This graph displays the distance variation between successive pairs of CA atoms
in the two extreme conformations that were computed for this mode (DQMIN/DQMAX).
Large distance variations can be an indicator for residue pairs that support the
important strain in that particular normal mode movement.
Note that residue pairs between chain breaks or at flexible ends of the protein
may also exhibit large CA-CA distance variations.
If more than one residues ae grouped together into a rigid block (NRBL>1), CA-CA distance variations
between CA atoms in the same block will be very low.
This feature is still experimental and will be further developped in the future.
CA i
CA i+1
vari
MET 1
VAL 2
-0.0001
VAL 2
ARG 3
0.0115
ARG 3
GLU 4
-0.0000
GLU 4
GLU 5
-0.0021
GLU 5
VAL 6
-0.0000
VAL 6
ALA 7
0.0160
ALA 7
GLY 8
-0.0000
GLY 8
SER 9
-0.0283
SER 9
THR 10
-0.0002
THR 10
GLN 11
-0.0111
GLN 11
THR 12
-0.0003
THR 12
LEU 13
0.0012
LEU 13
GLN 14
0.0000
GLN 14
TRP 15
-0.0196
TRP 15
LYS 16
0.0000
LYS 16
CYS 17
-0.0208
CYS 17
VAL 18
-0.0003
VAL 18
GLU 19
-0.0080
GLU 19
SER 20
-0.0002
SER 20
ARG 21
-0.0104
ARG 21
VAL 22
0.0005
VAL 22
ASP 23
0.0014
ASP 23
SER 24
0.0002
SER 24
LYS 25
-0.0019
LYS 25
ARG 26
-0.0002
ARG 26
LEU 27
0.0012
LEU 27
TYR 28
0.0000
TYR 28
TYR 29
-0.0022
TYR 29
GLY 30
0.0002
GLY 30
ARG 31
-0.0025
ARG 31
PHE 32
-0.0001
PHE 32
ILE 33
-0.0100
ILE 33
LEU 34
0.0000
LEU 34
SER 35
-0.0068
SER 35
PRO 36
-0.0001
PRO 36
LEU 37
0.0026
LEU 37
ARG 38
0.0004
ARG 38
LYS 39
0.0084
LYS 39
GLY 40
-0.0002
GLY 40
GLN 41
-0.0016
GLN 41
ALA 42
0.0004
ALA 42
ASP 43
0.0044
ASP 43
THR 44
0.0000
THR 44
VAL 45
0.0045
VAL 45
GLY 46
0.0004
GLY 46
ILE 47
-0.0001
ILE 47
ALA 48
-0.0003
ALA 48
LEU 49
-0.0077
LEU 49
ARG 50
0.0006
ARG 50
ARG 51
-0.0002
ARG 51
ALA 52
-0.0004
ALA 52
LEU 53
-0.0006
LEU 53
LEU 54
0.0001
LEU 54
GLY 55
0.0068
GLY 55
GLU 56
0.0002
GLU 56
ILE 57
0.0064
ILE 57
GLU 58
-0.0002
GLU 58
GLY 59
0.0053
GLY 59
ALA 60
-0.0003
ALA 60
CYS 61
0.0002
CYS 61
ILE 62
0.0000
ILE 62
THR 63
-0.0013
THR 63
ARG 64
0.0001
ARG 64
ALA 65
0.0018
ALA 65
LYS 66
0.0001
LYS 66
PHE 67
0.0007
PHE 67
GLY 68
-0.0000
GLY 68
SER 69
-0.0012
SER 69
VAL 70
-0.0002
VAL 70
PRO 71
0.0001
PRO 71
HIS 72
0.0002
HIS 72
GLU 73
-0.0001
GLU 73
TYR 74
0.0002
TYR 74
SER 75
-0.0003
SER 75
THR 76
-0.0001
THR 76
ILE 77
-0.0002
ILE 77
ALA 78
0.0003
ALA 78
GLY 79
-0.0000
GLY 79
ILE 80
-0.0006
ILE 80
GLU 81
-0.0001
GLU 81
GLU 82
0.0003
GLU 82
SER 83
0.0000
SER 83
VAL 84
-0.0000
VAL 84
GLN 85
-0.0002
GLN 85
GLU 86
0.0002
GLU 86
ILE 87
-0.0002
ILE 87
LEU 88
0.0004
LEU 88
LEU 89
-0.0006
LEU 89
ASN 90
-0.0000
ASN 90
LEU 91
-0.0000
LEU 91
LYS 92
0.0001
LYS 92
GLU 93
-0.0016
GLU 93
ILE 94
-0.0002
ILE 94
VAL 95
-0.0002
VAL 95
LEU 96
-0.0000
LEU 96
ARG 97
-0.0024
ARG 97
SER 98
0.0003
SER 98
ASN 99
0.0017
ASN 99
LEU 100
-0.0002
LEU 100
TYR 101
0.0023
TYR 101
GLY 102
-0.0001
GLY 102
