GPCompReports

ADA1A

Gene ADRA1A Adrenoceptors Aminergic receptors UniProt P35348
783
Total Contact Pairs
89
Significant Changes
7.75
Max Increase
-9.51
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 R55 12.48x48 R55 12.48x48 R H56 12.49x49 H56 12.49x49 H L57 12.50x50 L57 12.50x50 L H58 12.51x51 H58 12.51x51 H ICL1ECL1 Y91 23.49x49 Y91 23.49x49 Y W92 23.50x50 W92 23.50x50 W A93 23.51x51 A93 23.51x51 A F94 23.52x52 F94 23.52x52 F ECL1ICL2 P131 34.50x50 P131 34.50x50 P L132 34.51x51 L132 34.51x51 L R133 34.52x52 R133 34.52x52 R Y134 34.53x53 Y134 34.53x53 Y P135 34.54x54 P135 34.54x54 P T136 34.55x55 T136 34.55x55 T I137 34.56x56 I137 34.56x56 I V138 34.57x57 V138 34.57x57 V ICL2ECL2 R166 R166 R Q167 Q167 Q P168 P168 P A169 A169 A P170 P170 P E171 E171 E D172 D172 D E173 E173 E T174 T174 T I175 I175 I C176 45.50x50 C176 45.50x50 C Q177 45.51x51 Q177 45.51x51 Q I178 45.52x52 I178 45.52x52 I N179 N179 N E180 E180 E ECL2ICL3 K223 K223 K T224 T224 T D225 D225 D K226 K226 K S227 S227 S D228 D228 D S229 S229 S E230 E230 E Q231 Q231 Q V232 V232 V T233 T233 T L234 L234 L R235 R235 R I236 I236 I H237 H237 H R238 R238 R K239 K239 K N240 N240 N A241 A241 A P242 P242 P A243 A243 A G244 G244 G G245 G245 G S246 S246 S G247 G247 G M248 M248 M A249 A249 A S250 S250 S A251 A251 A K252 K252 K T253 T253 T K254 K254 K T255 T255 T H256 H256 H F257 F257 F S258 S258 S V259 V259 V R260 R260 R ICL3ECL3 P299 P299 P D300 D300 D F301 F301 F K302 K302 K P303 P303 P ECL3N-term M1 M1 M V2 V2 V F3 F3 F L4 L4 L S5 S5 S G6 G6 G N7 N7 N A8 A8 A S9 S9 S D10 D10 D S11 S11 S S12 S12 S N13 N13 N C14 C14 C T15 T15 T Q16 Q16 Q P17 P17 P P18 P18 P A19 A19 A N-termC-term I343 I343 I Q344 Q344 Q C345 C345 C L346 L346 L C347 C347 C R348 R348 R K349 K349 K Q350 Q350 Q S351 S351 S S352 S352 S K353 K353 K H354 H354 H A355 A355 A L356 L356 L G357 G357 G Y358 Y358 Y T359 T359 T L360 L360 L H361 H361 H P362 P362 P P363 P363 P S364 S364 S Q365 Q365 Q A366 A366 A V367 V367 V E368 E368 E G369 G369 G Q370 Q370 Q H371 H371 H K372 K372 K D373 D373 D M374 M374 M V375 V375 V R376 R376 R I377 I377 I P378 P378 P V379 V379 V G380 G380 G S381 S381 S R382 R382 R E383 E383 E T384 T384 T F385 F385 F Y386 Y386 Y R387 R387 R I388 I388 I S389 S389 S K390 K390 K T391 T391 T D392 D392 D G393 G393 G V394 V394 V C395 C395 C E396 E396 E W397 W397 W K398 K398 K F399 F399 F F400 F400 F S401 S401 S S402 S402 S M403 M403 M P404 P404 P R405 R405 R G406 G406 G S407 S407 S A408 A408 A R409 R409 R I410 I410 I T411 T411 T V412 V412 V S413 S413 S K414 K414 K D415 D415 D Q416 Q416 Q S417 S417 S S418 S418 S C419 C419 C T420 T420 T T421 T421 T A422 A422 A R423 R423 R V424 V424 V R425 R425 R S426 S426 S K427 K427 K S428 S428 S F429 F429 F L430 L430 L Q431 Q431 Q V432 V432 V C433 C433 C C434 C434 C C435 C435 C V436 V436 V G437 G437 G P438 P438 P S439 S439 S T440 T440 T P441 P441 P S442 S442 S L443 L443 L D444 D444 D K445 K445 K N446 N446 N H447 H447 H Q448 Q448 Q V449 V449 V P450 P450 P T451 T451 T I452 I452 I K453 K453 K V454 V454 V H455 H455 H T456 T456 T I457 I457 I S458 S458 S L459 L459 L S460 S460 S E461 E461 E N462 N462 N G463 G463 G E464 E464 E E465 E465 E V466 V466 V C-term P20 1.26x26 P20 1.26x26 P V21 1.27x27 V21 1.27x27 V N22 1.28x28 N22 1.28x28 N I23 1.29x29 I23 1.29x29 I S24 1.30x30 S24 1.30x30 S K25 1.31x31 K25 1.31x31 K A26 1.32x32 A26 1.32x32 A I27 1.33x33 I27 1.33x33 I L28 1.34x34 L28 1.34x34 L L29 1.35x35 L29 1.35x35 L G30 1.36x36 G30 1.36x36 G V31 1.37x37 V31 1.37x37 V I32 1.38x38 I32 1.38x38 I L33 1.39x39 L33 1.39x39 L G34 1.40x40 G34 1.40x40 G G35 1.41x41 G35 1.41x41 G L36 1.42x42 L36 1.42x42 L I37 1.43x43 I37 1.43x43 I L38 1.44x44 L38 1.44x44 L F39 1.45x45 F39 1.45x45 F G40 1.46x46 G40 1.46x46 G V41 1.47x47 V41 1.47x47 V L42 1.48x48 L42 1.48x48 L G43 1.49x49 G43 1.49x49 G N44 1.50x50 N44 1.50x50 N I45 1.51x51 I45 1.51x51 I L46 1.52x52 L46 1.52x52 L V47 1.53x53 V47 1.53x53 V I48 1.54x54 I48 1.54x54 I L49 1.55x55 L49 1.55x55 L S50 1.56x56 S50 1.56x56 S V51 1.57x57 V51 1.57x57 V A52 1.58x58 A52 1.58x58 A C53 1.59x59 C53 1.59x59 C H54 1.60x60 H54 1.60x60 H S59 2.37x37 S59 2.37x37 S V60 2.38x38 V60 2.38x38 V T61 2.39x39 T61 2.39x39 T H62 2.40x40 H62 2.40x40 H Y63 2.41x41 Y63 2.41x41 Y Y64 2.42x42 Y64 2.42x42 Y I65 2.43x43 I65 2.43x43 I V66 2.44x44 V66 2.44x44 V N67 2.45x45 N67 2.45x45 N L68 2.46x46 L68 2.46x46 L A69 2.47x47 A69 2.47x47 A V70 2.48x48 V70 2.48x48 V A71 2.49x49 A71 2.49x49 A D72 2.50x50 D72 2.50x50 D L73 2.51x51 L73 2.51x51 L L74 2.52x52 L74 2.52x52 L L75 2.53x53 L75 2.53x53 L T76 2.54x54 T76 2.54x54 T S77 2.55x55 S77 2.55x55 S T78 2.56x551 T78 2.56x551 T V79 2.57x56 V79 2.57x56 V L80 2.58x57 L80 2.58x57 L P81 2.59x58 P81 2.59x58 P F82 2.60x59 F82 2.60x59 F S83 2.61x60 S83 2.61x60 S A84 2.62x61 A84 2.62x61 A I85 2.63x62 I85 2.63x62 I F86 2.64x63 F86 2.64x63 F E87 2.65x64 E87 2.65x64 E V88 2.66x65 V88 2.66x65 V L89 2.67x66 L89 2.67x66 L G90 2.68x67 G90 2.68x67 G G95 3.21x21 G95 3.21x21 G R96 3.22x22 R96 3.22x22 R V97 3.23x23 V97 3.23x23 V F98 3.24x24 F98 3.24x24 F C99 3.25x25 C99 3.25x25 C N100 3.26x26 N100 3.26x26 N I101 3.27x27 I101 3.27x27 I W102 3.28x28 W102 3.28x28 W A103 3.29x29 A103 3.29x29 A A104 3.30x30 A104 3.30x30 A V105 3.31x31 V105 3.31x31 V D106 3.32x32 D106 3.32x32 D V107 3.33x33 V107 3.33x33 V L108 3.34x34 L108 3.34x34 L C109 3.35x35 C109 3.35x35 C C110 3.36x36 C110 3.36x36 C T111 3.37x37 T111 3.37x37 T A112 3.38x38 A112 3.38x38 A S113 3.39x39 S113 3.39x39 S I114 3.40x40 I114 3.40x40 I M115 3.41x41 M115 3.41x41 M G116 3.42x42 G116 3.42x42 G L117 3.43x43 L117 3.43x43 L C118 3.44x44 C118 3.44x44 C I119 3.45x45 I119 3.45x45 I I120 3.46x46 I120 3.46x46 I S121 3.47x47 S121 3.47x47 S I122 3.48x48 I122 3.48x48 I D123 3.49x49 D123 3.49x49 D R124 3.50x50 R124 3.50x50 R Y125 3.51x51 Y125 3.51x51 Y I126 3.52x52 I126 3.52x52 I G127 3.53x53 G127 3.53x53 G V128 3.54x54 V128 3.54x54 V S129 3.55x55 S129 3.55x55 S Y130 3.56x56 Y130 3.56x56 Y T139 4.38x38 T139 4.38x38 T Q140 4.39x39 Q140 4.39x39 Q R141 4.40x40 R141 4.40x40 R R142 4.41x41 R142 4.41x41 R G143 4.42x42 G143 4.42x42 G L144 4.43x43 L144 4.43x43 L M145 4.44x44 M145 4.44x44 M A146 4.45x45 A146 4.45x45 A L147 4.46x46 L147 4.46x46 L L148 4.47x47 L148 4.47x47 L C149 4.48x48 C149 4.48x48 C V150 4.49x49 V150 4.49x49 V W151 4.50x50 W151 4.50x50 W A152 4.51x51 A152 4.51x51 A L153 4.52x52 L153 4.52x52 L S154 4.53x53 S154 4.53x53 S L155 