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 16 ---

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 -0.0001

ARG 2 TRP 3 0.0001

TRP 3 SER 4 0.2033

SER 4 GLU 5 -0.0001

GLU 5 TRP 6 -0.0002

TRP 6 ALA 7 0.0509

ALA 7 SER 8 -0.0000

SER 8 GLY 9 0.0000

GLY 9 LYS 10 0.1663

LYS 10 VAL 11 0.0000

VAL 11 LEU 12 0.0001

LEU 12 CYS 13 -0.1083

CYS 13 LEU 14 -0.0000

LEU 14 LEU 15 -0.0001

LEU 15 ASP 16 -0.0270

ASP 16 PRO 17 0.0002

PRO 17 LEU 18 -0.0003

LEU 18 ASP 19 -0.0448

ASP 19 GLY 20 0.0002

GLY 20 VAL 21 0.0000

VAL 21 TYR 22 -0.1615

TYR 22 ASN 23 0.0002

ASN 23 TYR 24 -0.0001

TYR 24 LEU 25 0.0516

LEU 25 ALA 26 0.0002

ALA 26 GLN 27 -0.0003

GLN 27 GLN 28 0.1255

GLN 28 ARG 29 0.0003

ARG 29 CYS 30 0.0001

CYS 30 ASN 31 0.3024

ASN 31 LEU 32 -0.0003

LEU 32 ASP 33 0.0000

ASP 33 ASP 34 -0.0420

ASP 34 THR 35 -0.0001

THR 35 TRP 36 0.0001

TRP 36 GLU 37 -0.0468

GLU 37 GLY 38 0.0002

GLY 38 LYS 39 -0.0000

LYS 39 ILE 40 0.0682

ILE 40 TYR 41 -0.0001

TYR 41 ARG 42 -0.0001

ARG 42 VAL 43 0.0126

VAL 43 LEU 44 0.0001

LEU 44 ALA 45 -0.0001

ALA 45 GLY 46 0.0766

GLY 46 ASN 47 0.0003

ASN 47 PRO 48 -0.0001

PRO 48 ALA 49 0.0895

ALA 49 LYS 50 0.0001

LYS 50 HIS 51 -0.0001

HIS 51 ASP 52 0.0216

ASP 52 LEU 53 -0.0002

LEU 53 ASP 54 -0.0001

ASP 54 ILE 55 0.1421

ILE 55 LYS 56 0.0005

LYS 56 PRO 57 0.0001

PRO 57 THR 58 -0.1337

THR 58 VAL 59 -0.0001

VAL 59 ILE 60 -0.0002

ILE 60 SER 61 -0.1585

SER 61 HIS 62 -0.0001

HIS 62 ARG 63 0.0004

ARG 63 LEU 64 -0.1894

LEU 64 HIS 65 0.0000

HIS 65 PHE 66 -0.0001

PHE 66 PRO 67 -0.0459

PRO 67 GLU 68 0.0002

GLU 68 GLY 69 -0.0000

GLY 69 GLY 70 -0.0644

GLY 70 SER 71 -0.0002

SER 71 LEU 72 -0.0001

LEU 72 ALA 73 0.0193

ALA 73 ALA 74 0.0004

ALA 74 LEU 75 0.0004

LEU 75 THR 76 0.0104

THR 76 ALA 77 0.0001

ALA 77 HIS 78 -0.0003

HIS 78 GLN 79 -0.0241

GLN 79 ALA 80 0.0001

ALA 80 CYS 81 0.0002

CYS 81 HIS 82 0.0557

HIS 82 LEU 83 -0.0002

LEU 83 PRO 84 0.0001

PRO 84 LEU 85 0.1220

LEU 85 GLU 86 0.0003

GLU 86 THR 87 -0.0003

THR 87 PHE 88 0.0749

PHE 88 THR 89 -0.0003

THR 89 ARG 90 0.0000

ARG 90 HIS 91 -0.1171

HIS 91 ARG 92 -0.0002

ARG 92 GLN 93 -0.0001

GLN 93 PRO 94 0.0990

PRO 94 ARG 95 -0.0000

ARG 95 GLY 96 -0.0001

GLY 96 TRP 97 -0.0215

TRP 97 GLU 98 -0.0001

GLU 98 GLN 99 -0.0002

GLN 99 LEU 100 -0.0187

LEU 100 GLU 101 0.0002

GLU 101 GLN 102 0.0002

GLN 102 CYS 103 -0.0215

CYS 103 GLY 104 0.0003

GLY 104 TYR 105 -0.0000

TYR 105 PRO 106 0.1471

PRO 106 VAL 107 0.0001

VAL 107 GLN 108 -0.0000

GLN 108 ARG 109 0.0600

ARG 109 LEU 110 -0.0002

LEU 110 VAL 111 -0.0003

