GPCompReports

DRD2

Gene DRD2 Dopamine receptors Aminergic receptors UniProt P14416
699
Total Contact Pairs
75
Significant Changes
12.59
Max Increase
-7.81
Max Decrease

Interactive snake plot

GPCRdb-style topology. Click the view buttons to recolor residues by different data layers. Toggle contact links to draw significant residue-residue contacts as arcs. Click loop labels (ICL/ECL) to expand or collapse loop regions.

Color convention: blue = active-favoring, red = inactive-favoring.

ICL1 K63 12.48x48 K63 12.48x48 K A64 12.49x49 A64 12.49x49 A L65 12.50x50 L65 12.50x50 L Q66 12.51x51 Q66 12.51x51 Q ICL1ECL1 E99 23.49x49 E99 23.49x49 E W100 23.50x50 W100 23.50x50 W K101 23.51x51 K101 23.51x51 K F102 23.52x52 F102 23.52x52 F ECL1ICL2 P139 34.50x50 P139 34.50x50 P M140 34.51x51 M140 34.51x51 M L141 34.52x52 L141 34.52x52 L Y142 34.53x53 Y142 34.53x53 Y N143 34.54x54 N143 34.54x54 N ICL2ECL2 L174 L174 L N175 N175 N N176 N176 N A177 A177 A D178 D178 D Q179 Q179 Q N180 N180 N E181 E181 E C182 45.50x50 C182 45.50x50 C I183 45.51x51 I183 45.51x51 I I184 45.52x52 I184 45.52x52 I A185 A185 A ECL2ICL3 R227 R227 R S228 S228 S S229 S229 S R230 R230 R A231 A231 A F232 F232 F R233 R233 R A234 A234 A H235 H235 H L236 L236 L R237 R237 R A238 A238 A P239 P239 P L240 L240 L K241 K241 K G242 G242 G N243 N243 N C244 C244 C T245 T245 T H246 H246 H P247 P247 P E248 E248 E D249 D249 D M250 M250 M K251 K251 K L252 L252 L C253 C253 C T254 T254 T V255 V255 V I256 I256 I M257 M257 M K258 K258 K S259 S259 S N260 N260 N G261 G261 G S262 S262 S F263 F263 F P264 P264 P V265 V265 V N266 N266 N R267 R267 R R268 R268 R R269 R269 R V270 V270 V E271 E271 E A272 A272 A A273 A273 A R274 R274 R R275 R275 R A276 A276 A Q277 Q277 Q E278 E278 E L279 L279 L E280 E280 E M281 M281 M E282 E282 E M283 M283 M L284 L284 L S285 S285 S S286 S286 S T287 T287 T S288 S288 S P289 P289 P P290 P290 P E291 E291 E R292 R292 R T293 T293 T R294 R294 R Y295 Y295 Y S296 S296 S P297 P297 P I298 I298 I P299 P299 P P300 P300 P S301 S301 S H302 H302 H H303 H303 H Q304 Q304 Q L305 L305 L T306 T306 T L307 L307 L P308 P308 P D309 D309 D P310 P310 P S311 S311 S H312 H312 H H313 H313 H G314 G314 G L315 L315 L H316 H316 H S317 S317 S T318 T318 T P319 P319 P D320 D320 D S321 S321 S P322 P322 P A323 A323 A K324 K324 K P325 P325 P E326 E326 E K327 K327 K N328 N328 N G329 G329 G H330 H330 H A331 A331 A K332 K332 K D333 D333 D H334 H334 H P335 P335 P K336 K336 K I337 I337 I A338 A338 A K339 K339 K I340 I340 I F341 F341 F E342 E342 E I343 I343 I Q344 Q344 Q T345 T345 T M346 M346 M P347 P347 P N348 N348 N G349 G349 G K350 K350 K T351 T351 T R352 R352 R T353 T353 T S354 S354 S L355 L355 L K356 K356 K T357 T357 T M358 M358 M S359 S359 S R360 R360 R R361 R361 R ICL3ECL3 D400 D400 D C401 C401 C N402 N402 N I403 I403 I ECL3N-term M1 M1 M D2 D2 D P3 P3 P L4 L4 L N5 N5 N L6 L6 L S7 S7 S W8 W8 W Y9 Y9 Y D10 D10 D D11 D11 D D12 D12 D L13 L13 L E14 E14 E R15 R15 R Q16 Q16 Q N17 N17 N W18 W18 W S19 S19 S R20 R20 R P21 P21 P F22 F22 F N23 N23 N G24 G24 G S25 S25 S D26 D26 D G27 G27 G K28 K28 K A29 A29 A D30 D30 D N-termC-term C443 C443 C C-term R31 1.29x29 R31 1.29x29 R P32 1.30x30 P32 1.30x30 P H33 1.31x31 H33 1.31x31 H Y34 1.32x32 Y34 1.32x32 Y N35 1.33x33 N35 1.33x33 N Y36 1.34x34 Y36 1.34x34 Y Y37 1.35x35 Y37 1.35x35 Y A38 1.36x36 A38 1.36x36 A T39 1.37x37 T39 1.37x37 T L40 1.38x38 L40 1.38x38 L L41 1.39x39 L41 1.39x39 L T42 1.40x40 T42 1.40x40 T L43 1.41x41 L43 1.41x41 L L44 1.42x42 L44 1.42x42 L I45 1.43x43 I45 1.43x43 I A46 1.44x44 A46 1.44x44 A V47 1.45x45 V47 1.45x45 V I48 1.46x46 I48 1.46x46 I V49 1.47x47 V49 1.47x47 V F50 1.48x48 F50 1.48x48 F G51 1.49x49 G51 1.49x49 G N52 1.50x50 N52 1.50x50 N V53 1.51x51 V53 1.51x51 V L54 1.52x52 L54 1.52x52 L V55 1.53x53 V55 1.53x53 V C56 1.54x54 C56 1.54x54 C M57 1.55x55 M57 1.55x55 M A58 1.56x56 A58 1.56x56 A V59 1.57x57 V59 1.57x57 V S60 1.58x58 S60 1.58x58 S R61 1.59x59 R61 1.59x59 R E62 1.60x60 E62 1.60x60 E T67 2.37x37 T67 2.37x37 T T68 2.38x38 T68 2.38x38 T T69 2.39x39 T69 2.39x39 T N70 2.40x40 N70 2.40x40 N Y71 2.41x41 Y71 2.41x41 Y L72 2.42x42 L72 2.42x42 L I73 2.43x43 I73 2.43x43 I V74 2.44x44 V74 2.44x44 V S75 2.45x45 S75 2.45x45 S L76 2.46x46 L76 2.46x46 L A77 2.47x47 A77 2.47x47 A V78 2.48x48 V78 2.48x48 V A79 2.49x49 A79 2.49x49 A D80 2.50x50 D80 2.50x50 D L81 2.51x51 L81 2.51x51 L L82 2.52x52 L82 2.52x52 L V83 2.53x53 V83 2.53x53 V A84 2.54x54 A84 2.54x54 A T85 2.55x55 T85 2.55x55 T L86 2.56x551 L86 2.56x551 L V87 2.57x56 V87 2.57x56 V M88 2.58x57 M88 2.58x57 M P89 2.59x58 P89 2.59x58 P W90 2.60x59 W90 2.60x59 W V91 2.61x60 V91 2.61x60 V V92 2.62x61 V92 2.62x61 V Y93 2.63x62 Y93 2.63x62 Y L94 2.64x63 L94 2.64x63 L E95 2.65x64 E95 2.65x64 E V96 2.66x65 V96 2.66x65 V V97 2.67x66 V97 2.67x66 V G98 2.68x67 G98 2.68x67 G S103 3.21x21 S103 3.21x21 S R104 3.22x22 R104 3.22x22 R I105 3.23x23 I105 3.23x23 I H106 3.24x24 H106 3.24x24 H C107 3.25x25 C107 3.25x25 C D108 3.26x26 D108 3.26x26 D I109 3.27x27 I109 3.27x27 I F110 3.28x28 F110 3.28x28 F V111 3.29x29 V111 3.29x29 V T112 3.30x30 T112 3.30x30 T L113 3.31x31 L113 3.31x31 L D114 3.32x32 D114 3.32x32 D V115 3.33x33 V115 3.33x33 V M116 3.34x34 M116 3.34x34 M M117 3.35x35 M117 3.35x35 M C118 3.36x36 C118 3.36x36 C T119 3.37x37 T119 3.37x37 T A120 3.38x38 A120 3.38x38 A S121 3.39x39 S121 3.39x39 S I122 3.40x40 I122 3.40x40 I L123 3.41x41 L123 3.41x41 L N124 3.42x42 N124 3.42x42 N L125 3.43x43 L125 3.43x43 L C126 3.44x44 C126 3.44x44 C A127 3.45x45 A127 3.45x45 A I128 3.46x46 I128 3.46x46 I S129 3.47x47 S129 3.47x47 S I130 3.48x48 I130 3.48x48 I D131 3.49x49 D131 3.49x49 D R132 3.50x50 R132 3.50x50 R Y133 3.51x51 Y133 3.51x51 Y T134 3.52x52 T134 3.52x52 T A135 3.53x53 A135 3.53x53 A V136 3.54x54 V136 3.54x54 V A137 3.55x55 A137 3.55x55 A M138 3.56x56 M138 3.56x56 M T144 4.34x34 T144 4.34x34 T R145 4.35x35 R145 4.35x35 R Y146 4.36x36 Y146 4.36x36 Y S147 4.37x37 S147 4.37x37 S S148 4.38x38 S148 4.38x38 S K149 4.39x39 K149 4.39x39 K R150 4.40x40 R150 4.40x40 R R151 4.41x41 R151 4.41x41 R V152 4.42x42 V152 4.42x42 V T153 4.43x43 T153 4.43x43 T V154 4.44x44 V154 4.44x44 V M155 4.45x45 M155 4.45x45 M I156 4.46x46 I156 4.46x46 I S157 4.47x47 S157 4.47x47 S I158 4.48x48 I158 4.48x48 I V159 4.49x49 V159 4.49x49 V W160 4.50x50 W160 4.50x50 W V161 4.51x51 V161 4.51x51 V L162 4.52x52 L162 4.52x52 L S163 4.53x53 S163 4.53x53 S F164 4.54x54 F164 4.54x54 F T165 4.55x55 T165 4.55x55 T I166 4.56x56 I166 4.56x56 I S167 4.57x57 S167 4.57x57 S C168 4.58x59 C168 4.58x59 C P169 4.59x60 P169 4.59x60 P L170 4.60x61 L170 4.60x61 L L171 4.61x62 L171 4.61x62 L F172 4.62x63 F172 4.62x63 F G173 4.63x64 G173 4.63x64 G N186 5.35x36 N186 5.35x36 N P187 5.36x37 P187 5.36x37 P A188 5.37x38 A188 5.37x38 A F189 5.38x39 F189 5.38x39 F V190 5.39x40 V190 5.39x40 V V191 5.40x41 V191 5.40x41 V Y192 5.41x42 Y192 5.41x42 Y S193 5.42x43 S193 5.42x43 S S194 5.43x44 S194 5.43x44 S I195 5.44x45 I195 5.44x45 I V196 5.45x46 V196 5.45x46 V S197 5.46x461 S197 5.46x461 S F198 5.47x47 F198 5.47x47 F Y199 5.48x48 Y199 5.48x48 Y V200 5.49x49 V200 5.49x49 V P201 5.50x50 P201 5.50x50 P F202 5.51x51 F202 5.51x51 F I203 5.52x52 I203 5.52x52 I V204 5.53x53 V204 5.53x53 V T205 5.54x54 T205 5.54x54 T L206 5.55x55 L206 5.55x55 L L207 5.56x56 L207 5.56x56 L V208 5.57x57 V208 5.57x57 V Y209 5.58x58 Y209 5.58x58 Y I210 5.59x59 I210 5.59x59 I K211 5.60x60 K211 5.60x60 K I212 5.61x61 I212 5.61x61 I Y213 5.62x62 Y213 5.62x62 Y I214 5.63x63 I214 5.63x63 I V215 5.64x64 V215 5.64x64 V L216 5.65x65 L216 5.65x65 L R217 5.66x66 R217 5.66x66 R R218 5.67x67 R218 5.67x67 R R219 5.68x68 R219 5.68x68 R R220 5.69x69 R220 5.69x69 R K221 5.70x70 K221 5.70x70 K R222 5.71x71 R222 5.71x71 R V223 5.72x72 V223 5.72x72 V N224 5.73x73 N224 5.73x73 N T225 5.74x74 T225 5.74x74 T K226 5.75x75 K226 5.75x75 K K362 6.24x24 K362 6.24x24 K L363 6.25x25 L363 6.25x25 L S364 6.26x26 S364 6.26x26 S Q365 6.27x27 Q365 6.27x27 Q Q366 6.28x28 Q366 6.28x28 Q K367 6.29x29 K367 6.29x29 K E368 6.30x30 E368 6.30x30 E K369 6.31x31 K369 6.31x31 K K370 6.32x32 K370 6.32x32 K A371 6.33x33 A371 6.33x33 A T372 6.34x34 T372 6.34x34 T Q373 6.35x35 Q373 6.35x35 Q M374 6.36x36 M374 6.36x36 M L375 6.37x37 L375 6.37x37 L A376 6.38x38 A376 6.38x38 A I377 6.39x39 I377 6.39x39 I V378 6.40x40 V378 6.40x40 V L379 6.41x41 L379 6.41x41 L G380 6.42x42 G380 6.42x42 G V381 6.43x43 V381 6.43x43 V F382 6.44x44 F382 6.44x44 F I383 6.45x45 I383 6.45x45 I I384 6.46x46 I384 6.46x46 I C385 6.47x47 C385 6.47x47 C W386 6.48x48 W386 6.48x48 W L387 6.49x49 L387 6.49x49 L P388 6.50x50 P388 6.50x50 P F389 6.51x51 F389 6.51x51 F F390 6.52x52 F390 6.52x52 F I391 6.53x53 I391 6.53x53 I T392 6.54x54 T392 6.54x54 T H393 6.55x55 H393 6.55x55 H I394 6.56x56 I394 6.56x56 I L395 6.57x57 L395 6.57x57 L N396 6.58x58 N396 6.58x58 N I397 6.59x59 I397 6.59x59 I H398 6.60x60 H398 6.60x60 H C399 6.61x61 C399 6.61x61 C P404 7.31x30 P404 7.31x30 P P405 7.32x31 P405 7.32x31 P V406 7.33x32 V406 7.33x32 V L407 7.34x33 L407 7.34x33 L Y408 7.35x34 Y408 7.35x34 Y S409 7.36x35 S409 7.36x35 S A410 7.37x36 A410 7.37x36 A F411 7.38x37 F411 7.38x37 F T412 7.39x38 T412 7.39x38 T W413 7.40x39 W413 7.40x39 W L414 7.41x40 L414 7.41x40 L G415 7.42x41 G415 7.42x41 G Y416 7.43x42 Y416 7.43x42 Y V417 7.44x43 V417 7.44x43 V N418 7.45x45 N418 7.45x45 N S419 7.46x46 S419 7.46x46 S A420 7.47x47 A420 7.47x47 A V421 7.48x48 V421 7.48x48 V N422 7.49x49 N422 7.49x49 N P423 7.50x50 P423 7.50x50 P I424 7.51x51 I424 7.51x51 I I425 7.52x52 I425 7.52x52 I Y426 7.53x53 Y426 7.53x53 Y T427 7.54x54 T427 7.54x54 T T428 7.55x55 T428 7.55x55 T F429 7.56x56 F429 7.56x56 F N430 8.47x47 N430 8.47x47 N I431 8.48x48 I431 8.48x48 I E432 8.49x49 E432 8.49x49 E F437 8.54x54 F437 8.54x54 F L438 8.55x55 L438 8.55x55 L K439 8.56x56 K439 8.56x56 K F433 8.50x50 F433 8.50x50 F R434 8.51x51 R434 8.51x51 R K435 8.52x52 K435 8.52x52 K A436 8.53x53 A436 8.53x53 A I440 8.57x57 I440 8.57x57 I L441 8.58x58 L441 8.58x58 L H442 8.59x59 H442 8.59x59 H