4.54x54 L155 4.54x54 L V156 4.55x55 V156 4.55x55 V I157 4.56x56 I157 4.56x56 I S158 4.57x57 S158 4.57x57 S I159 4.58x58 I159 4.58x58 I G160 4.59x59 G160 4.59x59 G P161 4.60x60 P161 4.60x60 P L162 4.61x61 L162 4.61x61 L F163 4.62x62 F163 4.62x62 F G164 4.63x63 G164 4.63x63 G W165 4.64x64 W165 4.64x64 W E181 5.35x36 E181 5.35x36 E P182 5.36x37 P182 5.36x37 P G183 5.37x38 G183 5.37x38 G Y184 5.38x39 Y184 5.38x39 Y V185 5.39x40 V185 5.39x40 V L186 5.40x41 L186 5.40x41 L F187 5.41x42 F187 5.41x42 F S188 5.42x43 S188 5.42x43 S A189 5.43x44 A189 5.43x44 A L190 5.44x45 L190 5.44x45 L G191 5.45x46 G191 5.45x46 G S192 5.46x461 S192 5.46x461 S F193 5.47x47 F193 5.47x47 F Y194 5.48x48 Y194 5.48x48 Y L195 5.49x49 L195 5.49x49 L P196 5.50x50 P196 5.50x50 P L197 5.51x51 L197 5.51x51 L A198 5.52x52 A198 5.52x52 A I199 5.53x53 I199 5.53x53 I I200 5.54x54 I200 5.54x54 I L201 5.55x55 L201 5.55x55 L V202 5.56x56 V202 5.56x56 V M203 5.57x57 M203 5.57x57 M Y204 5.58x58 Y204 5.58x58 Y C205 5.59x59 C205 5.59x59 C R206 5.60x60 R206 5.60x60 R V207 5.61x61 V207 5.61x61 V Y208 5.62x62 Y208 5.62x62 Y V209 5.63x63 V209 5.63x63 V V210 5.64x64 V210 5.64x64 V A211 5.65x65 A211 5.65x65 A K212 5.66x66 K212 5.66x66 K R213 5.67x67 R213 5.67x67 R E214 5.68x68 E214 5.68x68 E S215 5.69x69 S215 5.69x69 S R216 5.70x70 R216 5.70x70 R G217 5.71x71 G217 5.71x71 G L218 5.72x72 L218 5.72x72 L K219 5.73x73 K219 5.73x73 K S220 5.74x74 S220 5.74x74 S G221 5.75x75 G221 5.75x75 G L222 5.76x76 L222 5.76x76 L L261 6.24x24 L261 6.24x24 L L262 6.25x25 L262 6.25x25 L K263 6.26x26 K263 6.26x26 K F264 6.27x27 F264 6.27x27 F S265 6.28x28 S265 6.28x28 S R266 6.29x29 R266 6.29x29 R E267 6.30x30 E267 6.30x30 E K268 6.31x31 K268 6.31x31 K K269 6.32x32 K269 6.32x32 K A270 6.33x33 A270 6.33x33 A A271 6.34x34 A271 6.34x34 A K272 6.35x35 K272 6.35x35 K T273 6.36x36 T273 6.36x36 T L274 6.37x37 L274 6.37x37 L G275 6.38x38 G275 6.38x38 G I276 6.39x39 I276 6.39x39 I V277 6.40x40 V277 6.40x40 V V278 6.41x41 V278 6.41x41 V G279 6.42x42 G279 6.42x42 G C280 6.43x43 C280 6.43x43 C F281 6.44x44 F281 6.44x44 F V282 6.45x45 V282 6.45x45 V L283 6.46x46 L283 6.46x46 L C284 6.47x47 C284 6.47x47 C W285 6.48x48 W285 6.48x48 W L286 6.49x49 L286 6.49x49 L P287 6.50x50 P287 6.50x50 P F288 6.51x51 F288 6.51x51 F F289 6.52x52 F289 6.52x52 F L290 6.53x53 L290 6.53x53 L V291 6.54x54 V291 6.54x54 V M292 6.55x55 M292 6.55x55 M P293 6.56x56 P293 6.56x56 P I294 6.57x57 I294 6.57x57 I G295 6.58x58 G295 6.58x58 G S296 6.59x59 S296 6.59x59 S F297 6.60x60 F297 6.60x60 F F298 6.61x61 F298 6.61x61 F S304 7.31x30 S304 7.31x30 S E305 7.32x31 E305 7.32x31 E T306 7.33x32 T306 7.33x32 T V307 7.34x33 V307 7.34x33 V F308 7.35x34 F308 7.35x34 F K309 7.36x35 K309 7.36x35 K I310 7.37x36 I310 7.37x36 I V311 7.38x37 V311 7.38x37 V F312 7.39x38 F312 7.39x38 F W313 7.40x39 W313 7.40x39 W L314 7.41x40 L314 7.41x40 L G315 7.42x41 G315 7.42x41 G Y316 7.43x42 Y316 7.43x42 Y L317 7.44x43 L317 7.44x43 L N318 7.45x45 N318 7.45x45 N S319 7.46x46 S319 7.46x46 S C320 7.47x47 C320 7.47x47 C I321 7.48x48 I321 7.48x48 I N322 7.49x49 N322 7.49x49 N P323 7.50x50 P323 7.50x50 P I324 7.51x51 I324 7.51x51 I I325 7.52x52 I325 7.52x52 I Y326 7.53x53 Y326 7.53x53 Y P327 7.54x54 P327 7.54x54 P C328 7.55x55 C328 7.55x55 C S329 7.56x56 S329 7.56x56 S S330 8.47x47 S330 8.47x47 S Q331 8.48x48 Q331 8.48x48 Q E332 8.49x49 E332 8.49x49 E F337 8.54x54 F337 8.54x54 F Q338 8.55x55 Q338 8.55x55 Q N339 8.56x56 N339 8.56x56 N F333 8.50x50 F333 8.50x50 F K334 8.51x51 K334 8.51x51 K K335 8.52x52 K335 8.52x52 K A336 8.53x53 A336 8.53x53 A V340 8.57x57 V340 8.57x57 V L341 8.58x58 L341 8.58x58 L R342 8.59x59 R342 8.59x59 R

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 ARG238 GLU461 0.000 9.514 -9.514 HIGH
2 PHE281 (6.44x44) TRP285 (6.48x48) 2.261 10.513 -8.252 HIGH
3 THR273 (6.36x36) SER329 (7.56x56) 0.000 8.163 -8.163 HIGH
4 PRO327 (7.54x54) PHE333 (8.50x50) 8.483 0.731 +7.753 HIGH
5 PHE82 (2.60x59) PHE98 (3.24x24) 0.000 7.245 -7.245 HIGH
6 LEU57 (12.50x50) HIS62 (2.40x40) 8.418 15.208 -6.791 HIGH
7 GLY221 (5.75x75) ILE236 0.000 6.684 -6.684 HIGH
8 ASP72 (2.50x50) SER319 (7.46x46) 10.457 3.872 +6.584 HIGH
9 ASN339 (8.56x56) GLN344 0.000 5.911 -5.911 HIGH
10 HIS371 LYS372 5.862 0.000 +5.862 HIGH
11 PHE281 (6.44x44) ASN318 (7.45x45) 0.649 6.389 -5.740 HIGH
12 SER458 VAL466 4.085 9.700 -5.615 HIGH
13 PHE385 PHE399 0.000 5.604 -5.604 HIGH
14 SER215 (5.69x69) LYS263 (6.26x26) 5.521 0.000 +5.521 HIGH
15 LEU132 (34.51x51) ARG260 0.000 5.457 -5.457 HIGH
16 HIS237 LEU459 0.000 5.033 -5.033 HIGH
17 ASP172 THR174 5.577 0.561 +5.015 HIGH
18 SER215 (5.69x69) GLU267 (6.30x30) 4.993 0.000 +4.993 MED
19 ILE114 (3.40x40) TRP285 (6.48x48) 4.923 0.000 +4.923 MED
20 THR61 (2.39x39) ARG124 (3.50x50) 0.000 4.907 -4.907 MED
21 VAL47 (1.53x53) PHE333 (8.50x50) 4.839 0.000 +4.839 MED
22 HIS58 (12.51x51) TYR63 (2.41x41) 4.727 0.000 +4.727 MED
23 TYR204 (5.58x58) GLY275 (6.38x38) 0.000 4.610 -4.610 MED
24 LEU117 (3.43x43) TYR326 (7.53x53) 4.579 0.000 +4.579 MED
25 LYS223 LEU234 0.000 4.479 -4.479 MED
26 GLY217 (5.71x71) LEU222 (5.76x76) 0.000 4.437 -4.437 MED
27 TYR125 (3.51x51) ARG206 (5.60x60) 6.879 2.501 +4.378 MED
28 GLU214 (5.68x68) LYS223 0.000 4.328 -4.328 MED
29 ASP123 (3.49x49) ARG124 (3.50x50) 0.000 4.195 -4.195 MED
30 ARG376 TYR386 0.000 4.173 -4.173 MED
31 CYS53 (1.59x59) CYS345 0.000 4.129 -4.129 MED
32 LEU218 (5.72x72) LYS263 (6.26x26) 4.017 0.000 +4.017 MED
33 TYR326 (7.53x53) PHE333 (8.50x50) 0.000 3.945 -3.945 MED
34 TRP285 (6.48x48) GLY315 (7.42x41) 4.768 8.702 -3.934 MED
35 PRO327 (7.54x54) PHE337 (8.54x54) 0.000 3.815 -3.815 MED
36 GLU214 (5.68x68) PHE264 (6.27x27) 0.000 3.721 -3.721 MED
37 ASN318 (7.45x45) ASN322 (7.49x49) 4.116 0.474 +3.642 MED
38 PRO327 (7.54x54) LYS334 (8.51x51) 0.496 4.091 -3.595 MED
39 ARG96 (3.22x22) ILE175 3.557 0.000 +3.557 MED
40 LEU222 (5.76x76) LEU234 0.000 3.531 -3.531 MED
41 ASN44 (1.50x50) ASP72 (2.50x50) 6.230 2.786 +3.444 MED
42 TYR204 (5.58x58) LEU274 (6.37x37) 2.034 5.462 -3.429 MED
43 TYR204 (5.58x58) VAL278 (6.41x41) 1.684 5.107 -3.423 MED
44 TYR125 (3.51x51) MET203 (5.57x57) 4.775 1.368 +3.407 MED
45 HIS237 SER460 0.000 3.340 -3.340 MED
46 ARG124 (3.50x50) LEU274 (6.37x37) 0.000 3.247 -3.247 MED
47 ARG166 GLU181 (5.35x36) 3.235 0.000 +3.235 MED
48 PRO182 (5.36x37) SER296 (6.59x59) 0.549 3.739 -3.190 MED
49 ARG260 PHE429 0.000 3.178 -3.178 MED
