Should you encounter any unexpected behaviour,
please let us know.

* EXP_1IKQ_unrelaxed_rank_001_alphafold2_ptm_model_3_seed_000 *

CA strain for 24021912353031383

--- normal mode 9 ---

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
LYS 1 ARG 2 0.0000

ARG 2 TRP 3 0.0001

TRP 3 SER 4 -0.0687

SER 4 GLU 5 0.0001

GLU 5 TRP 6 -0.0001

TRP 6 ALA 7 0.0544

ALA 7 SER 8 0.0000

SER 8 GLY 9 0.0003

GLY 9 LYS 10 -0.0035

LYS 10 VAL 11 -0.0002

VAL 11 LEU 12 0.0000

LEU 12 CYS 13 0.0187

CYS 13 LEU 14 -0.0001

LEU 14 LEU 15 0.0004

LEU 15 ASP 16 0.0227

ASP 16 PRO 17 0.0000

PRO 17 LEU 18 0.0000

LEU 18 ASP 19 0.0048

ASP 19 GLY 20 0.0002

GLY 20 VAL 21 0.0003

VAL 21 TYR 22 -0.0627

TYR 22 ASN 23 0.0001

ASN 23 TYR 24 0.0001

TYR 24 LEU 25 0.0693

LEU 25 ALA 26 0.0004

ALA 26 GLN 27 -0.0000

GLN 27 GLN 28 0.0999

GLN 28 ARG 29 -0.0001

ARG 29 CYS 30 -0.0004

CYS 30 ASN 31 0.0175

ASN 31 LEU 32 -0.0000

LEU 32 ASP 33 -0.0002

ASP 33 ASP 34 -0.1037

ASP 34 THR 35 0.0001

THR 35 TRP 36 0.0002

TRP 36 GLU 37 -0.0141

GLU 37 GLY 38 0.0004

GLY 38 LYS 39 0.0000

LYS 39 ILE 40 0.0046

ILE 40 TYR 41 -0.0001

TYR 41 ARG 42 -0.0001

ARG 42 VAL 43 -0.0114

VAL 43 LEU 44 -0.0001

LEU 44 ALA 45 0.0000

ALA 45 GLY 46 0.0451

GLY 46 ASN 47 -0.0001

ASN 47 PRO 48 -0.0000

PRO 48 ALA 49 0.0497

ALA 49 LYS 50 -0.0001

LYS 50 HIS 51 -0.0002

HIS 51 ASP 52 0.0391

ASP 52 LEU 53 0.0000

LEU 53 ASP 54 0.0001

ASP 54 ILE 55 0.1056

ILE 55 LYS 56 -0.0001

LYS 56 PRO 57 0.0003

PRO 57 THR 58 0.0343

THR 58 VAL 59 -0.0003

VAL 59 ILE 60 -0.0002

ILE 60 SER 61 0.1979

SER 61 HIS 62 -0.0003

HIS 62 ARG 63 0.0003

ARG 63 LEU 64 0.0240

LEU 64 HIS 65 -0.0002

HIS 65 PHE 66 -0.0002

PHE 66 PRO 67 0.0073

PRO 67 GLU 68 -0.0001

GLU 68 GLY 69 0.0001

GLY 69 GLY 70 0.0123

GLY 70 SER 71 -0.0001

SER 71 LEU 72 0.0002

LEU 72 ALA 73 0.0048

ALA 73 ALA 74 0.0001

ALA 74 LEU 75 0.0005

LEU 75 THR 76 0.0041

THR 76 ALA 77 0.0002

ALA 77 HIS 78 0.0002

HIS 78 GLN 79 0.0059

GLN 79 ALA 80 0.0002

ALA 80 CYS 81 -0.0001

CYS 81 HIS 82 -0.0029

HIS 82 LEU 83 -0.0001

LEU 83 PRO 84 0.0002

PRO 84 LEU 85 0.0211

LEU 85 GLU 86 0.0001

GLU 86 THR 87 -0.0002

THR 87 PHE 88 -0.0049

PHE 88 THR 89 -0.0000

THR 89 ARG 90 0.0002

ARG 90 HIS 91 0.0179