Top 100 conformational changes

Residue pairs with the largest RRCS changes between active and inactive states. GPCRdb numbering in parentheses. Highlighted rows exceed the significance threshold.

Rank Residue 1 Residue 2 Active RRCS Inactive RRCS ΔRRCS Magnitude
1 TRP90 (2.60x59) HIS106 (3.24x24) 12.725 0.134 +12.592 HIGH
2 THR427 (7.54x54) PHE433 (8.50x50) 8.818 0.000 +8.818 HIGH
3 THR69 (2.39x39) ARG132 (3.50x50) 0.000 7.814 -7.814 HIGH
4 HIS302 HIS303 0.000 7.675 -7.675 HIGH
5 ARG222 (5.71x71) GLU280 0.000 7.613 -7.613 HIGH
6 GLU14 ARG15 0.000 7.402 -7.402 HIGH
7 TRP386 (6.48x48) GLY415 (7.42x41) 2.014 9.191 -7.178 HIGH
8 ASN396 (6.58x58) TYR408 (7.35x34) 6.573 0.000 +6.573 HIGH
9 THR428 (7.55x55) ARG434 (8.51x51) 5.634 0.000 +5.634 HIGH
10 PHE341 ILE343 5.362 0.000 +5.362 HIGH
11 ARG104 (3.22x22) ALA177 0.713 5.961 -5.248 HIGH
12 TYR209 (5.58x58) LEU375 (6.37x37) 2.099 7.253 -5.154 HIGH
13 ASP131 (3.49x49) TYR142 (34.53x53) 3.820 8.890 -5.070 HIGH
14 HIS303 GLN304 0.000 5.048 -5.048 HIGH
15 THR392 (6.54x54) TYR408 (7.35x34) 5.228 0.181 +5.047 HIGH
16 ASP131 (3.49x49) ARG132 (3.50x50) 0.000 5.029 -5.029 HIGH
17 GLU62 (1.60x60) LYS439 (8.56x56) 5.037 0.196 +4.841 MED
18 ASN418 (7.45x45) ASN422 (7.49x49) 5.252 0.472 +4.780 MED
19 ARG31 (1.29x29) VAL97 (2.67x66) 4.749 0.000 +4.749 MED
20 ARG220 (5.69x69) GLU368 (6.30x30) 4.662 0.000 +4.662 MED
21 ARG233 GLU280 4.541 0.000 +4.541 MED
22 VAL265 ARG269 0.000 4.235 -4.235 MED
23 TRP386 (6.48x48) ASN418 (7.45x45) 6.181 2.153 +4.028 MED
24 TYR37 (1.35x35) GLU95 (2.65x64) 0.180 4.113 -3.933 MED
25 ASN175 ALA185 3.966 0.133 +3.834 MED
26 THR428 (7.55x55) PHE429 (7.56x56) 0.000 3.643 -3.643 MED
27 THR427 (7.54x54) ARG434 (8.51x51) 0.000 3.602 -3.602 MED
28 ASN5 SER7 3.584 0.000 +3.584 MED
29 PHE382 (6.44x44) ASN418 (7.45x45) 0.000 3.439 -3.439 MED
30 ARG132 (3.50x50) TYR142 (34.53x53) 0.000 3.414 -3.414 MED
31 ARG104 (3.22x22) ASN175 0.000 3.414 -3.414 MED
32 ASN175 ILE183 (45.51x51) 3.741 0.381 +3.359 MED
33 ARG132 (3.50x50) TYR209 (5.58x58) 3.348 0.000 +3.348 MED
34 ILE122 (3.40x40) TRP386 (6.48x48) 3.271 0.000 +3.271 MED
35 PHE202 (5.51x51) PHE382 (6.44x44) 3.247 0.000 +3.247 MED
36 LEU125 (3.43x43) TYR426 (7.53x53) 3.244 0.000 +3.244 MED
37 GLN16 TRP18 3.476 0.238 +3.238 MED
38 VAL378 (6.40x40) TYR426 (7.53x53) 3.364 0.132 +3.232 MED
39 PHE198 (5.47x47) PHE202 (5.51x51) 3.159 0.000 +3.159 MED
40 PHE341 LEU355 0.000 3.126 -3.126 MED
41 ARG132 (3.50x50) LEU375 (6.37x37) 0.000 3.119 -3.119 MED
42 ILE73 (2.43x43) TYR426 (7.53x53) 0.863 3.954 -3.091 MED
43 VAL136 (3.54x54) ARG219 (5.68x68) 2.542 5.566 -3.024 MED
44 PHE382 (6.44x44) TRP386 (6.48x48) 2.339 5.339 -2.999 MED
45 VAL115 SER167 0.486 3.476 -2.990 MED
46 LYS339 GLU342 0.000 2.968 -2.968 MED
47 VAL190 HIS393 5.917 3.022 +2.895 MED
48 ARG31 (1.29x29) TYR34 2.894 0.000 +2.894 MED
49 ARG132 (3.50x50) TYR426 (7.53x53) 2.881 0.000 +2.881 MED
50 TYR93 LYS101 1.068 3.947 -2.879 MED
51 LEU41 TRP413 11.114 8.252 +2.862 MED
52 TYR199 ILE394 5.087 2.246 +2.841 MED
53 LYS339 ILE340 2.820 0.000 +2.820 MED
54 ILE377 PHE429 (7.56x56) 0.000 2.675 -2.675 MED
55 THR119 SER163 1.785 4.442 -2.657 MED
56 LEU4 ASN5 0.000 2.649 -2.649 MED
57 HIS312 HIS313 5.338 7.954 -2.616 MED
58 TYR209 (5.58x58) VAL378 (6.40x40) 2.602 0.000 +2.602 MED
59 TYR34 TYR36 0.000 2.576 -2.576 MED
60 TYR142 (34.53x53) ARG151 3.282 5.832 -2.550 MED
61 SER229 ARG233 2.526 0.012 +2.514 MED
62 PRO139 ARG219 (5.68x68) 0.000 2.513 -2.513 MED
63 SER364 GLU368 (6.30x30) 0.085 2.591 -2.505 MED
64 ALA137 ARG219 (5.68x68) 0.000 2.503 -2.503 MED
65 LYS367 GLU432 0.000 2.468 -2.468 MED
66 MET88 TYR416 0.852 3.308 -2.456 MED
67 ASN70 PHE433 (8.50x50) 3.650 1.195 +2.454 MED
68 CYS399 CYS401 1.173 3.605 -2.433 MED
69 VAL55 THR427 (7.54x54) 2.357 0.000 +2.357 MED
70 GLY51 PRO423 1.751 4.097 -2.346 MED
71 ALA127 MET155 0.386 2.726 -2.340 MED
72 TYR142 (34.53x53) SER148 2.974 0.679 +2.296 MED
73 TRP100 CYS182 6.712 4.420 +2.292 MED
74 PHE50 LEU54 0.024 2.305 -2.281 MED
75 THR134 ARG151 2.278 0.000 +2.278 MED
76 ARG104 (3.22x22) ASN176 0.103 2.300 -2.197 LOW
77 THR112 LEU171 2.986 5.176 -2.190 LOW
78 ARG31 (1.29x29) VAL96 2.189 0.000 +2.189 LOW
79 TYR426 (7.53x53) PHE433 (8.50x50) 0.000 2.184 -2.184 LOW
80 LEU307 PRO308 2.150 0.000 +2.150 LOW
81 LEU76 SER121 1.838 3.924 -2.086 LOW
82 ILE424 PHE429 (7.56x56) 2.083 0.000 +2.083 LOW
83 SER129 TYR209 (5.58x58) 2.945 4.979 -2.034 LOW
84 LEU170 PHE189 5.625 3.607 +2.018 LOW
85 ASN422 (7.49x49) TYR426 (7.53x53) 0.455 2.458 -2.004 LOW
86 ASP108 ASN175 1.368 3.358 -1.990 LOW
87 LEU379 ILE383 0.000 1.978 -1.978 LOW
88 SER311 HIS312 3.217 5.187 -1.970 LOW
89 PHE389 TYR408 (7.35x34) 0.050 1.987 -1.937 LOW
90 THR351 THR353 1.926 0.000 +1.926 LOW
91 THR112 SER167 4.636 2.719 +1.917 LOW
92 ILE343 THR345 2.082 0.180 +1.902 LOW
93 SER103 HIS106 (3.24x24) 0.731 2.621 -1.889 LOW
94 ASP80 ASN422 (7.49x49) 4.894 3.031 +1.863 LOW
95 ASN52 ALA77 6.146 4.291 +1.855 LOW
96 TRP90 (2.60x59) PHE110 2.485 4.326 -1.841 LOW
97 ASN396 (6.58x58) ILE403 3.518 1.709 +1.810 LOW
98 ASN17 SER19 1.806 0.000 +1.806 LOW
99 PRO297 ILE298 0.000 1.784 -1.784 LOW
100 ARG31 (1.29x29) GLY98 1.784 0.000 +1.784 LOW