50 PHE193 (5.47x47) PHE289 (6.52x52) 12.991 16.099 -3.108 MED
51 TRP165 (4.64x64) GLU181 (5.35x36) 8.358 5.259 +3.099 MED
52 ASN44 (1.50x50) LEU73 (2.51x51) 4.199 1.170 +3.029 MED
53 ARG124 (3.50x50) GLU267 (6.30x30) 0.000 3.022 -3.022 MED
54 GLN167 GLU181 (5.35x36) 0.964 3.963 -2.999 MED
55 HIS54 ASN339 (8.56x56) 1.064 4.053 -2.988 MED
56 GLY221 (5.75x75) ARG235 0.000 2.965 -2.965 MED
57 ARG124 (3.50x50) SER329 (7.56x56) 2.951 0.000 +2.951 MED
58 ARG124 (3.50x50) TYR204 (5.58x58) 3.304 0.358 +2.946 MED
59 ALA104 SER158 5.344 2.427 +2.917 MED
60 GLY160 TRP165 (4.64x64) 4.990 2.117 +2.873 MED
61 LYS219 LYS263 (6.26x26) 2.844 0.000 +2.844 MED
62 PHE94 PHE98 (3.24x24) 0.925 3.698 -2.773 MED
63 ILE236 LEU459 0.000 2.752 -2.752 MED
64 PHE337 (8.54x54) LEU341 2.744 0.000 +2.744 MED
65 LEU117 (3.43x43) PHE281 (6.44x44) 1.592 4.314 -2.722 MED
66 ARG166 ASN179 8.346 5.682 +2.664 MED
67 TYR130 ARG133 2.976 0.313 +2.663 MED
68 GLN167 GLU180 4.228 6.882 -2.655 MED
69 PHE312 TYR316 6.048 8.648 -2.600 MED
70 VAL60 GLN140 3.829 1.252 +2.577 MED
71 CYS284 ASN318 (7.45x45) 3.590 1.016 +2.573 MED
72 ARG96 (3.22x22) ALA169 0.838 3.391 -2.553 MED
73 TYR208 LYS212 0.828 3.332 -2.504 MED
74 HIS237 SER458 0.000 2.502 -2.502 MED
75 HIS56 GLU332 0.685 3.174 -2.489 MED
76 HIS256 ARG260 6.543 8.996 -2.452 MED
77 ILE119 ALA146 0.000 2.451 -2.451 MED
78 SER83 TYR316 3.911 1.465 +2.446 MED
79 PHE288 MET292 0.288 2.710 -2.422 MED
80 ARG216 LYS263 (6.26x26) 2.340 0.000 +2.340 MED
81 ILE410 THR411 0.055 2.393 -2.339 MED
82 SER129 VAL210 0.147 2.455 -2.308 MED
83 TYR64 ILE119 2.723 5.019 -2.296 MED
84 TRP285 (6.48x48) ASN318 (7.45x45) 5.504 3.241 +2.264 MED
85 TYR208 LEU274 (6.37x37) 2.228 0.000 +2.228 MED
86 ARG166 GLN177 2.378 0.155 +2.223 MED
87 CYS118 PRO196 1.350 3.569 -2.219 MED
88 PRO170 GLN177 2.212 0.000 +2.212 MED
89 LEU218 (5.72x72) LEU261 0.000 2.200 -2.200 MED
90 SER460 GLU464 0.565 2.726 -2.161 LOW
91 ILE65 TYR326 (7.53x53) 0.025 2.184 -2.159 LOW
92 PHE39 CYS320 1.544 3.671 -2.127 LOW
93 GLY43 PRO323 2.383 4.498 -2.115 LOW
94 SER413 LYS414 1.094 3.209 -2.115 LOW
95 GLU181 (5.35x36) PRO182 (5.36x37) 0.917 3.027 -2.110 LOW
96 TRP165 (4.64x64) GLY183 0.000 2.087 -2.087 LOW
97 TRP92 CYS176 4.728 6.807 -2.079 LOW
98 VAL340 CYS345 0.000 2.064 -2.064 LOW
99 CYS284 LEU314 5.649 7.702 -2.053 LOW
100 LEU459 GLU464 2.874 4.912 -2.038 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| ≥ 2.19 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 44-53 47 (4.8), 44 (3.4) 2 53 (-4.1) 1
TM2 61-82 72 (6.6), 63 (4.7), 73 (3.0) 3 82 (-7.2), 62 (-6.8), 61 (-4.9) 3
TM3 96-125 114 (4.9), 117 (4.6), 125 (4.4), 96 (3.6) 4 98 (-7.2), 124 (-4.9), 123 (-4.2) 3
TM4 165-165 165 (3.1) 1 - 0
TM5 181-222 215 (5.5), 206 (4.4), 218 (4.0), 203 (3.4), 181 (3.2) 5 221 (-6.7), 204 (-4.6), 217 (-4.4), 222 (-4.4), 214 (-4.3), 182 (-3.2), 193 (-3.1) 7
TM6 263-296 263 (5.5), 267 (5.0) 2 281 (-8.3), 285 (-8.3), 273 (-8.2), 275 (-4.6), 264 (-3.7), 274 (-3.4), 278 (-3.4), 296 (-3.2), 289 (-3.1) 9
TM7 315-329 327 (7.8), 319 (6.6), 326 (4.6), 322 (3.6) 4 329 (-8.2), 318 (-5.7), 315 (-3.9) 3
Intracellular / Extracellular loops & H8
ICL1 57-58 58 (4.7) 1 57 (-6.8) 1
ICL2 132-132 - 0 132 (-5.5) 1
ICL3 223-260 - 0 238 (-9.5), 236 (-6.7), 260 (-5.5), 237 (-5.0), 223 (-4.5), 234 (-4.5) 6
ECL1 - - 0 - 0
ECL2 166-175 172 (5.0), 174 (5.0), 175 (3.6), 166 (3.2) 4 - 0
ECL3 - - 0 - 0
H8 333-339 333 (7.8) 1 339 (-5.9), 337 (-3.8), 334 (-3.6) 3

Interactive visualizations

ΔRRCS distribution

Active vs inactive comparison

Residue-wise changes

TM domain breakdown

Variants of interest

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

Position Protein change DNA change Allele freq Het / Hom ΔRRCS AM score Pathogenicity Conservation dbSNP
238 p.Arg238Leu c.713G>T 6.84e-07 1 / 0 9.51 0.527 AMBIGUOUS 0.51
238 p.Arg238Trp c.712C>T 6.16e-06 9 / 0 9.51 - nan - rs141722973
281 p.Phe281Leu c.843C>A 6.84e-07 1 / 0 8.25 0.999 PATHOGENIC 0.95 rs1307815039
285 p.Trp285Cys c.855G>T 6.84e-07 1 / 0 8.25 0.996 PATHOGENIC 0.95 rs532108221
281 p.Phe281Ser c.842T>C 6.84e-07 1 / 0 8.25 - nan -
281 p.Phe281Val c.841T>G 6.84e-07 1 / 0 8.25 - nan - rs916744865
281 p.Phe281Leu c.841T>C 6.84e-07 1 / 0 8.25 - nan -
273 p.Thr273Met c.818C>T 2.05e-06 3 / 0 8.16 0.630 PATHOGENIC 0.90 rs1218686921
329 p.Ser329Phe c.986C>T 6.84e-07 1 / 0 8.16 0.229 BENIGN 0.49
329 p.Ser329Ala c.985T>G 6.57e-06 1 / 0 8.16 - nan - rs544693873
329 p.Ser329Pro c.985T>C 6.84e-07 1 / 0 8.16 - nan -
333 p.Val333Ala c.998T>C 1.09e-05 6 / 0 7.75 0.992 PATHOGENIC 0.88 rs781403607
62 p.His62Arg c.185A>G 1.37e-06 2 / 0 6.79 0.895 PATHOGENIC 0.67 rs1813775984
221 p.Gly221Ser c.661G>A 4.10e-06 6 / 0 6.68 0.769 PATHOGENIC 0.81 rs201098896
72 p.Asp72Glu c.216C>A 5.47e-06 8 / 0 6.58 0.997 PATHOGENIC 1.00 rs1455659706
319 p.Ser319Ile c.956G>T 6.84e-07 1 / 0 6.58 0.976 PATHOGENIC 0.97
319 p.Ser319Gly c.955A>G 1.37e-06 2 / 0 6.58 - nan -
319 p.Val319Met c.955G>A 3.63e-06 2 / 0 6.58 - nan -
72 p.Asp72His c.214G>C 9.58e-06 12 / 1 6.58 - nan - rs748400751
72 p.Asp72Asn c.214G>A 1.37e-06 2 / 0 6.58 - nan - rs748400751
339 p.Asn339Lys c.1017T>G 6.84e-07 1 / 0 5.91 0.438 AMBIGUOUS 0.51 rs1174794179
339 p.Asn339Thr c.1016A>C 6.84e-07 1 / 0 5.91 - nan -
339 p.Cys339Ser c.1015T>A 1.82e-06 1 / 0 5.91 - nan -
371 p.His371Asp c.1111C>G 6.84e-07 1 / 0 5.86 0.088 BENIGN 0.32 rs749700097
318 p.Ala318Val c.953C>T 1.82e-06 1 / 0 5.74 0.986 PATHOGENIC 0.95
318 p.Ala318Thr c.952G>A 6.57e-06 1 / 0 5.74 - nan - rs1714236088
458 p.Ser458Pro c.1372T>C 6.58e-06 1 / 0 5.62 0.906 PATHOGENIC 0.96 rs1204162907
466 p.Cys466Tyr c.1397G>A 3.69e-06 1 / 0 5.62 0.670 PATHOGENIC 0.94 rs1804793057
399 p.Phe399Leu c.1195T>C 6.84e-07 1 / 0 5.60 0.338 BENIGN 0.49 rs1563237725
263 p.Lys263Asn c.789G>T 6.84e-07 1 / 0 5.52 0.979 PATHOGENIC 0.77
215 p.Ser215Asn c.644G>A 2.33e-05 34 / 0 5.52 0.171 BENIGN 0.51 rs749902900
260 p.Arg260Trp c.778A>T 6.84e-07 1 / 0 5.46 0.660 PATHOGENIC 0.69
237 p.His237Arg c.710A>G 6.84e-07 1 / 0 5.03 0.971 PATHOGENIC 0.80 rs1262421772
459 p.Ala459Val c.1376C>T 4.20e-06 1 / 0 5.03 0.094 BENIGN 0.73 rs1231983964
459 p.Ala459Glu c.1376C>A 1.26e-05 3 / 0 5.03 - nan - rs1231983964
459 p.Leu459Arg c.1376T>G 7.07e-07 1 / 0 5.03 - nan -
459 p.Leu459Val c.1375C>G 7.06e-07 1 / 0 5.03 - nan -
174 p.Thr174Ile c.521C>T 6.84e-07 1 / 0 5.02 0.482 AMBIGUOUS 0.40 rs1813726916