HIS 91 ARG 92 -0.0001

ARG 92 GLN 93 0.0004

GLN 93 PRO 94 -0.0832

PRO 94 ARG 95 0.0003

ARG 95 GLY 96 0.0000

GLY 96 TRP 97 -0.0408

TRP 97 GLU 98 0.0003

GLU 98 GLN 99 -0.0002

GLN 99 LEU 100 0.0134

LEU 100 GLU 101 0.0006

GLU 101 GLN 102 0.0001

GLN 102 CYS 103 -0.0045

CYS 103 GLY 104 -0.0002

GLY 104 TYR 105 0.0002

TYR 105 PRO 106 -0.0341

PRO 106 VAL 107 0.0000

VAL 107 GLN 108 0.0003

GLN 108 ARG 109 -0.0221

ARG 109 LEU 110 -0.0002

LEU 110 VAL 111 0.0003

VAL 111 ALA 112 0.0121

ALA 112 LEU 113 -0.0001

LEU 113 TYR 114 -0.0002

TYR 114 LEU 115 0.0172

LEU 115 ALA 116 -0.0000

ALA 116 ALA 117 -0.0001

ALA 117 ARG 118 0.0020

ARG 118 LEU 119 0.0001

LEU 119 SER 120 0.0000

SER 120 TRP 121 0.0041

TRP 121 ASN 122 0.0003

ASN 122 GLN 123 0.0001

GLN 123 VAL 124 0.0007

VAL 124 ASP 125 -0.0004

ASP 125 GLN 126 -0.0002

GLN 126 VAL 127 0.0050

VAL 127 ILE 128 -0.0003

ILE 128 ARG 129 0.0005

ARG 129 ASN 130 0.0012

ASN 130 ALA 131 0.0001

ALA 131 LEU 132 0.0003

LEU 132 ALA 133 -0.0135

ALA 133 SER 134 0.0000

SER 134 PRO 135 -0.0001

PRO 135 GLY 136 0.0082

GLY 136 SER 137 0.0001

SER 137 GLY 138 -0.0000

GLY 138 GLY 139 -0.0126

GLY 139 ASP 140 -0.0001

ASP 140 LEU 141 -0.0002

LEU 141 GLY 142 0.0019

GLY 142 GLU 143 0.0000

GLU 143 ALA 144 -0.0000

ALA 144 ILE 145 -0.0007

ILE 145 ARG 146 -0.0000

ARG 146 GLU 147 -0.0002

GLU 147 GLN 148 -0.0063

GLN 148 PRO 149 -0.0003

PRO 149 GLU 150 -0.0000

GLU 150 GLN 151 0.0255

GLN 151 ALA 152 -0.0003

ALA 152 ARG 153 -0.0005

ARG 153 LEU 154 -0.0012

LEU 154 ALA 155 -0.0001

ALA 155 LEU 156 0.0001

LEU 156 THR 157 -0.0063

THR 157 LEU 158 0.0001

LEU 158 ALA 159 0.0001

ALA 159 ALA 160 -0.0071

ALA 160 ALA 161 -0.0001

ALA 161 GLU 162 -0.0001

GLU 162 SER 163 -0.0192

SER 163 GLU 164 -0.0000

GLU 164 ARG 165 -0.0004

ARG 165 PHE 166 -0.0245

PHE 166 VAL 167 -0.0001

VAL 167 ARG 168 0.0004

ARG 168 GLN 169 -0.0013

GLN 169 GLY 170 -0.0003

GLY 170 THR 171 0.0001

THR 171 GLY 172 0.0037

GLY 172 ASN 173 0.0002

ASN 173 ASP 174 -0.0003

ASP 174 GLU 175 0.0218

GLU 175 ALA 176 -0.0000

ALA 176 GLY 177 -0.0001

GLY 177 ALA 178 0.0131

ALA 178 ALA 179 0.0002

ALA 179 ASN 180 -0.0001

ASN 180 ALA 181 0.0266

ALA 181 ASP 182 0.0002

ASP 182 VAL 183 -0.0002