Transmembrane domain analysis

Active-favoring residues form stronger contacts in the active state (positive ΔRRCS). Inactive-favoring residues form stronger contacts in the inactive state (negative ΔRRCS). Only residues with |ΔRRCS| ≥ 2.21 are shown (per-receptor significance threshold = max(mean(|Δ|) + σ, 0.2)).

Per-segment summary
Segment Range Active-favoring residues Count Inactive-favoring residues Count
TM1 31-62 62 (4.8), 31 (4.7) 2 37 (-3.9) 1
TM2 69-97 90 (12.6), 97 (4.7) 2 69 (-7.8), 95 (-3.9), 73 (-3.1) 3
TM3 104-136 106 (12.6), 122 (3.3), 125 (3.2) 3 132 (-7.8), 104 (-5.2), 131 (-5.1), 136 (-3.0) 4
TM4 - - 0 - 0
TM5 198-222 220 (4.7), 202 (3.2), 198 (3.2) 3 222 (-7.6), 209 (-5.2), 219 (-3.0) 3
TM6 368-396 396 (6.6), 392 (5.0), 368 (4.7), 378 (3.2) 4 386 (-7.2), 375 (-5.2), 382 (-3.4) 3
TM7 408-429 427 (8.8), 408 (6.6), 428 (5.6), 418 (4.8), 422 (4.8), 426 (3.2) 6 415 (-7.2), 429 (-3.6) 2
Intracellular / Extracellular loops & H8
ICL1 - - 0 - 0
ICL2 142-142 - 0 142 (-5.1) 1
ICL3 233-355 341 (5.4), 343 (5.4), 233 (4.5) 3 302 (-7.7), 303 (-7.7), 280 (-7.6), 304 (-5.0), 265 (-4.2), 269 (-4.2), 355 (-3.1) 7
ECL1 - - 0 - 0
ECL2 175-185 175 (3.8), 185 (3.8), 183 (3.4) 3 177 (-5.2) 1
ECL3 - - 0 - 0
H8 433-439 433 (8.8), 434 (5.6), 439 (4.8) 3 - 0

Interactive visualizations

ΔRRCS distribution

Active vs inactive comparison

Residue-wise changes

TM domain breakdown

Variants of interest

49 variants mapped to contact positions, sorted by |ΔRRCS| impact.

Position Protein change DNA change Allele freq Het / Hom ΔRRCS AM score Pathogenicity Conservation dbSNP
132 p.Arg132Ser c.396G>T 6.84e-07 1 / 0 7.81 1.000 PATHOGENIC 0.95
303 p.His303Asp c.907C>G 6.84e-07 1 / 0 7.67 0.096 BENIGN 0.49 rs1950782257
302 p.His302Pro c.905A>C 6.59e-06 1 / 0 7.67 0.069 BENIGN 0.39 rs1591272542
222 p.Arg222Pro c.665G>C 6.84e-07 1 / 0 7.61 0.910 PATHOGENIC 0.86 rs750647475
280 p.Glu280Ala c.839A>C 6.85e-07 1 / 0 7.61 0.269 BENIGN 0.52
280 p.Glu280Lys c.838G>A 6.16e-06 9 / 0 7.61 - nan - rs1950783306
222 p.Arg222Gln c.665G>A 1.30e-05 19 / 0 7.61 - nan - rs750647475
222 p.Arg222Gly c.664C>G 1.37e-06 2 / 0 7.61 - nan -
14 p.Glu14Gln c.40G>C 6.84e-07 1 / 0 7.40 0.074 BENIGN 0.44
408 p.Tyr408Cys c.1223A>G 6.84e-07 1 / 0 6.57 0.927 PATHOGENIC 0.88 rs1445212166
434 p.Arg434Leu c.1301G>T 6.84e-07 1 / 0 5.63 0.998 PATHOGENIC 1.00
434 p.Arg434His c.1301G>A 2.74e-06 4 / 0 5.63 - nan - rs1195929717
434 p.Arg434Cys c.1300C>T 1.37e-06 2 / 0 5.63 - nan -
341 p.Phe341Ser c.1022T>C 6.84e-07 1 / 0 5.36 0.594 PATHOGENIC 0.52
343 p.Ile343Thr c.1028T>C 6.84e-07 1 / 0 5.36 0.392 AMBIGUOUS 0.58
104 p.Arg104Ser c.312G>C 6.84e-07 1 / 0 5.25 0.384 AMBIGUOUS 0.63
177 p.Ala177Thr c.529G>A 2.53e-05 37 / 0 5.25 0.054 BENIGN 0.68 rs571869697
131 p.Asp131Asn c.391G>A 6.84e-07 1 / 0 5.07 0.998 PATHOGENIC 0.93 rs549053606
304 p.Gln304Lys c.910C>A 8.21e-06 12 / 0 5.05 0.090 BENIGN 0.56
392 p.Thr392Arg c.1175C>G 6.85e-07 1 / 0 5.05 0.943 PATHOGENIC 0.83
62 p.Glu62Asp c.186G>C 6.84e-07 1 / 0 4.84 0.901 PATHOGENIC 1.00 rs1950918416
62 p.Glu62Lys c.184G>A 6.84e-07 1 / 0 4.84 - nan - rs868401982
422 p.Asn422Thr c.1265A>C 6.85e-06 1 / 0 4.78 0.997 PATHOGENIC 1.00 rs1591270955
97 p.Val97Ala c.290T>C 1.37e-06 2 / 0 4.75 0.152 BENIGN 0.66 rs1231059179
31 p.Arg31Ile c.92G>T 6.84e-07 1 / 0 4.75 0.096 BENIGN 0.62
97 p.Gly97Arg c.289G>C 6.84e-07 1 / 0 4.75 - nan - rs907486029
31 p.Arg31Gly c.91A>G 1.37e-06 2 / 0 4.75 - nan -
368 p.Glu368Asp c.1104G>C 3.42e-06 5 / 0 4.66 0.993 PATHOGENIC 1.00 rs890174542
220 p.Arg220His c.659G>A 1.71e-05 25 / 0 4.66 0.304 BENIGN 0.67 rs557036496
368 p.Glu368Ala c.1103A>C 6.57e-06 1 / 0 4.66 - nan - rs1393695476
368 p.Glu368Gly c.1103A>G 6.84e-07 1 / 0 4.66 - nan -
220 p.Arg220Leu c.659G>T 6.84e-07 1 / 0 4.66 - nan -
220 p.Arg220Cys c.658C>T 1.37e-06 2 / 0 4.66 - nan - rs755559594
220 p.Arg220Ser c.658C>A 6.84e-07 1 / 0 4.66 - nan -
269 p.Arg269Lys c.806G>A 6.16e-06 9 / 0 4.24 0.071 BENIGN 0.54 rs146652676
269 p.Arg269Thr c.806G>C 6.57e-06 1 / 0 4.24 - nan - rs146652676
37 p.Tyr37Cys c.110A>G 4.79e-06 7 / 0 3.93 0.475 AMBIGUOUS 0.94 rs752405585
37 p.Tyr37His c.109T>C 6.84e-07 1 / 0 3.93 - nan -
175 p.Asn175Ser c.524A>G 6.84e-07 1 / 0 3.83 0.428 AMBIGUOUS 0.95 rs761794375
175 p.Asn175Asp c.523A>G 6.84e-07 1 / 0 3.83 - nan - rs769717591
7 p.Ser7Phe c.20C>T 1.37e-06 2 / 0 3.58 0.160 BENIGN 0.89 rs780510016
183 p.Ile183Asn c.548T>A 1.37e-06 2 / 0 3.36 0.209 BENIGN 0.52 rs1203831599
183 p.Ile183Phe c.547A>T 1.37e-06 2 / 0 3.36 - nan - rs938621123
16 p.Gln16His c.48G>C 2.05e-06 3 / 0 3.24 0.101 BENIGN 0.53 rs759561000
355 p.Leu355Val c.1063C>G 6.57e-06 1 / 0 3.13 0.084 BENIGN 0.67 rs1950779963
73 p.Ile73Met c.219C>G 6.84e-07 1 / 0 3.09 0.905 PATHOGENIC 0.84
136 p.Val136Ala c.407T>C 6.84e-07 1 / 0 3.02 0.986 PATHOGENIC 0.96
219 p.Arg219His c.656G>A 6.84e-07 1 / 0 3.02 0.725 PATHOGENIC 0.87 rs200148328
219 p.Arg219Cys c.655C>T 4.79e-06 7 / 0 3.02 - nan - rs987305741