172 p.Asp172Asn c.514G>A 6.57e-06 1 / 0 5.02 0.147 BENIGN 0.69 rs1250025758
174 p.Thr174Pro c.520A>C 6.84e-07 1 / 0 5.02 - nan -
267 p.Glu267Gln c.799G>C 2.74e-06 4 / 0 4.99 0.677 PATHOGENIC 0.87 rs1393618610
114 p.Ile114Asn c.341T>A 6.57e-06 1 / 0 4.92 0.982 PATHOGENIC 1.00 rs748982353
114 p.Ile114Thr c.341T>C 2.05e-06 3 / 0 4.92 - nan - rs748982353
114 p.Ile114Val c.340A>G 2.05e-06 3 / 0 4.92 - nan - rs1256300248
114 p.Ile114Phe c.340A>T 6.57e-06 1 / 0 4.92 - nan - rs1256300248
124 p.Arg124His c.371G>A 1.03e-05 15 / 0 4.91 0.970 PATHOGENIC 0.99
61 p.Thr61Arg c.182C>G 6.84e-07 1 / 0 4.91 0.931 PATHOGENIC 0.81
124 p.Arg124Cys c.370C>T 1.09e-05 16 / 0 4.91 - nan - rs747122943
124 p.Arg124Ser c.370C>A 3.42e-06 5 / 0 4.91 - nan - rs747122943
124 p.Arg124Gly c.370C>G 4.10e-06 6 / 0 4.91 - nan - rs747122943
47 p.Val47Ala c.140T>C 6.16e-06 9 / 0 4.84 0.984 PATHOGENIC 0.97 rs779890003
47 p.Val47Gly c.140T>G 6.84e-07 1 / 0 4.84 - nan -
47 p.Val47Met c.139G>A 1.31e-05 2 / 0 4.84 - nan - rs1243477642
63 p.Tyr63His c.187T>C 1.37e-06 2 / 0 4.73 0.490 AMBIGUOUS 0.71
58 p.His58Arg c.173A>G 6.84e-07 1 / 0 4.73 0.086 BENIGN 0.68
63 p.Tyr63Asn c.187T>A 6.84e-07 1 / 0 4.73 - nan -
58 p.His58Tyr c.172C>T 6.84e-07 1 / 0 4.73 - nan -
204 p.Tyr204His c.610T>C 6.84e-07 1 / 0 4.61 0.994 PATHOGENIC 0.98 rs1293034019
275 p.Gly275Val c.824G>T 6.84e-07 1 / 0 4.61 0.950 PATHOGENIC 0.74
275 p.Gly275Asp c.824G>A 2.05e-06 3 / 0 4.61 - nan -
275 p.Gly275Ser c.823G>A 4.72e-05 69 / 0 4.61 - nan - rs201224020
117 p.Leu117Arg c.350T>G 6.84e-07 1 / 0 4.58 0.991 PATHOGENIC 1.00 rs1813753776
326 p.Tyr326Cys c.977A>G 2.74e-06 4 / 0 4.58 0.990 PATHOGENIC 0.98
326 p.Tyr326His c.976T>C 6.57e-06 1 / 0 4.58 - nan - rs1326198666
326 p.Tyr326Asn c.976T>A 6.84e-07 1 / 0 4.58 - nan - rs1326198666
326 p.Glu326Lys c.976G>A 1.82e-06 1 / 0 4.58 - nan -
326 p.Glu326Gln c.976G>C 2.00e-05 11 / 0 4.58 - nan - rs1041635161
234 p.Leu234Phe c.700C>T 2.74e-06 4 / 0 4.48 0.888 PATHOGENIC 0.79
222 p.Leu222Pro c.665T>C 2.05e-06 3 / 0 4.44 0.816 PATHOGENIC 0.45 rs1406968822
217 p.Gly217Ala c.650G>C 4.17e-05 61 / 0 4.44 0.181 BENIGN 0.39 rs760453930
222 p.Leu222Phe c.664C>T 6.84e-07 1 / 0 4.44 - nan - rs1324162537
222 p.Leu222Ile c.664C>A 6.84e-07 1 / 0 4.44 - nan - rs1324162537
217 p.Gly217Val c.650G>T 6.84e-07 1 / 0 4.44 - nan -
217 p.Gly217Arg c.649G>C 1.37e-06 2 / 0 4.44 - nan - rs150544480
217 p.Gly217Ser c.649G>A 8.21e-06 12 / 0 4.44 - nan - rs150544480
125 p.Tyr125His c.373T>C 6.84e-07 1 / 0 4.38 0.927 PATHOGENIC 0.97
206 p.Arg206Gly c.616C>G 1.37e-06 2 / 0 4.38 0.643 PATHOGENIC 0.82 rs1285479324
214 p.Glu214Gly c.641A>G 6.84e-07 1 / 0 4.33 0.695 PATHOGENIC 0.47
214 p.Glu214Gln c.640G>C 6.84e-07 1 / 0 4.33 - nan -
123 p.Asp123Asn c.367G>A 4.79e-06 7 / 0 4.19 0.990 PATHOGENIC 0.96 rs61757010
123 p.Asp123Tyr c.367G>T 1.09e-05 16 / 0 4.19 - nan - rs61757010
386 p.Tyr386Cys c.1157A>G 6.84e-07 1 / 0 4.17 0.176 BENIGN 0.64 rs759652152
376 p.Arg376His c.1127G>A 3.22e-05 47 / 0 4.17 0.112 BENIGN 0.61 rs140512348
386 p.Tyr386His c.1156T>C 5.47e-06 8 / 0 4.17 - nan - rs1806052198
376 p.Arg376Pro c.1127G>C 6.57e-06 1 / 0 4.17 - nan - rs140512348
376 p.Arg376Leu c.1127G>T 5.47e-06 8 / 0 4.17 - nan - rs140512348
376 p.Arg376Cys c.1126C>T 3.28e-05 44 / 2 4.17 - nan - rs1496121
376 p.Arg376Ser c.1126C>A 6.84e-07 1 / 0 4.17 - nan - rs1496121
376 p.Arg376Gly c.1126C>G 6.84e-07 1 / 0 4.17 - nan - rs1496121
53 p.Cys53Arg c.157T>C 2.05e-06 3 / 0 4.13 0.645 PATHOGENIC 0.44
345 p.Cys345Arg c.1033T>C 2.74e-06 4 / 0 4.13 0.333 BENIGN 0.77
218 p.Leu218Val c.652C>G 5.47e-06 8 / 0 4.02 0.516 AMBIGUOUS 0.74 rs766542151
315 p.Gly315Arg c.943G>A 1.30e-05 19 / 0 3.93 0.998 PATHOGENIC 0.96 rs756970856
315 p.His315Arg c.944A>G 5.45e-06 3 / 0 3.93 - nan -
315 p.His315Asp c.943C>G 1.82e-06 1 / 0 3.93 - nan -
337 p.Asp337Ala c.1010A>C 1.82e-06 1 / 0 3.81 0.985 PATHOGENIC 0.94
337 p.Asp337His c.1009G>C 5.45e-06 3 / 0 3.81 - nan - rs1563246051
264 p.Phe264Leu c.792C>G 6.84e-07 1 / 0 3.72 0.998 PATHOGENIC 0.82
264 p.Phe264Leu c.790T>C 6.84e-07 1 / 0 3.72 - nan -
322 p.Asn322Lys c.966C>A 2.05e-06 3 / 0 3.64 0.998 PATHOGENIC 0.98 rs1315965898
322 p.Asn322Ser c.965A>G 1.09e-05 16 / 0 3.64 - nan - rs1458563910
334 p.Lys334Thr c.1001A>C 6.57e-06 1 / 0 3.60 0.801 PATHOGENIC 0.75 rs1313869976
334 p.Ser334Pro c.1000T>C 1.32e-05 2 / 0 3.60 - nan - rs988381380
96 p.Arg96Lys c.287G>A 6.57e-06 1 / 0 3.56 0.204 BENIGN 0.58 rs1813763764
175 p.Ile175Met c.525C>G 6.84e-06 10 / 0 3.56 0.131 BENIGN 0.44 rs756487113
175 p.Ile175Asn c.524T>A 1.37e-06 2 / 0 3.56 - nan - rs1347816678
175 p.Ile175Val c.523A>G 1.37e-06 2 / 0 3.56 - nan -
203 p.Met203Arg c.608T>G 1.37e-06 2 / 0 3.41 0.960 PATHOGENIC 0.66 rs1291020451
203 p.Met203Leu c.607A>C 6.84e-07 1 / 0 3.41 - nan - rs770251050
203 p.Met203Val c.607A>G 6.84e-07 1 / 0 3.41 - nan -
460 p.Ser460Ile c.1379G>T 7.08e-07 1 / 0 3.34 0.473 AMBIGUOUS 0.75 rs747894155
460 p.Ser460Thr c.1379G>C 7.08e-07 1 / 0 3.34 - nan -
460 p.Ser460Asn c.1379G>A 1.42e-06 2 / 0 3.34 - nan - rs747894155
181 p.Glu181Asp c.543G>T 6.84e-07 1 / 0 3.23 0.124 BENIGN 0.66
166 p.Arg166Lys c.497G>A 2.82e-03 4110 / 7 3.23 0.093 BENIGN 0.63 rs56233953
181 p.Glu181Lys c.541G>A 2.05e-06 3 / 0 3.23 - nan -
166 p.Arg166Gly c.496A>G 6.84e-07 1 / 0 3.23 - nan - rs1314932778
296 p.Glu296Lys c.886G>A 9.09e-06 5 / 0 3.19 0.936 PATHOGENIC 0.49 rs776089126
182 p.Pro182Ser c.544C>T 2.05e-06 3 / 0 3.19 0.338 BENIGN 0.51 rs551511934
429 p.Val429Ile c.1285G>A 4.24e-05 9 / 0 3.18 0.249 BENIGN 0.69 rs554972791
429 p.Val429Phe c.1285G>T 9.43e-06 2 / 0 3.18 - nan -
429 p.Arg429Gly c.1285A>G 6.86e-07 1 / 0 3.18 - nan - rs765906061
429 p.Phe429Leu c.1285T>C 6.84e-07 1 / 0 3.18 - nan -
289 p.Phe289Ser c.866T>C 3.42e-06 5 / 0 3.11 0.990 PATHOGENIC 0.96 rs772571115
289 p.Phe289Val c.865T>G 6.84e-07 1 / 0 3.11 - nan -
165 p.Trp165Cys c.495G>C 6.84e-07 1 / 0 3.10 0.996 PATHOGENIC 0.90 rs997765683
165 p.Trp165Gly c.493T>G 6.84e-07 1 / 0 3.10 - nan - rs1813730823
73 p.Leu73Pro c.218T>C 6.84e-07 1 / 0 3.03 0.997 PATHOGENIC 0.89 rs1177102605
73 p.Leu73His c.218T>A 4.10e-06 6 / 0 3.03 - nan - rs1177102605
73 p.Leu73Phe c.217C>T 2.74e-06 4 / 0 3.03 - nan - rs781501725
73 p.Leu73Ile c.217C>A 6.57e-06 1 / 0 3.03 - nan - rs781501725

Complete RRCS results

Top 1000 contact pairs by |ΔRRCS|. Significance threshold: |ΔRRCS| ≥ 2.19, computed as max(mean(|Δ|) + σ, 0.2). Highlighted rows indicate significant changes.

