CROSS-VALIDATION METHOD          : THROUGHOUT                      
REMARK   3   FREE R VALUE TEST SET SELECTION  : RANDOM                          
REMARK   3   R VALUE            (WORKING SET) : 0.229                           
REMARK   3   FREE R VALUE                     : 0.262                           
REMARK   3   FREE R VALUE TEST SET SIZE   (%) : 8.200                           
REMARK   3   FREE R VALUE TEST SET COUNT      : 1910                            
REMARK   3   ESTIMATED ERROR OF FREE R VALUE  : NULL                            
REMARK   3                                                                      
REMARK   3  FIT IN THE HIGHEST RESOLUTION BIN.                                  
REMARK   3   TOTAL NUMBER OF BINS USED           : 8                            
REMARK   3   BIN RESOLUTION RANGE HIGH       (A) : 1.90                         
REMARK   3   BIN RESOLUTION RANGE LOW        (A) : 1.99                         
REMARK   3   BIN COMPLETENESS (WORKING+TEST) (%) : 97.50                        
REMARK   3   REFLECTIONS IN BIN    (WORKING SET) : 2500                         
REMARK   3   BIN R VALUE           (WORKING SET) : 0.3650                       
REMARK   3   BIN FREE R VALUE                    : 0.3850                       
REMARK   3   BIN FREE R VALUE TEST SET SIZE  (%) : 8.30                         
REMARK   3   BIN FREE R VALUE TEST SET COUNT     : 232                          
REMARK   3   ESTIMATED ERROR OF BIN FREE R VALUE : NULL                         
REMARK   3                                                                      
REMARK   3  NUMBER OF NON-HYDROGEN ATOMS USED IN REFINEMENT.                    
REMARK   3   PROTEIN ATOMS            : 1932                                    
REMARK   3   NUCLEIC ACID ATOMS       : 0                                       
REMARK   3   HETEROGEN ATOMS          : 29                                      
REMARK   3   SOLVENT ATOMS            : 79                                      
REMARK   3                                                                      
REMARK   3  B VALUES.                                                           
REMARK   3   FROM WILSON PLOT           (A**2) : 33.70                          
REMARK   3   MEAN B VALUE      (OVERALL, A**2) : 40.40                          
REMARK   3   OVERALL ANISOTROPIC B VALUE.                                       
REMARK   3    B11 (A**2) : -2.86000                                             
REMARK   3    B22 (A**2) : -2.86000                                             
REMARK   3    B33 (A**2) : 5.72500                                              
REMARK   3    B12 (A**2) : -3.87000                                             
REMARK   3    B13 (A**2) : 0.00000                                              
REMARK   3    B23 (A**2) : 0.00000                                              
REMARK   3                                                                      
REMARK   3  ESTIMATED COORDINATE ERROR.                                         
REMARK   3   ESD FROM LUZZATI PLOT        (A) : NULL                            
REMARK   3   ESD FROM SIGMAA              (A) : NULL                            
REMARK   3   LOW RESOLUTION CUTOFF        (A) : NULL                            
REMARK   3                                                                      
REMARK   3  CROSS-VALIDATED ESTIMATED COORDINATE ERROR.                         
REMARK   3   ESD FROM C-V LUZZATI PLOT    (A) : NULL                            
REMARK   3   ESD FROM C-V SIGMAA          (A) : NULL                            
REMARK   3                                                                      
REMARK   3  RMS DEVIATIONS FROM IDEAL VALUES.                                   
REMARK   3   BOND LENGTHS                 (A) : 0.006                           
REMARK   3   BOND ANGLES            (DEGREES) : 0.980                           
REMARK   3   DIHEDRAL ANGLES        (DEGREES) : 21.80                           
REMARK   3   IMPROPER ANGLES        (DEGREES) : 0.594                           
REMARK   3                                                                      
REMARK   3  ISOTROPIC THERMAL MODEL : NULL                                      
REMARK   3                                                                      
REMARK   3  ISOTROPIC THERMAL FACTOR RESTRAINTS.    RMS    SIGMA                
REMARK   3   MAIN-CHAIN BOND              (A**2) : NULL  ; NULL                 
REMARK   3   MAIN-CHAIN ANGLE             (A**2) : NULL  ; NULL                 
REMARK   3   SIDE-CHAIN BOND              (A**2) : NULL  ; NULL                 
REMARK   3   SIDE-CHAIN ANGLE             (A**2) : NULL  ; NULL                 
REMARK   3                                                                      
REMARK   3  NCS MODEL : NULL                                                    
REMARK   3                                                                      
REMARK   3  NCS RESTRAINTS.                         RMS   SIGMA/WEIGHT          
REMARK   3   GROUP  1  POSITIONAL            (A) : NULL  ; NULL                 
REMARK   3   GROUP  1  B-FACTOR           (A**2) : NULL  ; NULL                 
REMARK   3                                                                      
REMARK   3  PARAMETER FILE  1  : PROTEIN_REP.PARAM                              
REMARK   3  PARAMETER FILE  2  : NULL                                           
REMARK   3  PARAMETER FILE  3  : NULL                                           
REMARK   3  TOPOLOGY FILE  1   : TOPHCSDX.PRO                                   
REMARK   3  TOPOLOGY FILE  2   : TOPH19.SOL                                     
REMARK   3  TOPOLOGY FILE  3   : NULL                                           
REMARK   3                                                                      
REMARK   3  OTHER REFINEMENT REMARKS: NULL                                      
REMARK   4                                                                      
REMARK   4 3ERT COMPLIES WITH FORMAT V. 3.30, 13-JUL-11                         
REMARK 100                                                                      
REMARK 100 THIS ENTRY HAS BEEN PROCESSED BY RCSB ON 31-MAR-99.                  
REMARK 100 THE DEPOSITION ID IS D_1000000760.                                   
REMARK 200                                                                      
REMARK 200 EXPERIMENTAL DETAILS                                                 
REMARK 200  EXPERIMENT TYPE                : X-RAY DIFFRACTION                  
REMARK 200  DATE OF DATA COLLECTION        : MAR-98                             
REMARK 200  TEMPERATURE           (KELVIN) : 100                                
REMARK 200  PH                             : 7.0                                
REMARK 200  NUMBER OF CRYSTALS USED        : 1                                  
REMARK 200                                                                      
REMARK 200  SYNCHROTRON              (Y/N) : Y                                  
REMARK 200  RADIATION SOURCE               : SSRL                               
REMARK 200  BEAMLINE                       : BL9-1                              
REMARK 200  X-RAY GENERATOR MODEL          : NULL                               
REMARK 200  MONOCHROMATIC OR LAUE    (M/L) : M                                  
REMARK 200  WAVELENGTH OR RANGE        (A) : 0.98                               
REMARK 200  MONOCHROMATOR                  : NULL                               
REMARK 200  OPTICS                         : NULL                               
REMARK 200                                                                      
REMARK 200  DETECTOR TYPE                  : IMAGE PLATE                        
REMARK 200  DETECTOR MANUFACTURER          : MARRESEARCH                        
REMARK 200  INTENSITY-INTEGRATION SOFTWARE : DENZO                              
REMARK 200  DATA SCALING SOFTWARE          : SCALEPACK                          
REMARK 200                                                                      
REMARK 200  NUMBER OF UNIQUE REFLECTIONS   : 23064                              
REMARK 200  RESOLUTION RANGE HIGH      (A) : 1.900                              
REMARK 200  RESOLUTION RANGE LOW       (A) : 41.000                             
REMARK 200  REJECTION CRITERIA  (SIGMA(I)) : -3.000                             
REMARK 200                                                                      
REMARK 200 OVERALL.                                                             
REMARK 200  COMPLETENESS FOR RANGE     (%) : 99.1                               
REMARK 200  DATA REDUNDANCY                : 11.70                              
REMARK 200  R MERGE                    (I) : NULL                               
REMARK 200  R SYM                      (I) : 0.07000                            
REMARK 200   FOR THE DATA SET  : 16.1000                            
REMARK 200                                                                      
REMARK 200 IN THE HIGHEST RESOLUTION SHELL.                                     
REMARK 200  HIGHEST RESOLUTION SHELL, RANGE HIGH (A) : 1.90                     
REMARK 200  HIGHEST RESOLUTION SHELL, RANGE LOW  (A) : 1.93                     
REMARK 200  COMPLETENESS FOR SHELL     (%) : 97.1                               
REMARK 200  DATA REDUNDANCY IN SHELL       : NULL                               
REMARK 200  R MERGE FOR SHELL          (I) : NULL                               
REMARK 200  R SYM FOR SHELL            (I) : 0.64600                            
REMARK 200   FOR SHELL         : 2.100                              
REMARK 200                                                                      
REMARK 200 DIFFRACTION PROTOCOL: SINGLE WAVELENGTH                              
REMARK 200 METHOD USED TO DETERMINE THE STRUCTURE: MOLECULAR REPLACEMENT        
REMARK 200 SOFTWARE USED: AMORE                                                 
REMARK 200 STARTING MODEL: 2LBD                                                 
REMARK 200                                                                      
REMARK 200 REMARK: NULL                                                         
REMARK 280                                                                      
REMARK 280 CRYSTAL                                                              
REMARK 280 SOLVENT CONTENT, VS   (%): 48.00                                     
REMARK 280 MATTHEWS COEFFICIENT, VM (ANGSTROMS**3/DA): 2.40                     
REMARK 280                                                                      
REMARK 280 CRYSTALLIZATION CONDITIONS: WELL: 25-27%(W/V) PEG 4000, 0.180 M      
REMARK 280  SODIUM ACETATE, 0.90 M TRIS PH 8.75-9.0 PROTEIN: 4.3 G/L            
REMARK 280  TEMPERATURE: 19-21 DEGREES C, PH 7.0                                
REMARK 290                                                                      
REMARK 290 CRYSTALLOGRAPHIC SYMMETRY                                            
REMARK 290 SYMMETRY OPERATORS FOR SPACE GROUP: P 65 2 2                         
REMARK 290                                                                      
REMARK 290      SYMOP   SYMMETRY                                                
REMARK 290     NNNMMM   OPERATOR                                                
REMARK 290       1555   X,Y,Z                                                   
REMARK 290       2555   -Y,X-Y,Z+2/3                                            
REMARK 290       3555   -X+Y,-X,Z+1/3                                           
REMARK 290       4555   -X,-Y,Z+1/2                                             
REMARK 290       5555   Y,-X+Y,Z+1/6                                            
REMARK 290       6555   X-Y,X,Z+5/6                                             
REMARK 290       7555   Y,X,-Z+2/3                                              
REMARK 290       8555   X-Y,-Y,-Z                                               
REMARK 290       9555   -X,-X+Y,-Z+1/3                                          
REMARK 290      10555   -Y,-X,-Z+1/6                                            
REMARK 290      11555   -X+Y,Y,-Z+1/2                                           
REMARK 290      12555   X,X-Y,-Z+5/6                                            
REMARK 290                                                                      
REMARK 290     WHERE NNN -> OPERATOR NUMBER                                     
REMARK 290           MMM -> TRANSLATION VECTOR                                  
REMARK 290                                                                      
REMARK 290 CRYSTALLOGRAPHIC SYMMETRY TRANSFORMATIONS                            
REMARK 290 THE FOLLOWING TRANSFORMATIONS OPERATE ON THE ATOM/HETATM             
REMARK 290 RECORDS IN THIS ENTRY TO PRODUCE CRYSTALLOGRAPHICALLY                
REMARK 290 RELATED MOLECULES.                                                   
REMARK 290   SMTRY1   1  1.000000  0.000000  0.000000        0.00000            
REMARK 290   SMTRY2   1  0.000000  1.000000  0.000000        0.00000            
REMARK 290   SMTRY3   1  0.000000  0.000000  1.000000        0.00000            
REMARK 290   SMTRY1   2 -0.500000 -0.866025  0.000000        0.00000            
REMARK 290   SMTRY2   2  0.866025 -0.500000  0.000000        0.00000            
REMARK 290   SMTRY3   2  0.000000  0.000000  1.000000      184.97800            
REMARK 290   SMTRY1   3 -0.500000  0.866025  0.000000        0.00000            
REMARK 290   SMTRY2   3 -0.866025 -0.500000  0.000000        0.00000            
REMARK 290   SMTRY3   3  0.000000  0.000000  1.000000       92.48900            
REMARK 290   SMTRY1   4 -1.000000  0.000000  0.000000        0.00000            
REMARK 290   SMTRY2   4  0.000000 -1.000000  0.000000        0.00000            
REMARK 290   SMTRY3   4  0.000000  0.000000  1.000000      138.73350            
REMARK 290   SMTRY1   5  0.500000  0.866025  0.000000        0.00000            
REMARK 290   SMTRY2   5 -0.866025  0.500000  0.000000        0.00000            
REMARK 290   SMTRY3   5  0.000000  0.000000  1.000000       46.24450            
REMARK 290   SMTRY1   6  0.500000 -0.866025  0.000000        0.00000            
REMARK 290   SMTRY2   6  0.866025  0.500000  0.000000        0.00000            
REMARK 290   SMTRY3   6  0.000000  0.000000  1.000000      231.22250            
REMARK 290   SMTRY1   7 -0.500000  0.866025  0.000000        0.00000            
REMARK 290   SMTRY2   7  0.866025  0.500000  0.000000        0.00000            
REMARK 290   SMTRY3   7  0.000000  0.000000 -1.000000      184.97800            
REMARK 290   SMTRY1   8  1.000000  0.000000  0.000000        0.00000            
REMARK 290   SMTRY2   8  0.000000 -1.000000  0.000000        0.00000            
REMARK 290   SMTRY3   8  0.000000  0.000000 -1.000000        0.00000            
REMARK 290   SMTRY1   9 -0.500000 -0.866025  0.000000        0.00000            
REMARK 290   SMTRY2   9 -0.866025  0.500000  0.000000        0.00000            
REMARK 290   SMTRY3   9  0.000000  0.000000 -1.000000       92.48900            
REMARK 290   SMTRY1  10  0.500000 -0.866025  0.000000        0.00000            
REMARK 290   SMTRY2  10 -0.866025 -0.500000  0.000000        0.00000            
REMARK 290   SMTRY3  10  0.000000  0.000000 -1.000000       46.24450            
REMARK 290   SMTRY1  11 -1.000000  0.000000  0.000000        0.00000            
REMARK 290   SMTRY2  11  0.000000  1.000000  0.000000        0.00000            
REMARK 290   SMTRY3  11  0.000000  0.000000 -1.000000      138.73350            
REMARK 290   SMTRY1  12  0.500000  0.866025  0.000000        0.00000            
REMARK 290   SMTRY2  12  0.866025 -0.500000  0.000000        0.00000            
REMARK 290   SMTRY3  12  0.000000  0.000000 -1.000000      231.22250            
REMARK 290                                                                      
REMARK 290 REMARK: NULL                                                         
REMARK 300                                                                      
REMARK 300 BIOMOLECULE: 1                                                       
REMARK 300 SEE REMARK 350 FOR THE AUTHOR PROVIDED AND/OR PROGRAM                
REMARK 300 GENERATED ASSEMBLY INFORMATION FOR THE STRUCTURE IN                  
REMARK 300 THIS ENTRY. THE REMARK MAY ALSO PROVIDE INFORMATION ON               
REMARK 300 BURIED SURFACE AREA.                                                 
REMARK 350                                                                      
REMARK 350 COORDINATES FOR A COMPLETE MULTIMER REPRESENTING THE KNOWN           
REMARK 350 BIOLOGICALLY SIGNIFICANT OLIGOMERIZATION STATE OF THE                
REMARK 350 MOLECULE CAN BE GENERATED BY APPLYING BIOMT TRANSFORMATIONS          
REMARK 350 GIVEN BELOW.  BOTH NON-CRYSTALLOGRAPHIC AND                          
REMARK 350 CRYSTALLOGRAPHIC OPERATIONS ARE GIVEN.                               
REMARK 350                                                                      
REMARK 350 BIOMOLECULE: 1                                                       
REMARK 350 AUTHOR DETERMINED BIOLOGICAL UNIT: DIMERIC                           
REMARK 350 APPLY THE FOLLOWING TO CHAINS: A                                     
REMARK 350   BIOMT1   1  1.000000  0.000000  0.000000        0.00000            
REMARK 350   BIOMT2   1  0.000000  1.000000  0.000000        0.00000            
REMARK 350   BIOMT3   1  0.000000  0.000000  1.000000        0.00000            
REMARK 350   BIOMT1   2  0.500000 -0.866025  0.000000       29.12100            
REMARK 350   BIOMT2   2 -0.866025 -0.500000  0.000000       50.43905            
REMARK 350   BIOMT3   2  0.000000  0.000000 -1.000000       46.24450            
REMARK 375                                                                      
REMARK 375 SPECIAL POSITION                                                     
REMARK 375 THE FOLLOWING ATOMS ARE FOUND TO BE WITHIN 0.15 ANGSTROMS            
REMARK 375 OF A SYMMETRY RELATED ATOM AND ARE ASSUMED TO BE ON SPECIAL          
REMARK 375 POSITIONS.                                                           
REMARK 375                                                                      
REMARK 375 ATOM RES CSSEQI                                                      
REMARK 375      HOH A   1  LIES ON A SPECIAL POSITION.                          
REMARK 375      HOH A   3  LIES ON A SPECIAL POSITION.                          
REMARK 465                                                                      
REMARK 465 MISSING RESIDUES                                                     
REMARK 465 THE FOLLOWING RESIDUES WERE NOT LOCATED IN THE                       
REMARK 465 EXPERIMENT. (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN               
REMARK 465 IDENTIFIER; SSSEQ=SEQUENCE NUMBER; I=INSERTION CODE.)                
REMARK 465                                                                      
REMARK 465   M RES C SSSEQI                                                     
REMARK 465     MET A   294                                                      
REMARK 465     ASP A   295                                                      
REMARK 465     PRO A   296                                                      
REMARK 465     MET A   297                                                      
REMARK 465     ILE A   298                                                      
REMARK 465     LYS A   299                                                      
REMARK 465     ARG A   300                                                      
REMARK 465     SER A   301                                                      
REMARK 465     LYS A   302                                                      
REMARK 465     LYS A   303                                                      
REMARK 465     ASN A   304                                                      
REMARK 465     SER A   305                                                      
REMARK 465     THR A   553                                                      
REMARK 465     SER A   554                                                      
REMARK 470                                                                      
REMARK 470 MISSING ATOM                                                         
REMARK 470 THE FOLLOWING RESIDUES HAVE MISSING ATOMS (M=MODEL NUMBER;           
REMARK 470 RES=RESIDUE NAME; C=CHAIN IDENTIFIER; SSEQ=SEQUENCE NUMBER;          
REMARK 470 I=INSERTION CODE):                                                   
REMARK 470   M RES CSSEQI  ATOMS                                                
REMARK 470     LEU A 306    CG   CD1  CD2                                       
REMARK 470     ARG A 335    CG   CD   NE   CZ   NH1  NH2                        
REMARK 470     MET A 437    CG   SD   CE                                        
REMARK 470     LEU A 462    CG   CD1  CD2                                       
REMARK 470     SER A 463    OG                                                  
REMARK 470     SER A 464    OG                                                  
REMARK 470     LYS A 481    CG   CD   CE   NZ                                   
REMARK 470     LYS A 529    CG   CD   CE   NZ                                   
REMARK 470     LYS A 531    CG   CD   CE   NZ                                   
REMARK 470     ASN A 532    CG   OD1  ND2                                       
REMARK 470     VAL A 534    CG1  CG2                                            
REMARK 470     PRO A 552    CA   C    O    CB   CG   CD                         
REMARK 500                                                                      
REMARK 500 GEOMETRY AND STEREOCHEMISTRY                                         
REMARK 500 SUBTOPIC: TORSION ANGLES                                             
REMARK 500                                                                      
REMARK 500 TORSION ANGLES OUTSIDE THE EXPECTED RAMACHANDRAN REGIONS:            
REMARK 500 (M=MODEL NUMBER; RES=RESIDUE NAME; C=CHAIN IDENTIFIER;               
REMARK 500 SSEQ=SEQUENCE NUMBER; I=INSERTION CODE).                             