Complete RRCS results

Top 1000 contact pairs by |ΔRRCS|. Significance threshold: |ΔRRCS| ≥ 2.21, computed as max(mean(|Δ|) + σ, 0.2). Highlighted rows indicate significant changes.

Res1 AA1 Res2 AA2 Active RRCS Inactive RRCS ΔRRCS |ΔRRCS|
90 TRP 106 HIS 12.725 0.134 12.592 12.592
427 THR 433 PHE 8.818 0.000 8.818 8.818
69 THR 132 ARG 0.000 7.814 -7.814 7.814
302 HIS 303 HIS 0.000 7.675 -7.675 7.675
222 ARG 280 GLU 0.000 7.613 -7.613 7.613
14 GLU 15 ARG 0.000 7.402 -7.402 7.402
386 TRP 415 GLY 2.014 9.191 -7.178 7.178
396 ASN 408 TYR 6.573 0.000 6.573 6.573
428 THR 434 ARG 5.634 0.000 5.634 5.634
341 PHE 343 ILE 5.362 0.000 5.362 5.362
104 ARG 177 ALA 0.713 5.961 -5.248 5.248
209 TYR 375 LEU 2.099 7.253 -5.154 5.154
131 ASP 142 TYR 3.820 8.890 -5.070 5.070
303 HIS 304 GLN 0.000 5.048 -5.048 5.048
392 THR 408 TYR 5.228 0.181 5.047 5.047
131 ASP 132 ARG 0.000 5.029 -5.029 5.029
62 GLU 439 LYS 5.037 0.196 4.841 4.841
418 ASN 422 ASN 5.252 0.472 4.780 4.780
31 ARG 97 VAL 4.749 0.000 4.749 4.749
220 ARG 368 GLU 4.662 0.000 4.662 4.662
233 ARG 280 GLU 4.541 0.000 4.541 4.541
265 VAL 269 ARG 0.000 4.235 -4.235 4.235
386 TRP 418 ASN 6.181 2.153 4.028 4.028
37 TYR 95 GLU 0.180 4.113 -3.933 3.933
175 ASN 185 ALA 3.966 0.133 3.834 3.834
428 THR 429 PHE 0.000 3.643 -3.643 3.643
427 THR 434 ARG 0.000 3.602 -3.602 3.602
5 ASN 7 SER 3.584 0.000 3.584 3.584
382 PHE 418 ASN 0.000 3.439 -3.439 3.439
132 ARG 142 TYR 0.000 3.414 -3.414 3.414
104 ARG 175 ASN 0.000 3.414 -3.414 3.414
175 ASN 183 ILE 3.741 0.381 3.359 3.359
132 ARG 209 TYR 3.348 0.000 3.348 3.348
122 ILE 386 TRP 3.271 0.000 3.271 3.271
202 PHE 382 PHE 3.247 0.000 3.247 3.247
125 LEU 426 TYR 3.244 0.000 3.244 3.244
16 GLN 18 TRP 3.476 0.238 3.238 3.238
378 VAL 426 TYR 3.364 0.132 3.232 3.232
198 PHE 202 PHE 3.159 0.000 3.159 3.159
341 PHE 355 LEU 0.000 3.126 -3.126 3.126
132 ARG 375 LEU 0.000 3.119 -3.119 3.119
73 ILE 426 TYR 0.863 3.954 -3.091 3.091
136 VAL 219 ARG 2.542 5.566 -3.024 3.024
382 PHE 386 TRP 2.339 5.339 -2.999 2.999
115 VAL 167 SER 0.486 3.476 -2.990 2.990
339 LYS 342 GLU 0.000 2.968 -2.968 2.968
190 VAL 393 HIS 5.917 3.022 2.895 2.895
31 ARG 34 TYR 2.894 0.000 2.894 2.894
132 ARG 426 TYR 2.881 0.000 2.881 2.881
93 TYR 101 LYS 1.068 3.947 -2.879 2.879
41 LEU 413 TRP 11.114 8.252 2.862 2.862
199 TYR 394 ILE 5.087 2.246 2.841 2.841
339 LYS 340 ILE 2.820 0.000 2.820 2.820
377 ILE 429 PHE 0.000 2.675 -2.675 2.675
119 THR 163 SER 1.785 4.442 -2.657 2.657
4 LEU 5 ASN 0.000 2.649 -2.649 2.649
312 HIS 313 HIS 5.338 7.954 -2.616 2.616
209 TYR 378 VAL 2.602 0.000 2.602 2.602
34 TYR 36 TYR 0.000 2.576 -2.576 2.576
142 TYR 151 ARG 3.282 5.832 -2.550 2.550
229 SER 233 ARG 2.526 0.012 2.514 2.514
139 PRO 219 ARG 0.000 2.513 -2.513 2.513
364 SER 368 GLU 0.085 2.591 -2.505 2.505
137 ALA 219 ARG 0.000 2.503 -2.503 2.503
367 LYS 432 GLU 0.000 2.468 -2.468 2.468
88 MET 416 TYR 0.852 3.308 -2.456 2.456
70 ASN 433 PHE 3.650 1.195 2.454 2.454
399 CYS 401 CYS 1.173 3.605 -2.433 2.433
55 VAL 427 THR 2.357 0.000 2.357 2.357
51 GLY 423 PRO 1.751 4.097 -2.346 2.346
127 ALA 155 MET 0.386 2.726 -2.340 2.340
142 TYR 148 SER 2.974 0.679 2.296 2.296
100 TRP 182 CYS 6.712 4.420 2.292 2.292
50 PHE 54 LEU 0.024 2.305 -2.281 2.281
134 THR 151 ARG 2.278 0.000 2.278 2.278
104 ARG 176 ASN 0.103 2.300 -2.197 2.197
112 THR 171 LEU 2.986 5.176 -2.190 2.190
31 ARG 96 VAL 2.189 0.000 2.189 2.189
426 TYR 433 PHE 0.000 2.184 -2.184 2.184
307 LEU 308 PRO 2.150 0.000 2.150 2.150
76 LEU 121 SER 1.838 3.924 -2.086 2.086
424 ILE 429 PHE 2.083 0.000 2.083 2.083
129 SER 209 TYR 2.945 4.979 -2.034 2.034
170 LEU 189 PHE 5.625 3.607 2.018 2.018
422 ASN 426 TYR 0.455 2.458 -2.004 2.004
108 ASP 175 ASN 1.368 3.358 -1.990 1.990
379 LEU 383 ILE 0.000 1.978 -1.978 1.978
311 SER 312 HIS 3.217 5.187 -1.970 1.970
389 PHE 408 TYR 0.050 1.987 -1.937 1.937
351 THR 353 THR 1.926 0.000 1.926 1.926
112 THR 167 SER 4.636 2.719 1.917 1.917
343 ILE 345 THR 2.082 0.180 1.902 1.902
103 SER 106 HIS 0.731 2.621 -1.889 1.889
80 ASP 422 ASN 4.894 3.031 1.863 1.863
52 ASN 77 ALA 6.146 4.291 1.855 1.855
90 TRP 110 PHE 2.485 4.326 -1.841 1.841
396 ASN 403 ILE 3.518 1.709 1.810 1.810
17 ASN 19 SER 1.806 0.000 1.806 1.806
297 PRO 298 ILE 0.000 1.784 -1.784 1.784
31 ARG 98 GLY 1.784 0.000 1.784 1.784
216 LEU 372 THR 0.000 1.780 -1.780 1.780
93 TYR 99 GLU 0.000 1.769 -1.769 1.769
134 THR 142 TYR 0.407 2.140 -1.733 1.733
69 THR 142 TYR 2.508 0.777 1.730 1.730
169 PRO 174 LEU 5.437 3.721 1.715 1.715
90 TRP 102 PHE 4.635 2.924 1.711 1.711
62 GLU 64 ALA 0.000 1.711 -1.711 1.711
59 VAL 70 ASN 0.149 1.855 -1.707 1.707
267 ARG 271 GLU 0.639 2.329 -1.690 1.690
386 TRP 390 PHE 1.207 2.879 -1.672 1.672
54 LEU 437 PHE 5.582 7.250 -1.668 1.668
432 GLU 435 LYS 5.296 3.634 1.662 1.662
397 ILE 398 HIS 0.000 1.652 -1.652 1.652
133 TYR 212 ILE 3.215 4.858 -1.643 1.643
175 ASN 186 ASN 1.642 0.000 1.642 1.642
385 CYS 414 LEU 5.234 6.867 -1.633 1.633
301 SER 302 HIS 0.087 1.715 -1.629 1.629
129 SER 208 VAL 3.966 2.347 1.620 1.620
68 THR 151 ARG 0.000 1.618 -1.618 1.618
374 MET 429 PHE 0.634 2.241 -1.607 1.607
166 ILE 193 SER 1.569 0.000 1.569 1.569
184 ILE 190 VAL 1.112 2.670 -1.558 1.558
57 MET 440 ILE 0.894 2.420 -1.526 1.526
324 LYS 325 PRO 1.578 0.071 1.507 1.507
198 PHE 199 TYR 2.875 4.370 -1.495 1.495
374 MET 378 VAL 1.494 0.000 1.494 1.494
100 TRP 102 PHE 3.498 2.006 1.492 1.492
148 SER 151 ARG 2.710 1.219 1.492 1.492
37 TYR 413 TRP 4.509 3.018 1.491 1.491
248 GLU 251 LYS 0.000 1.488 -1.488 1.488
192 TYR 196 VAL 0.000 1.488 -1.488 1.488
198 PHE 382 PHE 0.895 2.382 -1.486 1.486
55 VAL 437 PHE 1.623 3.104 -1.481 1.481
95 GLU 409 SER 3.262 4.744 -1.481 1.481
120 ALA 163 SER 2.796 4.268 -1.472 1.472
80 ASP 121 SER 1.379 2.829 -1.450 1.450
122 ILE 382 PHE 1.133 2.570 -1.437 1.437
304 GLN 305 LEU 0.000 1.431 -1.431 1.431
232 PHE 236 LEU 2.343 0.916 1.427 1.427
82 LEU 117 MET 2.394 3.821 -1.427 1.427
174 LEU 189 PHE 0.000 1.426 -1.426 1.426
52 ASN 80 ASP 3.852 2.427 1.425 1.425
136 VAL 216 LEU 0.000 1.402 -1.402 1.402
119 THR 197 SER 4.567 3.174 1.393 1.393
164 PHE 168 CYS 0.382 1.754 -1.373 1.373
305 LEU 306 THR 0.563 1.934 -1.371 1.371
94 LEU 100 TRP 1.283 2.641 -1.358 1.358
191 VAL 398 HIS 0.000 1.356 -1.356 1.356
128 ILE 132 ARG 1.702 0.349 1.353 1.353
213 TYR 217 ARG 1.608 2.956 -1.348 1.348
141 LEU 281 MET 0.000 1.348 -1.348 1.348
310 PRO 311 SER 0.111 1.458 -1.347 1.347
94 LEU 99 GLU 1.855 0.508 1.347 1.347
166 ILE 189 PHE 1.648 0.332 1.316 1.316
128 ILE 426 TYR 1.308 0.000 1.308 1.308
20 ARG 21 PRO 0.584 1.888 -1.303 1.303
116 MET 167 SER 3.672 4.970 -1.299 1.299
366 GLN 370 LYS 1.297 0.000 1.297 1.297
75 SER 124 ASN 7.124 8.420 -1.296 1.296
246 HIS 247 PRO 1.131 2.426 -1.296 1.296
213 TYR 372 THR 1.277 0.000 1.277 1.277
129 SER 205 THR 2.401 1.136 1.265 1.265
423 PRO 428 THR 1.260 0.000 1.260 1.260
337 ILE 339 LYS 1.247 0.000 1.247 1.247
243 ASN 245 THR 0.000 1.235 -1.235 1.235
296 SER 298 ILE 1.223 0.000 1.223 1.223
174 LEU 186 ASN 2.962 1.751 1.211 1.211
132 ARG 135 ALA 0.000 1.210 -1.210 1.210
392 THR 403 ILE 0.542 1.751 -1.209 1.209
378 VAL 425 ILE 1.010 2.212 -1.202 1.202