Res1 AA1 Res2 AA2 Active RRCS Inactive RRCS ΔRRCS |ΔRRCS|
238 ARG 461 GLU 0.000 9.514 -9.514 9.514
281 PHE 285 TRP 2.261 10.513 -8.252 8.252
273 THR 329 SER 0.000 8.163 -8.163 8.163
327 PRO 333 PHE 8.483 0.731 7.753 7.753
82 PHE 98 PHE 0.000 7.245 -7.245 7.245
57 LEU 62 HIS 8.418 15.208 -6.791 6.791
221 GLY 236 ILE 0.000 6.684 -6.684 6.684
72 ASP 319 SER 10.457 3.872 6.584 6.584
339 ASN 344 GLN 0.000 5.911 -5.911 5.911
371 HIS 372 LYS 5.862 0.000 5.862 5.862
281 PHE 318 ASN 0.649 6.389 -5.740 5.740
458 SER 466 VAL 4.085 9.700 -5.615 5.615
385 PHE 399 PHE 0.000 5.604 -5.604 5.604
215 SER 263 LYS 5.521 0.000 5.521 5.521
132 LEU 260 ARG 0.000 5.457 -5.457 5.457
237 HIS 459 LEU 0.000 5.033 -5.033 5.033
172 ASP 174 THR 5.577 0.561 5.015 5.015
215 SER 267 GLU 4.993 0.000 4.993 4.993
114 ILE 285 TRP 4.923 0.000 4.923 4.923
61 THR 124 ARG 0.000 4.907 -4.907 4.907
47 VAL 333 PHE 4.839 0.000 4.839 4.839
58 HIS 63 TYR 4.727 0.000 4.727 4.727
204 TYR 275 GLY 0.000 4.610 -4.610 4.610
117 LEU 326 TYR 4.579 0.000 4.579 4.579
223 LYS 234 LEU 0.000 4.479 -4.479 4.479
217 GLY 222 LEU 0.000 4.437 -4.437 4.437
125 TYR 206 ARG 6.879 2.501 4.378 4.378
214 GLU 223 LYS 0.000 4.328 -4.328 4.328
123 ASP 124 ARG 0.000 4.195 -4.195 4.195
376 ARG 386 TYR 0.000 4.173 -4.173 4.173
53 CYS 345 CYS 0.000 4.129 -4.129 4.129
218 LEU 263 LYS 4.017 0.000 4.017 4.017
326 TYR 333 PHE 0.000 3.945 -3.945 3.945
285 TRP 315 GLY 4.768 8.702 -3.934 3.934
327 PRO 337 PHE 0.000 3.815 -3.815 3.815
214 GLU 264 PHE 0.000 3.721 -3.721 3.721
318 ASN 322 ASN 4.116 0.474 3.642 3.642
327 PRO 334 LYS 0.496 4.091 -3.595 3.595
96 ARG 175 ILE 3.557 0.000 3.557 3.557
222 LEU 234 LEU 0.000 3.531 -3.531 3.531
44 ASN 72 ASP 6.230 2.786 3.444 3.444
204 TYR 274 LEU 2.034 5.462 -3.429 3.429
204 TYR 278 VAL 1.684 5.107 -3.423 3.423
125 TYR 203 MET 4.775 1.368 3.407 3.407
237 HIS 460 SER 0.000 3.340 -3.340 3.340
124 ARG 274 LEU 0.000 3.247 -3.247 3.247
166 ARG 181 GLU 3.235 0.000 3.235 3.235
182 PRO 296 SER 0.549 3.739 -3.190 3.190
260 ARG 429 PHE 0.000 3.178 -3.178 3.178
193 PHE 289 PHE 12.991 16.099 -3.108 3.108
165 TRP 181 GLU 8.358 5.259 3.099 3.099
44 ASN 73 LEU 4.199 1.170 3.029 3.029
124 ARG 267 GLU 0.000 3.022 -3.022 3.022
167 GLN 181 GLU 0.964 3.963 -2.999 2.999
54 HIS 339 ASN 1.064 4.053 -2.988 2.988
221 GLY 235 ARG 0.000 2.965 -2.965 2.965
124 ARG 329 SER 2.951 0.000 2.951 2.951
124 ARG 204 TYR 3.304 0.358 2.946 2.946
104 ALA 158 SER 5.344 2.427 2.917 2.917
160 GLY 165 TRP 4.990 2.117 2.873 2.873
219 LYS 263 LYS 2.844 0.000 2.844 2.844
94 PHE 98 PHE 0.925 3.698 -2.773 2.773
236 ILE 459 LEU 0.000 2.752 -2.752 2.752
337 PHE 341 LEU 2.744 0.000 2.744 2.744
117 LEU 281 PHE 1.592 4.314 -2.722 2.722
166 ARG 179 ASN 8.346 5.682 2.664 2.664
130 TYR 133 ARG 2.976 0.313 2.663 2.663
167 GLN 180 GLU 4.228 6.882 -2.655 2.655
312 PHE 316 TYR 6.048 8.648 -2.600 2.600
60 VAL 140 GLN 3.829 1.252 2.577 2.577
284 CYS 318 ASN 3.590 1.016 2.573 2.573
96 ARG 169 ALA 0.838 3.391 -2.553 2.553
208 TYR 212 LYS 0.828 3.332 -2.504 2.504
237 HIS 458 SER 0.000 2.502 -2.502 2.502
56 HIS 332 GLU 0.685 3.174 -2.489 2.489
256 HIS 260 ARG 6.543 8.996 -2.452 2.452
119 ILE 146 ALA 0.000 2.451 -2.451 2.451
83 SER 316 TYR 3.911 1.465 2.446 2.446
288 PHE 292 MET 0.288 2.710 -2.422 2.422
216 ARG 263 LYS 2.340 0.000 2.340 2.340
410 ILE 411 THR 0.055 2.393 -2.339 2.339
129 SER 210 VAL 0.147 2.455 -2.308 2.308
64 TYR 119 ILE 2.723 5.019 -2.296 2.296
285 TRP 318 ASN 5.504 3.241 2.264 2.264
208 TYR 274 LEU 2.228 0.000 2.228 2.228
166 ARG 177 GLN 2.378 0.155 2.223 2.223
118 CYS 196 PRO 1.350 3.569 -2.219 2.219
170 PRO 177 GLN 2.212 0.000 2.212 2.212
218 LEU 261 LEU 0.000 2.200 -2.200 2.200
460 SER 464 GLU 0.565 2.726 -2.161 2.161
65 ILE 326 TYR 0.025 2.184 -2.159 2.159
39 PHE 320 CYS 1.544 3.671 -2.127 2.127
43 GLY 323 PRO 2.383 4.498 -2.115 2.115
413 SER 414 LYS 1.094 3.209 -2.115 2.115
181 GLU 182 PRO 0.917 3.027 -2.110 2.110
165 TRP 183 GLY 0.000 2.087 -2.087 2.087
92 TRP 176 CYS 4.728 6.807 -2.079 2.079
340 VAL 345 CYS 0.000 2.064 -2.064 2.064
284 CYS 314 LEU 5.649 7.702 -2.053 2.053
459 LEU 464 GLU 2.874 4.912 -2.038 2.038
96 ARG 171 GLU 0.000 2.017 -2.017 2.017
200 ILE 281 PHE 2.017 0.000 2.017 2.017
133 ARG 427 LYS 0.000 2.015 -2.015 2.015
374 MET 376 ARG 1.996 0.000 1.996 1.996
72 ASP 322 ASN 4.716 2.759 1.957 1.957
277 VAL 325 ILE 0.819 2.750 -1.932 1.932
132 LEU 256 HIS 0.000 1.894 -1.894 1.894
44 ASN 69 ALA 5.923 4.041 1.882 1.882
396 GLU 398 LYS 3.466 1.588 1.878 1.878
100 ASN 166 ARG 4.708 6.586 -1.878 1.878
224 THR 232 VAL 0.000 1.873 -1.873 1.873
114 ILE 281 PHE 1.500 3.369 -1.868 1.868
118 CYS 199 ILE 1.990 0.123 1.867 1.867
288 PHE 289 PHE 2.356 0.495 1.860 1.860
189 ALA 289 PHE 2.331 0.489 1.842 1.842
120 ILE 274 LEU 0.000 1.828 -1.828 1.828
71 ALA 113 SER 0.925 2.741 -1.816 1.816
165 TRP 184 TYR 1.150 2.956 -1.806 1.806
208 TYR 271 ALA 1.793 0.000 1.793 1.793
221 GLY 234 LEU 0.000 1.772 -1.772 1.772
51 VAL 58 HIS 0.000 1.709 -1.709 1.709
47 VAL 337 PHE 0.735 2.442 -1.707 1.707
124 ARG 326 TYR 1.706 0.000 1.706 1.706
212 LYS 267 GLU 1.699 0.000 1.699 1.699
197 LEU 281 PHE 1.685 0.000 1.685 1.685
204 TYR 277 VAL 1.681 0.000 1.681 1.681
120 ILE 124 ARG 1.870 0.196 1.674 1.674
193 PHE 285 TRP 3.384 1.711 1.673 1.673
47 VAL 326 TYR 0.000 1.645 -1.645 1.645
117 LEU 322 ASN 1.641 0.000 1.641 1.641
63 TYR 140 GLN 3.141 1.500 1.641 1.641
161 PRO 184 TYR 6.917 8.548 -1.630 1.630
68 LEU 117 LEU 2.657 1.037 1.619 1.619
165 TRP 187 PHE 0.119 1.738 -1.619 1.619
222 LEU 233 THR 0.000 1.612 -1.612 1.612
157 ILE 184 TYR 3.244 1.639 1.605 1.605
317 LEU 321 ILE 1.599 0.000 1.599 1.599
58 HIS 140 GLN 1.877 0.282 1.596 1.596
161 PRO 166 ARG 2.129 0.539 1.591 1.591
211 ALA 264 PHE 0.000 1.590 -1.590 1.590
237 HIS 461 GLU 0.000 1.588 -1.588 1.588
388 ILE 396 GLU 0.000 1.587 -1.587 1.587
342 ARG 344 GLN 0.000 1.574 -1.574 1.574
92 TRP 98 PHE 1.679 3.239 -1.560 1.560
224 THR 233 THR 0.000 1.553 -1.553 1.553
180 GLU 296 SER 1.257 2.793 -1.537 1.537
96 ARG 172 ASP 2.528 0.993 1.535 1.535
180 GLU 292 MET 1.528 0.000 1.528 1.528
74 LEU 78 THR 1.499 0.000 1.499 1.499
62 HIS 333 PHE 0.180 1.677 -1.497 1.497
47 VAL 327 PRO 1.494 0.000 1.494 1.494
108 LEU 155 LEU 1.882 3.360 -1.478 1.478
167 GLN 178 ILE 1.463 0.000 1.463 1.463
96 ARG 173 GLU 3.742 2.295 1.447 1.447
313 TRP 316 TYR 2.407 1.003 1.404 1.404