VAL 183 VAL 184 0.0312

VAL 184 SER 185 -0.0001

SER 185 LEU 186 0.0001

LEU 186 THR 187 0.0076

THR 187 CYS 188 0.0000

CYS 188 PRO 189 0.0001

PRO 189 VAL 190 -0.0428

VAL 190 ALA 191 -0.0000

ALA 191 ALA 192 -0.0000

ALA 192 GLY 193 -0.0416

GLY 193 GLU 194 0.0000

GLU 194 CYS 195 0.0000

CYS 195 ALA 196 -0.0540

ALA 196 GLY 197 -0.0002

GLY 197 PRO 198 -0.0000

PRO 198 ALA 199 0.0265

ALA 199 ASP 200 0.0002

ASP 200 SER 201 0.0002

SER 201 GLY 202 0.0133

GLY 202 ASP 203 -0.0001

ASP 203 ALA 204 0.0000

ALA 204 LEU 205 -0.0060

LEU 205 LEU 206 -0.0002

LEU 206 GLU 207 0.0001

GLU 207 ARG 208 -0.0251

ARG 208 ASN 209 0.0001

ASN 209 TYR 210 0.0004

TYR 210 PRO 211 0.0394

PRO 211 THR 212 -0.0001

THR 212 GLY 213 -0.0003

GLY 213 ALA 214 0.0163

ALA 214 GLU 215 -0.0003

GLU 215 PHE 216 0.0002

PHE 216 LEU 217 -0.0282

LEU 217 GLY 218 0.0000

GLY 218 ASP 219 -0.0003

ASP 219 GLY 220 -0.0043

GLY 220 GLY 221 -0.0002

GLY 221 ASP 222 -0.0002

ASP 222 VAL 223 -0.0085

VAL 223 SER 224 0.0002

SER 224 PHE 225 -0.0000

PHE 225 SER 226 0.0153

SER 226 THR 227 0.0003

THR 227 ARG 228 0.0000

ARG 228 GLY 229 -0.0223

GLY 229 THR 230 -0.0003

THR 230 GLN 231 0.0001

GLN 231 ASN 232 -0.0227

ASN 232 TRP 233 -0.0000

TRP 233 THR 234 0.0000

THR 234 VAL 235 0.0053

VAL 235 GLU 236 0.0001

GLU 236 ARG 237 0.0003

ARG 237 LEU 238 -0.0022

LEU 238 LEU 239 -0.0002

LEU 239 GLN 240 -0.0001

GLN 240 ALA 241 0.0039

ALA 241 HIS 242 0.0003

HIS 242 ARG 243 -0.0000

ARG 243 GLN 244 0.0028

GLN 244 LEU 245 -0.0004

LEU 245 GLU 246 0.0002

GLU 246 GLU 247 0.0294

GLU 247 ARG 248 -0.0003

ARG 248 GLY 249 0.0004

GLY 249 TYR 250 0.0369

TYR 250 VAL 251 -0.0001

VAL 251 PHE 252 -0.0000

PHE 252 VAL 253 0.0016

VAL 253 GLY 254 0.0001

GLY 254 TYR 255 -0.0001

TYR 255 HIS 256 0.0046

HIS 256 GLY 257 -0.0003

GLY 257 THR 258 0.0000

THR 258 PHE 259 0.0098

PHE 259 LEU 260 0.0001

LEU 260 GLU 261 -0.0004

GLU 261 ALA 262 -0.0127

ALA 262 ALA 263 0.0003

ALA 263 GLN 264 0.0002

GLN 264 SER 265 -0.0040

SER 265 ILE 266 0.0001

ILE 266 VAL 267 -0.0001

VAL 267 PHE 268 0.0457

PHE 268 GLY 269 0.0001

GLY 269 GLY 270 -0.0002

GLY 270 VAL 271 0.0278

VAL 271 ARG 272 -0.0004

ARG 272 ALA 273 -0.0001

ALA 273 ARG 274 0.0197

ARG 274 SER 275 0.0002