385 CYS 418 ASN 3.629 2.431 1.198 1.198
57 MET 61 ARG 2.474 1.276 1.198 1.198
80 ASP 419 SER 10.542 9.345 1.196 1.196
198 PHE 387 LEU 3.958 2.780 1.179 1.179
37 TYR 41 LEU 4.751 3.587 1.164 1.164
37 TYR 409 SER 0.286 1.427 -1.141 1.141
403 ILE 408 TYR 1.370 0.234 1.136 1.136
60 SER 66 GLN 0.825 1.949 -1.124 1.124
239 PRO 241 LYS 1.120 0.000 1.120 1.120
181 GLU 183 ILE 0.527 1.647 -1.119 1.119
55 VAL 426 TYR 0.000 1.115 -1.115 1.115
54 LEU 440 ILE 2.077 0.972 1.105 1.105
114 ASP 416 TYR 5.147 4.052 1.095 1.095
330 HIS 331 ALA 0.000 1.094 -1.094 1.094
59 VAL 66 GLN 1.345 2.436 -1.091 1.091
88 MET 413 TRP 1.335 0.245 1.090 1.090
408 TYR 412 THR 0.000 1.087 -1.087 1.087
189 PHE 193 SER 2.583 1.498 1.085 1.085
126 CYS 204 VAL 1.065 0.000 1.065 1.065
325 PRO 326 GLU 1.058 0.000 1.058 1.058
68 THR 142 TYR 1.833 2.889 -1.056 1.056
126 CYS 201 PRO 1.794 2.835 -1.041 1.041
116 MET 164 PHE 1.911 2.949 -1.038 1.038
323 ALA 324 LYS 1.030 0.000 1.030 1.030
123 LEU 162 LEU 2.013 0.983 1.030 1.030
116 MET 117 MET 2.010 0.982 1.029 1.029
141 LEU 151 ARG 1.017 0.000 1.017 1.017
386 TRP 389 PHE 0.000 1.014 -1.014 1.014
158 ILE 162 LEU 0.000 1.013 -1.013 1.013
100 TRP 106 HIS 3.943 2.933 1.009 1.009
122 ILE 390 PHE 1.009 0.025 0.984 0.984
76 LEU 124 ASN 4.026 5.007 -0.981 0.981
170 LEU 175 ASN 0.625 1.598 -0.974 0.974
130 ILE 155 MET 0.988 0.018 0.970 0.970
32 PRO 34 TYR 0.000 0.962 -0.962 0.962
209 TYR 376 ALA 0.000 0.953 -0.953 0.953
7 SER 8 TRP 0.953 0.000 0.953 0.953
316 HIS 317 SER 2.383 1.440 0.943 0.943
141 LEU 148 SER 0.935 0.000 0.935 0.935
136 VAL 215 VAL 1.236 2.171 -0.935 0.935
162 LEU 166 ILE 1.059 0.127 0.932 0.932
138 MET 141 LEU 1.623 0.692 0.931 0.931
177 ALA 185 ALA 0.735 1.665 -0.930 0.930
206 LEU 379 LEU 0.966 0.036 0.930 0.930
199 TYR 391 ILE 2.549 1.624 0.924 0.924
309 ASP 310 PRO 3.878 2.956 0.922 0.922
116 MET 160 TRP 0.921 0.000 0.921 0.921
176 ASN 186 ASN 0.920 0.000 0.920 0.920
175 ASN 177 ALA 0.918 0.000 0.918 0.918
429 PHE 434 ARG 0.918 0.000 0.918 0.918
125 LEU 378 VAL 0.000 0.906 -0.906 0.906
87 VAL 110 PHE 1.753 2.650 -0.897 0.897
433 PHE 437 PHE 1.755 0.859 0.897 0.897
430 ASN 433 PHE 2.399 3.293 -0.893 0.893
393 HIS 408 TYR 4.454 3.564 0.891 0.891
315 LEU 316 HIS 3.753 4.642 -0.889 0.889
202 PHE 383 ILE 1.201 2.084 -0.883 0.883
279 LEU 282 GLU 0.179 1.060 -0.881 0.881
49 VAL 81 LEU 1.720 2.599 -0.879 0.879
190 VAL 397 ILE 1.375 2.249 -0.874 0.874
194 SER 394 ILE 0.000 0.870 -0.870 0.870
44 LEU 88 MET 0.863 0.000 0.863 0.863
412 THR 416 TYR 2.184 1.330 0.855 0.855
263 PHE 268 ARG 0.000 0.850 -0.850 0.850
138 MET 281 MET 0.000 0.847 -0.847 0.847
263 PHE 265 VAL 0.000 0.843 -0.843 0.843
384 ILE 414 LEU 1.819 0.977 0.842 0.842
352 ARG 354 SER 0.000 0.841 -0.841 0.841
318 THR 319 PRO 3.744 2.913 0.831 0.831
58 ALA 433 PHE 0.117 0.946 -0.829 0.829
425 ILE 426 TYR 0.879 0.052 0.827 0.827
275 ARG 278 GLU 0.106 0.930 -0.825 0.825
95 GLU 413 TRP 4.015 4.838 -0.824 0.824
403 ILE 407 LEU 1.028 0.206 0.823 0.823
170 LEU 184 ILE 0.000 0.811 -0.811 0.811
111 VAL 175 ASN 0.807 0.000 0.807 0.807
357 THR 361 ARG 0.807 0.000 0.807 0.807
212 ILE 375 LEU 0.782 0.000 0.782 0.782
83 VAL 88 MET 4.557 5.338 -0.781 0.781
396 ASN 401 CYS 0.779 0.000 0.779 0.779
75 SER 156 ILE 1.827 2.606 -0.779 0.779
61 ARG 440 ILE 0.306 1.080 -0.774 0.774
45 ILE 84 ALA 1.014 1.783 -0.769 0.769
125 LEU 422 ASN 0.766 0.000 0.766 0.766
189 PHE 192 TYR 0.000 0.765 -0.765 0.765
374 MET 426 TYR 0.000 0.761 -0.761 0.761
123 LEU 163 SER 0.592 1.350 -0.758 0.758
413 TRP 416 TYR 1.097 1.853 -0.756 0.756
230 ARG 361 ARG 0.755 0.000 0.755 0.755
54 LEU 441 LEU 0.000 0.755 -0.755 0.755
125 LEU 382 PHE 1.514 2.260 -0.747 0.747
116 MET 163 SER 4.362 3.618 0.744 0.744
385 CYS 415 GLY 2.088 2.832 -0.743 0.743
128 ILE 375 LEU 0.000 0.743 -0.743 0.743
99 GLU 180 ASN 0.900 0.158 0.742 0.742
151 ARG 155 MET 1.846 1.106 0.740 0.740
244 CYS 253 CYS 0.000 0.734 -0.734 0.734
363 LEU 367 LYS 0.731 0.000 0.731 0.731
224 ASN 365 GLN 0.725 0.000 0.725 0.725
72 LEU 128 ILE 2.395 3.114 -0.720 0.720
135 ALA 142 TYR 7.131 7.846 -0.714 0.714
108 ASP 171 LEU 0.000 0.707 -0.707 0.707
246 HIS 248 GLU 0.000 0.702 -0.702 0.702
263 PHE 264 PRO 1.977 1.277 0.700 0.700
51 GLY 437 PHE 0.000 0.699 -0.699 0.699
395 LEU 399 CYS 0.698 0.000 0.698 0.698
383 ILE 388 PRO 1.208 0.524 0.684 0.684
141 LEU 147 SER 0.683 0.000 0.683 0.683
94 LEU 110 PHE 0.000 0.681 -0.681 0.681
217 ARG 221 LYS 0.676 0.000 0.676 0.676
72 LEU 131 ASP 1.500 0.825 0.675 0.675
166 ILE 197 SER 1.682 1.017 0.665 0.665
108 ASP 170 LEU 1.142 0.478 0.664 0.664
213 TYR 375 LEU 0.659 0.000 0.659 0.659
205 THR 379 LEU 0.280 0.937 -0.658 0.658
73 ILE 427 THR 0.655 0.000 0.655 0.655
209 TYR 379 LEU 3.667 3.019 0.649 0.649
300 PRO 301 SER 0.000 0.645 -0.645 0.645
175 ASN 184 ILE 3.855 3.217 0.638 0.638
76 LEU 422 ASN 2.521 1.884 0.637 0.637
274 ARG 278 GLU 3.944 4.579 -0.635 0.635
55 VAL 73 ILE 0.327 0.959 -0.632 0.632
428 THR 437 PHE 0.626 0.000 0.626 0.626
288 SER 289 PRO 0.000 0.626 -0.626 0.626
93 TYR 102 PHE 4.818 5.444 -0.625 0.625
246 HIS 249 ASP 0.480 1.100 -0.620 0.620
407 LEU 411 PHE 3.900 3.285 0.615 0.615
35 ASN 38 ALA 0.000 0.601 -0.601 0.601
68 THR 149 LYS 0.599 0.000 0.599 0.599
404 PRO 407 LEU 0.000 0.597 -0.597 0.597
83 VAL 416 TYR 0.768 1.363 -0.595 0.595
389 PHE 393 HIS 0.000 0.591 -0.591 0.591
177 ALA 183 ILE 1.260 0.670 0.591 0.591
334 HIS 335 PRO 1.211 1.801 -0.590 0.590
68 THR 131 ASP 0.146 0.732 -0.585 0.585
427 THR 437 PHE 2.798 3.374 -0.577 0.577
93 TYR 100 TRP 0.000 0.575 -0.575 0.575
132 ARG 212 ILE 1.174 0.600 0.574 0.574
56 CYS 74 VAL 0.233 0.805 -0.572 0.572
392 THR 407 LEU 0.570 0.000 0.570 0.570
220 ARG 224 ASN 0.570 0.000 0.570 0.570
126 CYS 205 THR 2.538 3.106 -0.568 0.568
100 TRP 107 CYS 6.470 5.908 0.561 0.561
112 THR 170 LEU 2.708 3.269 -0.561 0.561
130 ILE 208 VAL 0.414 0.975 -0.561 0.561
104 ARG 108 ASP 1.149 1.709 -0.559 0.559
198 PHE 386 TRP 2.770 2.212 0.558 0.558
216 LEU 375 LEU 0.558 0.000 0.558 0.558
306 THR 307 LEU 0.556 0.000 0.556 0.556
104 ARG 173 GLY 0.553 0.000 0.553 0.553
196 VAL 201 PRO 2.172 2.722 -0.549 0.549
76 LEU 125 LEU 1.459 0.916 0.544 0.544
2 ASP 3 PRO 0.609 1.151 -0.542 0.542
374 MET 430 ASN 0.000 0.538 -0.538 0.538
18 TRP 19 SER 0.000 0.537 -0.537 0.537
69 THR 131 ASP 4.247 3.711 0.536 0.536
202 PHE 206 LEU 0.247 0.783 -0.536 0.536
99 GLU 101 LYS 8.202 7.667 0.535 0.535
52 ASN 419 SER 1.726 2.260 -0.534 0.534
59 VAL 65 LEU 2.255 1.721 0.534 0.534
68 THR 148 SER 3.681 3.151 0.530 0.530
131 ASP 155 MET 0.374 0.894 -0.520 0.520
139 PRO 140 MET 0.000 0.518 -0.518 0.518
209 TYR 426 TYR 0.506 0.000 0.506 0.506
136 VAL 212 ILE 0.230 0.729 -0.500 0.500
79 ALA 117 MET 0.253 0.751 -0.498 0.498
378 VAL 422 ASN 0.000 0.492 -0.492 0.492
115 VAL 184 ILE 0.491 0.000 0.491 0.491
194 SER 390 PHE 2.036 1.548 0.488 0.488
215 VAL 219 ARG 1.492 1.005 0.487 0.487
191 VAL 397 ILE 0.781 0.296 0.485 0.485
326 GLU 327 LYS 0.485 0.000 0.485 0.485
389 PHE 411 PHE 3.964 3.485 0.478 0.478
87 VAL 114 ASP 4.608 4.132 0.476 0.476
35 ASN 96 VAL 0.000 0.471 -0.471 0.471
45 ILE 89 PRO 0.789 0.321 0.469 0.469