257 PHE 261 LEU 3.183 4.580 -1.397 1.397
56 HIS 57 LEU 4.504 5.899 -1.395 1.395
96 ARG 100 ASN 1.634 0.240 1.394 1.394
288 PHE 312 PHE 1.826 3.205 -1.379 1.379
375 VAL 387 ARG 0.000 1.378 -1.378 1.378
120 ILE 326 TYR 1.371 0.000 1.371 1.371
79 VAL 102 TRP 3.533 4.904 -1.371 1.371
225 ASP 232 VAL 0.000 1.368 -1.368 1.368
411 THR 412 VAL 0.613 1.976 -1.363 1.363
200 ILE 278 VAL 0.007 1.367 -1.360 1.360
236 ILE 257 PHE 0.000 1.316 -1.316 1.316
114 ILE 192 SER 3.146 4.461 -1.314 1.314
284 CYS 315 GLY 1.008 2.310 -1.301 1.301
458 SER 465 GLU 0.306 1.605 -1.300 1.300
51 VAL 333 PHE 1.737 0.453 1.283 1.283
127 GLY 267 GLU 0.000 1.257 -1.257 1.257
202 VAL 206 ARG 1.302 0.048 1.254 1.254
49 LEU 340 VAL 0.556 1.806 -1.249 1.249
415 ASP 416 GLN 1.310 0.071 1.240 1.240
54 HIS 336 ALA 5.974 7.210 -1.236 1.236
189 ALA 194 TYR 4.621 5.847 -1.225 1.225
225 ASP 429 PHE 0.000 1.208 -1.208 1.208
227 SER 228 ASP 1.206 0.000 1.206 1.206
167 GLN 177 GLN 1.186 0.000 1.186 1.186
46 LEU 344 GLN 1.171 0.000 1.171 1.171
389 SER 391 THR 1.169 0.000 1.169 1.169
277 VAL 326 TYR 1.890 0.721 1.169 1.169
239 LYS 240 ASN 1.167 0.000 1.167 1.167
92 TRP 99 CYS 7.475 6.311 1.164 1.164
305 GLU 309 LYS 2.950 4.107 -1.157 1.157
104 ALA 162 LEU 1.152 0.000 1.152 1.152
96 ARG 170 PRO 6.341 5.194 1.147 1.147
384 THR 386 TYR 0.000 1.140 -1.140 1.140
7 ASN 8 ALA 0.000 1.139 -1.139 1.139
192 SER 289 PHE 2.550 1.412 1.138 1.138
193 PHE 194 TYR 2.201 1.068 1.133 1.133
361 HIS 362 PRO 1.591 0.458 1.133 1.133
74 LEU 109 CYS 2.097 0.978 1.119 1.119
172 ASP 175 ILE 2.572 1.454 1.118 1.118
277 VAL 322 ASN 0.000 1.111 -1.111 1.111
64 TYR 123 ASP 4.491 3.386 1.105 1.105
254 LYS 258 SER 0.000 1.105 -1.105 1.105
41 VAL 76 THR 4.626 3.525 1.100 1.100
44 ASN 323 PRO 4.644 3.555 1.088 1.088
60 VAL 64 TYR 3.252 2.164 1.088 1.088
128 VAL 264 PHE 0.000 1.076 -1.076 1.076
112 ALA 150 VAL 0.508 1.579 -1.071 1.071
124 ARG 270 ALA 0.000 1.067 -1.067 1.067
292 MET 296 SER 1.066 0.000 1.066 1.066
215 SER 268 LYS 0.000 1.050 -1.050 1.050
193 PHE 281 PHE 1.507 0.457 1.050 1.050
44 ASN 319 SER 1.531 2.564 -1.033 1.033
182 PRO 297 PHE 3.648 2.615 1.033 1.033
100 ASN 162 LEU 1.039 0.009 1.029 1.029
124 ARG 271 ALA 0.000 1.028 -1.028 1.028
330 SER 333 PHE 1.152 2.163 -1.011 1.011
197 LEU 282 VAL 0.586 1.594 -1.008 1.008
460 SER 466 VAL 1.834 0.831 1.003 1.003
29 LEU 87 GLU 0.443 1.444 -1.001 1.001
128 VAL 267 GLU 0.000 0.998 -0.998 0.998
118 CYS 200 ILE 2.547 3.541 -0.994 0.994
60 VAL 138 VAL 1.671 2.653 -0.982 0.982
444 ASP 445 LYS 0.000 0.973 -0.973 0.973
225 ASP 428 SER 0.000 0.971 -0.971 0.971
285 TRP 288 PHE 0.000 0.970 -0.970 0.970
50 SER 340 VAL 2.279 1.312 0.967 0.967
67 ASN 151 TRP 4.356 3.393 0.962 0.962
76 THR 319 SER 0.228 1.177 -0.949 0.949
343 ILE 346 LEU 0.000 0.947 -0.947 0.947
95 GLY 173 GLU 1.080 0.140 0.940 0.940
285 TRP 316 TYR 0.000 0.936 -0.936 0.936
51 VAL 62 HIS 0.178 1.112 -0.933 0.933
235 ARG 459 LEU 0.000 0.930 -0.930 0.930
124 ARG 134 TYR 0.000 0.928 -0.928 0.928
414 LYS 415 ASP 6.153 5.229 0.924 0.924
159 ILE 162 LEU 0.000 0.919 -0.919 0.919
442 SER 443 LEU 0.915 0.000 0.915 0.915
371 HIS 374 MET 0.000 0.915 -0.915 0.915
79 VAL 106 ASP 4.248 3.334 0.914 0.914
62 HIS 332 GLU 0.914 0.000 0.914 0.914
113 SER 322 ASN 0.898 0.000 0.898 0.898
181 GLU 296 SER 0.000 0.888 -0.888 0.888
121 SER 203 MET 3.033 2.147 0.886 0.886
137 ILE 142 ARG 4.480 3.599 0.881 0.881
85 ILE 94 PHE 0.800 1.679 -0.880 0.880
222 LEU 224 THR 0.000 0.876 -0.876 0.876
194 TYR 289 PHE 3.902 3.036 0.866 0.866
374 MET 386 TYR 0.000 0.866 -0.866 0.866
384 THR 400 PHE 0.000 0.864 -0.864 0.864
379 VAL 385 PHE 0.000 0.863 -0.863 0.863
75 LEU 109 CYS 3.230 2.369 0.861 0.861
185 VAL 296 SER 2.343 1.491 0.852 0.852
106 ASP 312 PHE 1.352 0.507 0.845 0.845
376 ARG 385 PHE 0.024 0.864 -0.839 0.839
323 PRO 337 PHE 0.000 0.836 -0.836 0.836
222 LEU 235 ARG 0.000 0.835 -0.835 0.835
159 ILE 163 PHE 2.994 2.160 0.834 0.834
108 LEU 158 SER 3.609 2.782 0.827 0.827
322 ASN 327 PRO 0.827 0.000 0.827 0.827
282 VAL 286 LEU 1.201 0.374 0.826 0.826
36 LEU 320 CYS 2.236 1.411 0.824 0.824
157 ILE 187 PHE 1.035 0.211 0.824 0.824
37 ILE 80 LEU 3.582 2.780 0.802 0.802
155 LEU 159 ILE 0.915 0.114 0.801 0.801
223 LYS 233 THR 0.000 0.799 -0.799 0.799
373 ASP 387 ARG 0.000 0.797 -0.797 0.797
333 PHE 337 PHE 1.063 0.273 0.791 0.791
191 GLY 196 PRO 1.695 2.484 -0.788 0.788
235 ARG 458 SER 0.000 0.782 -0.782 0.782
223 LYS 232 VAL 0.000 0.782 -0.782 0.782
36 LEU 317 LEU 0.673 1.447 -0.774 0.774
276 ILE 325 ILE 0.409 1.181 -0.772 0.772
72 ASP 113 SER 3.631 2.862 0.769 0.769
280 CYS 325 ILE 1.553 0.786 0.767 0.767
362 PRO 363 PRO 1.008 0.244 0.763 0.763
122 ILE 199 ILE 1.029 0.272 0.757 0.757
178 ILE 308 PHE 1.011 0.258 0.753 0.753
87 GLU 309 LYS 7.612 8.358 -0.746 0.746
204 TYR 326 TYR 0.738 0.000 0.738 0.738
161 PRO 179 ASN 1.481 0.747 0.734 0.734
65 ILE 333 PHE 0.539 1.270 -0.731 0.731
236 ILE 237 HIS 0.730 0.000 0.730 0.730
102 TRP 178 ILE 0.000 0.722 -0.722 0.722
160 GLY 184 TYR 0.650 1.369 -0.720 0.720
179 ASN 184 TYR 4.571 3.860 0.710 0.710
128 VAL 211 ALA 0.000 0.707 -0.707 0.707
68 LEU 72 ASP 1.829 1.129 0.700 0.700
22 ASN 25 LYS 1.646 2.337 -0.692 0.692
322 ASN 326 TYR 1.330 0.640 0.690 0.690
292 MET 308 PHE 0.684 0.000 0.684 0.684
21 VAL 88 VAL 0.000 0.684 -0.684 0.684
130 TYR 137 ILE 1.109 0.426 0.683 0.683
68 LEU 113 SER 2.547 3.229 -0.681 0.681
378 PRO 385 PHE 0.679 0.000 0.679 0.679
52 ALA 58 HIS 0.000 0.677 -0.677 0.677
375 VAL 386 TYR 0.000 0.676 -0.676 0.676
82 PHE 94 PHE 3.564 4.229 -0.666 0.666
44 ASN 76 THR 0.718 0.056 0.662 0.662
288 PHE 308 PHE 0.095 0.756 -0.661 0.661
280 CYS 321 ILE 0.139 0.796 -0.657 0.657
178 ILE 312 PHE 1.639 0.982 0.656 0.656
74 LEU 151 TRP 0.272 0.925 -0.653 0.653
255 THR 459 LEU 0.000 0.648 -0.648 0.648
216 ARG 267 GLU 0.646 0.000 0.646 0.646
272 LYS 276 ILE 0.927 0.282 0.645 0.645
201 LEU 278 VAL 0.642 0.000 0.642 0.642
53 CYS 54 HIS 0.374 1.016 -0.642 0.642
57 LEU 332 GLU 0.824 0.186 0.638 0.638
50 SER 333 PHE 1.605 0.970 0.635 0.635
383 GLU 385 PHE 0.000 0.633 -0.633 0.633
325 ILE 326 TYR 0.633 0.000 0.633 0.633
273 THR 325 ILE 0.000 0.629 -0.629 0.629
68 LEU 120 ILE 0.842 0.216 0.626 0.626
285 TRP 289 PHE 2.608 3.232 -0.625 0.625
2 VAL 3 PHE 0.000 0.614 -0.614 0.614
54 HIS 340 VAL 0.609 0.000 0.609 0.609
417 SER 418 SER 0.000 0.607 -0.607 0.607
86 PHE 176 CYS 1.669 1.066 0.603 0.603