VAL 103
0.0004
VAL 103
ARG 104
0.0001
ARG 104
ASP 105
0.0001
ASP 105
ALA 106
0.0000
ALA 106
SER 107
0.0014
SER 107
ILE 108
0.0004
ILE 108
CYS 109
0.0007
CYS 109
VAL 110
0.0004
VAL 110
LYS 111
0.0002
LYS 111
GLY 112
-0.0001
GLY 112
PRO 113
0.0004
PRO 113
ARG 114
-0.0002
ARG 114
TYR 115
-0.0003
TYR 115
ILE 116
0.0003
ILE 116
THR 117
-0.0008
THR 117
ALA 118
-0.0003
ALA 118
GLN 119
0.0005
GLN 119
ASP 120
-0.0003
ASP 120
ILE 121
0.0006
ILE 121
ILE 122
0.0005
ILE 122
LEU 123
-0.0010
LEU 123
PRO 124
0.0001
PRO 124
PRO 125
-0.0007
PRO 125
SER 126
0.0001
SER 126
VAL 127
0.0003
VAL 127
GLU 128
-0.0000
GLU 128
ILE 129
0.0011
ILE 129
VAL 130
-0.0002
VAL 130
ASP 131
-0.0007
ASP 131
THR 132
-0.0001
THR 132
ALA 133
0.0004
ALA 133
GLN 134
-0.0001
GLN 134
PRO 135
-0.0013
PRO 135
ILE 136
0.0001
ILE 136
ALA 137
0.0001
ALA 137
ASN 138
-0.0001
ASN 138
LEU 139
0.0004
LEU 139
THR 140
-0.0001
THR 140
GLU 141
0.0004
GLU 141
PRO 142
0.0001
PRO 142
ILE 143
0.0002
ILE 143
ASP 144
0.0005
ASP 144
PHE 145
0.0007
PHE 145
CYS 146
0.0004
CYS 146
ILE 147
0.0018
ILE 147
ASP 148
-0.0002
ASP 148
LEU 149
0.0013
LEU 149
GLN 150
-0.0003
GLN 150
ILE 151
-0.0001
ILE 151
LYS 152
0.0002
LYS 152
ARG 153
0.0022
ARG 153
ASP 154
0.0000
ASP 154
ARG 155
0.0071
ARG 155
GLY 156
0.0000
GLY 156
TYR 157
0.0090
TYR 157
GLN 158
-0.0003
GLN 158
THR 159
0.0028
THR 159
GLU 160
0.0002
GLU 160
LEU 161
0.0010
LEU 161
ARG 162
-0.0002
ARG 162
LYS 163
0.0000
LYS 163
ASN 164
0.0001
ASN 164
TYR 165
-0.0006
TYR 165
GLN 166
-0.0001
GLN 166
ASP 167
-0.0002
ASP 167
GLY 168
0.0001
GLY 168
SER 169
0.0015
SER 169
TYR 170
-0.0000
TYR 170
PRO 171
0.0026
PRO 171
ILE 172
-0.0002
ILE 172
ASP 173
0.0022
ASP 173
ALA 174
0.0002
ALA 174
VAL 175
0.0035
VAL 175
SER 176
-0.0002
SER 176
MET 177
0.0048
MET 177
PRO 178
0.0001
PRO 178
VAL 179
0.0030
VAL 179
ARG 180
-0.0002
ARG 180
ASN 181
0.0123
ASN 181
VAL 182
-0.0005
VAL 182
ASN 183
0.0156
ASN 183
TYR 184
-0.0000
TYR 184
SER 185
0.0090
SER 185
ILE 186
-0.0002
ILE 186
PHE 187
-0.0026
PHE 187
SER 188
-0.0000
SER 188
CYS 189
0.0106
CYS 189
GLY 190
-0.0001
GLY 190
ASN 191
0.0025
ASN 191
GLY 192
0.0003
GLY 192
ASN 193
0.0009
ASN 193
GLU 194
-0.0004
GLU 194
LYS 195
0.0006
LYS 195
HIS 196
-0.0002
HIS 196
GLU 197
0.0049
GLU 197
ILE 198
-0.0003
ILE 198
LEU 199
0.0004
LEU 199
PHE 200
0.0000
PHE 200
LEU 201
0.0047
LEU 201
GLU 202
0.0000
GLU 202
ILE 203
0.0071
ILE 203
TRP 204
-0.0001
TRP 204
THR 205
0.0048
THR 205
ASN 206
0.0001
ASN 206
GLY 207
-0.0005
GLY 207
SER 208
0.0001
SER 208
LEU 209
-0.0032
LEU 209
THR 210
0.0004
THR 210
PRO 211
-0.0070
PRO 211
LYS 212
-0.0001
LYS 212
GLU 213
-0.0024
GLU 213
ALA 214
0.0001
ALA 214
LEU 215
-0.0070
LEU 215
TYR 216
-0.0002
TYR 216
GLU 217
-0.0057
GLU 217
ALA 218
-0.0003
ALA 218
SER 219
-0.0066
SER 219
ARG 220
-0.0000
ARG 220
ASN 221
-0.0022
ASN 221
LEU 222
0.0003
LEU 222
ILE 223
-0.0017
ILE 223
ASP 224
0.0002