52 ASN 81 LEU 2.554 2.086 0.468 0.468
48 ILE 419 SER 3.060 2.596 0.464 0.464
83 VAL 87 VAL 0.037 0.500 -0.462 0.462
31 ARG 32 PRO 0.021 0.484 -0.462 0.462
118 CYS 416 TYR 0.678 0.216 0.462 0.462
160 TRP 163 SER 0.459 0.000 0.459 0.459
212 ILE 372 THR 0.000 0.456 -0.456 0.456
44 LEU 48 ILE 0.885 1.339 -0.455 0.455
72 LEU 124 ASN 0.338 0.789 -0.452 0.452
268 ARG 271 GLU 0.000 0.451 -0.451 0.451
137 ALA 215 VAL 0.000 0.451 -0.451 0.451
83 VAL 419 SER 0.450 0.000 0.450 0.450
118 CYS 386 TRP 2.232 1.782 0.450 0.450
76 LEU 426 TYR 0.538 0.988 -0.450 0.450
126 CYS 130 ILE 0.445 0.000 0.445 0.445
87 VAL 113 LEU 1.022 1.467 -0.444 0.444
438 LEU 442 HIS 0.000 0.444 -0.444 0.444
386 TRP 416 TYR 0.000 0.439 -0.439 0.439
55 VAL 77 ALA 0.493 0.927 -0.434 0.434
73 ILE 433 PHE 0.009 0.443 -0.434 0.434
55 VAL 433 PHE 0.256 0.688 -0.432 0.432
387 LEU 391 ILE 1.522 1.952 -0.430 0.430
132 ARG 378 VAL 0.424 0.000 0.424 0.424
113 LEU 116 MET 0.000 0.419 -0.419 0.419
50 PHE 441 LEU 0.294 0.712 -0.417 0.417
134 THR 138 MET 0.312 0.726 -0.414 0.414
199 TYR 390 PHE 4.392 3.978 0.413 0.413
129 SER 130 ILE 0.407 0.000 0.407 0.407
91 VAL 413 TRP 2.714 3.121 -0.407 0.407
340 ILE 342 GLU 0.403 0.000 0.403 0.403
247 PRO 248 GLU 0.000 0.403 -0.403 0.403
31 ARG 95 GLU 0.403 0.000 0.403 0.403
54 LEU 57 MET 0.000 0.396 -0.396 0.396
374 MET 377 ILE 0.396 0.000 0.396 0.396
125 LEU 418 ASN 0.394 0.000 0.394 0.394
79 ALA 121 SER 2.133 2.526 -0.394 0.394
49 VAL 85 THR 0.000 0.382 -0.382 0.382
111 VAL 170 LEU 1.817 1.436 0.381 0.381
34 TYR 95 GLU 0.380 0.000 0.380 0.380
115 VAL 170 LEU 1.378 0.998 0.380 0.380
79 ALA 120 ALA 0.284 0.662 -0.378 0.378
133 TYR 137 ALA 1.884 1.510 0.374 0.374
184 ILE 189 PHE 0.111 0.485 -0.374 0.374
403 ILE 404 PRO 1.078 0.705 0.373 0.373
427 THR 428 THR 0.560 0.188 0.372 0.372
62 GLU 65 LEU 1.345 1.716 -0.371 0.371
115 VAL 197 SER 0.000 0.369 -0.369 0.369
97 VAL 101 LYS 0.432 0.797 -0.365 0.365
84 ALA 89 PRO 1.910 1.546 0.364 0.364
100 TRP 180 ASN 3.766 3.402 0.364 0.364
115 VAL 193 SER 0.477 0.839 -0.361 0.361
206 LEU 210 ILE 0.984 0.624 0.359 0.359
373 GLN 429 PHE 0.000 0.359 -0.359 0.359
424 ILE 428 THR 0.664 0.306 0.358 0.358
100 TRP 110 PHE 1.365 1.013 0.353 0.353
44 LEU 417 VAL 1.262 0.911 0.351 0.351
430 ASN 432 GLU 0.866 1.216 -0.350 0.350
79 ALA 160 TRP 2.057 2.403 -0.347 0.347
107 CYS 175 ASN 0.346 0.000 0.346 0.346
226 LYS 230 ARG 0.000 0.341 -0.341 0.341
133 TYR 208 VAL 1.387 1.049 0.339 0.339
335 PRO 336 LYS 0.645 0.978 -0.333 0.333
52 ASN 423 PRO 3.698 4.031 -0.332 0.332
48 ILE 80 ASP 1.161 0.833 0.329 0.329
124 ASN 159 VAL 3.440 3.759 -0.319 0.319
317 SER 318 THR 0.319 0.000 0.319 0.319
71 TYR 152 VAL 0.914 0.596 0.318 0.318
108 ASP 173 GLY 0.315 0.000 0.315 0.315
60 SER 61 ARG 0.000 0.313 -0.313 0.313
110 PHE 111 VAL 0.490 0.800 -0.310 0.310
308 PRO 309 ASP 0.306 0.000 0.306 0.306
389 PHE 390 PHE 1.778 2.080 -0.302 0.302
62 GLU 63 LYS 0.000 0.302 -0.302 0.302
204 VAL 208 VAL 0.366 0.065 0.301 0.301
110 PHE 182 CYS 0.609 0.904 -0.295 0.295
107 CYS 182 CYS 6.670 6.964 -0.295 0.295
226 LYS 283 MET 0.294 0.000 0.294 0.294
73 ILE 128 ILE 0.820 1.111 -0.291 0.291
58 ALA 436 ALA 0.705 0.995 -0.290 0.290
62 GLU 436 ALA 0.715 0.428 0.286 0.286
78 VAL 160 TRP 0.005 0.290 -0.285 0.285
137 ALA 138 MET 0.217 0.500 -0.282 0.282
373 GLN 377 ILE 0.953 0.671 0.282 0.282
385 CYS 386 TRP 0.251 0.531 -0.280 0.280
120 ALA 160 TRP 1.516 1.790 -0.274 0.274
168 CYS 172 PHE 1.334 1.064 0.270 0.270
69 THR 128 ILE 0.000 0.270 -0.270 0.270
63 LYS 66 GLN 0.335 0.604 -0.269 0.269
365 GLN 368 GLU 0.000 0.268 -0.268 0.268
294 ARG 295 TYR 0.266 0.000 0.266 0.266
78 VAL 82 LEU 0.280 0.546 -0.266 0.266
194 SER 199 TYR 4.332 4.066 0.266 0.266
401 CYS 403 ILE 0.415 0.149 0.266 0.266
191 VAL 195 ILE 0.509 0.773 -0.264 0.264
65 LEU 432 GLU 1.598 1.861 -0.263 0.263
351 THR 354 SER 0.261 0.000 0.261 0.261
52 ASN 55 VAL 0.000 0.261 -0.261 0.261
93 TYR 97 VAL 3.385 3.644 -0.260 0.260
35 ASN 39 THR 0.258 0.000 0.258 0.258
169 PRO 189 PHE 1.431 1.174 0.257 0.257
409 SER 413 TRP 1.698 1.441 0.257 0.257
374 MET 425 ILE 1.696 1.439 0.256 0.256
179 GLN 180 ASN 0.268 0.523 -0.255 0.255
67 THR 70 ASN 4.365 4.110 0.255 0.255
123 LEU 201 PRO 0.696 0.947 -0.252 0.252
369 LYS 373 GLN 0.000 0.250 -0.250 0.250
382 PHE 387 LEU 0.415 0.165 0.249 0.249
100 TRP 179 GLN 0.399 0.150 0.249 0.249
331 ALA 332 LYS 0.000 0.245 -0.245 0.245
134 THR 139 PRO 0.426 0.188 0.238 0.238
214 ILE 218 ARG 1.895 2.133 -0.238 0.238
47 VAL 420 ALA 0.378 0.140 0.238 0.238
381 VAL 385 CYS 0.350 0.588 -0.238 0.238
55 VAL 423 PRO 0.808 1.045 -0.237 0.237
87 VAL 416 TYR 0.936 1.173 -0.237 0.237
227 ARG 365 GLN 0.232 0.000 0.232 0.232
58 ALA 437 PHE 0.961 1.190 -0.229 0.229
321 SER 322 PRO 2.142 1.919 0.224 0.224
133 TYR 215 VAL 0.000 0.223 -0.223 0.223
130 ILE 204 VAL 0.220 0.000 0.220 0.220
209 TYR 212 ILE 0.769 0.549 0.220 0.220
83 VAL 121 SER 0.220 0.000 0.220 0.220
82 LEU 86 LEU 0.773 0.992 -0.219 0.219
85 THR 86 LEU 0.753 0.971 -0.218 0.218
320 ASP 321 SER 0.632 0.415 0.218 0.218
1 MET 2 ASP 0.000 0.217 -0.217 0.217
133 TYR 211 LYS 2.155 2.372 -0.216 0.216
122 ILE 198 PHE 0.456 0.669 -0.213 0.213
159 VAL 163 SER 0.000 0.211 -0.211 0.211
425 ILE 430 ASN 0.000 0.210 -0.210 0.210
147 SER 151 ARG 0.000 0.209 -0.209 0.209
68 THR 69 THR 0.177 0.381 -0.203 0.203
53 VAL 57 MET 0.870 0.667 0.203 0.203
374 MET 375 LEU 0.000 0.203 -0.203 0.203
271 GLU 275 ARG 0.000 0.202 -0.202 0.202
48 ILE 420 ALA 2.832 2.631 0.201 0.201
87 VAL 91 VAL 0.459 0.258 0.201 0.201
49 VAL 53 VAL 0.435 0.236 0.199 0.199
102 PHE 106 HIS 0.968 0.771 0.197 0.197
122 ILE 197 SER 2.781 2.975 -0.194 0.194
370 LYS 429 PHE 0.000 0.194 -0.194 0.194
93 TYR 94 LEU 0.000 0.193 -0.193 0.193
82 LEU 160 TRP 0.835 0.644 0.192 0.192
58 ALA 440 ILE 1.876 1.685 0.191 0.191
395 LEU 403 ILE 0.526 0.335 0.191 0.191
216 LEU 371 ALA 0.190 0.000 0.190 0.190
111 VAL 184 ILE 1.226 1.416 -0.190 0.190
129 SER 212 ILE 0.404 0.594 -0.190 0.190
114 ASP 118 CYS 1.295 1.483 -0.188 0.188
252 LEU 256 ILE 0.285 0.099 0.187 0.187
123 LEU 126 CYS 0.000 0.186 -0.186 0.186
162 LEU 196 VAL 0.186 0.000 0.186 0.186
44 LEU 413 TRP 0.603 0.788 -0.184 0.184
340 ILE 341 PHE 0.000 0.182 -0.182 0.182
65 LEU 70 ASN 6.309 6.491 -0.182 0.182
123 LEU 166 ILE 0.000 0.182 -0.182 0.182
91 VAL 95 GLU 0.000 0.181 -0.181 0.181
346 MET 347 PRO 0.565 0.743 -0.177 0.177
348 ASN 350 LYS 0.000 0.175 -0.175 0.175
385 CYS 411 PHE 0.173 0.345 -0.172 0.172
79 ALA 124 ASN 0.416 0.247 0.169 0.169
131 ASP 151 ARG 2.881 2.713 0.169 0.169
38 ALA 92 VAL 0.344 0.176 0.168 0.168
91 VAL 416 TYR 2.153 2.320 -0.167 0.167
100 TRP 181 GLU 0.166 0.000 0.166 0.166
69 THR 73 ILE 0.163 0.000 0.163 0.163
194 SER 393 HIS 0.522 0.683 -0.161 0.161
250 MET 254 THR 0.000 0.161 -0.161 0.161
58 ALA 65 LEU 2.232 2.393 -0.161 0.161
74 VAL 78 VAL 0.304 0.144 0.160 0.160
92 VAL 96 VAL 0.052 0.209 -0.157 0.157
97 VAL 99 GLU 0.669 0.514 0.155 0.155
434 ARG 438 LEU 0.000 0.154 -0.154 0.154
205 THR 209 TYR 1.556 1.403 0.154 0.154
72 LEU 152 VAL 0.560 0.713 -0.153 0.153
193 SER 198 PHE 0.058 0.210 -0.152 0.152