REMARK 500                                                                      
REMARK 500 STANDARD TABLE:                                                      
REMARK 500 FORMAT:(10X,I3,1X,A3,1X,A1,I4,A1,4X,F7.2,3X,F7.2)                    
REMARK 500                                                                      
REMARK 500 EXPECTED VALUES: GJ KLEYWEGT AND TA JONES (1996). PHI/PSI-           
REMARK 500 CHOLOGY: RAMACHANDRAN REVISITED. STRUCTURE 4, 1395 - 1400            
REMARK 500                                                                      
REMARK 500  M RES CSSEQI        PSI       PHI                                   
REMARK 500    SER A 456      -72.77    -27.73                                   
REMARK 500    LEU A 462      -89.75    -39.06                                   
REMARK 500    SER A 463     -146.75   -115.17                                   
REMARK 500    LYS A 531     -116.92    -95.40                                   
REMARK 500    ASN A 532       55.06    -55.28                                   
REMARK 500    ALA A 551       38.68    -73.35                                   
REMARK 500                                                                      
REMARK 500 REMARK: NULL                                                         
REMARK 800                                                                      
REMARK 800 SITE                                                                 
REMARK 800 SITE_IDENTIFIER: AC1                                                 
REMARK 800 EVIDENCE_CODE: SOFTWARE                                              
REMARK 800 SITE_DESCRIPTION: BINDING SITE FOR RESIDUE OHT A 600                 
DBREF  3ERT A  294   554  UNP    P03372   ESR1_HUMAN     294    554             
SEQADV 3ERT MET A  294  UNP  P03372    SER   294 CLONING ARTIFACT               
SEQADV 3ERT ASP A  295  UNP  P03372    PRO   295 CLONING ARTIFACT               
SEQADV 3ERT PRO A  296  UNP  P03372    LEU   296 CLONING ARTIFACT               
SEQRES   1 A  261  MET ASP PRO MET ILE LYS ARG SER LYS LYS ASN SER LEU          
SEQRES   2 A  261  ALA LEU SER LEU THR ALA ASP GLN MET VAL SER ALA LEU          
SEQRES   3 A  261  LEU ASP ALA GLU PRO PRO ILE LEU TYR SER GLU TYR ASP          
SEQRES   4 A  261  PRO THR ARG PRO PHE SER GLU ALA SER MET MET GLY LEU          
SEQRES   5 A  261  LEU THR ASN LEU ALA ASP ARG GLU LEU VAL HIS MET ILE          
SEQRES   6 A  261  ASN TRP ALA LYS ARG VAL PRO GLY PHE VAL ASP LEU THR          
SEQRES   7 A  261  LEU HIS ASP GLN VAL HIS LEU LEU GLU CYS ALA TRP LEU          
SEQRES   8 A  261  GLU ILE LEU MET ILE GLY LEU VAL TRP ARG SER MET GLU          
SEQRES   9 A  261  HIS PRO GLY LYS LEU LEU PHE ALA PRO ASN LEU LEU LEU          
SEQRES  10 A  261  ASP ARG ASN GLN GLY LYS CYS VAL GLU GLY MET VAL GLU          
SEQRES  11 A  261  ILE PHE ASP MET LEU LEU ALA THR SER SER ARG PHE ARG          
SEQRES  12 A  261  MET MET ASN LEU GLN GLY GLU GLU PHE VAL CYS LEU LYS          
SEQRES  13 A  261  SER ILE ILE LEU LEU ASN SER GLY VAL TYR THR PHE LEU          
SEQRES  14 A  261  SER SER THR LEU LYS SER LEU GLU GLU LYS ASP HIS ILE          
SEQRES  15 A  261  HIS ARG VAL LEU ASP LYS ILE THR ASP THR LEU ILE HIS          
SEQRES  16 A  261  LEU MET ALA LYS ALA GLY LEU THR LEU GLN GLN GLN HIS          
SEQRES  17 A  261  GLN ARG LEU ALA GLN LEU LEU LEU ILE LEU SER HIS ILE          
SEQRES  18 A  261  ARG HIS MET SER ASN LYS GLY MET GLU HIS LEU TYR SER          
SEQRES  19 A  261  MET LYS CYS LYS ASN VAL VAL PRO LEU TYR ASP LEU LEU          
SEQRES  20 A  261  LEU GLU MET LEU ASP ALA HIS ARG LEU HIS ALA PRO THR          
SEQRES  21 A  261  SER                                                          
HET    OHT  A 600      29                                                       
HETNAM     OHT 4-HYDROXYTAMOXIFEN                                               
FORMUL   2  OHT    C26 H29 N O2                                                 
FORMUL   3  HOH   *79(H2 O)                                                     
HELIX    1   1 ALA A  307  SER A  309  1                                   3
HELIX    2   2 ALA A  312  ALA A  322  1                                  11
HELIX    3   3 MET A  342  ARG A  363  1                                  22
HELIX    4   4 PHE A  367  ASP A  369  1                                   3
HELIX    5   5 LEU A  372  SER A  395  1                                  24
HELIX    6   6 ARG A  412  CYS A  417  1                                   6
HELIX    7   7 ILE A  424  MET A  438  1                                  15
HELIX    8   8 GLY A  442  ASN A  455  1                                  14
HELIX    9   9 LEU A  466  LYS A  492  1                                  27
HELIX   10  10 LEU A  497  MET A  528  1                                  32
HELIX   11  11 LEU A  536  LEU A  544  1                                   9
SHEET    1   1 1 LYS A 401  ALA A 405  0
SHEET    2   2 1 LEU A 408  ASP A 411  0
SITE     1 AC1 10 HOH A   2  HOH A  58  LEU A 346  ALA A 350                    
SITE     2 AC1 10 ASP A 351  GLU A 353  LEU A 387  ARG A 394                    
SITE     3 AC1 10 MET A 421  GLY A 521                                          
CRYST1   58.242   58.242  277.467  90.00  90.00 120.00 P 65 2 2     12          
ORIGX1      1.000000  0.000000  0.000000        0.00000                         
ORIGX2      0.000000  1.000000  0.000000        0.00000                         
ORIGX3      0.000000  0.000000  1.000000        0.00000                         
SCALE1      0.017170  0.009913  0.000000        0.00000                         
SCALE2      0.000000  0.019826  0.000000        0.00000                         
SCALE3      0.000000  0.000000  0.003604        0.00000                         
ATOM      1  N   LEU A 306       6.369   9.127   4.589  1.00 62.53           N
ATOM      2  CA  LEU A 306       7.232  10.329   4.754  1.00 61.71           C
ATOM      3  C   LEU A 306       7.381  10.684   6.231  1.00 61.99           C
ATOM      4  O   LEU A 306       6.407  11.019   6.906  1.00 62.55           O
ATOM      5  CB  LEU A 306       6.640  11.504   4.009  1.00  0.00           C
ATOM      6  CG  LEU A 306       6.639  11.222   2.510  1.00  0.00           C
ATOM      7  CD2 LEU A 306       8.077  11.130   2.010  1.00  0.00           C
ATOM      8  CD1 LEU A 306       5.919  12.351   1.780  1.00  0.00           C
ATOM      9  N   ALA A 307       8.609  10.605   6.730  1.00 61.40           N
ATOM     10  CA  ALA A 307       8.891  10.912   8.125  1.00 59.75           C
ATOM     11  C   ALA A 307       8.693  12.393   8.429  1.00 58.63           C
ATOM     12  O   ALA A 307       8.451  12.770   9.574  1.00 58.72           O
ATOM     13  CB  ALA A 307      10.319  10.501   8.465  1.00 60.90           C
ATOM     14  N   LEU A 308       8.789  13.228   7.400  1.00 56.65           N
ATOM     15  CA  LEU A 308       8.638  14.668   7.573  1.00 57.08           C
ATOM     16  C   LEU A 308       7.190  15.130   7.710  1.00 56.98           C
ATOM     17  O   LEU A 308       6.935  16.307   7.960  1.00 55.81           O
ATOM     18  CB  LEU A 308       9.298  15.403   6.406  1.00 57.80           C
ATOM     19  CG  LEU A 308      10.637  14.822   5.948  1.00 59.39           C
ATOM     20  CD1 LEU A 308      10.474  14.189   4.569  1.00 59.98           C
ATOM     21  CD2 LEU A 308      11.695  15.921   5.933  1.00 58.57           C
ATOM     22  N   SER A 309       6.246  14.208   7.545  1.00 57.39           N
ATOM     23  CA  SER A 309       4.828  14.543   7.657  1.00 56.94           C
ATOM     24  C   SER A 309       4.260  14.095   9.002  1.00 56.55           C
ATOM     25  O   SER A 309       3.165  14.506   9.397  1.00 55.25           O
ATOM     26  CB  SER A 309       4.035  13.896   6.513  1.00 57.36           C
ATOM     27  OG  SER A 309       4.071  12.479   6.588  1.00 58.17           O
ATOM     28  N   LEU A 310       5.015  13.257   9.706  1.00 54.85           N
ATOM     29  CA  LEU A 310       4.590  12.749  11.004  1.00 54.34           C
ATOM     30  C   LEU A 310       4.330  13.865  12.003  1.00 53.98           C
ATOM     31  O   LEU A 310       4.993  14.904  11.984  1.00 53.98           O
ATOM     32  CB  LEU A 310       5.651  11.810  11.582  1.00 55.32           C
ATOM     33  CG  LEU A 310       5.586  10.332  11.189  1.00 57.72           C
ATOM     34  CD1 LEU A 310       5.530  10.200   9.676  1.00 58.32           C
ATOM     35  CD2 LEU A 310       6.808   9.610  11.739  1.00 58.40           C
ATOM     36  N   THR A 311       3.353  13.641  12.874  1.00 52.35           N
ATOM     37  CA  THR A 311       3.018  14.604  13.912  1.00 50.26           C
ATOM     38  C   THR A 311       3.815  14.200  15.146  1.00 49.15           C
ATOM     39  O   THR A 311       4.370  13.103  15.197  1.00 47.08           O
ATOM     40  CB  THR A 311       1.527  14.554  14.274  1.00 49.13           C
ATOM     41  OG1 THR A 311       1.242  13.311  14.930  1.00 46.82           O
ATOM     42  CG2 THR A 311       0.666  14.688  13.026  1.00 50.77           C
ATOM     43  N   ALA A 312       3.857  15.079  16.141  1.00 49.08           N
ATOM     44  CA  ALA A 312       4.589  14.798  17.369  1.00 47.76           C
ATOM     45  C   ALA A 312       4.170  13.461  17.965  1.00 47.42           C
ATOM     46  O   ALA A 312       5.009  12.610  18.263  1.00 45.47           O
ATOM     47  CB  ALA A 312       4.359  15.910  18.379  1.00 46.87           C
ATOM     48  N   ASP A 313       2.868  13.275  18.143  1.00 47.63           N
ATOM     49  CA  ASP A 313       2.367  12.033  18.714  1.00 47.86           C
ATOM     50  C   ASP A 313       2.745  10.846  17.836  1.00 44.39           C
ATOM     51  O   ASP A 313       2.958   9.741  18.332  1.00 45.23           O
ATOM     52  CB  ASP A 313       0.848  12.100  18.879  1.00 52.55           C
ATOM     53  CG  ASP A 313       0.430  12.873  20.119  1.00 56.88           C
ATOM     54  OD1 ASP A 313       1.314  13.235  20.929  1.00 56.80           O
ATOM     55  OD2 ASP A 313      -0.785  13.119  20.281  1.00 59.89           O
ATOM     56  N   GLN A 314       2.826  11.081  16.531  1.00 44.95           N
ATOM     57  CA  GLN A 314       3.182  10.028  15.588  1.00 45.18           C
ATOM     58  C   GLN A 314       4.673   9.722  15.707  1.00 43.55           C
ATOM     59  O   GLN A 314       5.100   8.580  15.556  1.00 44.72           O
ATOM     60  CB  GLN A 314       2.849  10.464  14.156  1.00 45.61           C
ATOM     61  CG  GLN A 314       1.534   9.885  13.625  1.00 48.66           C
ATOM     62  CD  GLN A 314       0.982  10.646  12.428  1.00 50.81           C
ATOM     63  OE1 GLN A 314       1.648  11.515  11.857  1.00 49.68           O
ATOM     64  NE2 GLN A 314      -0.248  10.318  12.042  1.00 51.73           N
ATOM     65  N   MET A 315       5.458  10.757  15.981  1.00 42.83           N
ATOM     66  CA  MET A 315       6.901  10.606  16.130  1.00 41.38           C
ATOM     67  C   MET A 315       7.219   9.792  17.379  1.00 39.06           C
ATOM     68  O   MET A 315       8.002   8.841  17.336  1.00 40.22           O
ATOM     69  CB  MET A 315       7.565  11.985  16.223  1.00 42.97           C
ATOM     70  CG  MET A 315       9.081  11.939  16.355  1.00 42.63           C
ATOM     71  SD  MET A 315       9.907  11.190  14.923  1.00 46.66           S
ATOM     72  CE  MET A 315       9.546  12.409  13.680  1.00 37.59           C
ATOM     73  N   VAL A 316       6.599  10.165  18.491  1.00 37.61           N
ATOM     74  CA  VAL A 316       6.818   9.475  19.755  1.00 39.70           C
ATOM     75  C   VAL A 316       6.403   8.010  19.667  1.00 40.03           C
ATOM     76  O   VAL A 316       7.144   7.117  20.074  1.00 38.03           O
ATOM     77  CB  VAL A 316       6.023  10.135  20.897  1.00 38.86           C
ATOM     78  CG1 VAL A 316       6.246   9.372  22.191  1.00 44.45           C
ATOM     79  CG2 VAL A 316       6.446  11.582  21.059  1.00 40.78           C
ATOM     80  N   SER A 317       5.205   7.761  19.150  1.00 41.68           N
ATOM     81  CA  SER A 317       4.726   6.390  19.026  1.00 41.28           C
ATOM     82  C   SER A 317       5.683   5.599  18.133  1.00 39.39           C
ATOM     83  O   SER A 317       5.994   4.439  18.411  1.00 39.78           O
ATOM     84  CB  SER A 317       3.301   6.382  18.453  1.00 43.50           C
ATOM     85  OG  SER A 317       3.233   5.664  17.232  1.00 48.44           O
ATOM     86  N   ALA A 318       6.166   6.230  17.068  1.00 38.29           N
ATOM     87  CA  ALA A 318       7.093   5.559  16.167  1.00 37.12           C
ATOM     88  C   ALA A 318       8.359   5.150  16.922  1.00 38.44           C
ATOM     89  O   ALA A 318       8.800   4.004  16.836  1.00 33.68           O
ATOM     90  CB  ALA A 318       7.455   6.476  15.004  1.00 38.81           C
ATOM     91  N   LEU A 319       8.932   6.091  17.669  1.00 36.70           N
ATOM     92  CA  LEU A 319      10.158   5.823  18.421  1.00 38.11           C
ATOM     93  C   LEU A 319       9.971   4.804  19.541  1.00 38.06           C
ATOM     94  O   LEU A 319      10.790   3.898  19.715  1.00 34.07           O
ATOM     95  CB  LEU A 319      10.719   7.134  18.981  1.00 39.14           C
ATOM     96  CG  LEU A 319      11.167   8.131  17.905  1.00 36.41           C
ATOM     97  CD1 LEU A 319      11.723   9.382  18.558  1.00 41.11           C
ATOM     98  CD2 LEU A 319      12.218   7.486  17.014  1.00 39.34           C
ATOM     99  N   LEU A 320       8.890   4.946  20.301  1.00 37.65           N
ATOM    100  CA  LEU A 320       8.619   4.014  21.388  1.00 41.40           C
ATOM    101  C   LEU A 320       8.495   2.600  20.833  1.00 40.92           C
ATOM    102  O   LEU A 320       9.003   1.644  21.414  1.00 41.75           O
ATOM    103  CB  LEU A 320       7.324   4.402  22.110  1.00 38.37           C
ATOM    104  CG  LEU A 320       7.396   5.607  23.048  1.00 42.86           C
ATOM    105  CD1 LEU A 320       6.017   5.874  23.635  1.00 45.04           C
ATOM    106  CD2 LEU A 320       8.401   5.350  24.161  1.00 42.57           C
ATOM    107  N   ASP A 321       7.820   2.482  19.696  1.00 43.79           N
ATOM    108  CA  ASP A 321       7.606   1.197  19.042  1.00 44.69           C
ATOM    109  C   ASP A 321       8.904   0.562  18.542  1.00 44.42           C
ATOM    110  O   ASP A 321       9.020  -0.662  18.474  1.00 44.27           O
ATOM    111  CB  ASP A 321       6.655   1.378  17.857  1.00 48.21           C
ATOM    112  CG  ASP A 321       5.194   1.302  18.259  1.00 52.96           C
ATOM    113  OD1 ASP A 321       4.892   1.417  19.467  1.00 54.01           O
ATOM    114  OD2 ASP A 321       4.346   1.128  17.354  1.00 56.46           O
ATOM    115  N   ALA A 322       9.877   1.398  18.192  1.00 40.76           N
ATOM    116  CA  ALA A 322      11.151   0.910  17.677  1.00 38.37           C
ATOM    117  C   ALA A 322      12.154   0.525  18.757  1.00 35.96           C
ATOM    118  O   ALA A 322      13.233   0.011  18.452  1.00 36.07           O
ATOM    119  CB  ALA A 322      11.759   1.956  16.757  1.00 38.60           C
ATOM    120  N   GLU A 323      11.801   0.765  20.015  1.00 36.05           N
ATOM    121  CA  GLU A 323      12.706   0.460  21.115  1.00 36.99           C
ATOM    122  C   GLU A 323      13.205  -0.978  21.110  1.00 38.00           C
ATOM    123  O   GLU A 323      12.424  -1.930  20.998  1.00 38.43           O
ATOM    124  CB  GLU A 323      12.041   0.767  22.459  1.00 35.53           C
ATOM    125  CG  GLU A 323      12.209   2.210  22.898  1.00 37.90           C
ATOM    126  CD  GLU A 323      13.657   2.569  23.199  1.00 36.89           C
ATOM    127  OE1 GLU A 323      14.134   2.246  24.308  1.00 38.05           O
ATOM    128  OE2 GLU A 323      14.314   3.172  22.325  1.00 33.17           O
ATOM    129  N   PRO A 324      14.527  -1.151  21.224  1.00 35.60           N
ATOM    130  CA  PRO A 324      15.158  -2.474  21.240  1.00 36.13           C
ATOM    131  C   PRO A 324      14.940  -3.162  22.583  1.00 35.54           C
ATOM    132  O   PRO A 324      14.617  -2.516  23.579  1.00 34.31           O
ATOM    133  CB  PRO A 324      16.633  -2.167  21.003  1.00 35.61           C
ATOM    134  CG  PRO A 324      16.811  -0.807  21.610  1.00 35.33           C
ATOM    135  CD  PRO A 324      15.522  -0.069  21.345  1.00 36.42           C
ATOM    136  N   PRO A 325      15.134  -4.485  22.631  1.00 35.25           N
ATOM    137  CA  PRO A 325      14.941  -5.208  23.889  1.00 34.63           C
ATOM    138  C   PRO A 325      16.132  -5.070  24.824  1.00 34.91           C
ATOM    139  O   PRO A 325      17.237  -4.728  24.398  1.00 30.41           O
ATOM    140  CB  PRO A 325      14.753  -6.652  23.439  1.00 35.59           C
ATOM    141  CG  PRO A 325      15.590  -6.743  22.200  1.00 34.91           C
ATOM    142  CD  PRO A 325      15.529  -5.386  21.534  1.00 37.08           C
ATOM    143  N   ILE A 326      15.899  -5.322  26.106  1.00 33.87           N
ATOM    144  CA  ILE A 326      16.975  -5.266  27.075  1.00 35.60           C
ATOM    145  C   ILE A 326      17.568  -6.669  27.103  1.00 34.48           C
ATOM    146  O   ILE A 326      16.876  -7.634  27.427  1.00 35.42           O
ATOM    147  CB  ILE A 326      16.458  -4.891  28.474  1.00 38.46           C
ATOM    148  CG1 ILE A 326      15.988  -3.430  28.465  1.00 41.41           C
ATOM    149  CG2 ILE A 326      17.558  -5.110  29.505  1.00 39.11           C
ATOM    150  CD1 ILE A 326      16.035  -2.746  29.815  1.00 44.19           C
ATOM    151  N   LEU A 327      18.840  -6.784  26.746  1.00 29.97           N
ATOM    152  CA  LEU A 327      19.494  -8.083  26.717  1.00 29.47           C
ATOM    153  C   LEU A 327      20.157  -8.438  28.030  1.00 31.35           C
ATOM    154  O   LEU A 327      20.393  -7.579  28.891  1.00 29.58           O
ATOM    155  CB  LEU A 327      20.528  -8.134  25.587  1.00 27.62           C
ATOM    156  CG  LEU A 327      19.978  -7.798  24.196  1.00 29.99           C
ATOM    157  CD1 LEU A 327      21.066  -7.991  23.138  1.00 29.85           C
ATOM    158  CD2 LEU A 327      18.775  -8.687  23.891  1.00 31.34           C
ATOM    159  N   TYR A 328      20.446  -9.725  28.182  1.00 30.84           N
ATOM    160  CA  TYR A 328      21.087 -10.228  29.382  1.00 30.73           C
ATOM    161  C   TYR A 328      22.529 -10.519  29.067  1.00 33.71           C
ATOM    162  O   TYR A 328      22.884 -10.744  27.909  1.00 34.62           O
ATOM    163  CB  TYR A 328      20.410 -11.520  29.842  1.00 33.42           C
ATOM    164  CG  TYR A 328      19.193 -11.273  30.685  1.00 33.15           C
ATOM    165  CD1 TYR A 328      17.996 -10.862  30.110  1.00 35.96           C
ATOM    166  CD2 TYR A 328      19.253 -11.399  32.071  1.00 31.43           C
ATOM    167  CE1 TYR A 328      16.881 -10.574  30.899  1.00 37.22           C
ATOM    168  CE2 TYR A 328      18.151 -11.116  32.864  1.00 36.16           C
ATOM    169  CZ  TYR A 328      16.972 -10.701  32.274  1.00 37.50           C
ATOM    170  OH  TYR A 328      15.895 -10.396  33.071  1.00 45.01           O
ATOM    171  N   SER A 329      23.359 -10.496  30.102  1.00 34.04           N
ATOM    172  CA  SER A 329      24.766 -10.800  29.961  1.00 37.10           C
ATOM    173  C   SER A 329      24.836 -12.317  29.831  1.00 40.31           C
ATOM    174  O   SER A 329      23.981 -13.028  30.363  1.00 39.69           O
ATOM    175  CB  SER A 329      25.526 -10.341  31.204  1.00 36.73           C
ATOM    176  OG  SER A 329      26.788 -10.964  31.281  1.00 36.83           O
ATOM    177  N   GLU A 330      25.845 -12.810  29.127  1.00 41.02           N
ATOM    178  CA  GLU A 330      25.992 -14.242  28.928  1.00 47.08           C
ATOM    179  C   GLU A 330      26.999 -14.852  29.894  1.00 49.09           C
ATOM    180  O   GLU A 330      28.208 -14.741  29.697  1.00 49.92           O
ATOM    181  CB  GLU A 330      26.423 -14.525  27.484  1.00 48.23           C
ATOM    182  CG  GLU A 330      25.278 -14.869  26.542  1.00 49.68           C
ATOM    183  CD  GLU A 330      25.765 -15.404  25.198  1.00 52.51           C
ATOM    184  OE1 GLU A 330      26.002 -14.590  24.279  1.00 50.88           O
ATOM    185  OE2 GLU A 330      25.909 -16.639  25.061  1.00 52.21           O
ATOM    186  N   TYR A 331      26.498 -15.492  30.943  1.00 53.28           N
ATOM    187  CA  TYR A 331      27.373 -16.129  31.921  1.00 57.98           C
ATOM    188  C   TYR A 331      26.603 -17.080  32.823  1.00 58.95           C
ATOM    189  O   TYR A 331      25.393 -16.942  33.003  1.00 58.95           O
ATOM    190  CB  TYR A 331      28.092 -15.078  32.774  1.00 59.61           C
ATOM    191  CG  TYR A 331      27.239 -14.460  33.859  1.00 63.59           C
ATOM    192  CD1 TYR A 331      27.010 -15.128  35.064  1.00 64.20           C
ATOM    193  CD2 TYR A 331      26.656 -13.205  33.682  1.00 65.28           C
ATOM    194  CE1 TYR A 331      26.219 -14.563  36.065  1.00 66.65           C
ATOM    195  CE2 TYR A 331      25.864 -12.630  34.676  1.00 66.99           C
ATOM    196  CZ  TYR A 331      25.648 -13.314  35.864  1.00 68.22           C
ATOM    197  OH  TYR A 331      24.854 -12.753  36.839  1.00 68.80           O
ATOM    198  N   ASP A 332      27.320 -18.045  33.387  1.00 61.52           N
ATOM    199  CA  ASP A 332      26.719 -19.026  34.281  1.00 63.91           C
ATOM    200  C   ASP A 332      26.393 -18.371  35.619  1.00 62.92           C
ATOM    201  O   ASP A 332      27.292 -18.073  36.406  1.00 63.58           O
ATOM    202  CB  ASP A 332      27.681 -20.194  34.500  1.00 65.59           C
ATOM    203  CG  ASP A 332      26.961 -21.516  34.648  1.00 67.79           C
ATOM    204  OD1 ASP A 332      25.780 -21.506  35.061  1.00 66.95           O
ATOM    205  OD2 ASP A 332      27.575 -22.564  34.351  1.00 68.76           O
ATOM    206  N   PRO A 333      25.096 -18.148  35.896  1.00 63.46           N
ATOM    207  CA  PRO A 333      24.677 -17.521  37.154  1.00 63.51           C
ATOM    208  C   PRO A 333      25.010 -18.419  38.332  1.00 63.31           C
ATOM    209  O   PRO A 333      25.129 -17.964  39.468  1.00 63.62           O
ATOM    210  CB  PRO A 333      23.165 -17.334  36.993  1.00 63.80           C
ATOM    211  CG  PRO A 333      22.866 -17.612  35.556  1.00 64.09           C
ATOM    212  CD  PRO A 333      23.945 -18.509  35.053  1.00 64.09           C
ATOM    213  N   THR A 334      25.160 -19.704  38.037  1.00 64.22           N
ATOM    214  CA  THR A 334      25.476 -20.697  39.050  1.00 66.10           C
ATOM    215  C   THR A 334      26.982 -20.804  39.269  1.00 65.73           C
ATOM    216  O   THR A 334      27.432 -21.323  40.289  1.00 64.79           O
ATOM    217  CB  THR A 334      24.929 -22.080  38.645  1.00 67.21           C
ATOM    218  OG1 THR A 334      25.571 -22.513  37.439  1.00 68.35           O
ATOM    219  CG2 THR A 334      23.423 -22.012  38.412  1.00 67.77           C