VAL 111 ALA 112 -0.0312

ALA 112 LEU 113 0.0003

LEU 113 TYR 114 -0.0002

TYR 114 LEU 115 -0.0108

LEU 115 ALA 116 -0.0001

ALA 116 ALA 117 -0.0000

ALA 117 ARG 118 -0.0045

ARG 118 LEU 119 -0.0002

LEU 119 SER 120 0.0003

SER 120 TRP 121 -0.0227

TRP 121 ASN 122 0.0002

ASN 122 GLN 123 -0.0001

GLN 123 VAL 124 -0.0077

VAL 124 ASP 125 -0.0001

ASP 125 GLN 126 -0.0002

GLN 126 VAL 127 -0.0040

VAL 127 ILE 128 -0.0004

ILE 128 ARG 129 0.0003

ARG 129 ASN 130 -0.0116

ASN 130 ALA 131 0.0004

ALA 131 LEU 132 -0.0003

LEU 132 ALA 133 -0.0153

ALA 133 SER 134 -0.0001

SER 134 PRO 135 0.0001

PRO 135 GLY 136 0.0136

GLY 136 SER 137 0.0004

SER 137 GLY 138 -0.0002

GLY 138 GLY 139 -0.0089

GLY 139 ASP 140 0.0002

ASP 140 LEU 141 -0.0004

LEU 141 GLY 142 0.0075

GLY 142 GLU 143 -0.0003

GLU 143 ALA 144 0.0002

ALA 144 ILE 145 0.0122

ILE 145 ARG 146 0.0002

ARG 146 GLU 147 -0.0002

GLU 147 GLN 148 0.0232

GLN 148 PRO 149 -0.0001

PRO 149 GLU 150 -0.0000

GLU 150 GLN 151 0.0824

GLN 151 ALA 152 -0.0004

ALA 152 ARG 153 0.0003

ARG 153 LEU 154 -0.0074

LEU 154 ALA 155 -0.0000

ALA 155 LEU 156 0.0002

LEU 156 THR 157 -0.0231

THR 157 LEU 158 -0.0001

LEU 158 ALA 159 0.0002

ALA 159 ALA 160 0.0123

ALA 160 ALA 161 0.0002

ALA 161 GLU 162 0.0000

GLU 162 SER 163 -0.0283

SER 163 GLU 164 -0.0003

GLU 164 ARG 165 0.0001

ARG 165 PHE 166 -0.0494

PHE 166 VAL 167 -0.0003

VAL 167 ARG 168 0.0002

ARG 168 GLN 169 0.0012

GLN 169 GLY 170 0.0002

GLY 170 THR 171 0.0001

THR 171 GLY 172 0.0410

GLY 172 ASN 173 0.0002

ASN 173 ASP 174 0.0001

ASP 174 GLU 175 -0.0176

GLU 175 ALA 176 -0.0002

ALA 176 GLY 177 0.0001

GLY 177 ALA 178 -0.0564

ALA 178 ALA 179 -0.0002

ALA 179 ASN 180 -0.0000

ASN 180 ALA 181 -0.0253

ALA 181 ASP 182 -0.0000

ASP 182 VAL 183 -0.0007

VAL 183 VAL 184 -0.0791

VAL 184 SER 185 0.0002

SER 185 LEU 186 -0.0003

LEU 186 THR 187 0.0973

THR 187 CYS 188 0.0003

CYS 188 PRO 189 0.0002

PRO 189 VAL 190 -0.0517

VAL 190 ALA 191 0.0002

ALA 191 ALA 192 -0.0000

ALA 192 GLY 193 0.0198

GLY 193 GLU 194 -0.0000

GLU 194 CYS 195 0.0000

CYS 195 ALA 196 -0.1316

ALA 196 GLY 197 -0.0003

GLY 197 PRO 198 0.0001

PRO 198 ALA 199 0.0790

ALA 199 ASP 200 0.0001

ASP 200 SER 201 -0.0002

SER 201 GLY 202 0.0206

GLY 202 ASP 203 -0.0003

ASP 203 ALA 204 0.0002

ALA 204 LEU 205 -0.0274

LEU 205 LEU 206 -0.0001

LEU 206 GLU 207 -0.0002

GLU 207 ARG 208 -0.1110

ARG 208 ASN 209 0.0004

ASN 209 TYR 210 -0.0002

TYR 210 PRO 211 -0.0420

PRO 211 THR 212 -0.0001

THR 212 GLY 213 0.0001

GLY 213 ALA 214 0.0143

ALA 214 GLU 215 0.0003

GLU 215 PHE 216 -0.0004

PHE 216 LEU 217 0.0042