SER 275 GLN 276 0.0002

GLN 276 ASP 277 0.0010

ASP 277 LEU 278 0.0000

LEU 278 ASP 279 -0.0000

ASP 279 ALA 280 0.0428

ALA 280 ILE 281 0.0003

ILE 281 TRP 282 0.0003

TRP 282 ARG 283 -0.0175

ARG 283 GLY 284 -0.0000

GLY 284 PHE 285 0.0002

PHE 285 TYR 286 -0.0128

TYR 286 ILE 287 0.0004

ILE 287 ALA 288 -0.0002

ALA 288 GLY 289 -0.0258

GLY 289 ASP 290 -0.0004

ASP 290 PRO 291 0.0002

PRO 291 ALA 292 0.0005

ALA 292 LEU 293 -0.0000

LEU 293 ALA 294 -0.0003

ALA 294 TYR 295 0.0038

TYR 295 GLY 296 0.0001

GLY 296 TYR 297 0.0001

TYR 297 ALA 298 0.0167

ALA 298 GLN 299 0.0000

GLN 299 ASP 300 0.0005

ASP 300 GLN 301 -0.0430

GLN 301 GLU 302 0.0000

GLU 302 PRO 303 -0.0001

PRO 303 ASP 304 -0.0055

ASP 304 ALA 305 0.0001

ALA 305 ARG 306 -0.0001

ARG 306 GLY 307 0.0096

GLY 307 ARG 308 0.0000

ARG 308 ILE 309 0.0001

ILE 309 ARG 310 -0.0308

ARG 310 ASN 311 -0.0002

ASN 311 GLY 312 -0.0002

GLY 312 ALA 313 -0.0373

ALA 313 LEU 314 -0.0003

LEU 314 LEU 315 -0.0001

LEU 315 ARG 316 -0.0194

ARG 316 VAL 317 0.0001

VAL 317 TYR 318 0.0002

TYR 318 VAL 319 -0.0220

VAL 319 PRO 320 -0.0000

PRO 320 ARG 321 0.0000

ARG 321 SER 322 -0.0089

SER 322 SER 323 -0.0000

SER 323 LEU 324 -0.0001

LEU 324 PRO 325 -0.0293

PRO 325 GLY 326 -0.0000

GLY 326 PHE 327 -0.0001

PHE 327 TYR 328 -0.0076

TYR 328 ARG 329 -0.0001

ARG 329 THR 330 0.0002

THR 330 SER 331 -0.0016

SER 331 LEU 332 -0.0001

LEU 332 THR 333 0.0005

THR 333 LEU 334 -0.0169

LEU 334 ALA 335 -0.0000

ALA 335 ALA 336 -0.0000

ALA 336 PRO 337 0.0136

PRO 337 GLU 338 0.0001

GLU 338 ALA 339 -0.0000

ALA 339 ALA 340 -0.0153

ALA 340 GLY 341 0.0000

GLY 341 GLU 342 -0.0002

GLU 342 VAL 343 -0.0112

VAL 343 GLU 344 -0.0001

GLU 344 ARG 345 -0.0001

ARG 345 LEU 346 -0.0305

LEU 346 ILE 347 -0.0002

ILE 347 GLY 348 0.0000

GLY 348 HIS 349 0.0384

HIS 349 PRO 350 0.0001

PRO 350 LEU 351 0.0000

LEU 351 PRO 352 0.0104

PRO 352 LEU 353 -0.0001

LEU 353 ARG 354 0.0001

ARG 354 LEU 355 0.0080

LEU 355 ASP 356 -0.0001

ASP 356 ALA 357 0.0000

ALA 357 ILE 358 -0.0141

ILE 358 THR 359 -0.0001

THR 359 GLY 360 0.0003

GLY 360 PRO 361 -0.0196

PRO 361 GLU 362 0.0000

GLU 362 GLU 363 -0.0003

GLU 363 GLU 364 -0.0024

GLU 364 GLY 365 -0.0004

GLY 365 GLY 366 0.0003