ATOM    220  N   ARG A 335      27.759 -20.308  38.314  1.00 65.93           N
ATOM    221  CA  ARG A 335      29.214 -20.361  38.421  1.00 66.89           C
ATOM    222  C   ARG A 335      29.756 -19.113  39.124  1.00 67.37           C
ATOM    223  O   ARG A 335      29.099 -18.071  39.148  1.00 67.51           O
ATOM    224  CB  ARG A 335      29.840 -20.481  37.048  1.00  0.00           C
ATOM    225  CG  ARG A 335      31.342 -20.702  37.196  1.00  0.00           C
ATOM    226  CD  ARG A 335      31.962 -20.923  35.821  1.00  0.00           C
ATOM    227  NE  ARG A 335      31.887 -19.692  35.002  1.00  0.00           N
ATOM    228  CZ  ARG A 335      32.216 -19.658  33.714  1.00  0.00           C
ATOM    229  NH2 ARG A 335      32.111 -18.497  33.073  1.00  0.00           N
ATOM    230  NH1 ARG A 335      32.641 -20.739  33.066  1.00  0.00           N
ATOM    231  N   PRO A 336      30.968 -19.207  39.703  1.00 67.82           N
ATOM    232  CA  PRO A 336      31.601 -18.085  40.410  1.00 67.62           C
ATOM    233  C   PRO A 336      31.701 -16.828  39.562  1.00 68.28           C
ATOM    234  O   PRO A 336      31.996 -16.895  38.372  1.00 69.08           O
ATOM    235  CB  PRO A 336      32.982 -18.621  40.784  1.00 66.69           C
ATOM    236  CG  PRO A 336      32.829 -20.097  40.779  1.00 67.91           C
ATOM    237  CD  PRO A 336      31.820 -20.408  39.713  1.00 67.78           C
ATOM    238  N   PHE A 337      31.460 -15.681  40.183  1.00 69.80           N
ATOM    239  CA  PHE A 337      31.529 -14.408  39.480  1.00 71.77           C
ATOM    240  C   PHE A 337      32.985 -14.013  39.245  1.00 71.65           C
ATOM    241  O   PHE A 337      33.336 -13.486  38.189  1.00 71.97           O
ATOM    242  CB  PHE A 337      30.818 -13.323  40.294  1.00 72.73           C
ATOM    243  CG  PHE A 337      31.219 -11.924  39.920  1.00 73.83           C
ATOM    244  CD1 PHE A 337      30.632 -11.287  38.833  1.00 72.94           C
ATOM    245  CD2 PHE A 337      32.191 -11.245  40.652  1.00 73.88           C
ATOM    246  CE1 PHE A 337      31.006  -9.993  38.478  1.00 73.49           C
ATOM    247  CE2 PHE A 337      32.573  -9.950  40.306  1.00 73.09           C
ATOM    248  CZ  PHE A 337      31.979  -9.323  39.217  1.00 73.23           C
ATOM    249  N   SER A 338      33.825 -14.273  40.241  1.00 71.87           N
ATOM    250  CA  SER A 338      35.248 -13.947  40.173  1.00 71.24           C
ATOM    251  C   SER A 338      35.931 -14.504  38.924  1.00 71.32           C
ATOM    252  O   SER A 338      36.951 -13.972  38.475  1.00 71.42           O
ATOM    253  CB  SER A 338      35.957 -14.488  41.414  1.00 70.79           C
ATOM    254  OG  SER A 338      35.547 -15.819  41.679  1.00 70.19           O
ATOM    255  N   GLU A 339      35.368 -15.574  38.368  1.00 70.27           N
ATOM    256  CA  GLU A 339      35.930 -16.215  37.183  1.00 69.54           C
ATOM    257  C   GLU A 339      35.770 -15.386  35.910  1.00 68.28           C
ATOM    258  O   GLU A 339      36.722 -15.216  35.143  1.00 69.39           O
ATOM    259  CB  GLU A 339      35.280 -17.586  36.971  1.00 70.63           C
ATOM    260  CG  GLU A 339      35.996 -18.740  37.657  1.00 72.43           C
ATOM    261  CD  GLU A 339      35.383 -20.089  37.319  1.00 74.22           C
ATOM    262  OE1 GLU A 339      34.787 -20.219  36.228  1.00 73.47           O
ATOM    263  OE2 GLU A 339      35.497 -21.020  38.145  1.00 76.58           O
ATOM    264  N   ALA A 340      34.561 -14.875  35.694  1.00 64.61           N
ATOM    265  CA  ALA A 340      34.246 -14.083  34.507  1.00 60.82           C
ATOM    266  C   ALA A 340      35.096 -12.824  34.326  1.00 56.92           C
ATOM    267  O   ALA A 340      35.634 -12.270  35.287  1.00 57.19           O
ATOM    268  CB  ALA A 340      32.766 -13.710  34.523  1.00 61.70           C
ATOM    269  N   SER A 341      35.215 -12.388  33.076  1.00 52.02           N
ATOM    270  CA  SER A 341      35.972 -11.185  32.738  1.00 46.45           C
ATOM    271  C   SER A 341      34.955 -10.081  32.448  1.00 43.35           C
ATOM    272  O   SER A 341      34.091 -10.244  31.591  1.00 39.74           O
ATOM    273  CB  SER A 341      36.838 -11.439  31.497  1.00 47.97           C
ATOM    274  OG  SER A 341      37.185 -10.226  30.847  1.00 46.53           O
ATOM    275  N   MET A 342      35.043  -8.967  33.171  1.00 41.03           N
ATOM    276  CA  MET A 342      34.110  -7.863  32.962  1.00 42.56           C
ATOM    277  C   MET A 342      34.110  -7.360  31.516  1.00 40.21           C
ATOM    278  O   MET A 342      33.049  -7.139  30.932  1.00 39.70           O
ATOM    279  CB  MET A 342      34.437  -6.699  33.904  1.00 45.83           C
ATOM    280  CG  MET A 342      33.212  -6.069  34.550  1.00 53.83           C
ATOM    281  SD  MET A 342      31.821  -7.225  34.698  1.00 58.03           S
ATOM    282  CE  MET A 342      32.197  -7.967  36.259  1.00 59.19           C
ATOM    283  N   MET A 343      35.295  -7.183  30.936  1.00 38.44           N
ATOM    284  CA  MET A 343      35.385  -6.693  29.562  1.00 38.54           C
ATOM    285  C   MET A 343      34.866  -7.727  28.568  1.00 35.58           C
ATOM    286  O   MET A 343      34.320  -7.373  27.523  1.00 35.90           O
ATOM    287  CB  MET A 343      36.830  -6.309  29.223  1.00 41.23           C
ATOM    288  CG  MET A 343      37.019  -5.736  27.816  1.00 40.45           C
ATOM    289  SD  MET A 343      36.028  -4.251  27.439  1.00 45.40           S
ATOM    290  CE  MET A 343      36.126  -3.335  28.987  1.00 40.72           C
ATOM    291  N   GLY A 344      35.038  -9.005  28.896  1.00 35.52           N
ATOM    292  CA  GLY A 344      34.555 -10.061  28.024  1.00 33.57           C
ATOM    293  C   GLY A 344      33.037 -10.060  28.045  1.00 32.05           C
ATOM    294  O   GLY A 344      32.387 -10.235  27.015  1.00 30.12           O
ATOM    295  N   LEU A 345      32.469  -9.858  29.229  1.00 32.77           N
ATOM    296  CA  LEU A 345      31.019  -9.819  29.374  1.00 34.62           C
ATOM    297  C   LEU A 345      30.432  -8.615  28.622  1.00 33.51           C
ATOM    298  O   LEU A 345      29.485  -8.753  27.854  1.00 29.93           O
ATOM    299  CB  LEU A 345      30.638  -9.725  30.855  1.00 36.73           C
ATOM    300  CG  LEU A 345      30.900 -10.958  31.725  1.00 38.90           C
ATOM    301  CD1 LEU A 345      30.528 -10.640  33.162  1.00 39.87           C
ATOM    302  CD2 LEU A 345      30.090 -12.143  31.207  1.00 41.05           C
ATOM    303  N   LEU A 346      31.011  -7.440  28.853  1.00 30.40           N
ATOM    304  CA  LEU A 346      30.546  -6.211  28.216  1.00 31.83           C
ATOM    305  C   LEU A 346      30.716  -6.248  26.704  1.00 30.89           C
ATOM    306  O   LEU A 346      29.851  -5.780  25.967  1.00 29.05           O
ATOM    307  CB  LEU A 346      31.293  -5.008  28.796  1.00 28.45           C
ATOM    308  CG  LEU A 346      31.077  -4.753  30.294  1.00 29.67           C
ATOM    309  CD1 LEU A 346      31.805  -3.481  30.688  1.00 30.00           C
ATOM    310  CD2 LEU A 346      29.601  -4.631  30.613  1.00 34.45           C
ATOM    311  N   THR A 347      31.833  -6.802  26.246  1.00 30.56           N
ATOM    312  CA  THR A 347      32.096  -6.907  24.818  1.00 31.21           C
ATOM    313  C   THR A 347      31.051  -7.798  24.147  1.00 32.27           C
ATOM    314  O   THR A 347      30.538  -7.475  23.071  1.00 31.08           O
ATOM    315  CB  THR A 347      33.477  -7.512  24.555  1.00 30.45           C
ATOM    316  OG1 THR A 347      34.492  -6.594  24.983  1.00 35.51           O
ATOM    317  CG2 THR A 347      33.654  -7.797  23.078  1.00 34.59           C
ATOM    318  N   ASN A 348      30.750  -8.925  24.784  1.00 29.22           N
ATOM    319  CA  ASN A 348      29.776  -9.867  24.247  1.00 32.50           C
ATOM    320  C   ASN A 348      28.379  -9.252  24.258  1.00 28.57           C
ATOM    321  O   ASN A 348      27.585  -9.473  23.341  1.00 32.70           O
ATOM    322  CB  ASN A 348      29.779 -11.164  25.065  1.00 30.89           C
ATOM    323  CG  ASN A 348      28.643 -12.106  24.668  1.00 38.98           C
ATOM    324  OD1 ASN A 348      27.538 -12.026  25.205  1.00 41.49           O
ATOM    325  ND2 ASN A 348      28.913 -12.992  23.718  1.00 41.38           N
ATOM    326  N   LEU A 349      28.085  -8.479  25.300  1.00 28.41           N
ATOM    327  CA  LEU A 349      26.788  -7.826  25.418  1.00 28.17           C
ATOM    328  C   LEU A 349      26.650  -6.770  24.321  1.00 27.96           C
ATOM    329  O   LEU A 349      25.631  -6.709  23.628  1.00 24.77           O
ATOM    330  CB  LEU A 349      26.646  -7.170  26.794  1.00 26.08           C
ATOM    331  CG  LEU A 349      25.370  -6.349  27.035  1.00 33.54           C
ATOM    332  CD1 LEU A 349      24.137  -7.234  26.865  1.00 28.27           C
ATOM    333  CD2 LEU A 349      25.397  -5.753  28.438  1.00 32.73           C
ATOM    334  N   ALA A 350      27.686  -5.947  24.165  1.00 28.31           N
ATOM    335  CA  ALA A 350      27.683  -4.891  23.157  1.00 28.60           C
ATOM    336  C   ALA A 350      27.474  -5.472  21.760  1.00 29.14           C
ATOM    337  O   ALA A 350      26.641  -4.980  20.999  1.00 31.22           O
ATOM    338  CB  ALA A 350      28.995  -4.109  23.211  1.00 27.91           C
ATOM    339  N   ASP A 351      28.226  -6.515  21.427  1.00 27.38           N
ATOM    340  CA  ASP A 351      28.105  -7.157  20.124  1.00 29.86           C
ATOM    341  C   ASP A 351      26.671  -7.610  19.820  1.00 30.68           C
ATOM    342  O   ASP A 351      26.205  -7.466  18.693  1.00 28.04           O
ATOM    343  CB  ASP A 351      29.050  -8.360  20.034  1.00 34.42           C
ATOM    344  CG  ASP A 351      30.511  -7.952  19.969  1.00 38.17           C
ATOM    345  OD1 ASP A 351      30.794  -6.749  19.772  1.00 35.42           O
ATOM    346  OD2 ASP A 351      31.375  -8.840  20.116  1.00 38.36           O
ATOM    347  N   ARG A 352      25.975  -8.158  20.816  1.00 27.25           N
ATOM    348  CA  ARG A 352      24.600  -8.607  20.606  1.00 26.35           C
ATOM    349  C   ARG A 352      23.651  -7.416  20.502  1.00 27.34           C
ATOM    350  O   ARG A 352      22.710  -7.433  19.708  1.00 26.83           O
ATOM    351  CB  ARG A 352      24.153  -9.539  21.750  1.00 26.87           C
ATOM    352  CG  ARG A 352      24.559 -10.997  21.527  1.00 31.69           C
ATOM    353  CD  ARG A 352      24.122 -11.913  22.668  1.00 30.11           C
ATOM    354  NE  ARG A 352      24.907 -11.684  23.874  1.00 30.28           N
ATOM    355  CZ  ARG A 352      24.385 -11.372  25.055  1.00 32.45           C
ATOM    356  NH1 ARG A 352      23.072 -11.251  25.186  1.00 31.20           N
ATOM    357  NH2 ARG A 352      25.174 -11.164  26.101  1.00 32.69           N
ATOM    358  N   GLU A 353      23.907  -6.371  21.286  1.00 24.42           N
ATOM    359  CA  GLU A 353      23.055  -5.177  21.259  1.00 26.41           C
ATOM    360  C   GLU A 353      23.135  -4.456  19.919  1.00 23.96           C
ATOM    361  O   GLU A 353      22.171  -3.828  19.468  1.00 28.39           O
ATOM    362  CB  GLU A 353      23.474  -4.202  22.359  1.00 25.00           C
ATOM    363  CG  GLU A 353      23.150  -4.660  23.767  1.00 28.26           C
ATOM    364  CD  GLU A 353      23.420  -3.576  24.792  1.00 31.14           C
ATOM    365  OE1 GLU A 353      22.500  -2.776  25.072  1.00 30.57           O
ATOM    366  OE2 GLU A 353      24.553  -3.524  25.312  1.00 29.90           O
ATOM    367  N   LEU A 354      24.298  -4.540  19.291  1.00 26.66           N
ATOM    368  CA  LEU A 354      24.522  -3.873  18.017  1.00 26.81           C
ATOM    369  C   LEU A 354      23.558  -4.300  16.927  1.00 27.94           C
ATOM    370  O   LEU A 354      23.075  -3.475  16.153  1.00 24.16           O
ATOM    371  CB  LEU A 354      25.952  -4.120  17.543  1.00 26.59           C
ATOM    372  CG  LEU A 354      26.372  -3.257  16.352  1.00 30.23           C
ATOM    373  CD1 LEU A 354      26.242  -1.775  16.720  1.00 27.37           C
ATOM    374  CD2 LEU A 354      27.794  -3.606  15.963  1.00 29.39           C
ATOM    375  N   VAL A 355      23.290  -5.598  16.854  1.00 29.04           N
ATOM    376  CA  VAL A 355      22.386  -6.125  15.844  1.00 29.60           C
ATOM    377  C   VAL A 355      21.020  -5.499  16.034  1.00 27.33           C
ATOM    378  O   VAL A 355      20.381  -5.041  15.080  1.00 30.07           O
ATOM    379  CB  VAL A 355      22.259  -7.654  15.976  1.00 32.23           C
ATOM    380  CG1 VAL A 355      21.421  -8.206  14.835  1.00 33.88           C
ATOM    381  CG2 VAL A 355      23.649  -8.282  15.999  1.00 31.06           C
ATOM    382  N   HIS A 356      20.581  -5.473  17.288  1.00 27.41           N
ATOM    383  CA  HIS A 356      19.292  -4.907  17.626  1.00 27.75           C
ATOM    384  C   HIS A 356      19.300  -3.399  17.410  1.00 28.10           C
ATOM    385  O   HIS A 356      18.273  -2.813  17.097  1.00 28.67           O
ATOM    386  CB  HIS A 356      18.937  -5.232  19.079  1.00 30.67           C
ATOM    387  CG  HIS A 356      18.603  -6.675  19.307  1.00 35.49           C
ATOM    388  ND1 HIS A 356      17.364  -7.208  19.018  1.00 36.11           N
ATOM    389  CD2 HIS A 356      19.352  -7.701  19.780  1.00 33.24           C
ATOM    390  CE1 HIS A 356      17.365  -8.499  19.303  1.00 32.90           C
ATOM    391  NE2 HIS A 356      18.559  -8.823  19.767  1.00 31.57           N
ATOM    392  N   MET A 357      20.457  -2.765  17.573  1.00 25.15           N
ATOM    393  CA  MET A 357      20.525  -1.323  17.368  1.00 24.40           C
ATOM    394  C   MET A 357      20.255  -1.012  15.899  1.00 24.69           C
ATOM    395  O   MET A 357      19.619  -0.004  15.570  1.00 26.27           O
ATOM    396  CB  MET A 357      21.902  -0.789  17.767  1.00 23.28           C
ATOM    397  CG  MET A 357      22.013   0.735  17.703  1.00 24.04           C
ATOM    398  SD  MET A 357      23.734   1.287  17.863  1.00 26.74           S
ATOM    399  CE  MET A 357      24.138   0.672  19.515  1.00 23.67           C
ATOM    400  N   ILE A 358      20.756  -1.874  15.020  1.00 26.19           N
ATOM    401  CA  ILE A 358      20.552  -1.720  13.579  1.00 30.21           C
ATOM    402  C   ILE A 358      19.055  -1.721  13.309  1.00 32.18           C
ATOM    403  O   ILE A 358      18.519  -0.816  12.662  1.00 31.73           O
ATOM    404  CB  ILE A 358      21.204  -2.888  12.790  1.00 33.89           C
ATOM    405  CG1 ILE A 358      22.728  -2.799  12.875  1.00 36.80           C
ATOM    406  CG2 ILE A 358      20.758  -2.860  11.334  1.00 34.09           C
ATOM    407  CD1 ILE A 358      23.300  -1.468  12.450  1.00 38.71           C
ATOM    408  N   ASN A 359      18.381  -2.751  13.809  1.00 33.12           N
ATOM    409  CA  ASN A 359      16.937  -2.870  13.645  1.00 33.07           C
ATOM    410  C   ASN A 359      16.231  -1.634  14.141  1.00 32.46           C
ATOM    411  O   ASN A 359      15.263  -1.163  13.530  1.00 31.28           O
ATOM    412  CB  ASN A 359      16.428  -4.104  14.379  1.00 37.41           C
ATOM    413  CG  ASN A 359      16.737  -5.367  13.628  1.00 43.64           C
ATOM    414  OD1 ASN A 359      17.049  -5.325  12.431  1.00 43.63           O
ATOM    415  ND2 ASN A 359      16.677  -6.502  14.312  1.00 44.31           N
ATOM    416  N   TRP A 360      16.707  -1.106  15.263  1.00 27.76           N
ATOM    417  CA  TRP A 360      16.102   0.086  15.842  1.00 29.27           C
ATOM    418  C   TRP A 360      16.311   1.296  14.925  1.00 27.41           C
ATOM    419  O   TRP A 360      15.359   2.002  14.581  1.00 28.83           O
ATOM    420  CB  TRP A 360      16.704   0.347  17.228  1.00 27.48           C
ATOM    421  CG  TRP A 360      16.523   1.748  17.707  1.00 30.32           C
ATOM    422  CD1 TRP A 360      15.399   2.285  18.263  1.00 27.22           C
ATOM    423  CD2 TRP A 360      17.495   2.803  17.657  1.00 27.27           C
ATOM    424  NE1 TRP A 360      15.609   3.612  18.564  1.00 30.60           N
ATOM    425  CE2 TRP A 360      16.886   3.953  18.204  1.00 29.05           C
ATOM    426  CE3 TRP A 360      18.819   2.883  17.207  1.00 27.73           C
ATOM    427  CZ2 TRP A 360      17.559   5.179  18.309  1.00 27.53           C
ATOM    428  CZ3 TRP A 360      19.488   4.106  17.312  1.00 24.31           C
ATOM    429  CH2 TRP A 360      18.853   5.232  17.860  1.00 25.22           C
ATOM    430  N   ALA A 361      17.559   1.520  14.523  1.00 28.02           N
ATOM    431  CA  ALA A 361      17.894   2.637  13.646  1.00 28.73           C
ATOM    432  C   ALA A 361      17.006   2.684  12.403  1.00 31.15           C
ATOM    433  O   ALA A 361      16.531   3.746  12.011  1.00 30.83           O
ATOM    434  CB  ALA A 361      19.345   2.539  13.220  1.00 28.75           C
ATOM    435  N   LYS A 362      16.795   1.526  11.784  1.00 31.09           N
ATOM    436  CA  LYS A 362      15.981   1.443  10.581  1.00 34.13           C
ATOM    437  C   LYS A 362      14.545   1.872  10.814  1.00 35.78           C
ATOM    438  O   LYS A 362      13.821   2.168   9.859  1.00 37.73           O
ATOM    439  CB  LYS A 362      16.012   0.016  10.023  1.00 33.81           C
ATOM    440  CG  LYS A 362      17.252  -0.280   9.198  1.00 39.52           C
ATOM    441  CD  LYS A 362      17.547  -1.773   9.135  1.00 43.74           C
ATOM    442  CE  LYS A 362      18.851  -2.045   8.389  1.00 47.20           C
ATOM    443  NZ  LYS A 362      19.177  -3.506   8.288  1.00 50.74           N
ATOM    444  N   ARG A 363      14.133   1.921  12.078  1.00 34.25           N
ATOM    445  CA  ARG A 363      12.769   2.313  12.409  1.00 35.90           C
ATOM    446  C   ARG A 363      12.654   3.742  12.943  1.00 37.56           C
ATOM    447  O   ARG A 363      11.567   4.198  13.303  1.00 38.56           O
ATOM    448  CB  ARG A 363      12.177   1.306  13.390  1.00 36.72           C
ATOM    449  CG  ARG A 363      12.168  -0.111  12.826  1.00 40.31           C
ATOM    450  CD  ARG A 363      11.469  -1.087  13.748  1.00 42.11           C
ATOM    451  NE  ARG A 363      10.160  -0.588  14.157  1.00 45.53           N
ATOM    452  CZ  ARG A 363       9.315  -1.261  14.931  1.00 49.83           C
ATOM    453  NH1 ARG A 363       9.642  -2.467  15.374  1.00 48.73           N
ATOM    454  NH2 ARG A 363       8.143  -0.729  15.261  1.00 52.28           N
ATOM    455  N   VAL A 364      13.785   4.442  13.003  1.00 35.66           N
ATOM    456  CA  VAL A 364      13.803   5.835  13.432  1.00 34.26           C
ATOM    457  C   VAL A 364      13.360   6.590  12.171  1.00 33.08           C
ATOM    458  O   VAL A 364      14.030   6.531  11.147  1.00 32.75           O
ATOM    459  CB  VAL A 364      15.230   6.272  13.827  1.00 33.90           C
ATOM    460  CG1 VAL A 364      15.292   7.779  13.995  1.00 31.21           C
ATOM    461  CG2 VAL A 364      15.643   5.571  15.112  1.00 31.12           C
ATOM    462  N   PRO A 365      12.225   7.309  12.234  1.00 34.88           N
ATOM    463  CA  PRO A 365      11.724   8.049  11.069  1.00 36.29           C
ATOM    464  C   PRO A 365      12.756   8.878  10.321  1.00 37.63           C
ATOM    465  O   PRO A 365      13.428   9.726  10.906  1.00 40.79           O
ATOM    466  CB  PRO A 365      10.608   8.917  11.645  1.00 37.35           C
ATOM    467  CG  PRO A 365      10.136   8.157  12.842  1.00 40.17           C
ATOM    468  CD  PRO A 365      11.358   7.490  13.412  1.00 34.02           C
ATOM    469  N   GLY A 366      12.878   8.624   9.023  1.00 35.14           N
ATOM    470  CA  GLY A 366      13.816   9.371   8.212  1.00 34.09           C
ATOM    471  C   GLY A 366      15.168   8.722   8.007  1.00 35.28           C
ATOM    472  O   GLY A 366      15.858   9.036   7.035  1.00 37.90           O
ATOM    473  N   PHE A 367      15.554   7.814   8.901  1.00 33.88           N
ATOM    474  CA  PHE A 367      16.860   7.164   8.787  1.00 32.68           C
ATOM    475  C   PHE A 367      17.032   6.333   7.525  1.00 32.03           C
ATOM    476  O   PHE A 367      18.073   6.403   6.883  1.00 32.31           O
ATOM    477  CB  PHE A 367      17.138   6.292  10.016  1.00 30.70           C
ATOM    478  CG  PHE A 367      18.545   5.773  10.080  1.00 30.66           C
ATOM    479  CD1 PHE A 367      19.589   6.601  10.485  1.00 29.31           C
ATOM    480  CD2 PHE A 367      18.828   4.447   9.751  1.00 32.59           C
ATOM    481  CE1 PHE A 367      20.896   6.121  10.568  1.00 27.92           C
ATOM    482  CE2 PHE A 367      20.133   3.951   9.828  1.00 28.73           C
ATOM    483  CZ  PHE A 367      21.171   4.791  10.240  1.00 25.63           C
ATOM    484  N   VAL A 368      16.026   5.541   7.166  1.00 35.55           N
ATOM    485  CA  VAL A 368      16.123   4.718   5.960  1.00 39.35           C
ATOM    486  C   VAL A 368      15.966   5.524   4.674  1.00 40.45           C
ATOM    487  O   VAL A 368      16.157   4.992   3.580  1.00 42.42           O
ATOM    488  CB  VAL A 368      15.077   3.584   5.945  1.00 40.93           C
ATOM    489  CG1 VAL A 368      15.543   2.448   6.843  1.00 41.96           C
ATOM    490  CG2 VAL A 368      13.717   4.114   6.390  1.00 41.64           C
ATOM    491  N   ASP A 369      15.606   6.798   4.798  1.00 38.83           N
ATOM    492  CA  ASP A 369      15.464   7.646   3.621  1.00 37.70           C
ATOM    493  C   ASP A 369      16.855   8.010   3.136  1.00 35.79           C
ATOM    494  O   ASP A 369      17.037   8.431   1.995  1.00 35.32           O
ATOM    495  CB  ASP A 369      14.700   8.929   3.953  1.00 39.93           C
ATOM    496  CG  ASP A 369      13.253   8.672   4.302  1.00 46.04           C
ATOM    497  OD1 ASP A 369      12.686   7.672   3.807  1.00 46.14           O
ATOM    498  OD2 ASP A 369      12.681   9.472   5.075  1.00 49.54           O
ATOM    499  N   LEU A 370      17.839   7.840   4.015  1.00 32.51           N
ATOM    500  CA  LEU A 370      19.230   8.152   3.704  1.00 28.18           C
ATOM    501  C   LEU A 370      19.884   7.042   2.893  1.00 31.17           C
ATOM    502  O   LEU A 370      19.342   5.943   2.784  1.00 31.55           O
ATOM    503  CB  LEU A 370      20.021   8.339   5.003  1.00 28.86           C
ATOM    504  CG  LEU A 370      19.523   9.395   5.999  1.00 28.79           C
ATOM    505  CD1 LEU A 370      20.317   9.274   7.298  1.00 30.61           C
ATOM    506  CD2 LEU A 370      19.692  10.791   5.405  1.00 29.75           C
ATOM    507  N   THR A 371      21.053   7.333   2.331  1.00 28.71           N
ATOM    508  CA  THR A 371      21.793   6.336   1.569  1.00 32.78           C
ATOM    509  C   THR A 371      22.373   5.315   2.540  1.00 35.35           C
ATOM    510  O   THR A 371      22.535   5.591   3.735  1.00 31.03           O