ASP 224
LEU 225
-0.0093
LEU 225
PHE 226
0.0002
PHE 226
LEU 227
-0.0260
LEU 227
PRO 228
0.0000
PRO 228
PHE 229
0.0350
PHE 229
LEU 230
-0.0001
LEU 230
HIS 231
-0.0546
HIS 231
ALA 232
-0.0001
ALA 232
GLU 233
-0.0428
GLU 233
GLU 234
0.0001
GLU 234
GLU 235
0.0051
GLU 235
GLY 236
-0.0001
GLY 236
ALA 237
0.0273
ALA 237
SER 238
-0.0002
SER 238
PHE 239
0.0081
PHE 239
GLU 240
-0.0004
GLU 240
GLU 241
-0.0004
GLU 241
ASN 242
-0.0001
ASN 242
LYS 243
-0.0045
LYS 243
ASN 244
-0.0002
ASN 244
ARG 245
0.0109
ARG 245
PHE 246
-0.0003
PHE 246
THR 247
0.0155
THR 247
PRO 248
0.0001
PRO 248
PRO 249
-0.0049
PRO 249
LEU 250
-0.0002
LEU 250
PHE 251
-0.0173
PHE 251
THR 252
0.0001
THR 252
PHE 253
-0.0141
PHE 253
GLN 254
0.0000
GLN 254
LYS 255
-0.0142
LYS 255
ARG 256
-0.0003
ARG 256
LEU 257
0.0008
LEU 257
THR 258
-0.0000
THR 258
ASN 259
0.0066
ASN 259
LEU 260
0.0002
LEU 260
LYS 261
-0.0077
LYS 261
LYS 262
-0.0003
LYS 262
ASN 263
0.0085
ASN 263
LYS 264
0.0001
LYS 264
LYS 265
0.0300
LYS 265
GLY 266
0.0002
GLY 266
ILE 267
0.0320
ILE 267
PRO 268
-0.0003
PRO 268
LEU 269
-0.0047
LEU 269
ASN 270
-0.0001
ASN 270
CYS 271
-0.0044
CYS 271
ILE 272
-0.0003
ILE 272
PHE 273
0.0033
PHE 273
ILE 274
0.0003
ILE 274
ASP 275
0.0025
ASP 275
GLN 276
-0.0000
GLN 276
LEU 277
0.0034
LEU 277
GLU 278
0.0001
GLU 278
LEU 279
-0.0006
LEU 279
THR 280
0.0000
THR 280
SER 281
-0.0005
SER 281
ARG 282
-0.0002
ARG 282
THR 283
0.0000
THR 283
TYR 284
0.0002
TYR 284
ASN 285
0.0018
ASN 285
CYS 286
-0.0001
CYS 286
LEU 287
-0.0010
LEU 287
LYS 288
0.0001
LYS 288
ARG 289
0.0011
ARG 289
ALA 290
0.0001
ALA 290
ASN 291
-0.0017
ASN 291
ILE 292
-0.0002
ILE 292
HIS 293
-0.0011
HIS 293
THR 294
0.0002
THR 294
LEU 295
-0.0023
LEU 295
LEU 296
-0.0003
LEU 296
ASP 297
-0.0031
ASP 297
LEU 298
0.0003
LEU 298
LEU 299
0.0011
LEU 299
SER 300
0.0001
SER 300
LYS 301
-0.0046
LYS 301
THR 302
-0.0003
THR 302
GLU 303
-0.0012
GLU 303
GLU 304
-0.0000
GLU 304
ASP 305
-0.0002
ASP 305
LEU 306
-0.0000
LEU 306
LEU 307
-0.0006
LEU 307
ARG 308
-0.0004
ARG 308
ILE 309
0.0007
ILE 309
ASP 310
-0.0002
ASP 310
SER 311
-0.0002
SER 311
PHE 312
-0.0001
PHE 312
ARG 313
-0.0000
ARG 313
MET 314
0.0001
MET 314
GLU 315
-0.0008
GLU 315
ASP 316
-0.0001
ASP 316
ARG 317
0.0005
ARG 317
LYS 318
0.0003
LYS 318
HIS 319
-0.0004
HIS 319
ILE 320
0.0001
ILE 320
TRP 321
-0.0002
TRP 321
ASP 322
0.0005
ASP 322
THR 323
0.0003
THR 323
LEU 324
0.0003
LEU 324
GLU 325
-0.0021
GLU 325
LYS 326
-0.0001
LYS 326
HIS 327
0.0007
HIS 327
LEU 328
-0.0000
LEU 328
PRO 329
-0.0015
PRO 329
ILE 330
-0.0002
ILE 330
ASP 331
-0.0004
ASP 331
LEU 332
-0.0004
LEU 332
LEU 333
0.0041
LEU 333
LYS 334
-0.0002
LYS 334
ASN 335
-0.0005
ASN 335
LYS 336
0.0004
LYS 336
LEU 337
-0.0004
LEU 337
SER 338
0.0003
SER 338
PHE 339
0.0004
If you find results from this site helpful for your research, please cite one of our papers:
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.