269 LYS 329 SER 0.000 0.597 -0.597 0.597
127 GLY 134 TYR 3.476 2.880 0.596 0.596
41 VAL 73 LEU 1.757 2.352 -0.595 0.595
234 LEU 257 PHE 0.000 0.595 -0.595 0.595
113 SER 319 SER 0.590 0.000 0.590 0.590
29 LEU 33 LEU 1.543 0.955 0.588 0.588
55 ARG 58 HIS 0.657 0.071 0.586 0.586
365 GLN 366 ALA 0.585 0.000 0.585 0.585
122 ILE 203 MET 1.133 1.712 -0.579 0.579
76 THR 81 PRO 1.612 2.188 -0.576 0.576
75 LEU 80 LEU 5.695 5.121 0.574 0.574
459 LEU 465 GLU 1.126 1.699 -0.572 0.572
61 THR 123 ASP 5.550 4.978 0.572 0.572
200 ILE 204 TYR 1.349 0.780 0.569 0.569
234 LEU 457 ILE 0.000 0.568 -0.568 0.568
294 ILE 301 PHE 0.983 0.416 0.567 0.567
181 GLU 184 TYR 0.369 0.936 -0.566 0.566
428 SER 429 PHE 0.000 0.558 -0.558 0.558
47 VAL 323 PRO 1.527 0.971 0.556 0.556
370 GLN 371 HIS 0.552 0.000 0.552 0.552
124 ARG 207 VAL 0.807 1.357 -0.550 0.550
71 ALA 109 CYS 0.842 1.392 -0.550 0.550
125 TYR 207 VAL 2.110 2.657 -0.548 0.548
210 VAL 214 GLU 0.613 0.067 0.546 0.546
220 SER 222 LEU 0.000 0.543 -0.543 0.543
282 VAL 287 PRO 0.778 0.235 0.542 0.542
75 LEU 319 SER 1.499 0.956 0.542 0.542
180 GLU 302 LYS 3.883 4.425 -0.542 0.542
339 ASN 345 CYS 0.000 0.536 -0.536 0.536
64 TYR 147 LEU 2.528 1.992 0.536 0.536
128 VAL 271 ALA 0.000 0.536 -0.536 0.536
288 PHE 311 VAL 4.162 3.634 0.528 0.528
59 SER 140 GLN 0.525 0.000 0.525 0.525
1 MET 305 GLU 0.524 0.000 0.524 0.524
207 VAL 274 LEU 0.523 0.000 0.523 0.523
227 SER 428 SER 0.000 0.523 -0.523 0.523
71 ALA 151 TRP 1.388 0.869 0.519 0.519
375 VAL 385 PHE 0.000 0.518 -0.518 0.518
207 VAL 271 ALA 0.000 0.518 -0.518 0.518
92 TRP 102 TRP 4.827 4.309 0.517 0.517
284 CYS 321 ILE 0.212 0.723 -0.510 0.510
39 PHE 324 ILE 1.868 2.376 -0.508 0.508
115 MET 153 LEU 1.106 0.599 0.507 0.507
204 TYR 271 ALA 0.000 0.502 -0.502 0.502
158 SER 159 ILE 0.000 0.500 -0.500 0.500
255 THR 258 SER 0.000 0.500 -0.500 0.500
21 VAL 89 LEU 0.000 0.498 -0.498 0.498
193 PHE 197 LEU 1.915 1.419 0.496 0.496
416 GLN 417 SER 0.678 0.185 0.492 0.492
259 VAL 263 LYS 0.991 0.501 0.491 0.491
40 GLY 320 CYS 1.432 0.942 0.490 0.490
107 VAL 188 SER 0.000 0.488 -0.488 0.488
63 TYR 147 LEU 0.359 0.846 -0.487 0.487
117 LEU 277 VAL 0.000 0.486 -0.486 0.486
89 LEU 91 TYR 2.279 2.765 -0.485 0.485
50 SER 337 PHE 3.266 2.785 0.481 0.481
383 GLU 399 PHE 0.000 0.479 -0.479 0.479
352 SER 353 LYS 0.477 0.000 0.477 0.477
61 THR 274 LEU 0.000 0.477 -0.477 0.477
157 ILE 191 GLY 1.187 1.662 -0.476 0.476
424 VAL 426 SER 0.000 0.473 -0.473 0.473
96 ARG 176 CYS 0.473 0.000 0.473 0.473
139 THR 142 ARG 2.155 2.621 -0.465 0.465
387 ARG 395 CYS 0.000 0.465 -0.465 0.465
50 SER 51 VAL 0.000 0.464 -0.464 0.464
75 LEU 110 CYS 1.595 1.138 0.458 0.458
412 VAL 413 SER 1.831 1.374 0.457 0.457
64 TYR 146 ALA 0.547 0.091 0.456 0.456
102 TRP 106 ASP 0.456 0.000 0.456 0.456
194 TYR 293 PRO 0.000 0.455 -0.455 0.455
114 ILE 193 PHE 0.065 0.519 -0.454 0.454
126 ILE 134 TYR 1.252 0.798 0.454 0.454
128 VAL 210 VAL 2.079 1.629 0.449 0.449
78 THR 105 VAL 0.522 0.971 -0.449 0.449
67 ASN 112 ALA 0.000 0.446 -0.446 0.446
86 PHE 91 TYR 5.499 5.939 -0.440 0.440
51 VAL 66 VAL 2.164 1.726 0.439 0.439
125 TYR 129 SER 4.739 4.300 0.439 0.439
60 VAL 134 TYR 0.092 0.526 -0.434 0.434
218 LEU 264 PHE 0.000 0.433 -0.433 0.433
51 VAL 57 LEU 2.607 2.181 0.425 0.425
121 SER 199 ILE 0.425 0.000 0.425 0.425
65 ILE 120 ILE 0.523 0.099 0.424 0.424
136 THR 142 ARG 0.721 0.300 0.421 0.421
190 LEU 196 PRO 0.241 0.662 -0.421 0.421
3 PHE 4 LEU 0.000 0.419 -0.419 0.419
117 LEU 318 ASN 0.418 0.000 0.418 0.418
276 ILE 329 SER 0.000 0.416 -0.416 0.416
193 PHE 286 LEU 4.630 4.217 0.413 0.413
202 VAL 203 MET 0.140 0.552 -0.413 0.413
269 LYS 331 GLN 0.000 0.412 -0.412 0.412
128 VAL 207 VAL 0.420 0.829 -0.409 0.409
29 LEU 88 VAL 0.029 0.430 -0.401 0.401
199 ILE 203 MET 0.712 0.311 0.401 0.401
186 LEU 297 PHE 1.509 1.906 -0.398 0.398
71 ALA 112 ALA 1.013 0.617 0.396 0.396
80 LEU 316 TYR 3.988 3.597 0.391 0.391
38 LEU 42 LEU 1.425 1.813 -0.389 0.389
343 ILE 347 CYS 0.386 0.000 0.386 0.386
185 VAL 292 MET 1.565 1.948 -0.382 0.382
119 ILE 150 VAL 1.081 1.462 -0.382 0.382
395 CYS 397 TRP 0.448 0.067 0.380 0.380
121 SER 200 ILE 2.953 3.332 -0.379 0.379
30 GLY 88 VAL 1.225 0.847 0.377 0.377
236 ILE 460 SER 0.000 0.368 -0.368 0.368
230 GLU 231 GLN 0.366 0.000 0.366 0.366
111 THR 154 SER 4.848 5.212 -0.363 0.363
93 ALA 94 PHE 0.471 0.113 0.358 0.358
59 SER 62 HIS 4.060 3.702 0.358 0.358
53 CYS 340 VAL 0.000 0.357 -0.357 0.357
224 THR 231 GLN 0.000 0.357 -0.357 0.357
83 SER 312 PHE 0.000 0.355 -0.355 0.355
255 THR 257 PHE 0.000 0.355 -0.355 0.355
117 LEU 278 VAL 0.000 0.353 -0.353 0.353
440 THR 441 PRO 0.848 1.199 -0.351 0.351
398 LYS 400 PHE 0.970 1.321 -0.351 0.351
82 PHE 102 TRP 1.148 0.799 0.349 0.349
179 ASN 185 VAL 0.895 1.243 -0.348 0.348
258 SER 259 VAL 0.000 0.347 -0.347 0.347
102 TRP 316 TYR 0.577 0.233 0.344 0.344
167 GLN 179 ASN 2.480 2.136 0.344 0.344
67 ASN 147 LEU 3.557 3.899 -0.342 0.342
228 ASP 229 SER 0.000 0.339 -0.339 0.339
70 VAL 74 LEU 0.000 0.336 -0.336 0.336
102 TRP 312 PHE 0.395 0.731 -0.335 0.335
278 VAL 282 VAL 0.395 0.060 0.335 0.335
219 LYS 256 HIS 0.331 0.000 0.331 0.331
107 VAL 158 SER 1.270 1.601 -0.331 0.331
65 ILE 274 LEU 0.000 0.329 -0.329 0.329
121 SER 122 ILE 0.328 0.000 0.328 0.328
175 ILE 177 GLN 1.227 1.550 -0.323 0.323
185 VAL 293 PRO 1.385 1.707 -0.322 0.322
117 LEU 200 ILE 1.485 1.805 -0.320 0.320
28 LEU 32 ILE 0.773 1.091 -0.318 0.318
295 GLY 302 LYS 0.641 0.324 0.317 0.317
188 SER 192 SER 0.000 0.316 -0.316 0.316
458 SER 464 GLU 0.154 0.470 -0.316 0.316
239 LYS 242 PRO 0.000 0.314 -0.314 0.314
117 LEU 120 ILE 0.000 0.312 -0.312 0.312
118 CYS 122 ILE 0.311 0.000 0.311 0.311
75 LEU 106 ASP 1.107 1.411 -0.304 0.304
76 THR 320 CYS 0.301 0.000 0.301 0.301
32 ILE 36 LEU 0.000 0.299 -0.299 0.299
449 VAL 450 PRO 1.569 1.271 0.298 0.298
215 SER 264 PHE 0.000 0.297 -0.297 0.297
133 ARG 136 THR 0.578 0.873 -0.295 0.295
87 GLU 313 TRP 1.372 1.666 -0.294 0.294
46 LEU 337 PHE 2.094 1.801 0.293 0.293
129 SER 130 TYR 1.393 1.683 -0.291 0.291
218 LEU 257 PHE 0.000 0.290 -0.290 0.290
179 ASN 181 GLU 1.750 1.461 0.290 0.290
304 SER 307 VAL 1.681 1.392 0.289 0.289
237 HIS 466 VAL 0.000 0.285 -0.285 0.285
96 ARG 99 CYS 0.285 0.000 0.285 0.285
212 LYS 216 ARG 3.291 3.575 -0.284 0.284
364 SER 365 GLN 0.000 0.281 -0.281 0.281
419 CYS 420 THR 0.280 0.000 0.280 0.280
286 LEU 290 LEU 2.245 1.966 0.279 0.279