ATOM    511  CB  THR A 371      22.979   6.945   0.817  1.00 33.56           C
ATOM    512  OG1 THR A 371      23.880   7.525   1.765  1.00 34.32           O
ATOM    513  CG2 THR A 371      22.514   8.003  -0.177  1.00 32.26           C
ATOM    514  N   LEU A 372      22.702   4.141   2.015  1.00 34.53           N
ATOM    515  CA  LEU A 372      23.274   3.073   2.822  1.00 35.63           C
ATOM    516  C   LEU A 372      24.587   3.547   3.444  1.00 37.02           C
ATOM    517  O   LEU A 372      24.813   3.374   4.643  1.00 35.12           O
ATOM    518  CB  LEU A 372      23.519   1.841   1.943  1.00 38.17           C
ATOM    519  CG  LEU A 372      24.363   0.705   2.515  1.00 43.11           C
ATOM    520  CD1 LEU A 372      23.689   0.146   3.758  1.00 46.30           C
ATOM    521  CD2 LEU A 372      24.535  -0.384   1.456  1.00 45.27           C
ATOM    522  N   HIS A 373      25.442   4.159   2.627  1.00 35.74           N
ATOM    523  CA  HIS A 373      26.729   4.656   3.099  1.00 36.63           C
ATOM    524  C   HIS A 373      26.575   5.669   4.243  1.00 36.33           C
ATOM    525  O   HIS A 373      27.350   5.649   5.200  1.00 32.95           O
ATOM    526  CB  HIS A 373      27.506   5.282   1.935  1.00 43.90           C
ATOM    527  CG  HIS A 373      28.538   6.280   2.360  1.00 50.58           C
ATOM    528  ND1 HIS A 373      28.245   7.612   2.561  1.00 53.54           N
ATOM    529  CD2 HIS A 373      29.857   6.138   2.637  1.00 54.12           C
ATOM    530  CE1 HIS A 373      29.339   8.248   2.944  1.00 56.79           C
ATOM    531  NE2 HIS A 373      30.331   7.377   2.998  1.00 56.68           N
ATOM    532  N   ASP A 374      25.579   6.548   4.147  1.00 31.98           N
ATOM    533  CA  ASP A 374      25.341   7.541   5.195  1.00 30.61           C
ATOM    534  C   ASP A 374      24.805   6.876   6.472  1.00 30.35           C
ATOM    535  O   ASP A 374      25.151   7.275   7.586  1.00 26.86           O
ATOM    536  CB  ASP A 374      24.354   8.603   4.712  1.00 29.83           C
ATOM    537  CG  ASP A 374      25.018   9.672   3.859  1.00 35.85           C
ATOM    538  OD1 ASP A 374      26.265   9.744   3.842  1.00 34.37           O
ATOM    539  OD2 ASP A 374      24.293  10.440   3.197  1.00 35.21           O
ATOM    540  N   GLN A 375      23.944   5.876   6.309  1.00 25.64           N
ATOM    541  CA  GLN A 375      23.403   5.156   7.453  1.00 26.64           C
ATOM    542  C   GLN A 375      24.556   4.501   8.214  1.00 25.39           C
ATOM    543  O   GLN A 375      24.586   4.513   9.442  1.00 28.40           O
ATOM    544  CB  GLN A 375      22.425   4.077   6.990  1.00 30.05           C
ATOM    545  CG  GLN A 375      21.101   4.615   6.485  1.00 29.52           C
ATOM    546  CD  GLN A 375      20.219   3.514   5.940  1.00 35.96           C
ATOM    547  OE1 GLN A 375      20.155   2.425   6.510  1.00 31.40           O
ATOM    548  NE2 GLN A 375      19.542   3.785   4.826  1.00 34.71           N
ATOM    549  N   VAL A 376      25.504   3.937   7.475  1.00 26.81           N
ATOM    550  CA  VAL A 376      26.660   3.281   8.071  1.00 29.45           C
ATOM    551  C   VAL A 376      27.527   4.285   8.821  1.00 31.00           C
ATOM    552  O   VAL A 376      27.953   4.028   9.948  1.00 29.87           O
ATOM    553  CB  VAL A 376      27.531   2.597   7.002  1.00 29.63           C
ATOM    554  CG1 VAL A 376      28.812   2.072   7.634  1.00 28.79           C
ATOM    555  CG2 VAL A 376      26.746   1.470   6.341  1.00 30.60           C
ATOM    556  N   HIS A 377      27.785   5.427   8.191  1.00 28.16           N
ATOM    557  CA  HIS A 377      28.602   6.457   8.813  1.00 28.74           C
ATOM    558  C   HIS A 377      27.983   6.954  10.114  1.00 25.27           C
ATOM    559  O   HIS A 377      28.676   7.101  11.117  1.00 25.93           O
ATOM    560  CB  HIS A 377      28.791   7.639   7.864  1.00 30.17           C
ATOM    561  CG  HIS A 377      29.508   8.791   8.488  1.00 33.85           C
ATOM    562  ND1 HIS A 377      30.844   8.739   8.823  1.00 37.73           N
ATOM    563  CD2 HIS A 377      29.072  10.017   8.864  1.00 35.24           C
ATOM    564  CE1 HIS A 377      31.200   9.884   9.378  1.00 35.49           C
ATOM    565  NE2 HIS A 377      30.144  10.676   9.413  1.00 35.00           N
ATOM    566  N   LEU A 378      26.678   7.206  10.106  1.00 24.52           N
ATOM    567  CA  LEU A 378      26.015   7.695  11.314  1.00 26.23           C
ATOM    568  C   LEU A 378      26.120   6.696  12.458  1.00 28.68           C
ATOM    569  O   LEU A 378      26.379   7.078  13.603  1.00 25.01           O
ATOM    570  CB  LEU A 378      24.543   8.001  11.026  1.00 26.16           C
ATOM    571  CG  LEU A 378      24.291   9.182  10.073  1.00 28.17           C
ATOM    572  CD1 LEU A 378      22.778   9.353   9.871  1.00 27.12           C
ATOM    573  CD2 LEU A 378      24.910  10.460  10.641  1.00 30.11           C
ATOM    574  N   LEU A 379      25.919   5.415  12.154  1.00 24.05           N
ATOM    575  CA  LEU A 379      26.000   4.389  13.183  1.00 27.15           C
ATOM    576  C   LEU A 379      27.430   4.177  13.672  1.00 27.01           C
ATOM    577  O   LEU A 379      27.655   3.981  14.868  1.00 25.57           O
ATOM    578  CB  LEU A 379      25.401   3.073  12.667  1.00 28.66           C
ATOM    579  CG  LEU A 379      23.875   3.024  12.845  1.00 31.43           C
ATOM    580  CD1 LEU A 379      23.248   1.944  11.963  1.00 33.24           C
ATOM    581  CD2 LEU A 379      23.565   2.760  14.311  1.00 29.58           C
ATOM    582  N   GLU A 380      28.401   4.236  12.763  1.00 25.93           N
ATOM    583  CA  GLU A 380      29.784   4.053  13.173  1.00 27.41           C
ATOM    584  C   GLU A 380      30.216   5.159  14.133  1.00 27.28           C
ATOM    585  O   GLU A 380      31.057   4.937  15.009  1.00 26.39           O
ATOM    586  CB  GLU A 380      30.730   4.034  11.969  1.00 30.40           C
ATOM    587  CG  GLU A 380      32.172   3.785  12.381  1.00 38.14           C
ATOM    588  CD  GLU A 380      33.079   3.471  11.210  1.00 45.72           C
ATOM    589  OE1 GLU A 380      32.868   4.047  10.120  1.00 42.83           O
ATOM    590  OE2 GLU A 380      34.005   2.648  11.387  1.00 46.08           O
ATOM    591  N  ACYS A 381      29.636   6.339  13.965  0.75 24.59           N
ATOM    592  CA ACYS A 381      29.968   7.466  14.825  0.75 23.86           C
ATOM    593  C  ACYS A 381      29.236   7.423  16.161  0.75 22.04           C
ATOM    594  O  ACYS A 381      29.812   7.731  17.205  0.75 21.56           O
ATOM    595  CB ACYS A 381      29.621   8.782  14.122  0.75 25.78           C
ATOM    596  SG ACYS A 381      30.696   9.195  12.733  0.75 31.22           S
ATOM    597  N   ALA A 382      27.973   7.015  16.127  1.00 23.72           N
ATOM    598  CA  ALA A 382      27.140   7.016  17.318  1.00 23.55           C
ATOM    599  C   ALA A 382      26.913   5.756  18.131  1.00 25.70           C
ATOM    600  O   ALA A 382      26.376   5.838  19.236  1.00 23.47           O
ATOM    601  CB  ALA A 382      25.785   7.586  16.950  1.00 25.98           C
ATOM    602  N   TRP A 383      27.311   4.603  17.616  1.00 26.12           N
ATOM    603  CA  TRP A 383      27.025   3.354  18.317  1.00 23.70           C
ATOM    604  C   TRP A 383      27.355   3.308  19.801  1.00 23.67           C
ATOM    605  O   TRP A 383      26.523   2.868  20.584  1.00 23.24           O
ATOM    606  CB  TRP A 383      27.669   2.173  17.578  1.00 22.32           C
ATOM    607  CG  TRP A 383      29.130   2.055  17.763  1.00 24.23           C
ATOM    608  CD1 TRP A 383      30.103   2.581  16.966  1.00 24.36           C
ATOM    609  CD2 TRP A 383      29.798   1.348  18.804  1.00 27.10           C
ATOM    610  NE1 TRP A 383      31.341   2.240  17.448  1.00 27.24           N
ATOM    611  CE2 TRP A 383      31.182   1.484  18.579  1.00 28.12           C
ATOM    612  CE3 TRP A 383      29.359   0.609  19.912  1.00 26.67           C
ATOM    613  CZ2 TRP A 383      32.133   0.908  19.419  1.00 28.64           C
ATOM    614  CZ3 TRP A 383      30.306   0.037  20.745  1.00 27.96           C
ATOM    615  CH2 TRP A 383      31.676   0.190  20.496  1.00 29.40           C
ATOM    616  N   LEU A 384      28.542   3.762  20.210  1.00 20.14           N
ATOM    617  CA  LEU A 384      28.864   3.711  21.638  1.00 22.53           C
ATOM    618  C   LEU A 384      28.074   4.731  22.452  1.00 19.31           C
ATOM    619  O   LEU A 384      27.706   4.460  23.594  1.00 23.35           O
ATOM    620  CB  LEU A 384      30.367   3.891  21.883  1.00 25.31           C
ATOM    621  CG  LEU A 384      30.823   3.645  23.335  1.00 27.52           C
ATOM    622  CD1 LEU A 384      30.272   2.305  23.853  1.00 29.59           C
ATOM    623  CD2 LEU A 384      32.336   3.645  23.397  1.00 26.28           C
ATOM    624  N   GLU A 385      27.807   5.909  21.885  1.00 20.65           N
ATOM    625  CA  GLU A 385      27.010   6.895  22.613  1.00 21.42           C
ATOM    626  C   GLU A 385      25.618   6.290  22.835  1.00 22.56           C
ATOM    627  O   GLU A 385      25.024   6.436  23.902  1.00 22.21           O
ATOM    628  CB  GLU A 385      26.860   8.180  21.802  1.00 21.86           C
ATOM    629  CG  GLU A 385      28.115   9.020  21.704  1.00 21.89           C
ATOM    630  CD  GLU A 385      27.882  10.255  20.858  1.00 29.10           C
ATOM    631  OE1 GLU A 385      27.375  11.255  21.399  1.00 31.02           O
ATOM    632  OE2 GLU A 385      28.188  10.219  19.655  1.00 30.17           O
ATOM    633  N   ILE A 386      25.101   5.618  21.810  1.00 22.15           N
ATOM    634  CA  ILE A 386      23.779   4.998  21.896  1.00 22.60           C
ATOM    635  C   ILE A 386      23.767   3.899  22.961  1.00 22.42           C
ATOM    636  O   ILE A 386      22.823   3.819  23.744  1.00 24.54           O
ATOM    637  CB  ILE A 386      23.328   4.456  20.500  1.00 23.18           C
ATOM    638  CG1 ILE A 386      23.088   5.651  19.562  1.00 24.99           C
ATOM    639  CG2 ILE A 386      22.010   3.645  20.620  1.00 24.17           C
ATOM    640  CD1 ILE A 386      22.989   5.293  18.076  1.00 26.40           C
ATOM    641  N   LEU A 387      24.812   3.072  23.021  1.00 22.41           N
ATOM    642  CA  LEU A 387      24.867   2.031  24.052  1.00 22.69           C
ATOM    643  C   LEU A 387      24.944   2.660  25.438  1.00 26.34           C
ATOM    644  O   LEU A 387      24.287   2.206  26.385  1.00 23.64           O
ATOM    645  CB  LEU A 387      26.093   1.130  23.864  1.00 24.48           C
ATOM    646  CG  LEU A 387      26.068   0.193  22.655  1.00 23.54           C
ATOM    647  CD1 LEU A 387      27.298  -0.709  22.707  1.00 26.24           C
ATOM    648  CD2 LEU A 387      24.792  -0.629  22.652  1.00 26.48           C
ATOM    649  N   MET A 388      25.750   3.714  25.555  1.00 23.89           N
ATOM    650  CA  MET A 388      25.923   4.387  26.834  1.00 24.06           C
ATOM    651  C   MET A 388      24.662   5.095  27.320  1.00 23.24           C
ATOM    652  O   MET A 388      24.340   5.024  28.504  1.00 25.46           O
ATOM    653  CB  MET A 388      27.088   5.379  26.760  1.00 23.83           C
ATOM    654  CG  MET A 388      28.439   4.718  26.748  1.00 23.85           C
ATOM    655  SD  MET A 388      29.731   5.988  26.735  1.00 26.91           S
ATOM    656  CE  MET A 388      31.134   5.045  27.078  1.00 21.70           C
ATOM    657  N   ILE A 389      23.937   5.777  26.436  1.00 24.00           N
ATOM    658  CA  ILE A 389      22.730   6.439  26.906  1.00 23.65           C
ATOM    659  C   ILE A 389      21.695   5.400  27.350  1.00 26.20           C
ATOM    660  O   ILE A 389      20.935   5.631  28.295  1.00 22.41           O
ATOM    661  CB  ILE A 389      22.131   7.439  25.851  1.00 26.69           C
ATOM    662  CG1 ILE A 389      21.187   8.405  26.583  1.00 24.89           C
ATOM    663  CG2 ILE A 389      21.411   6.704  24.707  1.00 23.85           C
ATOM    664  CD1 ILE A 389      20.431   9.379  25.683  1.00 24.87           C
ATOM    665  N   GLY A 390      21.682   4.245  26.690  1.00 26.99           N
ATOM    666  CA  GLY A 390      20.751   3.204  27.091  1.00 28.82           C
ATOM    667  C   GLY A 390      21.133   2.720  28.480  1.00 29.90           C
ATOM    668  O   GLY A 390      20.276   2.521  29.344  1.00 29.14           O
ATOM    669  N   LEU A 391      22.433   2.549  28.699  1.00 26.34           N
ATOM    670  CA  LEU A 391      22.956   2.091  29.984  1.00 29.31           C
ATOM    671  C   LEU A 391      22.605   3.070  31.105  1.00 30.72           C
ATOM    672  O   LEU A 391      22.155   2.671  32.185  1.00 28.73           O
ATOM    673  CB  LEU A 391      24.476   1.936  29.898  1.00 28.20           C
ATOM    674  CG  LEU A 391      25.206   1.655  31.209  1.00 31.08           C
ATOM    675  CD1 LEU A 391      24.718   0.331  31.793  1.00 26.14           C
ATOM    676  CD2 LEU A 391      26.708   1.620  30.958  1.00 25.10           C
ATOM    677  N   VAL A 392      22.817   4.356  30.850  1.00 28.58           N
ATOM    678  CA  VAL A 392      22.505   5.369  31.851  1.00 28.78           C
ATOM    679  C   VAL A 392      21.012   5.327  32.166  1.00 28.19           C
ATOM    680  O   VAL A 392      20.618   5.346  33.326  1.00 30.45           O
ATOM    681  CB  VAL A 392      22.923   6.771  31.354  1.00 29.86           C
ATOM    682  CG1 VAL A 392      22.329   7.853  32.238  1.00 31.71           C
ATOM    683  CG2 VAL A 392      24.442   6.870  31.372  1.00 28.88           C
ATOM    684  N   TRP A 393      20.190   5.240  31.126  1.00 27.80           N
ATOM    685  CA  TRP A 393      18.733   5.186  31.280  1.00 29.63           C
ATOM    686  C   TRP A 393      18.256   4.052  32.190  1.00 31.82           C
ATOM    687  O   TRP A 393      17.458   4.274  33.107  1.00 31.82           O
ATOM    688  CB  TRP A 393      18.067   5.046  29.906  1.00 29.83           C
ATOM    689  CG  TRP A 393      16.605   4.670  29.953  1.00 33.00           C
ATOM    690  CD1 TRP A 393      16.056   3.459  29.618  1.00 33.81           C
ATOM    691  CD2 TRP A 393      15.515   5.499  30.370  1.00 31.01           C
ATOM    692  NE1 TRP A 393      14.696   3.486  29.802  1.00 33.77           N
ATOM    693  CE2 TRP A 393      14.335   4.725  30.264  1.00 37.77           C
ATOM    694  CE3 TRP A 393      15.418   6.821  30.826  1.00 32.45           C
ATOM    695  CZ2 TRP A 393      13.072   5.232  30.597  1.00 37.46           C
ATOM    696  CZ3 TRP A 393      14.162   7.326  31.156  1.00 35.52           C
ATOM    697  CH2 TRP A 393      13.006   6.531  31.040  1.00 37.71           C
ATOM    698  N   ARG A 394      18.737   2.838  31.957  1.00 31.79           N
ATOM    699  CA  ARG A 394      18.287   1.729  32.786  1.00 36.71           C
ATOM    700  C   ARG A 394      18.911   1.698  34.180  1.00 36.66           C
ATOM    701  O   ARG A 394      18.446   0.966  35.049  1.00 37.10           O
ATOM    702  CB  ARG A 394      18.493   0.390  32.065  1.00 36.56           C
ATOM    703  CG  ARG A 394      19.914   0.010  31.764  1.00 36.81           C
ATOM    704  CD  ARG A 394      19.929  -1.131  30.747  1.00 36.79           C
ATOM    705  NE  ARG A 394      21.282  -1.559  30.417  1.00 34.16           N
ATOM    706  CZ  ARG A 394      21.864  -1.351  29.238  1.00 31.63           C
ATOM    707  NH1 ARG A 394      21.207  -0.716  28.280  1.00 31.81           N
ATOM    708  NH2 ARG A 394      23.098  -1.782  29.021  1.00 30.50           N
ATOM    709  N   SER A 395      19.954   2.493  34.395  1.00 33.07           N
ATOM    710  CA  SER A 395      20.603   2.564  35.701  1.00 35.21           C
ATOM    711  C   SER A 395      20.010   3.712  36.532  1.00 35.89           C
ATOM    712  O   SER A 395      20.390   3.915  37.687  1.00 38.54           O
ATOM    713  CB  SER A 395      22.112   2.784  35.539  1.00 32.91           C
ATOM    714  OG  SER A 395      22.696   1.811  34.688  1.00 32.01           O
ATOM    715  N   MET A 396      19.076   4.448  35.937  1.00 35.93           N
ATOM    716  CA  MET A 396      18.430   5.588  36.589  1.00 42.63           C
ATOM    717  C   MET A 396      17.906   5.304  37.992  1.00 45.50           C
ATOM    718  O   MET A 396      18.125   6.089  38.913  1.00 45.72           O
ATOM    719  CB  MET A 396      17.274   6.104  35.725  1.00 43.71           C
ATOM    720  CG  MET A 396      17.480   7.506  35.175  1.00 45.99           C
ATOM    721  SD  MET A 396      15.962   8.278  34.580  1.00 49.20           S
ATOM    722  CE  MET A 396      14.987   8.298  36.065  1.00 53.09           C
ATOM    723  N   GLU A 397      17.215   4.181  38.152  1.00 48.85           N
ATOM    724  CA  GLU A 397      16.645   3.822  39.444  1.00 51.77           C
ATOM    725  C   GLU A 397      17.548   2.934  40.283  1.00 52.81           C
ATOM    726  O   GLU A 397      17.071   2.187  41.139  1.00 54.25           O
ATOM    727  CB  GLU A 397      15.296   3.130  39.246  1.00 54.81           C
ATOM    728  CG  GLU A 397      14.165   4.073  38.874  1.00 57.72           C
ATOM    729  CD  GLU A 397      13.195   3.448  37.891  1.00 62.24           C
ATOM    730  OE1 GLU A 397      13.660   2.925  36.854  1.00 63.86           O
ATOM    731  OE2 GLU A 397      11.971   3.476  38.154  1.00 64.30           O
ATOM    732  N   HIS A 398      18.851   3.013  40.040  1.00 50.21           N
ATOM    733  CA  HIS A 398      19.813   2.220  40.792  1.00 49.35           C
ATOM    734  C   HIS A 398      20.999   3.083  41.196  1.00 47.30           C
ATOM    735  O   HIS A 398      22.122   2.887  40.730  1.00 44.60           O
ATOM    736  CB  HIS A 398      20.271   1.018  39.963  1.00 52.29           C
ATOM    737  CG  HIS A 398      19.187   0.017  39.721  1.00 54.08           C
ATOM    738  ND1 HIS A 398      18.373   0.054  38.608  1.00 56.22           N
ATOM    739  CD2 HIS A 398      18.750  -1.021  40.472  1.00 53.87           C
ATOM    740  CE1 HIS A 398      17.481  -0.917  38.685  1.00 55.41           C
ATOM    741  NE2 HIS A 398      17.689  -1.584  39.806  1.00 55.44           N
ATOM    742  N   PRO A 399      20.755   4.050  42.095  1.00 46.26           N
ATOM    743  CA  PRO A 399      21.785   4.968  42.586  1.00 45.23           C
ATOM    744  C   PRO A 399      23.087   4.270  42.957  1.00 44.55           C
ATOM    745  O   PRO A 399      23.079   3.233  43.626  1.00 46.42           O
ATOM    746  CB  PRO A 399      21.127   5.631  43.793  1.00 47.20           C
ATOM    747  CG  PRO A 399      19.660   5.560  43.504  1.00 47.65           C
ATOM    748  CD  PRO A 399      19.443   4.300  42.721  1.00 47.09           C
ATOM    749  N   GLY A 400      24.201   4.841  42.509  1.00 41.58           N
ATOM    750  CA  GLY A 400      25.507   4.282  42.812  1.00 39.71           C
ATOM    751  C   GLY A 400      25.907   3.047  42.022  1.00 37.71           C
ATOM    752  O   GLY A 400      27.027   2.561  42.175  1.00 40.43           O
ATOM    753  N   LYS A 401      25.012   2.537  41.180  1.00 36.36           N
ATOM    754  CA  LYS A 401      25.316   1.343  40.391  1.00 34.39           C
ATOM    755  C   LYS A 401      24.969   1.485  38.912  1.00 32.19           C
ATOM    756  O   LYS A 401      24.140   2.307  38.532  1.00 30.82           O
ATOM    757  CB  LYS A 401      24.562   0.130  40.947  1.00 35.96           C
ATOM    758  CG  LYS A 401      24.633  -0.008  42.466  1.00 39.09           C
ATOM    759  CD  LYS A 401      24.287  -1.429  42.904  1.00 44.30           C
ATOM    760  CE  LYS A 401      24.458  -1.605  44.408  1.00 46.81           C
ATOM    761  NZ  LYS A 401      24.969  -2.969  44.747  1.00 53.99           N
ATOM    762  N   LEU A 402      25.612   0.663  38.086  1.00 28.45           N
ATOM    763  CA  LEU A 402      25.358   0.659  36.648  1.00 28.70           C
ATOM    764  C   LEU A 402      24.754  -0.685  36.293  1.00 30.03           C
ATOM    765  O   LEU A 402      25.367  -1.727  36.537  1.00 31.28           O
ATOM    766  CB  LEU A 402      26.661   0.848  35.867  1.00 29.00           C
ATOM    767  CG  LEU A 402      27.279   2.241  36.030  1.00 24.46           C
ATOM    768  CD1 LEU A 402      28.624   2.309  35.311  1.00 27.56           C
ATOM    769  CD2 LEU A 402      26.313   3.278  35.484  1.00 25.05           C
ATOM    770  N   LEU A 403      23.552  -0.658  35.735  1.00 30.84           N
ATOM    771  CA  LEU A 403      22.872  -1.880  35.336  1.00 32.94           C
ATOM    772  C   LEU A 403      23.256  -2.219  33.900  1.00 30.07           C
ATOM    773  O   LEU A 403      22.543  -1.871  32.956  1.00 31.83           O
ATOM    774  CB  LEU A 403      21.361  -1.693  35.434  1.00 33.96           C
ATOM    775  CG  LEU A 403      20.551  -2.991  35.415  1.00 39.36           C
ATOM    776  CD1 LEU A 403      20.585  -3.637  36.806  1.00 43.68           C
ATOM    777  CD2 LEU A 403      19.129  -2.688  34.998  1.00 41.44           C
ATOM    778  N   PHE A 404      24.384  -2.892  33.734  1.00 29.38           N
ATOM    779  CA  PHE A 404      24.835  -3.256  32.403  1.00 29.27           C
ATOM    780  C   PHE A 404      23.809  -4.181  31.756  1.00 31.22           C
ATOM    781  O   PHE A 404      23.625  -4.177  30.539  1.00 28.10           O
ATOM    782  CB  PHE A 404      26.201  -3.929  32.493  1.00 29.92           C
ATOM    783  CG  PHE A 404      27.305  -2.997  32.926  1.00 30.81           C
ATOM    784  CD1 PHE A 404      27.848  -2.078  32.029  1.00 32.53           C
ATOM    785  CD2 PHE A 404      27.795  -3.032  34.228  1.00 32.51           C
ATOM    786  CE1 PHE A 404      28.864  -1.204  32.423  1.00 30.23           C
ATOM    787  CE2 PHE A 404      28.815  -2.159  34.637  1.00 34.86           C
ATOM    788  CZ  PHE A 404      29.350  -1.242  33.726  1.00 31.06           C
ATOM    789  N   ALA A 405      23.138  -4.967  32.594  1.00 30.15           N
ATOM    790  CA  ALA A 405      22.104  -5.910  32.163  1.00 29.83           C
ATOM    791  C   ALA A 405      21.309  -6.237  33.429  1.00 32.09           C
ATOM    792  O   ALA A 405      21.785  -5.994  34.535  1.00 32.39           O
ATOM    793  CB  ALA A 405      22.744  -7.172  31.597  1.00 30.09           C
ATOM    794  N   PRO A 406      20.088  -6.779  33.287  1.00 34.53           N
ATOM    795  CA  PRO A 406      19.303  -7.102  34.489  1.00 36.81           C
ATOM    796  C   PRO A 406      19.996  -8.085  35.433  1.00 37.55           C
ATOM    797  O   PRO A 406      19.698  -8.113  36.626  1.00 38.76           O
ATOM    798  CB  PRO A 406      17.985  -7.654  33.933  1.00 35.49           C
ATOM    799  CG  PRO A 406      17.923  -7.152  32.518  1.00 36.43           C
ATOM    800  CD  PRO A 406      19.356  -7.101  32.052  1.00 35.40           C
ATOM    801  N   ASN A 407      20.924  -8.877  34.901  1.00 37.04           N
ATOM    802  CA  ASN A 407      21.651  -9.847  35.711  1.00 39.46           C