113 LEU 117 MET 0.336 0.488 -0.152 0.152
84 ALA 88 MET 0.075 0.227 -0.152 0.152
441 LEU 442 HIS 0.000 0.152 -0.152 0.152
32 PRO 33 HIS 0.151 0.000 0.151 0.151
83 VAL 118 CYS 0.188 0.340 -0.151 0.151
48 ILE 52 ASN 0.958 0.807 0.151 0.151
68 THR 152 VAL 3.884 4.034 -0.150 0.150
76 LEU 128 ILE 0.539 0.390 0.149 0.149
411 PHE 414 LEU 0.373 0.225 0.148 0.148
423 PRO 437 PHE 0.000 0.147 -0.147 0.147
65 LEU 433 PHE 3.923 3.778 0.145 0.145
144 THR 146 TYR 0.000 0.144 -0.144 0.144
140 MET 277 GLN 0.000 0.144 -0.144 0.144
193 SER 197 SER 0.669 0.812 -0.143 0.143
379 LEU 382 PHE 0.000 0.142 -0.142 0.142
69 THR 70 ASN 0.032 0.173 -0.140 0.140
93 TYR 98 GLY 0.008 0.146 -0.138 0.138
107 CYS 183 ILE 0.000 0.137 -0.137 0.137
238 ALA 239 PRO 0.328 0.464 -0.136 0.136
82 LEU 87 VAL 0.843 0.978 -0.135 0.135
90 TRP 100 TRP 1.656 1.789 -0.133 0.133
383 ILE 387 LEU 0.684 0.813 -0.129 0.129
186 ASN 187 PRO 1.032 0.904 0.128 0.128
126 CYS 129 SER 0.127 0.000 0.127 0.127
125 LEU 205 THR 0.111 0.235 -0.124 0.124
195 ILE 200 VAL 4.298 4.176 0.122 0.122
66 GLN 71 TYR 2.908 3.029 -0.121 0.121
298 ILE 299 PRO 1.180 1.300 -0.119 0.119
392 THR 411 PHE 2.991 2.872 0.119 0.119
161 VAL 165 THR 0.415 0.296 0.119 0.119
94 LEU 182 CYS 0.117 0.000 0.117 0.117
65 LEU 430 ASN 0.000 0.117 -0.117 0.117
394 ILE 398 HIS 1.211 1.328 -0.117 0.117
120 ALA 159 VAL 1.314 1.198 0.116 0.116
86 LEU 113 LEU 0.189 0.305 -0.116 0.116
72 LEU 155 MET 0.707 0.822 -0.115 0.115
299 PRO 300 PRO 0.580 0.466 0.113 0.113
256 ILE 260 ASN 0.113 0.000 0.113 0.113
164 PHE 167 SER 0.111 0.000 0.111 0.111
391 ILE 395 LEU 1.043 0.932 0.111 0.111
388 PRO 411 PHE 6.189 6.079 0.110 0.110
168 CYS 169 PRO 0.810 0.701 0.110 0.110
176 ASN 185 ALA 1.038 1.147 -0.109 0.109
144 THR 147 SER 1.626 1.517 0.108 0.108
115 VAL 166 ILE 0.107 0.000 0.107 0.107
43 LEU 47 VAL 0.001 0.108 -0.107 0.107
80 ASP 423 PRO 0.106 0.000 0.106 0.106
210 ILE 214 ILE 0.719 0.614 0.105 0.105
127 ALA 159 VAL 0.444 0.549 -0.105 0.105
381 VAL 421 VAL 1.037 1.142 -0.105 0.105
266 ASN 269 ARG 0.104 0.000 0.104 0.104
42 THR 92 VAL 0.261 0.161 0.100 0.100
86 LEU 117 MET 0.000 0.099 -0.099 0.099
87 VAL 117 MET 0.099 0.000 0.099 0.099
208 VAL 212 ILE 0.418 0.320 0.098 0.098
83 VAL 89 PRO 0.025 0.123 -0.098 0.098
53 VAL 81 LEU 1.534 1.630 -0.097 0.097
75 SER 160 TRP 2.315 2.409 -0.094 0.094
150 ARG 154 VAL 0.071 0.163 -0.092 0.092
389 PHE 412 THR 3.804 3.894 -0.090 0.090
156 ILE 160 TRP 1.245 1.154 0.090 0.090
48 ILE 88 MET 1.504 1.417 0.086 0.086
122 ILE 201 PRO 0.976 1.061 -0.086 0.086
289 PRO 290 PRO 0.312 0.397 -0.085 0.085
6 LEU 8 TRP 0.000 0.085 -0.085 0.085
280 GLU 284 LEU 0.084 0.000 0.084 0.084
109 ILE 113 LEU 0.737 0.821 -0.083 0.083
45 ILE 88 MET 2.811 2.894 -0.083 0.083
117 MET 160 TRP 1.208 1.291 -0.082 0.082
107 CYS 111 VAL 0.391 0.473 -0.082 0.082
198 PHE 390 PHE 14.351 14.432 -0.081 0.081
72 LEU 127 ALA 1.137 1.218 -0.081 0.081
96 VAL 97 VAL 0.000 0.080 -0.080 0.080
56 CYS 81 LEU 0.304 0.225 0.079 0.079
56 CYS 78 VAL 0.269 0.191 0.078 0.078
109 ILE 171 LEU 0.394 0.471 -0.077 0.077
431 ILE 435 LYS 0.639 0.563 0.076 0.076
387 LEU 388 PRO 0.813 0.737 0.076 0.076
48 ILE 84 ALA 1.091 1.016 0.075 0.075
133 TYR 138 MET 0.204 0.130 0.074 0.074
111 VAL 182 CYS 0.534 0.607 -0.073 0.073
52 ASN 422 ASN 0.000 0.068 -0.068 0.068
138 MET 219 ARG 0.000 0.066 -0.066 0.066
67 THR 69 THR 0.000 0.065 -0.065 0.065
45 ILE 49 VAL 0.215 0.150 0.065 0.065
203 ILE 207 LEU 0.743 0.678 0.065 0.065
92 VAL 413 TRP 1.381 1.316 0.065 0.065
431 ILE 432 GLU 0.267 0.202 0.065 0.065
124 ASN 160 TRP 0.141 0.076 0.064 0.064
381 VAL 425 ILE 0.454 0.518 -0.064 0.064
38 ALA 96 VAL 0.884 0.820 0.064 0.064
363 LEU 366 GLN 0.253 0.194 0.060 0.060
119 THR 167 SER 0.000 0.060 -0.060 0.060
119 THR 166 ILE 0.594 0.653 -0.060 0.060
125 LEU 386 TRP 0.058 0.000 0.058 0.058
70 ASN 73 ILE 0.597 0.539 0.058 0.058
48 ILE 416 TYR 0.632 0.690 -0.058 0.058
71 TYR 156 ILE 0.731 0.788 -0.057 0.057
105 ILE 109 ILE 0.508 0.565 -0.056 0.056
88 MET 89 PRO 0.752 0.696 0.056 0.056
91 VAL 110 PHE 1.551 1.496 0.056 0.056
377 ILE 425 ILE 0.994 0.940 0.054 0.054
296 SER 297 PRO 0.043 0.097 -0.054 0.054
86 LEU 87 VAL 0.054 0.000 0.054 0.054
381 VAL 418 ASN 1.113 1.166 -0.053 0.053
123 LEU 159 VAL 4.013 4.066 -0.053 0.053
417 VAL 421 VAL 0.443 0.390 0.053 0.053
55 VAL 74 VAL 0.000 0.052 -0.052 0.052
59 VAL 71 TYR 0.000 0.052 -0.052 0.052
430 ASN 431 ILE 0.051 0.000 0.051 0.051
195 ILE 196 VAL 0.000 0.049 -0.049 0.049
187 PRO 397 ILE 1.771 1.820 -0.049 0.049
159 VAL 160 TRP 0.022 0.071 -0.049 0.049
200 VAL 201 PRO 1.407 1.455 -0.048 0.048
426 TYR 427 THR 0.046 0.000 0.046 0.046
114 ASP 119 THR 0.000 0.045 -0.045 0.045
388 PRO 414 LEU 0.289 0.333 -0.044 0.044
125 LEU 128 ILE 0.000 0.043 -0.043 0.043
44 LEU 420 ALA 0.510 0.468 0.042 0.042
166 ILE 167 SER 0.000 0.041 -0.041 0.041
195 ILE 199 TYR 0.041 0.000 0.041 0.041
82 LEU 85 THR 0.118 0.078 0.040 0.040
168 CYS 171 LEU 0.000 0.040 -0.040 0.040
183 ILE 185 ALA 0.040 0.000 0.040 0.040
200 VAL 204 VAL 0.013 0.053 -0.040 0.040
128 ILE 209 TYR 0.037 0.000 0.037 0.037
57 MET 62 GLU 0.000 0.036 -0.036 0.036
76 LEU 80 ASP 1.344 1.309 0.035 0.035
57 MET 60 SER 0.000 0.035 -0.035 0.035
166 ILE 196 VAL 1.872 1.838 0.034 0.034
72 LEU 156 ILE 0.888 0.854 0.033 0.033
83 VAL 117 MET 2.007 2.040 -0.033 0.033
33 HIS 35 ASN 0.000 0.033 -0.033 0.033
377 ILE 381 VAL 0.215 0.182 0.033 0.033
154 VAL 158 ILE 0.899 0.869 0.031 0.031
49 VAL 84 ALA 0.632 0.662 -0.030 0.030
138 MET 139 PRO 0.117 0.090 0.027 0.027
135 ALA 219 ARG 0.000 0.027 -0.027 0.027
422 ASN 423 PRO 0.982 1.008 -0.026 0.026
59 VAL 433 PHE 1.409 1.435 -0.026 0.026
143 ASN 148 SER 0.025 0.000 0.025 0.025
202 PHE 203 ILE 0.159 0.134 0.025 0.025
41 LEU 92 VAL 0.853 0.877 -0.024 0.024
89 PRO 90 TRP 0.023 0.000 0.023 0.023
302 HIS 304 GLN 0.000 0.023 -0.023 0.023
41 LEU 95 GLU 0.310 0.332 -0.022 0.022
195 ILE 201 PRO 0.314 0.336 -0.022 0.022
103 SER 105 ILE 0.479 0.501 -0.022 0.022
212 ILE 216 LEU 0.702 0.723 -0.021 0.021
370 LYS 431 ILE 0.000 0.021 -0.021 0.021
56 CYS 77 ALA 0.526 0.545 -0.020 0.020
190 VAL 194 SER 0.441 0.461 -0.019 0.019
186 ASN 189 PHE 1.998 1.980 0.019 0.019
119 THR 123 LEU 0.986 0.968 0.018 0.018
111 VAL 115 VAL 0.025 0.040 -0.015 0.015
425 ILE 429 PHE 0.469 0.454 0.015 0.015
419 SER 422 ASN 0.014 0.000 0.014 0.014
153 THR 157 SER 0.130 0.143 -0.013 0.013
199 TYR 387 LEU 0.000 0.012 -0.012 0.012
120 ALA 124 ASN 0.148 0.137 0.011 0.011
282 GLU 285 SER 0.010 0.000 0.010 0.010
130 ILE 134 THR 0.241 0.231 0.010 0.010
152 VAL 156 ILE 0.895 0.886 0.009 0.009
112 THR 168 CYS 0.000 0.009 -0.009 0.009
45 ILE 92 VAL 0.564 0.556 0.008 0.008
421 VAL 425 ILE 1.071 1.063 0.008 0.008
404 PRO 405 PRO 0.430 0.436 -0.006 0.006
382 PHE 383 ILE 0.000 0.006 -0.006 0.006
354 SER 357 THR 0.006 0.000 0.006 0.006
65 LEU 436 ALA 0.678 0.683 -0.005 0.005
59 VAL 74 VAL 1.970 1.975 -0.004 0.004
113 LEU 118 CYS 0.000 0.003 -0.003 0.003
48 ILE 81 LEU 0.080 0.077 0.003 0.003
186 ASN 188 ALA 0.758 0.761 -0.003 0.003
110 PHE 114 ASP 0.001 0.000 0.001 0.001
107 CYS 112 THR 0.000 0.001 -0.001 0.001
115 VAL 119 THR 0.369 0.369 0.000 0.000