GLY 366 ARG 367 0.0404

ARG 367 LEU 368 0.0003

LEU 368 GLU 369 0.0004

GLU 369 THR 370 -0.0208

THR 370 ILE 371 -0.0000

ILE 371 LEU 372 -0.0000

LEU 372 GLY 373 -0.0166

GLY 373 TRP 374 0.0001

TRP 374 PRO 375 0.0003

PRO 375 LEU 376 0.0219

LEU 376 ALA 377 0.0001

ALA 377 GLU 378 0.0001

GLU 378 ARG 379 0.0084

ARG 379 THR 380 0.0002

THR 380 VAL 381 0.0001

VAL 381 VAL 382 -0.0217

VAL 382 ILE 383 -0.0003

ILE 383 PRO 384 0.0001

PRO 384 SER 385 0.0205

SER 385 ALA 386 -0.0004

ALA 386 ILE 387 0.0000

ILE 387 PRO 388 -0.0269

PRO 388 THR 389 0.0001

THR 389 ASP 390 -0.0000

ASP 390 PRO 391 -0.0144

PRO 391 ARG 392 -0.0000

ARG 392 ASN 393 0.0002

ASN 393 VAL 394 -0.0022

VAL 394 GLY 395 0.0001

GLY 395 GLY 396 0.0002

GLY 396 ASP 397 0.0007

ASP 397 LEU 398 -0.0002

LEU 398 ASP 399 0.0001

ASP 399 PRO 400 0.0036

PRO 400 SER 401 0.0002

SER 401 SER 402 -0.0002

SER 402 ILE 403 -0.0095

ILE 403 PRO 404 0.0001

PRO 404 ASP 405 -0.0005

ASP 405 LYS 406 0.0028

LYS 406 GLU 407 0.0002

GLU 407 GLN 408 -0.0005

GLN 408 ALA 409 0.0043

ALA 409 ILE 410 -0.0001

ILE 410 SER 411 -0.0003

SER 411 ALA 412 -0.0094

ALA 412 LEU 413 0.0000

LEU 413 PRO 414 -0.0002

PRO 414 ASP 415 -0.0157

ASP 415 TYR 416 -0.0003

TYR 416 ALA 417 -0.0004

ALA 417 SER 418 0.0241

SER 418 GLN 419 -0.0001

GLN 419 PRO 420 -0.0000

PRO 420 GLY 421 0.0389

GLY 421 LYS 422 0.0001

If you find results from this site helpful for your research, please cite one of our papers:

K. Suhre & Y.H. Sanejouand, ElNemo: a normal mode web-server for protein movement analysis and the generation of templates for molecular replacement. Nucleic Acids Research, 32, W610-W614, 2004.
K. Suhre & Y.H. Sanejouand, On the potential of normal mode analysis for solving difficult molecular replacement problems. Acta Cryst. D vol.60, p796-799, 2004 © International Union of Crystallography.

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.

Should you encounter any unexpected behaviour, please let us know.

*** EXP_1IKQ_unrelaxed_rank_001_alphafold2_ptm_model_3_seed_000 ***

CA strain for 24021912353031383

--- normal mode 9 ---

Should you encounter any unexpected behaviour,
please let us know.

* EXP_1IKQ_unrelaxed_rank_001_alphafold2_ptm_model_3_seed_000 *