ATOM    803  C   ASN A 407      23.100  -9.435  35.874  1.00 38.64           C
ATOM    804  O   ASN A 407      23.964 -10.256  36.180  1.00 40.12           O
ATOM    805  CB  ASN A 407      21.581 -11.243  35.082  1.00 40.37           C
ATOM    806  CG  ASN A 407      22.232 -11.306  33.711  1.00 45.01           C
ATOM    807  OD1 ASN A 407      22.343 -10.296  33.009  1.00 38.16           O
ATOM    808  ND2 ASN A 407      22.659 -12.503  33.318  1.00 46.72           N
ATOM    809  N   LEU A 408      23.365  -8.149  35.671  1.00 38.20           N
ATOM    810  CA  LEU A 408      24.714  -7.631  35.800  1.00 36.91           C
ATOM    811  C   LEU A 408      24.670  -6.187  36.286  1.00 40.43           C
ATOM    812  O   LEU A 408      24.646  -5.248  35.490  1.00 38.16           O
ATOM    813  CB  LEU A 408      25.450  -7.720  34.460  1.00 36.14           C
ATOM    814  CG  LEU A 408      26.973  -7.609  34.550  1.00 35.02           C
ATOM    815  CD1 LEU A 408      27.525  -8.775  35.353  1.00 39.18           C
ATOM    816  CD2 LEU A 408      27.578  -7.589  33.157  1.00 37.45           C
ATOM    817  N   LEU A 409      24.644  -6.034  37.607  1.00 39.35           N
ATOM    818  CA  LEU A 409      24.606  -4.733  38.257  1.00 41.33           C
ATOM    819  C   LEU A 409      25.893  -4.566  39.060  1.00 42.00           C
ATOM    820  O   LEU A 409      26.177  -5.358  39.959  1.00 41.17           O
ATOM    821  CB  LEU A 409      23.392  -4.659  39.185  1.00 43.97           C
ATOM    822  CG  LEU A 409      23.163  -3.382  39.993  1.00 48.17           C
ATOM    823  CD1 LEU A 409      22.847  -2.233  39.058  1.00 47.51           C
ATOM    824  CD2 LEU A 409      22.014  -3.602  40.976  1.00 50.30           C
ATOM    825  N   LEU A 410      26.676  -3.544  38.727  1.00 39.21           N
ATOM    826  CA  LEU A 410      27.931  -3.295  39.423  1.00 40.72           C
ATOM    827  C   LEU A 410      27.946  -1.944  40.132  1.00 40.67           C
ATOM    828  O   LEU A 410      27.361  -0.970  39.652  1.00 40.36           O
ATOM    829  CB  LEU A 410      29.106  -3.353  38.442  1.00 41.68           C
ATOM    830  CG  LEU A 410      29.457  -4.660  37.716  1.00 45.37           C
ATOM    831  CD1 LEU A 410      30.972  -4.728  37.554  1.00 45.46           C
ATOM    832  CD2 LEU A 410      28.949  -5.872  38.484  1.00 47.47           C
ATOM    833  N   ASP A 411      28.611  -1.891  41.281  1.00 41.53           N
ATOM    834  CA  ASP A 411      28.717  -0.640  42.025  1.00 42.87           C
ATOM    835  C   ASP A 411      30.088  -0.016  41.779  1.00 43.94           C
ATOM    836  O   ASP A 411      30.934  -0.610  41.107  1.00 38.71           O
ATOM    837  CB  ASP A 411      28.490  -0.874  43.527  1.00 44.65           C
ATOM    838  CG  ASP A 411      29.655  -1.578  44.209  1.00 47.95           C
ATOM    839  OD1 ASP A 411      30.680  -1.862  43.553  1.00 49.39           O
ATOM    840  OD2 ASP A 411      29.537  -1.849  45.425  1.00 52.21           O
ATOM    841  N   ARG A 412      30.295   1.181  42.320  1.00 46.85           N
ATOM    842  CA  ARG A 412      31.555   1.904  42.171  1.00 50.13           C
ATOM    843  C   ARG A 412      32.771   1.026  42.429  1.00 50.26           C
ATOM    844  O   ARG A 412      33.626   0.865  41.560  1.00 50.96           O
ATOM    845  CB  ARG A 412      31.601   3.090  43.137  1.00 51.25           C
ATOM    846  CG  ARG A 412      30.971   4.363  42.614  1.00 55.04           C
ATOM    847  CD  ARG A 412      31.644   5.580  43.218  1.00 54.91           C
ATOM    848  NE  ARG A 412      33.071   5.615  42.913  1.00 56.32           N
ATOM    849  CZ  ARG A 412      33.826   6.708  42.984  1.00 62.05           C
ATOM    850  NH1 ARG A 412      33.290   7.866  43.356  1.00 63.21           N
ATOM    851  NH2 ARG A 412      35.120   6.646  42.681  1.00 60.49           N
ATOM    852  N   ASN A 413      32.844   0.469  43.633  1.00 52.17           N
ATOM    853  CA  ASN A 413      33.969  -0.375  44.022  1.00 53.24           C
ATOM    854  C   ASN A 413      34.235  -1.480  43.013  1.00 54.07           C
ATOM    855  O   ASN A 413      35.386  -1.743  42.660  1.00 53.64           O
ATOM    856  CB  ASN A 413      33.719  -0.980  45.403  1.00 55.67           C
ATOM    857  CG  ASN A 413      33.654   0.073  46.496  1.00 57.74           C
ATOM    858  OD1 ASN A 413      33.697   1.276  46.223  1.00 57.74           O
ATOM    859  ND2 ASN A 413      33.551  -0.375  47.742  1.00 57.50           N
ATOM    860  N   GLN A 414      33.173  -2.129  42.547  1.00 55.20           N
ATOM    861  CA  GLN A 414      33.323  -3.198  41.571  1.00 55.28           C
ATOM    862  C   GLN A 414      33.850  -2.631  40.259  1.00 55.43           C
ATOM    863  O   GLN A 414      34.654  -3.266  39.578  1.00 56.03           O
ATOM    864  CB  GLN A 414      31.986  -3.903  41.342  1.00 55.22           C
ATOM    865  CG  GLN A 414      31.653  -4.946  42.398  1.00 56.32           C
ATOM    866  CD  GLN A 414      30.203  -5.360  42.336  1.00 57.47           C
ATOM    867  OE1 GLN A 414      29.292  -4.538  42.399  1.00 58.75           O
ATOM    868  NE2 GLN A 414      29.977  -6.662  42.198  1.00 58.96           N
ATOM    869  N   GLY A 415      33.398  -1.430  39.910  1.00 57.08           N
ATOM    870  CA  GLY A 415      33.849  -0.806  38.680  1.00 58.77           C
ATOM    871  C   GLY A 415      35.350  -0.582  38.689  1.00 61.55           C
ATOM    872  O   GLY A 415      36.024  -0.748  37.671  1.00 60.27           O
ATOM    873  N   LYS A 416      35.877  -0.211  39.851  1.00 63.21           N
ATOM    874  CA  LYS A 416      37.305   0.041  40.011  1.00 65.92           C
ATOM    875  C   LYS A 416      38.159  -1.105  39.472  1.00 66.77           C
ATOM    876  O   LYS A 416      39.361  -0.946  39.269  1.00 67.12           O
ATOM    877  CB  LYS A 416      37.634   0.263  41.491  1.00 66.47           C
ATOM    878  CG  LYS A 416      38.121   1.662  41.823  1.00 69.48           C
ATOM    879  CD  LYS A 416      37.078   2.439  42.613  1.00 71.75           C
ATOM    880  CE  LYS A 416      37.404   2.448  44.100  1.00 72.86           C
ATOM    881  NZ  LYS A 416      36.225   2.079  44.933  1.00 72.46           N
ATOM    882  N   CYS A 417      37.539  -2.257  39.238  1.00 67.53           N
ATOM    883  CA  CYS A 417      38.270  -3.414  38.741  1.00 68.01           C
ATOM    884  C   CYS A 417      38.015  -3.736  37.270  1.00 67.49           C
ATOM    885  O   CYS A 417      38.632  -4.653  36.721  1.00 68.63           O
ATOM    886  CB  CYS A 417      37.951  -4.642  39.602  1.00 70.57           C
ATOM    887  SG  CYS A 417      38.591  -4.548  41.300  1.00 74.82           S
ATOM    888  N   VAL A 418      37.111  -2.994  36.632  1.00 64.53           N
ATOM    889  CA  VAL A 418      36.817  -3.226  35.218  1.00 59.58           C
ATOM    890  C   VAL A 418      37.739  -2.362  34.355  1.00 58.39           C
ATOM    891  O   VAL A 418      37.799  -1.140  34.513  1.00 55.79           O
ATOM    892  CB  VAL A 418      35.326  -2.918  34.879  1.00 59.07           C
ATOM    893  CG1 VAL A 418      34.971  -1.503  35.284  1.00 57.98           C
ATOM    894  CG2 VAL A 418      35.072  -3.121  33.391  1.00 53.22           C
ATOM    895  N   GLU A 419      38.463  -3.013  33.450  1.00 55.98           N
ATOM    896  CA  GLU A 419      39.403  -2.328  32.570  1.00 54.05           C
ATOM    897  C   GLU A 419      38.761  -1.280  31.662  1.00 51.61           C
ATOM    898  O   GLU A 419      37.665  -1.480  31.130  1.00 49.04           O
ATOM    899  CB  GLU A 419      40.149  -3.351  31.711  1.00 57.42           C
ATOM    900  CG  GLU A 419      39.385  -3.779  30.468  1.00 60.88           C
ATOM    901  CD  GLU A 419      40.178  -4.722  29.585  1.00 63.83           C
ATOM    902  OE1 GLU A 419      40.431  -5.870  30.012  1.00 64.75           O
ATOM    903  OE2 GLU A 419      40.546  -4.314  28.462  1.00 63.82           O
ATOM    904  N   GLY A 420      39.465  -0.165  31.491  1.00 48.86           N
ATOM    905  CA  GLY A 420      38.983   0.908  30.642  1.00 45.69           C
ATOM    906  C   GLY A 420      37.895   1.768  31.254  1.00 43.98           C
ATOM    907  O   GLY A 420      37.417   2.705  30.619  1.00 41.64           O
ATOM    908  N   MET A 421      37.503   1.471  32.488  1.00 42.80           N
ATOM    909  CA  MET A 421      36.449   2.247  33.123  1.00 42.06           C
ATOM    910  C   MET A 421      36.924   3.059  34.313  1.00 41.66           C
ATOM    911  O   MET A 421      36.113   3.512  35.112  1.00 39.99           O
ATOM    912  CB  MET A 421      35.306   1.326  33.554  1.00 42.34           C
ATOM    913  CG  MET A 421      34.589   0.636  32.395  1.00 37.93           C
ATOM    914  SD  MET A 421      32.928   0.103  32.845  1.00 38.77           S
ATOM    915  CE  MET A 421      32.002   1.699  32.766  1.00 35.99           C
ATOM    916  N   VAL A 422      38.232   3.256  34.430  1.00 43.36           N
ATOM    917  CA  VAL A 422      38.757   4.019  35.558  1.00 44.79           C
ATOM    918  C   VAL A 422      38.056   5.372  35.689  1.00 44.18           C
ATOM    919  O   VAL A 422      37.691   5.784  36.784  1.00 44.61           O
ATOM    920  CB  VAL A 422      40.285   4.247  35.433  1.00 46.45           C
ATOM    921  CG1 VAL A 422      40.594   5.087  34.206  1.00 48.35           C
ATOM    922  CG2 VAL A 422      40.813   4.920  36.697  1.00 45.98           C
ATOM    923  N   GLU A 423      37.846   6.055  34.570  1.00 42.20           N
ATOM    924  CA  GLU A 423      37.192   7.356  34.616  1.00 40.07           C
ATOM    925  C   GLU A 423      35.704   7.337  34.250  1.00 35.67           C
ATOM    926  O   GLU A 423      34.880   7.955  34.918  1.00 32.56           O
ATOM    927  CB  GLU A 423      37.909   8.337  33.684  1.00 43.94           C
ATOM    928  CG  GLU A 423      39.411   8.466  33.893  1.00 50.01           C
ATOM    929  CD  GLU A 423      40.097   9.158  32.719  1.00 55.54           C
ATOM    930  OE1 GLU A 423      39.539  10.155  32.205  1.00 56.27           O
ATOM    931  OE2 GLU A 423      41.188   8.704  32.306  1.00 57.91           O
ATOM    932  N   ILE A 424      35.345   6.618  33.197  1.00 36.15           N
ATOM    933  CA  ILE A 424      33.949   6.643  32.772  1.00 31.67           C
ATOM    934  C   ILE A 424      32.890   6.034  33.686  1.00 28.79           C
ATOM    935  O   ILE A 424      31.728   6.442  33.631  1.00 26.56           O
ATOM    936  CB  ILE A 424      33.802   6.087  31.347  1.00 34.01           C
ATOM    937  CG1 ILE A 424      34.203   4.617  31.296  1.00 35.31           C
ATOM    938  CG2 ILE A 424      34.640   6.935  30.395  1.00 33.32           C
ATOM    939  CD1 ILE A 424      33.857   3.955  29.978  1.00 35.84           C
ATOM    940  N   PHE A 425      33.261   5.091  34.543  1.00 29.17           N
ATOM    941  CA  PHE A 425      32.258   4.519  35.448  1.00 29.71           C
ATOM    942  C   PHE A 425      31.594   5.649  36.241  1.00 30.17           C
ATOM    943  O   PHE A 425      30.368   5.774  36.275  1.00 26.46           O
ATOM    944  CB  PHE A 425      32.903   3.529  36.424  1.00 30.98           C
ATOM    945  CG  PHE A 425      31.948   2.496  36.958  1.00 32.10           C
ATOM    946  CD1 PHE A 425      31.126   2.783  38.048  1.00 33.90           C
ATOM    947  CD2 PHE A 425      31.883   1.230  36.382  1.00 30.32           C
ATOM    948  CE1 PHE A 425      30.243   1.815  38.561  1.00 32.72           C
ATOM    949  CE2 PHE A 425      31.008   0.257  36.880  1.00 31.57           C
ATOM    950  CZ  PHE A 425      30.189   0.550  37.973  1.00 33.34           C
ATOM    951  N   ASP A 426      32.415   6.483  36.871  1.00 29.49           N
ATOM    952  CA  ASP A 426      31.893   7.587  37.661  1.00 32.03           C
ATOM    953  C   ASP A 426      31.133   8.593  36.806  1.00 28.94           C
ATOM    954  O   ASP A 426      30.155   9.177  37.256  1.00 31.27           O
ATOM    955  CB  ASP A 426      33.030   8.290  38.401  1.00 33.41           C
ATOM    956  CG  ASP A 426      33.455   7.547  39.655  1.00 39.39           C
ATOM    957  OD1 ASP A 426      32.766   6.576  40.038  1.00 38.69           O
ATOM    958  OD2 ASP A 426      34.479   7.936  40.256  1.00 39.54           O
ATOM    959  N   MET A 427      31.584   8.795  35.572  1.00 30.23           N
ATOM    960  CA  MET A 427      30.918   9.736  34.676  1.00 28.51           C
ATOM    961  C   MET A 427      29.525   9.202  34.324  1.00 29.02           C
ATOM    962  O   MET A 427      28.537   9.948  34.300  1.00 24.84           O
ATOM    963  CB  MET A 427      31.743   9.912  33.408  1.00 27.00           C
ATOM    964  CG  MET A 427      33.032  10.680  33.609  1.00 31.76           C
ATOM    965  SD  MET A 427      33.960  10.787  32.076  1.00 34.88           S
ATOM    966  CE  MET A 427      35.409  11.753  32.643  1.00 44.81           C
ATOM    967  N   LEU A 428      29.450   7.902  34.058  1.00 25.17           N
ATOM    968  CA  LEU A 428      28.172   7.292  33.730  1.00 27.57           C
ATOM    969  C   LEU A 428      27.210   7.411  34.916  1.00 29.58           C
ATOM    970  O   LEU A 428      26.042   7.742  34.744  1.00 26.50           O
ATOM    971  CB  LEU A 428      28.379   5.825  33.332  1.00 27.88           C
ATOM    972  CG  LEU A 428      29.039   5.683  31.957  1.00 26.58           C
ATOM    973  CD1 LEU A 428      29.677   4.304  31.782  1.00 27.69           C
ATOM    974  CD2 LEU A 428      27.993   5.928  30.894  1.00 25.60           C
ATOM    975  N   LEU A 429      27.701   7.146  36.126  1.00 30.29           N
ATOM    976  CA  LEU A 429      26.859   7.250  37.323  1.00 30.47           C
ATOM    977  C   LEU A 429      26.319   8.681  37.465  1.00 30.24           C
ATOM    978  O   LEU A 429      25.142   8.901  37.770  1.00 28.73           O
ATOM    979  CB  LEU A 429      27.675   6.883  38.571  1.00 31.65           C
ATOM    980  CG  LEU A 429      28.078   5.415  38.757  1.00 32.52           C
ATOM    981  CD1 LEU A 429      28.960   5.263  39.995  1.00 31.41           C
ATOM    982  CD2 LEU A 429      26.825   4.574  38.903  1.00 34.82           C
ATOM    983  N   ALA A 430      27.193   9.655  37.237  1.00 31.33           N
ATOM    984  CA  ALA A 430      26.807  11.058  37.332  1.00 29.99           C
ATOM    985  C   ALA A 430      25.696  11.387  36.344  1.00 30.92           C
ATOM    986  O   ALA A 430      24.754  12.107  36.674  1.00 30.72           O
ATOM    987  CB  ALA A 430      28.016  11.950  37.077  1.00 31.52           C
ATOM    988  N   THR A 431      25.801  10.854  35.128  1.00 30.31           N
ATOM    989  CA  THR A 431      24.786  11.106  34.112  1.00 28.70           C
ATOM    990  C   THR A 431      23.462  10.481  34.530  1.00 29.28           C
ATOM    991  O   THR A 431      22.402  11.099  34.397  1.00 25.59           O
ATOM    992  CB  THR A 431      25.208  10.534  32.736  1.00 30.74           C
ATOM    993  OG1 THR A 431      26.570  10.894  32.465  1.00 32.00           O
ATOM    994  CG2 THR A 431      24.320  11.087  31.631  1.00 26.11           C
ATOM    995  N   SER A 432      23.520   9.253  35.036  1.00 27.92           N
ATOM    996  CA  SER A 432      22.308   8.574  35.480  1.00 29.79           C
ATOM    997  C   SER A 432      21.651   9.400  36.587  1.00 31.28           C
ATOM    998  O   SER A 432      20.433   9.578  36.611  1.00 29.75           O
ATOM    999  CB  SER A 432      22.638   7.178  36.009  1.00 33.27           C
ATOM   1000  OG  SER A 432      21.453   6.414  36.137  1.00 37.05           O
ATOM   1001  N  ASER A 433      22.477   9.902  37.495  0.75 31.93           N
ATOM   1002  CA ASER A 433      22.002  10.714  38.605  0.75 35.66           C
ATOM   1003  C  ASER A 433      21.299  11.971  38.091  0.75 35.19           C
ATOM   1004  O  ASER A 433      20.257  12.374  38.613  0.75 35.25           O
ATOM   1005  CB ASER A 433      23.184  11.097  39.502  0.75 37.53           C
ATOM   1006  OG ASER A 433      22.823  12.091  40.442  0.75 44.47           O
ATOM   1007  N   ARG A 434      21.867  12.579  37.054  1.00 33.53           N
ATOM   1008  CA  ARG A 434      21.300  13.788  36.471  1.00 34.09           C
ATOM   1009  C   ARG A 434      19.936  13.491  35.872  1.00 33.57           C
ATOM   1010  O   ARG A 434      18.995  14.265  36.052  1.00 30.11           O
ATOM   1011  CB  ARG A 434      22.240  14.355  35.401  1.00 33.55           C
ATOM   1012  CG  ARG A 434      21.671  15.529  34.624  1.00 38.74           C
ATOM   1013  CD  ARG A 434      21.559  16.787  35.478  1.00 38.05           C
ATOM   1014  NE  ARG A 434      21.157  17.944  34.679  1.00 37.87           N
ATOM   1015  CZ  ARG A 434      20.487  18.995  35.149  1.00 41.41           C
ATOM   1016  NH1 ARG A 434      20.134  19.050  36.428  1.00 40.50           N
ATOM   1017  NH2 ARG A 434      20.175  19.998  34.338  1.00 38.62           N
ATOM   1018  N   PHE A 435      19.831  12.371  35.158  1.00 34.61           N
ATOM   1019  CA  PHE A 435      18.564  11.963  34.549  1.00 35.32           C
ATOM   1020  C   PHE A 435      17.527  11.780  35.657  1.00 35.66           C
ATOM   1021  O   PHE A 435      16.362  12.136  35.497  1.00 34.73           O
ATOM   1022  CB  PHE A 435      18.727  10.634  33.796  1.00 35.15           C
ATOM   1023  CG  PHE A 435      19.241  10.779  32.386  1.00 37.79           C
ATOM   1024  CD1 PHE A 435      19.459  12.035  31.824  1.00 42.06           C
ATOM   1025  CD2 PHE A 435      19.521   9.650  31.623  1.00 40.99           C
ATOM   1026  CE1 PHE A 435      19.955  12.163  30.522  1.00 43.38           C
ATOM   1027  CE2 PHE A 435      20.017   9.768  30.323  1.00 41.00           C
ATOM   1028  CZ  PHE A 435      20.233  11.029  29.775  1.00 40.56           C
ATOM   1029  N   ARG A 436      17.967  11.217  36.778  1.00 38.40           N
ATOM   1030  CA  ARG A 436      17.094  10.983  37.924  1.00 40.56           C
ATOM   1031  C   ARG A 436      16.577  12.302  38.493  1.00 40.49           C
ATOM   1032  O   ARG A 436      15.382  12.458  38.729  1.00 41.13           O
ATOM   1033  CB  ARG A 436      17.845  10.215  39.012  1.00 40.70           C
ATOM   1034  CG  ARG A 436      16.942   9.590  40.068  1.00 44.55           C
ATOM   1035  CD  ARG A 436      17.648   8.459  40.810  1.00 48.45           C
ATOM   1036  NE  ARG A 436      18.981   8.841  41.275  1.00 50.08           N
ATOM   1037  CZ  ARG A 436      20.119   8.362  40.776  1.00 51.91           C
ATOM   1038  NH1 ARG A 436      20.099   7.472  39.790  1.00 49.18           N
ATOM   1039  NH2 ARG A 436      21.283   8.770  41.266  1.00 51.82           N
ATOM   1040  N   MET A 437      17.478  13.251  38.707  1.00 40.04           N
ATOM   1041  CA  MET A 437      17.090  14.546  39.245  1.00 41.09           C
ATOM   1042  C   MET A 437      16.099  15.221  38.299  1.00 40.99           C
ATOM   1043  O   MET A 437      15.111  15.804  38.735  1.00 42.44           O
ATOM   1044  CB  MET A 437      18.307  15.431  39.424  1.00  0.00           C
ATOM   1045  CG  MET A 437      19.170  14.906  40.566  1.00  0.00           C
ATOM   1046  SD  MET A 437      20.698  15.870  40.682  1.00  0.00           S
ATOM   1047  CE  MET A 437      20.043  17.417  41.270  1.00  0.00           C
ATOM   1048  N   MET A 438      16.367  15.127  37.001  1.00 39.00           N
ATOM   1049  CA  MET A 438      15.510  15.733  35.988  1.00 40.08           C
ATOM   1050  C   MET A 438      14.221  14.964  35.783  1.00 37.67           C
ATOM   1051  O   MET A 438      13.305  15.451  35.125  1.00 36.69           O
ATOM   1052  CB  MET A 438      16.237  15.793  34.651  1.00 38.20           C
ATOM   1053  CG  MET A 438      17.354  16.794  34.601  1.00 41.97           C
ATOM   1054  SD  MET A 438      18.000  16.862  32.943  1.00 44.28           S
ATOM   1055  CE  MET A 438      16.698  17.749  32.097  1.00 39.75           C
ATOM   1056  N   ASN A 439      14.156  13.759  36.337  1.00 38.50           N
ATOM   1057  CA  ASN A 439      12.981  12.919  36.175  1.00 40.80           C
ATOM   1058  C   ASN A 439      12.725  12.744  34.678  1.00 39.21           C
ATOM   1059  O   ASN A 439      11.638  13.037  34.173  1.00 37.96           O
ATOM   1060  CB  ASN A 439      11.762  13.556  36.847  1.00 44.76           C
ATOM   1061  CG  ASN A 439      10.566  12.620  36.887  1.00 48.32           C
ATOM   1062  OD1 ASN A 439      10.721  11.399  36.964  1.00 48.80           O
ATOM   1063  ND2 ASN A 439       9.365  13.188  36.828  1.00 50.47           N
ATOM   1064  N   LEU A 440      13.749  12.275  33.972  1.00 37.61           N
ATOM   1065  CA  LEU A 440      13.655  12.052  32.532  1.00 35.21           C
ATOM   1066  C   LEU A 440      12.587  11.024  32.196  1.00 36.43           C
ATOM   1067  O   LEU A 440      12.518   9.967  32.826  1.00 37.60           O
ATOM   1068  CB  LEU A 440      14.999  11.575  31.986  1.00 34.42           C
ATOM   1069  CG  LEU A 440      15.021  11.467  30.462  1.00 34.99           C
ATOM   1070  CD1 LEU A 440      14.890  12.863  29.870  1.00 34.68           C
ATOM   1071  CD2 LEU A 440      16.295  10.795  30.001  1.00 34.20           C
ATOM   1072  N   GLN A 441      11.764  11.327  31.196  1.00 37.04           N
ATOM   1073  CA  GLN A 441      10.696  10.420  30.785  1.00 38.65           C
ATOM   1074  C   GLN A 441      11.098   9.565  29.585  1.00 38.85           C
ATOM   1075  O   GLN A 441      11.922   9.976  28.763  1.00 36.31           O
ATOM   1076  CB  GLN A 441       9.432  11.212  30.443  1.00 38.44           C
ATOM   1077  CG  GLN A 441       8.912  12.064  31.592  1.00 42.11           C
ATOM   1078  CD  GLN A 441       8.362  11.227  32.729  1.00 44.68           C
ATOM   1079  OE1 GLN A 441       7.268  10.668  32.629  1.00 46.70           O
ATOM   1080  NE2 GLN A 441       9.119  11.133  33.818  1.00 43.30           N
ATOM   1081  N   GLY A 442      10.499   8.377  29.494  1.00 36.19           N
ATOM   1082  CA  GLY A 442      10.791   7.468  28.401  1.00 38.09           C
ATOM   1083  C   GLY A 442      10.599   8.111  27.043  1.00 36.81           C
ATOM   1084  O   GLY A 442      11.381   7.877  26.122  1.00 34.16           O
ATOM   1085  N   GLU A 443       9.556   8.925  26.918  1.00 36.46           N
ATOM   1086  CA  GLU A 443       9.270   9.603  25.662  1.00 36.70           C
ATOM   1087  C   GLU A 443      10.409  10.551  25.312  1.00 34.74           C
ATOM   1088  O   GLU A 443      10.760  10.704  24.145  1.00 33.23           O
ATOM   1089  CB  GLU A 443       7.956  10.378  25.764  1.00 41.74           C
ATOM   1090  CG  GLU A 443       6.723   9.488  25.879  1.00 48.17           C
ATOM   1091  CD  GLU A 443       6.482   9.009  27.302  1.00 54.41           C
ATOM   1092  OE1 GLU A 443       7.159   9.516  28.224  1.00 56.84           O
ATOM   1093  OE2 GLU A 443       5.619   8.123  27.498  1.00 58.12           O
ATOM   1094  N   GLU A 444      10.985  11.179  26.332  1.00 31.62           N