RRCS change distribution

-0.06
Mean ΔRRCS
1.58
Std Dev
-0.04
Median

Magnitude classification

16
High (|Δ| ≥ 5.0)
59
Medium (2.2 ≤ |Δ| < 5.0)
624
Low (|Δ| < 2.2)

Methods

RRCS analysis. Residue-Residue Contact Scores (RRCS) were calculated for each conformational state based on inter-atomic distances. Changes (ΔRRCS) were computed by comparing active and inactive structures predicted by AlphaFold multistate (del Alamo et al., 2022).

Significance threshold. |ΔRRCS| ≥ 2.21, computed as max(mean(|Δ|) + σ, 0.2). The 0.2 floor ensures receptors with very small overall change still surface their largest contacts.

Variant data. Population frequencies from gnomAD v4; pathogenicity predictions from AlphaMissense; conservation from ProtVar / UniProt.

Structural annotation. TM domain boundaries and generic numbering from GPCRdb.

What is RRCS?

Residue-Residue Contact Score (RRCS) measures how strongly two amino acids interact in a protein structure. When a protein changes shape (from inactive to active), these contact strengths change.

ΔRRCS (Delta RRCS) shows the difference in contact strength between states:

  • Positive ΔRRCS. Contact is stronger in the active state.
  • Negative ΔRRCS. Contact is stronger in the inactive state.
  • Large |ΔRRCS|. Significant structural rearrangement.

Residues with large RRCS changes are critical for protein function. Mutations at these positions may disrupt the protein's ability to change shape properly.

Pathogenicity predictions

AlphaMissense predicts whether a mutation harms protein function:

  • Pathogenic (score ≥ 0.564): mutation likely damages function.
  • Ambiguous (0.34–0.563): effect uncertain.
  • Benign (< 0.34): mutation likely tolerated.

Conservation & population data

Conservation score. How well-preserved a position is across species (0 = variable, 1 = conserved). High conservation suggests the position is critical for function.

Allele frequency. How often a variant appears in the population. Rare variants (low frequency) may be more likely to be harmful.

Sources: AlphaFold multistate · RRCS · gnomAD v4 · AlphaMissense · GPCRdb · UniProt / ProtVar