LEU 217 GLY 218 -0.0002

GLY 218 ASP 219 -0.0003

ASP 219 GLY 220 -0.0054

GLY 220 GLY 221 0.0002

GLY 221 ASP 222 0.0002

ASP 222 VAL 223 -0.0113

VAL 223 SER 224 0.0004

SER 224 PHE 225 -0.0003

PHE 225 SER 226 0.0181

SER 226 THR 227 0.0001

THR 227 ARG 228 0.0003

ARG 228 GLY 229 -0.0113

GLY 229 THR 230 -0.0000

THR 230 GLN 231 0.0005

GLN 231 ASN 232 -0.0007

ASN 232 TRP 233 -0.0003

TRP 233 THR 234 0.0002

THR 234 VAL 235 0.0129

VAL 235 GLU 236 -0.0001

GLU 236 ARG 237 0.0000

ARG 237 LEU 238 0.0153

LEU 238 LEU 239 -0.0004

LEU 239 GLN 240 0.0000

GLN 240 ALA 241 -0.0104

ALA 241 HIS 242 0.0001

HIS 242 ARG 243 0.0000

ARG 243 GLN 244 -0.0355

GLN 244 LEU 245 0.0002

LEU 245 GLU 246 0.0001

GLU 246 GLU 247 -0.0443

GLU 247 ARG 248 -0.0003

ARG 248 GLY 249 0.0000

GLY 249 TYR 250 -0.0008

TYR 250 VAL 251 0.0002

VAL 251 PHE 252 -0.0002

PHE 252 VAL 253 0.0154

VAL 253 GLY 254 0.0003

GLY 254 TYR 255 -0.0000

TYR 255 HIS 256 0.0222

HIS 256 GLY 257 0.0002

GLY 257 THR 258 -0.0002

THR 258 PHE 259 0.0608

PHE 259 LEU 260 0.0003

LEU 260 GLU 261 -0.0003

GLU 261 ALA 262 0.0244

ALA 262 ALA 263 0.0002

ALA 263 GLN 264 -0.0004

GLN 264 SER 265 -0.0056

SER 265 ILE 266 -0.0002

ILE 266 VAL 267 0.0003

VAL 267 PHE 268 -0.0511

PHE 268 GLY 269 -0.0001

GLY 269 GLY 270 0.0002

GLY 270 VAL 271 -0.0238

VAL 271 ARG 272 -0.0001

ARG 272 ALA 273 -0.0001

ALA 273 ARG 274 0.0434

ARG 274 SER 275 0.0004

SER 275 GLN 276 -0.0000

GLN 276 ASP 277 0.0224

ASP 277 LEU 278 -0.0002

LEU 278 ASP 279 0.0004

ASP 279 ALA 280 0.0735

ALA 280 ILE 281 -0.0000

ILE 281 TRP 282 -0.0003

TRP 282 ARG 283 -0.0733

ARG 283 GLY 284 0.0000

GLY 284 PHE 285 0.0004

PHE 285 TYR 286 -0.0255

TYR 286 ILE 287 0.0001

ILE 287 ALA 288 0.0001

ALA 288 GLY 289 -0.0268

GLY 289 ASP 290 -0.0001

ASP 290 PRO 291 0.0000

PRO 291 ALA 292 -0.0137

ALA 292 LEU 293 0.0002

LEU 293 ALA 294 0.0003

ALA 294 TYR 295 -0.0148

TYR 295 GLY 296 -0.0001

GLY 296 TYR 297 0.0006

TYR 297 ALA 298 -0.0143

ALA 298 GLN 299 -0.0002

GLN 299 ASP 300 0.0002

ASP 300 GLN 301 -0.0522

GLN 301 GLU 302 0.0001

GLU 302 PRO 303 0.0001

PRO 303 ASP 304 -0.0295

ASP 304 ALA 305 -0.0001

ALA 305 ARG 306 0.0000

ARG 306 GLY 307 0.0071

GLY 307 ARG 308 0.0003

ARG 308 ILE 309 0.0001

ILE 309 ARG 310 -0.0002

ARG 310 ASN 311 0.0001

ASN 311 GLY 312 -0.0001

GLY 312 ALA 313 0.0193

ALA 313 LEU 314 0.0003

LEU 314 LEU 315 -0.0001

LEU 315 ARG 316 0.0258

ARG 316 VAL 317 0.0000

VAL 317 TYR 318 0.0003

TYR 318 VAL 319 -0.0026

VAL 319 PRO 320 -0.0001

PRO 320 ARG 321 0.0005

ARG 321 SER 322 0.0193

SER 322 SER 323 0.0004