ATOM   1095  CA  GLU A 444      12.097  12.095  26.126  1.00 33.92           C
ATOM   1096  C   GLU A 444      13.356  11.304  25.770  1.00 33.44           C
ATOM   1097  O   GLU A 444      14.086  11.668  24.841  1.00 33.43           O
ATOM   1098  CB  GLU A 444      12.332  12.925  27.387  1.00 34.92           C
ATOM   1099  CG  GLU A 444      11.168  13.844  27.732  1.00 38.39           C
ATOM   1100  CD  GLU A 444      11.383  14.610  29.023  1.00 38.06           C
ATOM   1101  OE1 GLU A 444      11.800  13.994  30.026  1.00 38.87           O
ATOM   1102  OE2 GLU A 444      11.133  15.835  29.035  1.00 40.56           O
ATOM   1103  N   PHE A 445      13.591  10.215  26.501  1.00 30.60           N
ATOM   1104  CA  PHE A 445      14.754   9.357  26.275  1.00 32.45           C
ATOM   1105  C   PHE A 445      14.850   8.885  24.829  1.00 31.56           C
ATOM   1106  O   PHE A 445      15.924   8.945  24.222  1.00 32.45           O
ATOM   1107  CB  PHE A 445      14.705   8.139  27.203  1.00 29.52           C
ATOM   1108  CG  PHE A 445      15.668   7.047  26.829  1.00 30.96           C
ATOM   1109  CD1 PHE A 445      17.037   7.202  27.030  1.00 28.24           C
ATOM   1110  CD2 PHE A 445      15.206   5.864  26.266  1.00 30.67           C
ATOM   1111  CE1 PHE A 445      17.934   6.194  26.675  1.00 28.46           C
ATOM   1112  CE2 PHE A 445      16.095   4.848  25.909  1.00 31.75           C
ATOM   1113  CZ  PHE A 445      17.461   5.015  26.112  1.00 30.50           C
ATOM   1114  N   VAL A 446      13.739   8.415  24.266  1.00 29.13           N
ATOM   1115  CA  VAL A 446      13.787   7.943  22.889  1.00 28.24           C
ATOM   1116  C   VAL A 446      14.100   9.064  21.900  1.00 27.40           C
ATOM   1117  O   VAL A 446      14.781   8.837  20.903  1.00 28.13           O
ATOM   1118  CB  VAL A 446      12.479   7.193  22.477  1.00 29.04           C
ATOM   1119  CG1 VAL A 446      12.318   5.938  23.342  1.00 30.07           C
ATOM   1120  CG2 VAL A 446      11.266   8.092  22.605  1.00 27.74           C
ATOM   1121  N   CYS A 447      13.619  10.275  22.165  1.00 29.09           N
ATOM   1122  CA  CYS A 447      13.919  11.393  21.272  1.00 29.04           C
ATOM   1123  C   CYS A 447      15.421  11.676  21.329  1.00 27.85           C
ATOM   1124  O   CYS A 447      16.065  11.882  20.302  1.00 28.91           O
ATOM   1125  CB  CYS A 447      13.157  12.652  21.693  1.00 29.45           C
ATOM   1126  SG  CYS A 447      11.389  12.589  21.309  1.00 35.65           S
ATOM   1127  N   LEU A 448      15.970  11.684  22.538  1.00 27.15           N
ATOM   1128  CA  LEU A 448      17.393  11.939  22.729  1.00 25.52           C
ATOM   1129  C   LEU A 448      18.246  10.902  22.008  1.00 28.04           C
ATOM   1130  O   LEU A 448      19.206  11.252  21.325  1.00 25.70           O
ATOM   1131  CB  LEU A 448      17.735  11.933  24.219  1.00 27.71           C
ATOM   1132  CG  LEU A 448      17.248  13.135  25.039  1.00 29.40           C
ATOM   1133  CD1 LEU A 448      17.806  13.043  26.455  1.00 30.97           C
ATOM   1134  CD2 LEU A 448      17.686  14.434  24.375  1.00 29.59           C
ATOM   1135  N   LYS A 449      17.904   9.622  22.161  1.00 25.11           N
ATOM   1136  CA  LYS A 449      18.673   8.569  21.507  1.00 26.68           C
ATOM   1137  C   LYS A 449      18.629   8.746  19.993  1.00 25.25           C
ATOM   1138  O   LYS A 449      19.610   8.488  19.296  1.00 25.57           O
ATOM   1139  CB  LYS A 449      18.135   7.184  21.900  1.00 29.00           C
ATOM   1140  CG  LYS A 449      19.135   6.052  21.694  1.00 34.55           C
ATOM   1141  CD  LYS A 449      18.738   4.789  22.459  1.00 32.96           C
ATOM   1142  CE  LYS A 449      17.267   4.420  22.221  1.00 31.25           C
ATOM   1143  NZ  LYS A 449      17.024   2.967  22.474  1.00 29.42           N
ATOM   1144  N   SER A 450      17.486   9.196  19.489  1.00 25.84           N
ATOM   1145  CA  SER A 450      17.323   9.416  18.063  1.00 27.06           C
ATOM   1146  C   SER A 450      18.175  10.592  17.612  1.00 26.62           C
ATOM   1147  O   SER A 450      18.761  10.573  16.529  1.00 25.89           O
ATOM   1148  CB  SER A 450      15.858   9.707  17.742  1.00 32.38           C
ATOM   1149  OG  SER A 450      15.108   8.515  17.746  1.00 35.80           O
ATOM   1150  N   ILE A 451      18.233  11.625  18.441  1.00 26.59           N
ATOM   1151  CA  ILE A 451      19.025  12.791  18.096  1.00 25.19           C
ATOM   1152  C   ILE A 451      20.495  12.386  17.975  1.00 24.26           C
ATOM   1153  O   ILE A 451      21.186  12.798  17.043  1.00 26.70           O
ATOM   1154  CB  ILE A 451      18.845  13.895  19.156  1.00 26.58           C
ATOM   1155  CG1 ILE A 451      17.509  14.607  18.911  1.00 25.61           C
ATOM   1156  CG2 ILE A 451      20.010  14.887  19.104  1.00 20.01           C
ATOM   1157  CD1 ILE A 451      16.935  15.269  20.138  1.00 28.41           C
ATOM   1158  N   ILE A 452      20.969  11.570  18.911  1.00 22.20           N
ATOM   1159  CA  ILE A 452      22.359  11.122  18.879  1.00 21.56           C
ATOM   1160  C   ILE A 452      22.656  10.426  17.555  1.00 22.97           C
ATOM   1161  O   ILE A 452      23.642  10.727  16.875  1.00 21.11           O
ATOM   1162  CB  ILE A 452      22.656  10.145  20.046  1.00 23.14           C
ATOM   1163  CG1 ILE A 452      22.724  10.929  21.372  1.00 22.06           C
ATOM   1164  CG2 ILE A 452      23.975   9.417  19.798  1.00 21.70           C
ATOM   1165  CD1 ILE A 452      22.752  10.036  22.617  1.00 25.94           C
ATOM   1166  N   LEU A 453      21.783   9.497  17.173  1.00 23.02           N
ATOM   1167  CA  LEU A 453      21.986   8.769  15.935  1.00 21.60           C
ATOM   1168  C   LEU A 453      22.092   9.688  14.717  1.00 23.50           C
ATOM   1169  O   LEU A 453      22.961   9.501  13.860  1.00 24.51           O
ATOM   1170  CB  LEU A 453      20.846   7.765  15.734  1.00 21.35           C
ATOM   1171  CG  LEU A 453      20.712   7.189  14.325  1.00 21.75           C
ATOM   1172  CD1 LEU A 453      21.814   6.166  14.109  1.00 25.05           C
ATOM   1173  CD2 LEU A 453      19.328   6.537  14.156  1.00 24.10           C
ATOM   1174  N   LEU A 454      21.219  10.687  14.639  1.00 26.56           N
ATOM   1175  CA  LEU A 454      21.233  11.599  13.494  1.00 26.28           C
ATOM   1176  C   LEU A 454      22.292  12.702  13.553  1.00 27.93           C
ATOM   1177  O   LEU A 454      22.781  13.144  12.513  1.00 28.71           O
ATOM   1178  CB  LEU A 454      19.852  12.242  13.331  1.00 25.57           C
ATOM   1179  CG  LEU A 454      18.737  11.224  13.052  1.00 30.38           C
ATOM   1180  CD1 LEU A 454      17.406  11.926  12.955  1.00 28.89           C
ATOM   1181  CD2 LEU A 454      19.040  10.478  11.761  1.00 32.96           C
ATOM   1182  N   ASN A 455      22.637  13.146  14.758  1.00 26.74           N
ATOM   1183  CA  ASN A 455      23.604  14.234  14.934  1.00 26.77           C
ATOM   1184  C   ASN A 455      25.062  13.782  14.953  1.00 31.04           C
ATOM   1185  O   ASN A 455      25.965  14.517  14.523  1.00 27.85           O
ATOM   1186  CB  ASN A 455      23.285  14.997  16.223  1.00 26.30           C
ATOM   1187  CG  ASN A 455      24.175  16.216  16.418  1.00 27.30           C
ATOM   1188  OD1 ASN A 455      24.174  17.133  15.600  1.00 30.35           O
ATOM   1189  ND2 ASN A 455      24.931  16.229  17.505  1.00 27.27           N
ATOM   1190  N   SER A 456      25.268  12.570  15.461  1.00 30.52           N
ATOM   1191  CA  SER A 456      26.572  11.928  15.578  1.00 35.67           C
ATOM   1192  C   SER A 456      27.627  12.344  14.563  1.00 35.82           C
ATOM   1193  O   SER A 456      28.598  13.041  14.886  1.00 33.05           O
ATOM   1194  CB  SER A 456      26.392  10.393  15.506  1.00 40.35           C
ATOM   1195  OG  SER A 456      25.872   9.953  14.244  1.00 31.28           O
ATOM   1196  N   GLY A 457      27.438  11.887  13.334  1.00 33.87           N
ATOM   1197  CA  GLY A 457      28.393  12.190  12.292  1.00 36.72           C
ATOM   1198  C   GLY A 457      27.876  13.018  11.136  1.00 36.75           C
ATOM   1199  O   GLY A 457      28.309  12.805  10.012  1.00 37.85           O
ATOM   1200  N   VAL A 458      26.967  13.957  11.393  1.00 38.90           N
ATOM   1201  CA  VAL A 458      26.438  14.802  10.317  1.00 43.53           C
ATOM   1202  C   VAL A 458      27.472  15.801   9.817  1.00 46.55           C
ATOM   1203  O   VAL A 458      27.392  16.265   8.681  1.00 46.60           O
ATOM   1204  CB  VAL A 458      25.231  15.648  10.756  1.00 43.93           C
ATOM   1205  CG1 VAL A 458      24.208  15.713   9.631  1.00 44.00           C
ATOM   1206  CG2 VAL A 458      24.638  15.097  12.012  1.00 50.45           C
ATOM   1207  N   TYR A 459      28.432  16.144  10.671  1.00 50.75           N
ATOM   1208  CA  TYR A 459      29.456  17.114  10.301  1.00 55.55           C
ATOM   1209  C   TYR A 459      30.791  16.490   9.928  1.00 57.45           C
ATOM   1210  O   TYR A 459      31.793  17.190   9.798  1.00 57.43           O
ATOM   1211  CB  TYR A 459      29.647  18.129  11.433  1.00 57.14           C
ATOM   1212  CG  TYR A 459      28.376  18.870  11.780  1.00 59.50           C
ATOM   1213  CD1 TYR A 459      27.430  19.175  10.796  1.00 62.29           C
ATOM   1214  CD2 TYR A 459      28.093  19.229  13.095  1.00 61.09           C
ATOM   1215  CE1 TYR A 459      26.234  19.813  11.117  1.00 64.09           C
ATOM   1216  CE2 TYR A 459      26.900  19.868  13.429  1.00 62.58           C
ATOM   1217  CZ  TYR A 459      25.976  20.153  12.437  1.00 63.12           C
ATOM   1218  OH  TYR A 459      24.790  20.765  12.767  1.00 62.47           O
ATOM   1219  N   THR A 460      30.800  15.173   9.750  1.00 59.47           N
ATOM   1220  CA  THR A 460      32.018  14.474   9.366  1.00 62.07           C
ATOM   1221  C   THR A 460      31.759  13.678   8.086  1.00 63.48           C
ATOM   1222  O   THR A 460      32.457  12.708   7.782  1.00 64.04           O
ATOM   1223  CB  THR A 460      32.503  13.531  10.499  1.00 62.71           C
ATOM   1224  OG1 THR A 460      33.473  12.612   9.982  1.00 67.02           O
ATOM   1225  CG2 THR A 460      31.345  12.760  11.084  1.00 58.30           C
ATOM   1226  N   PHE A 461      30.757  14.113   7.326  1.00 65.13           N
ATOM   1227  CA  PHE A 461      30.395  13.446   6.080  1.00 67.38           C
ATOM   1228  C   PHE A 461      31.463  13.604   5.004  1.00 69.06           C
ATOM   1229  O   PHE A 461      32.181  14.606   4.962  1.00 69.58           O
ATOM   1230  CB  PHE A 461      29.052  13.975   5.563  1.00 66.74           C
ATOM   1231  CG  PHE A 461      27.867  13.147   5.991  1.00 66.23           C
ATOM   1232  CD1 PHE A 461      27.963  11.760   6.085  1.00 66.35           C
ATOM   1233  CD2 PHE A 461      26.658  13.754   6.312  1.00 65.54           C
ATOM   1234  CE1 PHE A 461      26.872  10.994   6.494  1.00 66.22           C
ATOM   1235  CE2 PHE A 461      25.562  12.996   6.722  1.00 65.15           C
ATOM   1236  CZ  PHE A 461      25.670  11.615   6.813  1.00 64.46           C
ATOM   1237  N   LEU A 462      31.543  12.601   4.133  1.00 70.20           N
ATOM   1238  CA  LEU A 462      32.511  12.545   3.039  1.00 72.05           C
ATOM   1239  C   LEU A 462      32.810  13.856   2.304  1.00 72.77           C
ATOM   1240  O   LEU A 462      33.726  14.590   2.679  1.00 73.79           O
ATOM   1241  CB  LEU A 462      32.086  11.496   2.027  1.00  0.00           C
ATOM   1242  CG  LEU A 462      33.194  11.311   0.996  1.00  0.00           C
ATOM   1243  CD2 LEU A 462      32.744  10.306  -0.059  1.00  0.00           C
ATOM   1244  CD1 LEU A 462      34.451  10.793   1.688  1.00  0.00           C
ATOM   1245  N   SER A 463      32.043  14.141   1.253  1.00 73.47           N
ATOM   1246  CA  SER A 463      32.262  15.343   0.449  1.00 72.83           C
ATOM   1247  C   SER A 463      31.127  16.362   0.491  1.00 71.41           C
ATOM   1248  O   SER A 463      30.455  16.528   1.512  1.00 72.30           O
ATOM   1249  CB  SER A 463      32.530  14.956  -0.996  1.00  0.00           C
ATOM   1250  OG  SER A 463      31.317  14.490  -1.592  1.00  0.00           O
ATOM   1251  N   SER A 464      30.932  17.049  -0.633  1.00 69.33           N
ATOM   1252  CA  SER A 464      29.892  18.063  -0.759  1.00 66.56           C
ATOM   1253  C   SER A 464      29.108  17.886  -2.061  1.00 64.15           C
ATOM   1254  O   SER A 464      28.657  18.862  -2.663  1.00 63.20           O
ATOM   1255  CB  SER A 464      30.501  19.450  -0.722  1.00  0.00           C
ATOM   1256  OG  SER A 464      29.456  20.425  -0.761  1.00  0.00           O
ATOM   1257  N   THR A 465      28.954  16.638  -2.493  1.00 61.42           N
ATOM   1258  CA  THR A 465      28.206  16.343  -3.709  1.00 57.61           C
ATOM   1259  C   THR A 465      26.767  16.824  -3.523  1.00 55.05           C
ATOM   1260  O   THR A 465      26.349  17.130  -2.407  1.00 54.19           O
ATOM   1261  CB  THR A 465      28.185  14.825  -4.005  1.00 57.85           C
ATOM   1262  OG1 THR A 465      27.524  14.135  -2.935  1.00 54.49           O
ATOM   1263  CG2 THR A 465      29.606  14.287  -4.150  1.00 57.37           C
ATOM   1264  N   LEU A 466      26.013  16.892  -4.615  1.00 52.04           N
ATOM   1265  CA  LEU A 466      24.624  17.330  -4.551  1.00 49.16           C
ATOM   1266  C   LEU A 466      23.816  16.397  -3.650  1.00 47.86           C
ATOM   1267  O   LEU A 466      22.960  16.845  -2.883  1.00 45.26           O
ATOM   1268  CB  LEU A 466      24.012  17.349  -5.956  1.00 48.69           C
ATOM   1269  CG  LEU A 466      22.954  18.416  -6.253  1.00 48.43           C
ATOM   1270  CD1 LEU A 466      22.156  18.002  -7.482  1.00 48.08           C
ATOM   1271  CD2 LEU A 466      22.033  18.594  -5.057  1.00 47.75           C
ATOM   1272  N   LYS A 467      24.092  15.099  -3.751  1.00 45.82           N
ATOM   1273  CA  LYS A 467      23.399  14.100  -2.947  1.00 46.88           C
ATOM   1274  C   LYS A 467      23.737  14.284  -1.472  1.00 46.14           C
ATOM   1275  O   LYS A 467      22.885  14.107  -0.603  1.00 45.42           O
ATOM   1276  CB  LYS A 467      23.802  12.692  -3.394  1.00 48.65           C
ATOM   1277  CG  LYS A 467      22.829  11.603  -2.974  1.00 51.24           C
ATOM   1278  CD  LYS A 467      23.561  10.301  -2.682  1.00 54.68           C
ATOM   1279  CE  LYS A 467      23.105   9.179  -3.604  1.00 57.67           C
ATOM   1280  NZ  LYS A 467      24.149   8.118  -3.732  1.00 59.26           N
ATOM   1281  N   SER A 468      24.989  14.644  -1.202  1.00 45.24           N
ATOM   1282  CA  SER A 468      25.456  14.854   0.161  1.00 46.34           C
ATOM   1283  C   SER A 468      24.778  16.064   0.790  1.00 43.97           C
ATOM   1284  O   SER A 468      24.473  16.063   1.983  1.00 42.66           O
ATOM   1285  CB  SER A 468      26.975  15.050   0.173  1.00 47.39           C
ATOM   1286  OG  SER A 468      27.407  15.538   1.434  1.00 54.72           O
ATOM   1287  N   LEU A 469      24.547  17.099  -0.011  1.00 42.40           N
ATOM   1288  CA  LEU A 469      23.890  18.301   0.486  1.00 40.48           C
ATOM   1289  C   LEU A 469      22.423  17.996   0.786  1.00 39.09           C
ATOM   1290  O   LEU A 469      21.856  18.507   1.759  1.00 35.10           O
ATOM   1291  CB  LEU A 469      24.002  19.427  -0.545  1.00 44.66           C
ATOM   1292  CG  LEU A 469      25.438  19.874  -0.849  1.00 46.87           C
ATOM   1293  CD1 LEU A 469      25.514  20.477  -2.246  1.00 47.16           C
ATOM   1294  CD2 LEU A 469      25.890  20.883   0.198  1.00 47.40           C
ATOM   1295  N   GLU A 470      21.814  17.151  -0.045  1.00 35.00           N
ATOM   1296  CA  GLU A 470      20.417  16.769   0.146  1.00 34.05           C
ATOM   1297  C   GLU A 470      20.290  15.916   1.403  1.00 34.09           C
ATOM   1298  O   GLU A 470      19.321  16.034   2.157  1.00 32.06           O
ATOM   1299  CB  GLU A 470      19.913  15.964  -1.053  1.00 37.68           C
ATOM   1300  CG  GLU A 470      19.772  16.773  -2.330  1.00 42.65           C
ATOM   1301  CD  GLU A 470      19.339  15.922  -3.510  1.00 47.92           C
ATOM   1302  OE1 GLU A 470      19.671  14.716  -3.539  1.00 50.09           O
ATOM   1303  OE2 GLU A 470      18.666  16.462  -4.412  1.00 50.51           O
ATOM   1304  N   GLU A 471      21.274  15.047   1.606  1.00 34.62           N
ATOM   1305  CA  GLU A 471      21.309  14.162   2.766  1.00 35.57           C
ATOM   1306  C   GLU A 471      21.393  14.984   4.051  1.00 34.44           C
ATOM   1307  O   GLU A 471      20.594  14.795   4.969  1.00 31.97           O
ATOM   1308  CB  GLU A 471      22.515  13.222   2.670  1.00 34.51           C
ATOM   1309  CG  GLU A 471      22.377  12.122   1.614  1.00 38.39           C
ATOM   1310  CD  GLU A 471      21.475  10.989   2.063  1.00 40.17           C
ATOM   1311  OE1 GLU A 471      21.973  10.061   2.738  1.00 32.31           O
ATOM   1312  OE2 GLU A 471      20.268  11.027   1.742  1.00 41.38           O
ATOM   1313  N   LYS A 472      22.359  15.898   4.112  1.00 33.61           N
ATOM   1314  CA  LYS A 472      22.518  16.739   5.291  1.00 35.75           C
ATOM   1315  C   LYS A 472      21.237  17.522   5.581  1.00 34.73           C
ATOM   1316  O   LYS A 472      20.795  17.606   6.723  1.00 33.70           O
ATOM   1317  CB  LYS A 472      23.683  17.710   5.097  1.00 39.45           C
ATOM   1318  CG  LYS A 472      25.049  17.049   5.139  1.00 41.83           C
ATOM   1319  CD  LYS A 472      26.079  17.956   5.794  1.00 47.72           C
ATOM   1320  CE  LYS A 472      27.446  17.286   5.862  1.00 48.74           C
ATOM   1321  NZ  LYS A 472      27.850  16.700   4.548  1.00 52.16           N
ATOM   1322  N   ASP A 473      20.643  18.098   4.544  1.00 33.51           N
ATOM   1323  CA  ASP A 473      19.420  18.865   4.720  1.00 34.71           C
ATOM   1324  C   ASP A 473      18.338  17.999   5.338  1.00 33.01           C
ATOM   1325  O   ASP A 473      17.641  18.416   6.264  1.00 32.72           O
ATOM   1326  CB  ASP A 473      18.924  19.404   3.379  1.00 38.01           C
ATOM   1327  CG  ASP A 473      17.654  20.221   3.521  1.00 44.15           C
ATOM   1328  OD1 ASP A 473      17.750  21.396   3.931  1.00 46.70           O
ATOM   1329  OD2 ASP A 473      16.560  19.687   3.231  1.00 45.70           O
ATOM   1330  N   HIS A 474      18.198  16.785   4.826  1.00 32.98           N
ATOM   1331  CA  HIS A 474      17.185  15.882   5.343  1.00 32.20           C
ATOM   1332  C   HIS A 474      17.404  15.573   6.815  1.00 29.56           C
ATOM   1333  O   HIS A 474      16.460  15.542   7.597  1.00 29.92           O
ATOM   1334  CB  HIS A 474      17.184  14.576   4.567  1.00 33.08           C
ATOM   1335  CG  HIS A 474      16.047  13.674   4.926  1.00 36.18           C
ATOM   1336  ND1 HIS A 474      16.229  12.457   5.543  1.00 39.07           N
ATOM   1337  CD2 HIS A 474      14.711  13.814   4.751  1.00 37.92           C
ATOM   1338  CE1 HIS A 474      15.054  11.884   5.733  1.00 38.20           C
ATOM   1339  NE2 HIS A 474      14.117  12.686   5.262  1.00 37.37           N
ATOM   1340  N   ILE A 475      18.654  15.327   7.185  1.00 27.56           N
ATOM   1341  CA  ILE A 475      18.972  15.016   8.572  1.00 25.80           C
ATOM   1342  C   ILE A 475      18.576  16.202   9.459  1.00 27.92           C
ATOM   1343  O   ILE A 475      17.928  16.039  10.485  1.00 29.07           O
ATOM   1344  CB  ILE A 475      20.479  14.708   8.721  1.00 25.92           C
ATOM   1345  CG1 ILE A 475      20.786  13.341   8.095  1.00 26.26           C
ATOM   1346  CG2 ILE A 475      20.876  14.712  10.192  1.00 27.38           C
ATOM   1347  CD1 ILE A 475      22.259  13.072   7.848  1.00 27.11           C
ATOM   1348  N   HIS A 476      18.956  17.405   9.053  1.00 29.37           N
ATOM   1349  CA  HIS A 476      18.621  18.576   9.846  1.00 29.37           C
ATOM   1350  C   HIS A 476      17.120  18.811   9.948  1.00 31.21           C
ATOM   1351  O   HIS A 476      16.637  19.336  10.952  1.00 29.37           O
ATOM   1352  CB  HIS A 476      19.342  19.797   9.282  1.00 32.16           C
ATOM   1353  CG  HIS A 476      20.777  19.868   9.700  1.00 39.71           C
ATOM   1354  ND1 HIS A 476      21.809  20.068   8.809  1.00 39.97           N
ATOM   1355  CD2 HIS A 476      21.355  19.708  10.915  1.00 39.67           C
ATOM   1356  CE1 HIS A 476      22.960  20.027   9.457  1.00 39.84           C
ATOM   1357  NE2 HIS A 476      22.712  19.810  10.735  1.00 40.23           N
ATOM   1358  N   ARG A 477      16.373  18.395   8.929  1.00 31.74           N
ATOM   1359  CA  ARG A 477      14.928  18.571   8.957  1.00 31.49           C
ATOM   1360  C   ARG A 477      14.310  17.582   9.932  1.00 30.63           C
ATOM   1361  O   ARG A 477      13.360  17.904  10.650  1.00 30.20           O
ATOM   1362  CB  ARG A 477      14.341  18.376   7.558  1.00 34.84           C
ATOM   1363  CG  ARG A 477      14.424  19.626   6.698  1.00 40.41           C
ATOM   1364  CD  ARG A 477      13.698  19.445   5.370  1.00 45.06           C
ATOM   1365  NE  ARG A 477      14.107  20.456   4.399  1.00 53.08           N
ATOM   1366  CZ  ARG A 477      13.647  21.705   4.376  1.00 55.71           C
ATOM   1367  NH1 ARG A 477      12.756  22.106   5.274  1.00 56.59           N
ATOM   1368  NH2 ARG A 477      14.086  22.558   3.458  1.00 59.43           N
ATOM   1369  N   VAL A 478      14.862  16.375   9.973  1.00 29.94           N
ATOM   1370  CA  VAL A 478      14.350  15.369  10.886  1.00 29.96           C
ATOM   1371  C   VAL A 478      14.695  15.774  12.316  1.00 29.91           C
ATOM   1372  O   VAL A 478      13.860  15.677  13.221  1.00 29.92           O
ATOM   1373  CB  VAL A 478      14.937  13.976  10.575  1.00 32.63           C
ATOM   1374  CG1 VAL A 478      14.461  12.974  11.608  1.00 33.15           C
ATOM   1375  CG2 VAL A 478      14.505  13.529   9.169  1.00 31.21           C
ATOM   1376  N   LEU A 479      15.929  16.232  12.516  1.00 28.81           N
ATOM   1377  CA  LEU A 479      16.360  16.674  13.836  1.00 28.28           C
ATOM   1378  C   LEU A 479      15.410  17.776  14.312  1.00 29.35           C
ATOM   1379  O   LEU A 479      14.994  17.784  15.469  1.00 28.79           O
ATOM   1380  CB  LEU A 479      17.799  17.210  13.780  1.00 27.01           C
ATOM   1381  CG  LEU A 479      18.908  16.151  13.852  1.00 26.13           C
ATOM   1382  CD1 LEU A 479      20.230  16.770  13.394  1.00 26.15           C
ATOM   1383  CD2 LEU A 479      19.028  15.602  15.277  1.00 24.96           C
ATOM   1384  N   ASP A 480      15.077  18.703  13.416  1.00 31.18           N
ATOM   1385  CA  ASP A 480      14.163  19.800  13.742  1.00 33.61           C
ATOM   1386  C   ASP A 480      12.818  19.221  14.174  1.00 33.31           C
ATOM   1387  O   ASP A 480      12.185  19.724  15.105  1.00 33.80           O
ATOM   1388  CB  ASP A 480      13.944  20.712  12.528  1.00 33.94           C
ATOM   1389  CG  ASP A 480      15.055  21.743  12.345  1.00 36.01           C
ATOM   1390  OD1 ASP A 480      15.860  21.951  13.274  1.00 34.03           O
ATOM   1391  OD2 ASP A 480      15.120  22.353  11.257  1.00 36.50           O
ATOM   1392  N   LYS A 481      12.379  18.161  13.498  1.00 33.75           N
ATOM   1393  CA  LYS A 481      11.107  17.536  13.839  1.00 33.09           C
ATOM   1394  C   LYS A 481      11.163  16.895  15.224  1.00 33.78           C
ATOM   1395  O   LYS A 481      10.166  16.870  15.942  1.00 35.34           O
ATOM   1396  CB  LYS A 481      10.722  16.488  12.811  1.00  0.00           C
ATOM   1397  CG  LYS A 481      10.360  17.161  11.492  1.00  0.00           C
ATOM   1398  CD  LYS A 481      10.050  16.096  10.446  1.00  0.00           C
ATOM   1399  CE  LYS A 481       8.731  15.412  10.791  1.00  0.00           C
ATOM   1400  NZ  LYS A 481       7.625  16.365  10.618  1.00  0.00           N
ATOM   1401  N   ILE A 482      12.327  16.378  15.607  1.00 32.69           N
ATOM   1402  CA  ILE A 482      12.456  15.764  16.922  1.00 31.76           C
ATOM   1403  C   ILE A 482      12.454  16.853  17.992  1.00 31.55           C
ATOM   1404  O   ILE A 482      11.942  16.649  19.094  1.00 29.34           O
ATOM   1405  CB  ILE A 482      13.742  14.913  17.028  1.00 32.71           C
ATOM   1406  CG1 ILE A 482      13.696  13.785  15.994  1.00 33.41           C
ATOM   1407  CG2 ILE A 482      13.874  14.337  18.431  1.00 32.59           C
ATOM   1408  CD1 ILE A 482      14.977  12.968  15.908  1.00 33.82           C
ATOM   1409  N   THR A 483      13.026  18.012  17.679  1.00 31.10           N
ATOM   1410  CA  THR A 483      13.022  19.108  18.645  1.00 32.00           C
ATOM   1411  C   THR A 483      11.559  19.483  18.920  1.00 33.33           C
ATOM   1412  O   THR A 483      11.146  19.600  20.071  1.00 32.36           O
ATOM   1413  CB  THR A 483      13.756  20.350  18.110  1.00 32.89           C
ATOM   1414  OG1 THR A 483      15.111  20.011  17.789  1.00 30.04           O
ATOM   1415  CG2 THR A 483      13.755  21.451  19.161  1.00 30.65           C
ATOM   1416  N   ASP A 484      10.785  19.657  17.851  1.00 32.31           N
ATOM   1417  CA  ASP A 484       9.369  20.003  17.965  1.00 34.27           C
ATOM   1418  C   ASP A 484       8.658  18.985  18.840  1.00 33.42           C
ATOM   1419  O   ASP A 484       7.830  19.339  19.674  1.00 34.26           O
ATOM   1420  CB  ASP A 484       8.707  20.014  16.591  1.00 37.77           C
ATOM   1421  CG  ASP A 484       9.270  21.080  15.680  1.00 42.58           C
ATOM   1422  OD1 ASP A 484       9.871  22.045  16.199  1.00 43.65           O
ATOM   1423  OD2 ASP A 484       9.106  20.952  14.445  1.00 43.33           O
ATOM   1424  N   THR A 485       8.998  17.715  18.647  1.00 34.17           N
ATOM   1425  CA  THR A 485       8.397  16.635  19.414  1.00 34.41           C
ATOM   1426  C   THR A 485       8.709  16.756  20.904  1.00 35.12           C
ATOM   1427  O   THR A 485       7.819  16.596  21.745  1.00 31.86           O
ATOM   1428  CB  THR A 485       8.875  15.268  18.886  1.00 33.55           C
ATOM   1429  OG1 THR A 485       8.401  15.093  17.542  1.00 36.59           O
ATOM   1430  CG2 THR A 485       8.347  14.138  19.753  1.00 31.06           C
ATOM   1431  N   LEU A 486       9.966  17.046  21.229  1.00 33.65           N
ATOM   1432  CA  LEU A 486      10.368  17.192  22.621  1.00 34.31           C
ATOM   1433  C   LEU A 486       9.597  18.348  23.256  1.00 34.74           C
ATOM   1434  O   LEU A 486       9.078  18.224  24.363  1.00 35.84           O
ATOM   1435  CB  LEU A 486      11.880  17.449  22.721  1.00 32.27           C
ATOM   1436  CG  LEU A 486      12.777  16.202  22.754  1.00 35.79           C
ATOM   1437  CD1 LEU A 486      14.232  16.614  22.521  1.00 32.36           C
ATOM   1438  CD2 LEU A 486      12.635  15.482  24.105  1.00 29.60           C
ATOM   1439  N   ILE A 487       9.512  19.468  22.548  1.00 35.61           N
ATOM   1440  CA  ILE A 487       8.787  20.625  23.063  1.00 36.85           C
ATOM   1441  C   ILE A 487       7.315  20.258  23.276  1.00 38.35           C
ATOM   1442  O   ILE A 487       6.709  20.629  24.281  1.00 38.82           O
ATOM   1443  CB  ILE A 487       8.889  21.826  22.095  1.00 37.08           C
ATOM   1444  CG1 ILE A 487      10.291  22.443  22.181  1.00 35.53           C
ATOM   1445  CG2 ILE A 487       7.833  22.884  22.443  1.00 39.98           C
ATOM   1446  CD1 ILE A 487      10.634  23.040  23.544  1.00 33.39           C
ATOM   1447  N   HIS A 488       6.749  19.520  22.327  1.00 40.47           N
ATOM   1448  CA  HIS A 488       5.357  19.096  22.428  1.00 42.41           C
ATOM   1449  C   HIS A 488       5.154  18.254  23.685  1.00 42.55           C
ATOM   1450  O   HIS A 488       4.233  18.498  24.466  1.00 43.08           O
ATOM   1451  CB  HIS A 488       4.962  18.282  21.197  1.00 44.60           C
ATOM   1452  CG  HIS A 488       3.612  17.648  21.305  1.00 47.99           C
ATOM   1453  ND1 HIS A 488       3.440  16.299  21.533  1.00 51.01           N
ATOM   1454  CD2 HIS A 488       2.369  18.176  21.214  1.00 47.70           C
ATOM   1455  CE1 HIS A 488       2.149  16.023  21.577  1.00 51.12           C
ATOM   1456  NE2 HIS A 488       1.477  17.144  21.386  1.00 49.80           N
ATOM   1457  N   LEU A 489       6.022  17.267  23.880  1.00 39.61           N
ATOM   1458  CA  LEU A 489       5.936  16.399  25.048  1.00 39.43           C
ATOM   1459  C   LEU A 489       5.972  17.204  26.339  1.00 40.08           C
ATOM   1460  O   LEU A 489       5.267  16.890  27.297  1.00 38.41           O
ATOM   1461  CB  LEU A 489       7.087  15.396  25.049  1.00 38.64           C
ATOM   1462  CG  LEU A 489       6.961  14.242  24.056  1.00 38.19           C
ATOM   1463  CD1 LEU A 489       8.259  13.457  24.027  1.00 38.14           C
ATOM   1464  CD2 LEU A 489       5.799  13.345  24.459  1.00 41.04           C
ATOM   1465  N   MET A 490       6.798  18.246  26.353  1.00 39.67           N
ATOM   1466  CA  MET A 490       6.939  19.102  27.523  1.00 41.38           C
ATOM   1467  C   MET A 490       5.718  20.004  27.717  1.00 42.32           C
ATOM   1468  O   MET A 490       5.296  20.259  28.847  1.00 41.15           O
ATOM   1469  CB  MET A 490       8.207  19.953  27.395  1.00 39.18           C
ATOM   1470  CG  MET A 490       9.495  19.169  27.608  1.00 41.15           C
ATOM   1471  SD  MET A 490      10.978  20.104  27.158  1.00 35.78           S
ATOM   1472  CE  MET A 490      12.178  18.774  27.055  1.00 39.43           C
ATOM   1473  N   ALA A 491       5.161  20.496  26.615  1.00 43.36           N
ATOM   1474  CA  ALA A 491       3.983  21.350  26.693  1.00 44.40           C
ATOM   1475  C   ALA A 491       2.841  20.510  27.251  1.00 46.58           C
ATOM   1476  O   ALA A 491       2.073  20.968  28.095  1.00 45.09           O
ATOM   1477  CB  ALA A 491       3.622  21.878  25.311  1.00 43.76           C
ATOM   1478  N   LYS A 492       2.753  19.268  26.784  1.00 46.84           N
ATOM   1479  CA  LYS A 492       1.712  18.350  27.222  1.00 50.33           C
ATOM   1480  C   LYS A 492       1.842  18.024  28.701  1.00 51.70           C
ATOM   1481  O   LYS A 492       0.845  17.784  29.379  1.00 53.76           O
ATOM   1482  CB  LYS A 492       1.772  17.053  26.411  1.00 50.63           C
ATOM   1483  CG  LYS A 492       1.086  17.135  25.063  1.00 54.28           C
ATOM   1484  CD  LYS A 492      -0.001  16.084  24.929  1.00 59.35           C
ATOM   1485  CE  LYS A 492      -0.988  16.453  23.826  1.00 62.00           C
ATOM   1486  NZ  LYS A 492      -1.351  15.281  22.976  1.00 63.28           N
ATOM   1487  N   ALA A 493       3.072  18.012  29.199  1.00 50.34           N
ATOM   1488  CA  ALA A 493       3.319  17.709  30.599  1.00 49.44           C
ATOM   1489  C   ALA A 493       2.972  18.892  31.499  1.00 49.43           C
ATOM   1490  O   ALA A 493       3.087  18.801  32.721  1.00 51.71           O
ATOM   1491  CB  ALA A 493       4.776  17.314  30.794  1.00 50.68           C
ATOM   1492  N   GLY A 494       2.565  20.006  30.894  1.00 48.74           N
ATOM   1493  CA  GLY A 494       2.197  21.177  31.672  1.00 47.28           C
ATOM   1494  C   GLY A 494       3.330  22.130  32.007  1.00 46.03           C
ATOM   1495  O   GLY A 494       3.217  22.937  32.926  1.00 44.04           O
ATOM   1496  N   LEU A 495       4.436  22.040  31.278  1.00 45.47           N
ATOM   1497  CA  LEU A 495       5.556  22.934  31.532  1.00 43.33           C
ATOM   1498  C   LEU A 495       5.282  24.260  30.837  1.00 42.79           C
ATOM   1499  O   LEU A 495       4.670  24.291  29.767  1.00 43.07           O
ATOM   1500  CB  LEU A 495       6.853  22.332  30.986  1.00 44.68           C
ATOM   1501  CG  LEU A 495       7.682  21.464  31.936  1.00 43.93           C
ATOM   1502  CD1 LEU A 495       6.913  20.205  32.257  1.00 44.93           C
ATOM   1503  CD2 LEU A 495       9.028  21.115  31.289  1.00 42.99           C
ATOM   1504  N   THR A 496       5.725  25.355  31.443  1.00 43.17           N
ATOM   1505  CA  THR A 496       5.536  26.671  30.842  1.00 43.93           C
ATOM   1506  C   THR A 496       6.489  26.795  29.658  1.00 45.82           C
ATOM   1507  O   THR A 496       7.400  25.982  29.503  1.00 43.57           O
ATOM   1508  CB  THR A 496       5.867  27.791  31.832  1.00 46.56           C
ATOM   1509  OG1 THR A 496       7.229  27.655  32.259  1.00 44.36           O
ATOM   1510  CG2 THR A 496       4.945  27.724  33.038  1.00 46.02           C
ATOM   1511  N   LEU A 497       6.285  27.815  28.831  1.00 45.36           N
ATOM   1512  CA  LEU A 497       7.141  28.030  27.669  1.00 45.00           C
ATOM   1513  C   LEU A 497       8.605  28.139  28.084  1.00 44.68           C
ATOM   1514  O   LEU A 497       9.475  27.504  27.486  1.00 44.99           O
ATOM   1515  CB  LEU A 497       6.723  29.300  26.925  1.00 46.24           C
ATOM   1516  CG  LEU A 497       5.972  29.097  25.604  1.00 50.31           C
ATOM   1517  CD1 LEU A 497       5.892  30.426  24.862  1.00 50.88           C
ATOM   1518  CD2 LEU A 497       6.676  28.046  24.754  1.00 50.77           C
ATOM   1519  N   GLN A 498       8.873  28.941  29.110  1.00 40.83           N
ATOM   1520  CA  GLN A 498      10.233  29.113  29.601  1.00 40.37           C
ATOM   1521  C   GLN A 498      10.787  27.789  30.130  1.00 39.39           C
ATOM   1522  O   GLN A 498      11.938  27.441  29.870  1.00 35.20           O
ATOM   1523  CB  GLN A 498      10.260  30.162  30.706  1.00 43.45           C
ATOM   1524  CG  GLN A 498      11.595  30.288  31.410  1.00 42.62           C
ATOM   1525  CD  GLN A 498      11.542  31.269  32.564  1.00 46.58           C
ATOM   1526  OE1 GLN A 498      10.584  31.279  33.335  1.00 48.49           O
ATOM   1527  NE2 GLN A 498      12.568  32.099  32.688  1.00 43.65           N
ATOM   1528  N   GLN A 499       9.967  27.056  30.878  1.00 36.19           N
ATOM   1529  CA  GLN A 499      10.388  25.768  31.422  1.00 36.47           C
ATOM   1530  C   GLN A 499      10.651  24.782  30.283  1.00 35.02           C
ATOM   1531  O   GLN A 499      11.430  23.835  30.431  1.00 36.32           O
ATOM   1532  CB  GLN A 499       9.309  25.187  32.334  1.00 38.83           C
ATOM   1533  CG  GLN A 499       9.185  25.841  33.703  1.00 41.32           C
ATOM   1534  CD  GLN A 499       8.060  25.223  34.514  1.00 42.77           C
ATOM   1535  OE1 GLN A 499       7.032  24.832  33.961  1.00 45.79           O
ATOM   1536  NE2 GLN A 499       8.253  25.121  35.827  1.00 43.09           N
ATOM   1537  N   GLN A 500       9.980  24.998  29.158  1.00 34.11           N
ATOM   1538  CA  GLN A 500      10.135  24.137  27.989  1.00 34.25           C
ATOM   1539  C   GLN A 500      11.510  24.349  27.358  1.00 34.82           C
ATOM   1540  O   GLN A 500      12.254  23.386  27.123  1.00 30.54           O
ATOM   1541  CB  GLN A 500       9.042  24.435  26.958  1.00 33.52           C
ATOM   1542  CG  GLN A 500       7.672  23.873  27.316  1.00 35.93           C
ATOM   1543  CD  GLN A 500       6.557  24.418  26.435  1.00 39.67           C
ATOM   1544  OE1 GLN A 500       6.660  24.416  25.208  1.00 39.23           O
ATOM   1545  NE2 GLN A 500       5.482  24.886  27.063  1.00 41.77           N
ATOM   1546  N   HIS A 501      11.835  25.612  27.078  1.00 34.06           N
ATOM   1547  CA  HIS A 501      13.117  25.966  26.479  1.00 37.07           C
ATOM   1548  C   HIS A 501      14.255  25.542  27.395  1.00 35.52           C
ATOM   1549  O   HIS A 501      15.270  24.995  26.946  1.00 36.01           O
ATOM   1550  CB  HIS A 501      13.196  27.476  26.247  1.00 42.96           C
ATOM   1551  CG  HIS A 501      12.044  28.027  25.468  1.00 51.17           C
ATOM   1552  ND1 HIS A 501      11.264  29.068  25.927  1.00 54.39           N
ATOM   1553  CD2 HIS A 501      11.534  27.678  24.264  1.00 52.58           C
ATOM   1554  CE1 HIS A 501      10.325  29.336  25.037  1.00 54.49           C
ATOM   1555  NE2 HIS A 501      10.467  28.507  24.019  1.00 54.77           N
ATOM   1556  N   GLN A 502      14.086  25.798  28.685  1.00 33.87           N
ATOM   1557  CA  GLN A 502      15.110  25.437  29.649  1.00 32.34           C
ATOM   1558  C   GLN A 502      15.340  23.931  29.715  1.00 31.73           C
ATOM   1559  O   GLN A 502      16.484  23.478  29.767  1.00 27.69           O
ATOM   1560  CB  GLN A 502      14.739  25.977  31.031  1.00 35.85           C
ATOM   1561  CG  GLN A 502      14.787  27.498  31.112  1.00 32.50           C
ATOM   1562  CD  GLN A 502      14.420  28.028  32.484  1.00 36.54           C
ATOM   1563  OE1 GLN A 502      14.103  27.261  33.396  1.00 34.30           O
ATOM   1564  NE2 GLN A 502      14.462  29.347  32.639  1.00 35.78           N
ATOM   1565  N   ARG A 503      14.267  23.147  29.705  1.00 30.89           N
ATOM   1566  CA  ARG A 503      14.435  21.704  29.778  1.00 29.59           C
ATOM   1567  C   ARG A 503      15.049  21.152  28.496  1.00 29.74           C
ATOM   1568  O   ARG A 503      15.894  20.259  28.548  1.00 29.21           O
ATOM   1569  CB  ARG A 503      13.106  21.012  30.052  1.00 32.79           C
ATOM   1570  CG  ARG A 503      13.258  19.540  30.399  1.00 30.94           C
ATOM   1571  CD  ARG A 503      11.930  18.935  30.798  1.00 30.70           C
ATOM   1572  NE  ARG A 503      12.018  17.491  30.993  1.00 28.59           N
ATOM   1573  CZ  ARG A 503      12.489  16.908  32.092  1.00 29.24           C
ATOM   1574  NH1 ARG A 503      12.916  17.641  33.113  1.00 30.15           N
ATOM   1575  NH2 ARG A 503      12.514  15.584  32.180  1.00 33.56           N
ATOM   1576  N   LEU A 504      14.622  21.674  27.351  1.00 28.59           N
ATOM   1577  CA  LEU A 504      15.164  21.223  26.076  1.00 29.05           C
ATOM   1578  C   LEU A 504      16.681  21.419  26.090  1.00 29.65           C
ATOM   1579  O   LEU A 504      17.439  20.536  25.675  1.00 26.28           O
ATOM   1580  CB  LEU A 504      14.566  22.023  24.916  1.00 28.23           C
ATOM   1581  CG  LEU A 504      15.327  21.899  23.593  1.00 31.18           C
ATOM   1582  CD1 LEU A 504      15.252  20.452  23.117  1.00 32.07           C
ATOM   1583  CD2 LEU A 504      14.742  22.842  22.542  1.00 30.80           C
ATOM   1584  N   ALA A 505      17.114  22.584  26.567  1.00 28.51           N
ATOM   1585  CA  ALA A 505      18.535  22.899  26.632  1.00 25.86           C
ATOM   1586  C   ALA A 505      19.261  21.976  27.604  1.00 26.31           C
ATOM   1587  O   ALA A 505      20.338  21.462  27.288  1.00 25.65           O
ATOM   1588  CB  ALA A 505      18.736  24.360  27.039  1.00 30.14           C
ATOM   1589  N   GLN A 506      18.679  21.772  28.784  1.00 23.47           N
ATOM   1590  CA  GLN A 506      19.300  20.906  29.785  1.00 27.71           C
ATOM   1591  C   GLN A 506      19.501  19.507  29.216  1.00 24.37           C
ATOM   1592  O   GLN A 506      20.537  18.887  29.440  1.00 26.17           O
ATOM   1593  CB  GLN A 506      18.434  20.797  31.043  1.00 27.55           C
ATOM   1594  CG  GLN A 506      18.414  22.026  31.946  1.00 32.68           C
ATOM   1595  CD  GLN A 506      17.111  22.116  32.736  1.00 39.13           C
ATOM   1596  OE1 GLN A 506      16.321  21.167  32.754  1.00 35.96           O
ATOM   1597  NE2 GLN A 506      16.879  23.257  33.386  1.00 38.38           N
ATOM   1598  N   LEU A 507      18.505  19.016  28.485  1.00 26.51           N
ATOM   1599  CA  LEU A 507      18.577  17.677  27.902  1.00 26.00           C
ATOM   1600  C   LEU A 507      19.649  17.585  26.819  1.00 25.87           C
ATOM   1601  O   LEU A 507      20.421  16.625  26.771  1.00 27.36           O
ATOM   1602  CB  LEU A 507      17.225  17.285  27.294  1.00 31.64           C
ATOM   1603  CG  LEU A 507      16.053  16.961  28.229  1.00 33.10           C
ATOM   1604  CD1 LEU A 507      14.835  16.562  27.388  1.00 33.43           C
ATOM   1605  CD2 LEU A 507      16.432  15.840  29.172  1.00 31.19           C
ATOM   1606  N   LEU A 508      19.704  18.587  25.953  1.00 24.61           N
ATOM   1607  CA  LEU A 508      20.677  18.572  24.865  1.00 23.73           C
ATOM   1608  C   LEU A 508      22.114  18.742  25.345  1.00 22.69           C
ATOM   1609  O   LEU A 508      23.048  18.224  24.730  1.00 20.82           O
ATOM   1610  CB  LEU A 508      20.319  19.646  23.834  1.00 24.04           C
ATOM   1611  CG  LEU A 508      18.981  19.453  23.114  1.00 25.14           C
ATOM   1612  CD1 LEU A 508      18.882  20.433  21.960  1.00 25.24           C
ATOM   1613  CD2 LEU A 508      18.871  18.013  22.594  1.00 27.55           C
ATOM   1614  N   LEU A 509      22.297  19.448  26.454  1.00 23.84           N
ATOM   1615  CA  LEU A 509      23.642  19.642  26.987  1.00 25.83           C
ATOM   1616  C   LEU A 509      24.159  18.317  27.540  1.00 25.79           C
ATOM   1617  O   LEU A 509      25.360  18.062  27.547  1.00 24.19           O
ATOM   1618  CB  LEU A 509      23.636  20.720  28.076  1.00 26.13           C
ATOM   1619  CG  LEU A 509      23.486  22.151  27.547  1.00 28.90           C
ATOM   1620  CD1 LEU A 509      23.524  23.140  28.710  1.00 32.36           C
ATOM   1621  CD2 LEU A 509      24.595  22.455  26.551  1.00 29.11           C
ATOM   1622  N   ILE A 510      23.257  17.456  27.995  1.00 24.51           N
ATOM   1623  CA  ILE A 510      23.704  16.168  28.505  1.00 25.38           C
ATOM   1624  C   ILE A 510      24.326  15.344  27.371  1.00 23.69           C
ATOM   1625  O   ILE A 510      25.206  14.520  27.611  1.00 23.76           O
ATOM   1626  CB  ILE A 510      22.547  15.381  29.170  1.00 28.93           C
ATOM   1627  CG1 ILE A 510      22.127  16.082  30.466  1.00 31.44           C
ATOM   1628  CG2 ILE A 510      23.007  13.973  29.517  1.00 32.28           C
ATOM   1629  CD1 ILE A 510      20.698  15.790  30.896  1.00 37.15           C
ATOM   1630  N   LEU A 511      23.889  15.586  26.136  1.00 24.71           N
ATOM   1631  CA  LEU A 511      24.420  14.862  24.978  1.00 26.02           C
ATOM   1632  C   LEU A 511      25.912  15.151  24.769  1.00 27.11           C
ATOM   1633  O   LEU A 511      26.641  14.332  24.214  1.00 25.33           O
ATOM   1634  CB  LEU A 511      23.629  15.226  23.714  1.00 23.65           C
ATOM   1635  CG  LEU A 511      22.154  14.800  23.657  1.00 26.14           C
ATOM   1636  CD1 LEU A 511      21.649  14.921  22.222  1.00 26.66           C
ATOM   1637  CD2 LEU A 511      21.990  13.365  24.145  1.00 25.69           C
ATOM   1638  N   SER A 512      26.372  16.318  25.211  1.00 25.04           N
ATOM   1639  CA  SER A 512      27.787  16.638  25.077  1.00 23.76           C
ATOM   1640  C   SER A 512      28.597  15.767  26.049  1.00 23.56           C
ATOM   1641  O   SER A 512      29.745  15.387  25.769  1.00 21.88           O
ATOM   1642  CB  SER A 512      28.023  18.130  25.357  1.00 26.90           C
ATOM   1643  OG  SER A 512      29.271  18.327  25.986  1.00 37.54           O
ATOM   1644  N  BHIS A 513      28.010  15.453  27.201  0.50 21.24           N
ATOM   1645  CA BHIS A 513      28.696  14.606  28.173  0.50 21.24           C
ATOM   1646  C  BHIS A 513      28.719  13.170  27.651  0.50 19.58           C
ATOM   1647  O  BHIS A 513      29.708  12.457  27.807  0.50 22.85           O
ATOM   1648  CB BHIS A 513      27.991  14.636  29.534  0.50 21.70           C
ATOM   1649  CG BHIS A 513      28.800  14.031  30.642  0.50 24.54           C
ATOM   1650  ND1BHIS A 513      28.285  13.106  31.523  0.50 27.35           N
ATOM   1651  CD2BHIS A 513      30.095  14.211  31.001  0.50 24.48           C
ATOM   1652  CE1BHIS A 513      29.226  12.741  32.377  0.50 25.16           C
ATOM   1653  NE2BHIS A 513      30.334  13.397  32.082  0.50 25.92           N
ATOM   1654  N   ILE A 514      27.630  12.751  27.018  1.00 20.33           N
ATOM   1655  CA  ILE A 514      27.570  11.393  26.492  1.00 20.85           C
ATOM   1656  C   ILE A 514      28.640  11.256  25.397  1.00 20.53           C
ATOM   1657  O   ILE A 514      29.302  10.228  25.288  1.00 22.18           O
ATOM   1658  CB  ILE A 514      26.156  11.087  25.952  1.00 27.44           C
ATOM   1659  CG1 ILE A 514      25.186  10.964  27.137  1.00 27.75           C
ATOM   1660  CG2 ILE A 514      26.169   9.802  25.124  1.00 29.04           C
ATOM   1661  CD1 ILE A 514      23.752  10.649  26.753  1.00 34.22           C
ATOM   1662  N   ARG A 515      28.822  12.292  24.587  1.00 20.27           N
ATOM   1663  CA  ARG A 515      29.861  12.243  23.553  1.00 21.61           C
ATOM   1664  C   ARG A 515      31.222  12.090  24.223  1.00 21.27           C
ATOM   1665  O   ARG A 515      32.075  11.312  23.787  1.00 19.99           O
ATOM   1666  CB  ARG A 515      29.861  13.536  22.728  1.00 22.65           C
ATOM   1667  CG  ARG A 515      31.002  13.612  21.735  1.00 25.99           C
ATOM   1668  CD  ARG A 515      30.665  12.819  20.488  1.00 28.63           C
ATOM   1669  NE  ARG A 515      29.581  13.481  19.787  1.00 36.02           N
ATOM   1670  CZ  ARG A 515      29.616  13.826  18.508  1.00 38.91           C
ATOM   1671  NH1 ARG A 515      30.689  13.566  17.776  1.00 35.03           N
ATOM   1672  NH2 ARG A 515      28.580  14.458  17.973  1.00 40.02           N
ATOM   1673  N   HIS A 516      31.419  12.843  25.295  1.00 23.09           N
ATOM   1674  CA  HIS A 516      32.674  12.812  26.034  1.00 24.63           C
ATOM   1675  C   HIS A 516      32.963  11.391  26.537  1.00 24.14           C
ATOM   1676  O   HIS A 516      34.056  10.855  26.360  1.00 23.87           O
ATOM   1677  CB  HIS A 516      32.565  13.791  27.206  1.00 24.19           C
ATOM   1678  CG  HIS A 516      33.825  13.946  27.990  1.00 31.41           C