SER 323 LEU 324 0.0001

LEU 324 PRO 325 0.0651

PRO 325 GLY 326 0.0002

GLY 326 PHE 327 0.0001

PHE 327 TYR 328 0.0480

TYR 328 ARG 329 -0.0003

ARG 329 THR 330 -0.0001

THR 330 SER 331 -0.0314

SER 331 LEU 332 -0.0001

LEU 332 THR 333 0.0002

THR 333 LEU 334 -0.0028

LEU 334 ALA 335 -0.0000

ALA 335 ALA 336 -0.0001

ALA 336 PRO 337 0.0109

PRO 337 GLU 338 -0.0002

GLU 338 ALA 339 0.0002

ALA 339 ALA 340 0.0383

ALA 340 GLY 341 0.0002

GLY 341 GLU 342 0.0004

GLU 342 VAL 343 0.0157

VAL 343 GLU 344 0.0000

GLU 344 ARG 345 -0.0002

ARG 345 LEU 346 0.0407

LEU 346 ILE 347 -0.0000

ILE 347 GLY 348 -0.0003

GLY 348 HIS 349 0.0908

HIS 349 PRO 350 -0.0002

PRO 350 LEU 351 0.0001

LEU 351 PRO 352 -0.0222

PRO 352 LEU 353 0.0000

LEU 353 ARG 354 -0.0001

ARG 354 LEU 355 0.0408

LEU 355 ASP 356 0.0000

ASP 356 ALA 357 -0.0001

ALA 357 ILE 358 -0.0229

ILE 358 THR 359 -0.0003

THR 359 GLY 360 0.0001

GLY 360 PRO 361 -0.0117

PRO 361 GLU 362 -0.0001

GLU 362 GLU 363 0.0005

GLU 363 GLU 364 0.0265

GLU 364 GLY 365 0.0000

GLY 365 GLY 366 0.0000

GLY 366 ARG 367 -0.0213

ARG 367 LEU 368 -0.0000

LEU 368 GLU 369 0.0002

GLU 369 THR 370 -0.0155

THR 370 ILE 371 0.0001

ILE 371 LEU 372 -0.0000

LEU 372 GLY 373 -0.0379

GLY 373 TRP 374 -0.0002

TRP 374 PRO 375 -0.0002

PRO 375 LEU 376 0.0236

LEU 376 ALA 377 -0.0005

ALA 377 GLU 378 -0.0004

GLU 378 ARG 379 -0.0085

ARG 379 THR 380 0.0000

THR 380 VAL 381 -0.0001

VAL 381 VAL 382 -0.0123

VAL 382 ILE 383 -0.0000

ILE 383 PRO 384 0.0004

PRO 384 SER 385 -0.0292

SER 385 ALA 386 -0.0000

ALA 386 ILE 387 -0.0004

ILE 387 PRO 388 0.0093

PRO 388 THR 389 -0.0001

THR 389 ASP 390 -0.0000

ASP 390 PRO 391 0.0071

PRO 391 ARG 392 -0.0001

ARG 392 ASN 393 0.0002

ASN 393 VAL 394 0.0188

VAL 394 GLY 395 -0.0001

GLY 395 GLY 396 -0.0002

GLY 396 ASP 397 0.0516

ASP 397 LEU 398 0.0001

LEU 398 ASP 399 0.0002

ASP 399 PRO 400 0.0265

PRO 400 SER 401 -0.0001

SER 401 SER 402 -0.0001

SER 402 ILE 403 -0.0085

ILE 403 PRO 404 -0.0003

PRO 404 ASP 405 -0.0001

ASP 405 LYS 406 -0.0105

LYS 406 GLU 407 0.0001

GLU 407 GLN 408 0.0002

GLN 408 ALA 409 -0.0001

ALA 409 ILE 410 0.0001

ILE 410 SER 411 -0.0001

SER 411 ALA 412 0.0403

ALA 412 LEU 413 0.0002

LEU 413 PRO 414 0.0001

PRO 414 ASP 415 0.0723

ASP 415 TYR 416 0.0001

TYR 416 ALA 417 0.0002

ALA 417 SER 418 0.1808

SER 418 GLN 419 0.0001

GLN 419 PRO 420 0.0003

PRO 420 GLY 421 0.0206

GLY 421 LYS 422 0.0002

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 16 ---

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

* EXP_1IKQ_unrelaxed_rank_001_alphafold2_ptm_model_3_seed_000 *