ATOM   1679  ND1 HIS A 516      34.935  14.584  27.488  1.00 33.24           N
ATOM   1680  CD2 HIS A 516      34.138  13.586  29.257  1.00 35.85           C
ATOM   1681  CE1 HIS A 516      35.880  14.614  28.410  1.00 35.06           C
ATOM   1682  NE2 HIS A 516      35.422  14.014  29.494  1.00 33.03           N
ATOM   1683  N   MET A 517      31.966  10.786  27.167  1.00 20.92           N
ATOM   1684  CA  MET A 517      32.107   9.435  27.684  1.00 24.40           C
ATOM   1685  C   MET A 517      32.398   8.449  26.565  1.00 23.30           C
ATOM   1686  O   MET A 517      33.211   7.548  26.730  1.00 25.85           O
ATOM   1687  CB  MET A 517      30.835   9.036  28.426  1.00 24.01           C
ATOM   1688  CG  MET A 517      30.604   9.904  29.651  1.00 26.93           C
ATOM   1689  SD  MET A 517      29.437   9.221  30.788  1.00 26.57           S
ATOM   1690  CE  MET A 517      27.912   9.383  29.807  1.00 23.58           C
ATOM   1691  N   SER A 518      31.735   8.614  25.424  1.00 21.99           N
ATOM   1692  CA  SER A 518      31.978   7.718  24.302  1.00 22.86           C
ATOM   1693  C   SER A 518      33.432   7.863  23.812  1.00 25.47           C
ATOM   1694  O   SER A 518      34.109   6.868  23.534  1.00 22.52           O
ATOM   1695  CB  SER A 518      30.977   8.025  23.174  1.00 21.98           C
ATOM   1696  OG  SER A 518      31.281   7.335  21.976  1.00 23.80           O
ATOM   1697  N   ASN A 519      33.924   9.098  23.712  1.00 22.61           N
ATOM   1698  CA  ASN A 519      35.298   9.309  23.260  1.00 21.92           C
ATOM   1699  C   ASN A 519      36.295   8.644  24.202  1.00 21.21           C
ATOM   1700  O   ASN A 519      37.255   8.018  23.754  1.00 23.20           O
ATOM   1701  CB  ASN A 519      35.609  10.806  23.157  1.00 24.63           C
ATOM   1702  CG  ASN A 519      34.866  11.468  22.022  1.00 29.01           C
ATOM   1703  OD1 ASN A 519      34.662  10.863  20.966  1.00 31.82           O
ATOM   1704  ND2 ASN A 519      34.458  12.712  22.226  1.00 28.48           N
ATOM   1705  N   LYS A 520      36.072   8.782  25.504  1.00 22.92           N
ATOM   1706  CA  LYS A 520      36.965   8.171  26.487  1.00 26.24           C
ATOM   1707  C   LYS A 520      36.899   6.646  26.374  1.00 27.50           C
ATOM   1708  O   LYS A 520      37.914   5.959  26.497  1.00 27.06           O
ATOM   1709  CB  LYS A 520      36.581   8.592  27.912  1.00 27.26           C
ATOM   1710  CG  LYS A 520      36.617  10.100  28.173  1.00 33.46           C
ATOM   1711  CD  LYS A 520      37.961  10.710  27.811  1.00 41.95           C
ATOM   1712  CE  LYS A 520      39.048  10.307  28.801  1.00 43.37           C
ATOM   1713  NZ  LYS A 520      39.859  11.479  29.254  1.00 47.41           N
ATOM   1714  N   GLY A 521      35.704   6.118  26.140  1.00 25.41           N
ATOM   1715  CA  GLY A 521      35.562   4.678  26.002  1.00 26.36           C
ATOM   1716  C   GLY A 521      36.254   4.169  24.752  1.00 26.92           C
ATOM   1717  O   GLY A 521      36.923   3.128  24.774  1.00 26.76           O
ATOM   1718  N  AMET A 522      36.101   4.894  23.650  0.50 25.73           N
ATOM   1719  CA AMET A 522      36.727   4.491  22.401  0.50 27.77           C
ATOM   1720  C  AMET A 522      38.242   4.532  22.511  0.50 29.26           C
ATOM   1721  O  AMET A 522      38.939   3.743  21.870  0.50 31.90           O
ATOM   1722  CB AMET A 522      36.267   5.395  21.258  0.50 27.02           C
ATOM   1723  CG AMET A 522      34.827   5.161  20.864  0.50 26.41           C
ATOM   1724  SD AMET A 522      34.584   3.586  20.020  0.50 27.30           S
ATOM   1725  CE AMET A 522      33.141   4.017  19.031  0.50 32.89           C
ATOM   1726  N   GLU A 523      38.749   5.452  23.324  1.00 30.76           N
ATOM   1727  CA  GLU A 523      40.189   5.576  23.514  1.00 34.04           C
ATOM   1728  C   GLU A 523      40.717   4.260  24.060  1.00 34.32           C
ATOM   1729  O   GLU A 523      41.733   3.748  23.594  1.00 33.65           O
ATOM   1730  CB  GLU A 523      40.515   6.726  24.480  1.00 35.76           C
ATOM   1731  CG  GLU A 523      40.658   8.079  23.784  1.00 43.15           C
ATOM   1732  CD  GLU A 523      40.560   9.265  24.739  1.00 46.75           C
ATOM   1733  OE1 GLU A 523      41.212   9.225  25.805  1.00 43.28           O
ATOM   1734  OE2 GLU A 523      39.832  10.240  24.417  1.00 47.72           O
ATOM   1735  N   HIS A 524      40.021   3.699  25.042  1.00 36.18           N
ATOM   1736  CA  HIS A 524      40.455   2.427  25.607  1.00 39.13           C
ATOM   1737  C   HIS A 524      40.290   1.281  24.613  1.00 37.99           C
ATOM   1738  O   HIS A 524      41.225   0.520  24.371  1.00 37.67           O
ATOM   1739  CB  HIS A 524      39.678   2.092  26.877  1.00 40.53           C
ATOM   1740  CG  HIS A 524      40.061   0.773  27.473  1.00 48.63           C
ATOM   1741  ND1 HIS A 524      39.246  -0.337  27.412  1.00 49.43           N
ATOM   1742  CD2 HIS A 524      41.192   0.375  28.104  1.00 49.07           C
ATOM   1743  CE1 HIS A 524      39.858  -1.362  27.979  1.00 51.20           C
ATOM   1744  NE2 HIS A 524      41.040  -0.956  28.407  1.00 52.58           N
ATOM   1745  N   LEU A 525      39.101   1.161  24.035  1.00 36.91           N
ATOM   1746  CA  LEU A 525      38.832   0.093  23.084  1.00 36.90           C
ATOM   1747  C   LEU A 525      39.859   0.057  21.954  1.00 41.08           C
ATOM   1748  O   LEU A 525      40.244  -1.016  21.487  1.00 40.27           O
ATOM   1749  CB  LEU A 525      37.417   0.241  22.514  1.00 35.59           C
ATOM   1750  CG  LEU A 525      36.268   0.108  23.526  1.00 32.63           C
ATOM   1751  CD1 LEU A 525      34.936   0.246  22.811  1.00 31.11           C
ATOM   1752  CD2 LEU A 525      36.342  -1.240  24.238  1.00 35.59           C
ATOM   1753  N   TYR A 526      40.314   1.227  21.522  1.00 43.53           N
ATOM   1754  CA  TYR A 526      41.300   1.297  20.448  1.00 48.93           C
ATOM   1755  C   TYR A 526      42.671   0.871  20.964  1.00 50.04           C
ATOM   1756  O   TYR A 526      43.472   0.303  20.224  1.00 50.70           O
ATOM   1757  CB  TYR A 526      41.375   2.722  19.890  1.00 51.41           C
ATOM   1758  CG  TYR A 526      42.305   2.878  18.704  1.00 57.28           C
ATOM   1759  CD1 TYR A 526      43.653   3.200  18.884  1.00 58.08           C
ATOM   1760  CD2 TYR A 526      41.834   2.718  17.400  1.00 58.41           C
ATOM   1761  CE1 TYR A 526      44.510   3.359  17.789  1.00 60.63           C
ATOM   1762  CE2 TYR A 526      42.681   2.875  16.304  1.00 60.68           C
ATOM   1763  CZ  TYR A 526      44.016   3.195  16.504  1.00 60.54           C
ATOM   1764  OH  TYR A 526      44.850   3.343  15.417  1.00 63.20           O
ATOM   1765  N   SER A 527      42.930   1.139  22.240  1.00 52.68           N
ATOM   1766  CA  SER A 527      44.205   0.791  22.857  1.00 56.06           C
ATOM   1767  C   SER A 527      44.365  -0.718  23.054  1.00 60.72           C
ATOM   1768  O   SER A 527      45.398  -1.185  23.535  1.00 61.12           O
ATOM   1769  CB  SER A 527      44.351   1.517  24.199  1.00 55.23           C
ATOM   1770  OG  SER A 527      43.752   0.789  25.257  1.00 52.55           O
ATOM   1771  N   MET A 528      43.336  -1.472  22.678  1.00 64.25           N
ATOM   1772  CA  MET A 528      43.347  -2.930  22.788  1.00 67.77           C
ATOM   1773  C   MET A 528      42.727  -3.502  21.513  1.00 70.29           C
ATOM   1774  O   MET A 528      42.170  -4.602  21.513  1.00 71.92           O
ATOM   1775  CB  MET A 528      42.534  -3.381  24.008  1.00 67.55           C
ATOM   1776  CG  MET A 528      41.237  -2.607  24.222  1.00 69.58           C
ATOM   1777  SD  MET A 528      39.895  -3.569  24.983  1.00 70.27           S
ATOM   1778  CE  MET A 528      39.231  -4.413  23.554  1.00 71.44           C
ATOM   1779  N   LYS A 529      42.835  -2.739  20.428  1.00 71.60           N
ATOM   1780  CA  LYS A 529      42.274  -3.122  19.136  1.00 72.45           C
ATOM   1781  C   LYS A 529      42.812  -4.438  18.587  1.00 72.87           C
ATOM   1782  O   LYS A 529      43.989  -4.762  18.752  1.00 70.54           O
ATOM   1783  CB  LYS A 529      42.512  -2.022  18.118  1.00  0.00           C
ATOM   1784  CG  LYS A 529      41.755  -2.351  16.835  1.00  0.00           C
ATOM   1785  CD  LYS A 529      41.967  -1.234  15.819  1.00  0.00           C
ATOM   1786  CE  LYS A 529      41.132  -1.514  14.574  1.00  0.00           C
ATOM   1787  NZ  LYS A 529      41.678  -2.686  13.873  1.00  0.00           N
ATOM   1788  N   CYS A 530      41.928  -5.188  17.932  1.00 74.83           N
ATOM   1789  CA  CYS A 530      42.277  -6.474  17.327  1.00 76.93           C
ATOM   1790  C   CYS A 530      43.102  -6.222  16.063  1.00 78.24           C
ATOM   1791  O   CYS A 530      43.241  -5.078  15.627  1.00 79.14           O
ATOM   1792  CB  CYS A 530      41.002  -7.245  16.952  1.00 77.24           C
ATOM   1793  SG  CYS A 530      40.448  -8.492  18.148  1.00 79.18           S
ATOM   1794  N   LYS A 531      43.648  -7.290  15.482  1.00 78.41           N
ATOM   1795  CA  LYS A 531      44.433  -7.185  14.263  1.00 78.19           C
ATOM   1796  C   LYS A 531      43.502  -7.473  13.063  1.00 78.13           C
ATOM   1797  O   LYS A 531      42.532  -6.734  12.834  1.00 78.16           O
ATOM   1798  CB  LYS A 531      45.574  -8.177  14.291  1.00  0.00           C
ATOM   1799  CG  LYS A 531      46.548  -7.821  15.410  1.00  0.00           C
ATOM   1800  CD  LYS A 531      47.382  -6.614  14.993  1.00  0.00           C
ATOM   1801  CE  LYS A 531      46.799  -5.352  15.619  1.00  0.00           C
ATOM   1802  NZ  LYS A 531      45.777  -4.789  14.725  1.00  0.00           N
ATOM   1803  N   ASN A 532      43.782  -8.537  12.320  1.00 77.76           N
ATOM   1804  CA  ASN A 532      42.981  -8.904  11.154  1.00 77.32           C
ATOM   1805  C   ASN A 532      41.483  -9.083  11.428  1.00 77.43           C
ATOM   1806  O   ASN A 532      40.892 -10.126  11.119  1.00 78.14           O
ATOM   1807  CB  ASN A 532      43.533 -10.160  10.526  1.00  0.00           C
ATOM   1808  CG  ASN A 532      42.932 -10.387   9.146  1.00  0.00           C
ATOM   1809  OD1 ASN A 532      43.505  -9.973   8.140  1.00  0.00           O
ATOM   1810  ND2 ASN A 532      41.774 -11.049   9.099  1.00  0.00           N
ATOM   1811  N   VAL A 533      40.867  -8.054  11.994  1.00 76.36           N
ATOM   1812  CA  VAL A 533      39.442  -8.096  12.280  1.00 74.13           C
ATOM   1813  C   VAL A 533      38.687  -7.143  11.350  1.00 73.10           C
ATOM   1814  O   VAL A 533      39.023  -5.960  11.252  1.00 74.20           O
ATOM   1815  CB  VAL A 533      39.154  -7.716  13.750  1.00 74.37           C
ATOM   1816  CG1 VAL A 533      39.690  -6.327  14.046  1.00 73.93           C
ATOM   1817  CG2 VAL A 533      37.662  -7.781  14.020  1.00 74.71           C
ATOM   1818  N   VAL A 534      37.671  -7.666  10.664  1.00 69.94           N
ATOM   1819  CA  VAL A 534      36.866  -6.866   9.746  1.00 66.83           C
ATOM   1820  C   VAL A 534      36.463  -5.540  10.392  1.00 64.14           C
ATOM   1821  O   VAL A 534      35.895  -5.519  11.485  1.00 63.77           O
ATOM   1822  CB  VAL A 534      35.620  -7.626   9.337  1.00  0.00           C
ATOM   1823  CG1 VAL A 534      34.722  -6.710   8.512  1.00  0.00           C
ATOM   1824  CG2 VAL A 534      36.004  -8.845   8.506  1.00  0.00           C
ATOM   1825  N   PRO A 535      36.756  -4.415   9.718  1.00 61.33           N
ATOM   1826  CA  PRO A 535      36.424  -3.077  10.229  1.00 57.05           C
ATOM   1827  C   PRO A 535      34.944  -2.903  10.571  1.00 52.97           C
ATOM   1828  O   PRO A 535      34.068  -3.462   9.908  1.00 52.05           O
ATOM   1829  CB  PRO A 535      36.867  -2.135   9.106  1.00 59.19           C
ATOM   1830  CG  PRO A 535      37.024  -3.008   7.893  1.00 62.48           C
ATOM   1831  CD  PRO A 535      37.424  -4.354   8.407  1.00 61.73           C
ATOM   1832  N   LEU A 536      34.672  -2.120  11.609  1.00 48.72           N
ATOM   1833  CA  LEU A 536      33.301  -1.874  12.042  1.00 44.88           C
ATOM   1834  C   LEU A 536      32.434  -1.432  10.871  1.00 43.08           C
ATOM   1835  O   LEU A 536      31.287  -1.862  10.734  1.00 41.47           O
ATOM   1836  CB  LEU A 536      33.280  -0.796  13.128  1.00 43.92           C
ATOM   1837  CG  LEU A 536      32.267  -0.911  14.273  1.00 42.93           C
ATOM   1838  CD1 LEU A 536      31.919   0.490  14.744  1.00 43.00           C
ATOM   1839  CD2 LEU A 536      31.021  -1.654  13.835  1.00 39.75           C
ATOM   1840  N   TYR A 537      32.992  -0.575  10.024  1.00 42.64           N
ATOM   1841  CA  TYR A 537      32.269  -0.065   8.866  1.00 42.83           C
ATOM   1842  C   TYR A 537      31.683  -1.199   8.031  1.00 42.74           C
ATOM   1843  O   TYR A 537      30.499  -1.191   7.696  1.00 41.40           O
ATOM   1844  CB  TYR A 537      33.200   0.786   7.997  1.00 44.70           C
ATOM   1845  CG  TYR A 537      32.483   1.558   6.914  1.00 47.92           C
ATOM   1846  CD1 TYR A 537      32.190   0.964   5.687  1.00 48.97           C
ATOM   1847  CD2 TYR A 537      32.073   2.876   7.123  1.00 50.33           C
ATOM   1848  CE1 TYR A 537      31.503   1.660   4.693  1.00 53.03           C
ATOM   1849  CE2 TYR A 537      31.383   3.584   6.135  1.00 54.33           C
ATOM   1850  CZ  TYR A 537      31.101   2.967   4.924  1.00 54.79           C
ATOM   1851  OH  TYR A 537      30.400   3.647   3.952  1.00 56.57           O
ATOM   1852  N   ASP A 538      32.521  -2.176   7.703  1.00 44.45           N
ATOM   1853  CA  ASP A 538      32.097  -3.309   6.894  1.00 45.31           C
ATOM   1854  C   ASP A 538      31.070  -4.195   7.588  1.00 43.38           C
ATOM   1855  O   ASP A 538      30.176  -4.738   6.940  1.00 43.81           O
ATOM   1856  CB  ASP A 538      33.322  -4.126   6.480  1.00 51.36           C
ATOM   1857  CG  ASP A 538      34.361  -3.284   5.748  1.00 56.66           C
ATOM   1858  OD1 ASP A 538      34.096  -2.079   5.526  1.00 59.90           O
ATOM   1859  OD2 ASP A 538      35.436  -3.820   5.397  1.00 57.52           O
ATOM   1860  N   LEU A 539      31.193  -4.344   8.902  1.00 41.49           N
ATOM   1861  CA  LEU A 539      30.244  -5.157   9.655  1.00 39.01           C
ATOM   1862  C   LEU A 539      28.891  -4.451   9.652  1.00 36.21           C
ATOM   1863  O   LEU A 539      27.848  -5.069   9.437  1.00 35.21           O
ATOM   1864  CB  LEU A 539      30.734  -5.350  11.093  1.00 41.82           C
ATOM   1865  CG  LEU A 539      29.770  -6.065  12.044  1.00 46.43           C
ATOM   1866  CD1 LEU A 539      29.298  -7.378  11.424  1.00 47.48           C
ATOM   1867  CD2 LEU A 539      30.473  -6.319  13.378  1.00 46.30           C
ATOM   1868  N   LEU A 540      28.918  -3.146   9.895  1.00 35.34           N
ATOM   1869  CA  LEU A 540      27.702  -2.336   9.903  1.00 35.63           C
ATOM   1870  C   LEU A 540      27.059  -2.414   8.510  1.00 35.37           C
ATOM   1871  O   LEU A 540      25.845  -2.583   8.371  1.00 33.34           O
ATOM   1872  CB  LEU A 540      28.062  -0.877  10.219  1.00 37.58           C
ATOM   1873  CG  LEU A 540      27.856  -0.252  11.605  1.00 40.77           C
ATOM   1874  CD1 LEU A 540      27.526  -1.299  12.644  1.00 39.41           C
ATOM   1875  CD2 LEU A 540      29.114   0.505  11.984  1.00 41.38           C
ATOM   1876  N   LEU A 541      27.892  -2.289   7.483  1.00 36.97           N
ATOM   1877  CA  LEU A 541      27.418  -2.339   6.101  1.00 38.74           C
ATOM   1878  C   LEU A 541      26.723  -3.676   5.833  1.00 39.91           C
ATOM   1879  O   LEU A 541      25.616  -3.714   5.298  1.00 36.84           O
ATOM   1880  CB  LEU A 541      28.591  -2.152   5.146  1.00 40.23           C
ATOM   1881  CG  LEU A 541      28.301  -2.111   3.643  1.00 41.66           C
ATOM   1882  CD1 LEU A 541      27.184  -1.130   3.349  1.00 42.94           C
ATOM   1883  CD2 LEU A 541      29.572  -1.715   2.908  1.00 44.17           C
ATOM   1884  N   GLU A 542      27.366  -4.770   6.229  1.00 41.06           N
ATOM   1885  CA  GLU A 542      26.790  -6.097   6.037  1.00 41.85           C
ATOM   1886  C   GLU A 542      25.414  -6.196   6.691  1.00 41.71           C
ATOM   1887  O   GLU A 542      24.472  -6.721   6.101  1.00 42.92           O
ATOM   1888  CB  GLU A 542      27.718  -7.169   6.621  1.00 44.09           C
ATOM   1889  CG  GLU A 542      27.009  -8.456   7.053  1.00 50.07           C
ATOM   1890  CD  GLU A 542      26.434  -9.244   5.887  1.00 55.43           C
ATOM   1891  OE1 GLU A 542      26.841  -8.995   4.728  1.00 56.08           O
ATOM   1892  OE2 GLU A 542      25.570 -10.118   6.130  1.00 58.38           O
ATOM   1893  N   MET A 543      25.298  -5.686   7.914  1.00 40.11           N
ATOM   1894  CA  MET A 543      24.036  -5.732   8.633  1.00 36.25           C
ATOM   1895  C   MET A 543      23.000  -4.769   8.072  1.00 34.96           C
ATOM   1896  O   MET A 543      21.807  -5.073   8.048  1.00 35.38           O
ATOM   1897  CB  MET A 543      24.270  -5.425  10.111  1.00 39.67           C
ATOM   1898  CG  MET A 543      25.136  -6.459  10.808  1.00 41.70           C
ATOM   1899  SD  MET A 543      24.917  -6.444  12.603  1.00 46.63           S
ATOM   1900  CE  MET A 543      25.324  -4.749  12.964  1.00 39.79           C
ATOM   1901  N   LEU A 544      23.457  -3.605   7.630  1.00 32.95           N
ATOM   1902  CA  LEU A 544      22.559  -2.602   7.074  1.00 37.21           C
ATOM   1903  C   LEU A 544      22.148  -2.940   5.640  1.00 39.34           C
ATOM   1904  O   LEU A 544      20.971  -2.842   5.294  1.00 39.73           O
ATOM   1905  CB  LEU A 544      23.225  -1.225   7.111  1.00 34.70           C
ATOM   1906  CG  LEU A 544      23.269  -0.563   8.491  1.00 32.55           C
ATOM   1907  CD1 LEU A 544      24.285   0.563   8.479  1.00 32.86           C
ATOM   1908  CD2 LEU A 544      21.897  -0.028   8.845  1.00 29.13           C
ATOM   1909  N   ASP A 545      23.117  -3.337   4.817  1.00 40.98           N
ATOM   1910  CA  ASP A 545      22.850  -3.685   3.418  1.00 41.02           C
ATOM   1911  C   ASP A 545      22.116  -5.015   3.349  1.00 42.71           C
ATOM   1912  O   ASP A 545      22.680  -6.029   2.929  1.00 44.00           O
ATOM   1913  CB  ASP A 545      24.160  -3.780   2.620  1.00 38.26           C
ATOM   1914  CG  ASP A 545      23.922  -3.937   1.120  1.00 36.06           C
ATOM   1915  OD1 ASP A 545      22.768  -3.735   0.690  1.00 31.07           O
ATOM   1916  OD2 ASP A 545      24.881  -4.264   0.380  1.00 33.25           O
ATOM   1917  N   ALA A 546      20.853  -5.009   3.755  1.00 43.05           N
ATOM   1918  CA  ALA A 546      20.069  -6.229   3.746  1.00 46.42           C
ATOM   1919  C   ALA A 546      19.193  -6.361   2.508  1.00 49.31           C
ATOM   1920  O   ALA A 546      18.804  -5.368   1.884  1.00 48.78           O
ATOM   1921  CB  ALA A 546      19.212  -6.304   5.006  1.00 47.29           C
ATOM   1922  N   HIS A 547      18.895  -7.605   2.152  1.00 50.91           N
ATOM   1923  CA  HIS A 547      18.042  -7.884   1.006  1.00 53.96           C
ATOM   1924  C   HIS A 547      16.603  -7.937   1.518  1.00 55.78           C
ATOM   1925  O   HIS A 547      16.361  -7.795   2.720  1.00 54.50           O
ATOM   1926  CB  HIS A 547      18.431  -9.223   0.368  1.00 53.20           C
ATOM   1927  CG  HIS A 547      18.395 -10.382   1.317  1.00 55.99           C
ATOM   1928  ND1 HIS A 547      19.395 -11.329   1.371  1.00 56.95           N
ATOM   1929  CD2 HIS A 547      17.477 -10.753   2.241  1.00 54.90           C
ATOM   1930  CE1 HIS A 547      19.095 -12.232   2.287  1.00 56.10           C
ATOM   1931  NE2 HIS A 547      17.936 -11.906   2.829  1.00 58.13           N
ATOM   1932  N   ARG A 548      15.653  -8.140   0.612  1.00 57.17           N
ATOM   1933  CA  ARG A 548      14.245  -8.212   0.986  1.00 61.03           C
ATOM   1934  C   ARG A 548      13.695  -9.608   0.710  1.00 62.23           C
ATOM   1935  O   ARG A 548      12.501  -9.781   0.466  1.00 62.67           O
ATOM   1936  CB  ARG A 548      13.432  -7.171   0.208  1.00 63.32           C
ATOM   1937  CG  ARG A 548      14.272  -6.222  -0.636  1.00 68.10           C
ATOM   1938  CD  ARG A 548      13.447  -5.061  -1.170  1.00 72.46           C
ATOM   1939  NE  ARG A 548      13.701  -3.826  -0.432  1.00 77.05           N
ATOM   1940  CZ  ARG A 548      14.863  -3.177  -0.429  1.00 79.49           C
ATOM   1941  NH1 ARG A 548      15.891  -3.643  -1.128  1.00 81.30           N
ATOM   1942  NH2 ARG A 548      15.001  -2.062   0.278  1.00 80.06           N
ATOM   1943  N   LEU A 549      14.576 -10.603   0.756  1.00 63.08           N
ATOM   1944  CA  LEU A 549      14.188 -11.985   0.507  1.00 64.86           C
ATOM   1945  C   LEU A 549      13.431 -12.574   1.702  1.00 67.38           C
ATOM   1946  O   LEU A 549      12.759 -13.600   1.578  1.00 68.08           O
ATOM   1947  CB  LEU A 549      15.433 -12.828   0.195  1.00 63.02           C
ATOM   1948  CG  LEU A 549      16.461 -12.191  -0.753  1.00 61.37           C
ATOM   1949  CD1 LEU A 549      17.700 -13.074  -0.878  1.00 58.84           C
ATOM   1950  CD2 LEU A 549      15.823 -11.972  -2.108  1.00 59.03           C
ATOM   1951  N   HIS A 550      13.541 -11.920   2.856  1.00 68.31           N
ATOM   1952  CA  HIS A 550      12.858 -12.378   4.065  1.00 70.20           C
ATOM   1953  C   HIS A 550      11.557 -11.602   4.275  1.00 71.50           C
ATOM   1954  O   HIS A 550      10.940 -11.684   5.340  1.00 71.14           O
ATOM   1955  CB  HIS A 550      13.753 -12.190   5.298  1.00 70.78           C
ATOM   1956  CG  HIS A 550      14.977 -13.054   5.306  1.00 71.14           C
ATOM   1957  ND1 HIS A 550      15.793 -13.172   6.411  1.00 71.10           N
ATOM   1958  CD2 HIS A 550      15.538 -13.821   4.341  1.00 70.70           C
ATOM   1959  CE1 HIS A 550      16.805 -13.972   6.126  1.00 71.37           C
ATOM   1960  NE2 HIS A 550      16.674 -14.380   4.876  1.00 69.93           N
ATOM   1961  N   ALA A 551      11.143 -10.851   3.258  1.00 72.40           N
ATOM   1962  CA  ALA A 551       9.919 -10.056   3.339  1.00 73.79           C
ATOM   1963  C   ALA A 551       8.658 -10.920   3.266  1.00 74.86           C
ATOM   1964  O   ALA A 551       7.684 -10.473   2.622  1.00 75.80           O
ATOM   1965  CB  ALA A 551       9.904  -9.013   2.221  1.00 73.27           C
ATOM   1966  N   PRO A 552       8.651 -12.026   3.852  1.00 73.88           N
TER    1967      PRO A 552
END



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elNémo is maintained by Yves-Henri Sanejouand.
It was developed by Karsten Suhre.
Between 2003 and 2014, it was hosted by IGS (Marseille).
Last modification: April 25th, 2023.