33 LEU 313 TRP 5.560 5.839 -0.279 0.279
110 CYS 285 TRP 2.498 2.776 -0.278 0.278
194 TYR 290 LEU 1.821 1.544 0.277 0.277
255 THR 463 GLY 0.000 0.277 -0.277 0.277
155 LEU 158 SER 0.000 0.275 -0.275 0.275
48 ILE 70 VAL 1.335 1.060 0.275 0.275
107 VAL 184 TYR 0.938 1.213 -0.275 0.275
33 LEU 84 ALA 1.378 1.652 -0.274 0.274
377 ILE 379 VAL 0.000 0.273 -0.273 0.273
61 THR 134 TYR 1.894 2.166 -0.272 0.272
60 VAL 139 THR 0.875 1.145 -0.271 0.271
236 ILE 461 GLU 0.000 0.268 -0.268 0.268
460 SER 462 ASN 0.333 0.601 -0.268 0.268
280 CYS 318 ASN 0.828 0.563 0.265 0.265
391 THR 392 ASP 1.533 1.798 -0.264 0.264
111 THR 192 SER 2.120 2.384 -0.264 0.264
48 ILE 73 LEU 0.708 0.445 0.264 0.264
121 SER 204 TYR 4.420 4.157 0.263 0.263
92 TRP 94 PHE 3.187 2.925 0.262 0.262
102 TRP 176 CYS 1.328 1.067 0.262 0.262
211 ALA 270 ALA 0.261 0.000 0.261 0.261
303 PRO 307 VAL 0.649 0.910 -0.261 0.261
157 ILE 188 SER 1.129 1.390 -0.260 0.260
430 LEU 432 VAL 0.364 0.110 0.254 0.254
372 LYS 373 ASP 0.254 0.000 0.254 0.254
178 ILE 292 MET 0.000 0.252 -0.252 0.252
91 TYR 93 ALA 0.304 0.556 -0.252 0.252
358 TYR 359 THR 0.000 0.252 -0.252 0.252
106 ASP 110 CYS 1.405 1.153 0.252 0.252
215 SER 216 ARG 0.252 0.000 0.252 0.252
54 HIS 56 HIS 3.508 3.759 -0.251 0.251
180 GLU 185 VAL 1.771 1.522 0.249 0.249
67 ASN 116 GLY 0.019 0.268 -0.249 0.249
108 LEU 151 TRP 0.795 0.547 0.248 0.248
116 GLY 150 VAL 0.326 0.573 -0.248 0.248
114 ILE 200 ILE 0.142 0.387 -0.244 0.244
133 ARG 137 ILE 0.763 1.007 -0.244 0.244
75 LEU 79 VAL 1.771 1.527 0.243 0.243
8 ALA 9 SER 0.000 0.239 -0.239 0.239
73 LEU 77 SER 0.238 0.000 0.238 0.238
57 LEU 333 PHE 0.000 0.234 -0.234 0.234
377 ILE 384 THR 0.000 0.234 -0.234 0.234
331 GLN 334 LYS 0.234 0.000 0.234 0.234
281 PHE 282 VAL 0.275 0.041 0.234 0.234
68 LEU 322 ASN 2.025 1.793 0.232 0.232
386 TYR 397 TRP 0.027 0.258 -0.231 0.231
223 LYS 257 PHE 0.000 0.230 -0.230 0.230
374 MET 387 ARG 0.000 0.230 -0.230 0.230
386 TYR 398 LYS 0.000 0.229 -0.229 0.229
452 ILE 454 VAL 0.438 0.209 0.228 0.228
121 SER 278 VAL 0.000 0.226 -0.226 0.226
21 VAL 26 ALA 0.438 0.663 -0.225 0.225
269 LYS 273 THR 0.225 0.000 0.225 0.225
126 ILE 138 VAL 1.122 0.899 0.224 0.224
112 ALA 151 TRP 2.146 1.922 0.224 0.224
274 LEU 326 TYR 0.000 0.223 -0.223 0.223
453 LYS 455 HIS 0.399 0.176 0.223 0.223
115 MET 154 SER 0.300 0.078 0.222 0.222
131 PRO 263 LYS 0.000 0.221 -0.221 0.221
54 HIS 57 LEU 0.928 1.149 -0.221 0.221
107 VAL 157 ILE 0.715 0.494 0.221 0.221
292 MET 293 PRO 1.070 1.288 -0.217 0.217
241 ALA 242 PRO 0.474 0.257 0.217 0.217
325 ILE 329 SER 0.000 0.216 -0.216 0.216
48 ILE 66 VAL 0.108 0.320 -0.212 0.212
330 SER 332 GLU 0.764 0.975 -0.211 0.211
119 ILE 147 LEU 0.472 0.261 0.211 0.211
334 LYS 338 GLN 1.417 1.208 0.209 0.209
291 VAL 308 PHE 0.673 0.466 0.208 0.208
70 VAL 151 TRP 0.024 0.231 -0.206 0.206
92 TRP 174 THR 6.506 6.305 0.201 0.201
105 VAL 158 SER 0.199 0.000 0.199 0.199
387 ARG 397 TRP 0.000 0.199 -0.199 0.199
324 ILE 328 CYS 0.000 0.195 -0.195 0.195
9 SER 10 ASP 0.081 0.276 -0.195 0.195
134 TYR 138 VAL 4.100 4.293 -0.193 0.193
68 LEU 277 VAL 0.000 0.192 -0.192 0.192
123 ASP 134 TYR 6.193 6.384 -0.191 0.191
46 LEU 341 LEU 1.023 0.834 0.189 0.189
158 SER 184 TYR 0.801 0.613 0.188 0.188
41 VAL 77 SER 0.896 0.709 0.187 0.187
37 ILE 81 PRO 1.462 1.649 -0.187 0.187
186 LEU 190 LEU 1.580 1.766 -0.186 0.186
225 ASP 227 SER 0.000 0.182 -0.182 0.182
293 PRO 297 PHE 0.156 0.338 -0.181 0.181
52 ALA 349 LYS 0.000 0.178 -0.178 0.178
92 TRP 173 GLU 1.085 1.263 -0.178 0.178
261 LEU 461 GLU 0.177 0.000 0.177 0.177
37 ILE 76 THR 1.079 0.903 0.176 0.176
350 GLN 354 HIS 0.176 0.000 0.176 0.176
41 VAL 45 ILE 0.790 0.615 0.175 0.175
26 ALA 88 VAL 2.040 1.866 0.174 0.174
62 HIS 65 ILE 0.000 0.174 -0.174 0.174
60 VAL 143 GLY 0.623 0.450 0.173 0.173
225 ASP 231 GLN 0.000 0.172 -0.172 0.172
314 LEU 317 LEU 0.272 0.103 0.170 0.170
215 SER 219 LYS 0.000 0.169 -0.169 0.169
124 ARG 277 VAL 0.167 0.000 0.167 0.167
388 ILE 395 CYS 0.000 0.167 -0.167 0.167
438 PRO 439 SER 0.166 0.000 0.166 0.166
33 LEU 87 GLU 0.323 0.159 0.164 0.164
83 SER 313 TRP 1.424 1.588 -0.164 0.164
388 ILE 394 VAL 0.000 0.162 -0.162 0.162
283 LEU 314 LEU 0.433 0.595 -0.162 0.162
287 PRO 311 VAL 2.601 2.440 0.161 0.161
157 ILE 192 SER 0.623 0.463 0.160 0.160
121 SER 207 VAL 0.000 0.159 -0.159 0.159
125 TYR 126 ILE 0.241 0.082 0.159 0.159
120 ILE 204 TYR 0.482 0.323 0.159 0.159
212 LYS 215 SER 0.156 0.000 0.156 0.156
190 LEU 195 LEU 2.801 2.957 -0.156 0.156
86 PHE 92 TRP 5.427 5.582 -0.156 0.156
33 LEU 36 LEU 0.000 0.154 -0.154 0.154
122 ILE 126 ILE 0.768 0.614 0.153 0.153
377 ILE 385 PHE 2.859 2.706 0.153 0.153
68 LEU 326 TYR 1.055 0.902 0.152 0.152
291 VAL 303 PRO 1.641 1.489 0.152 0.152
126 ILE 137 ILE 1.117 1.269 -0.152 0.152
114 ILE 196 PRO 1.204 1.356 -0.151 0.151
427 LYS 428 SER 0.147 0.000 0.147 0.147
197 LEU 286 LEU 0.000 0.146 -0.146 0.146
166 ARG 167 GLN 0.146 0.000 0.146 0.146
264 PHE 268 LYS 0.236 0.092 0.144 0.144
112 ALA 154 SER 3.763 3.621 0.142 0.142
126 ILE 130 TYR 0.190 0.048 0.141 0.141
287 PRO 314 LEU 0.503 0.643 -0.141 0.141
304 SER 306 THR 0.322 0.462 -0.140 0.140
150 VAL 154 SER 0.256 0.395 -0.139 0.139
83 SER 102 TRP 4.009 4.147 -0.139 0.139
284 CYS 285 TRP 0.139 0.277 -0.138 0.138
64 TYR 143 GLY 3.891 3.755 0.136 0.136
144 LEU 148 LEU 0.137 0.001 0.136 0.136
189 ALA 293 PRO 0.439 0.304 0.135 0.135
389 SER 392 ASP 0.135 0.000 0.135 0.135
310 ILE 314 LEU 0.135 0.000 0.135 0.135
78 THR 102 TRP 0.000 0.134 -0.134 0.134
366 ALA 367 VAL 0.733 0.599 0.133 0.133
136 THR 137 ILE 0.254 0.386 -0.132 0.132
284 CYS 311 VAL 0.111 0.241 -0.130 0.130
125 TYR 210 VAL 0.000 0.130 -0.130 0.130
302 LYS 303 PRO 0.978 0.848 0.129 0.129
113 SER 318 ASN 0.128 0.000 0.128 0.128
65 ILE 327 PRO 0.127 0.000 0.127 0.127
373 ASP 389 SER 0.000 0.127 -0.127 0.127
308 PHE 312 PHE 0.127 0.000 0.127 0.127
141 ARG 145 MET 0.125 0.000 0.125 0.125
22 ASN 24 SER 0.121 0.000 0.121 0.121
67 ASN 119 ILE 0.120 0.000 0.120 0.120
45 ILE 49 LEU 1.044 0.924 0.120 0.120
235 ARG 237 HIS 0.000 0.119 -0.119 0.119
300 ASP 301 PHE 0.421 0.302 0.119 0.119
99 CYS 100 ASN 0.258 0.376 -0.118 0.118
225 ASP 230 GLU 0.000 0.118 -0.118 0.118
312 PHE 313 TRP 0.000 0.115 -0.115 0.115
290 LEU 294 ILE 0.114 0.000 0.114 0.114
439 SER 440 THR 0.112 0.000 0.112 0.112
99 CYS 176 CYS 6.070 5.961 0.109 0.109
10 ASP 12 SER 0.000 0.108 -0.108 0.108
218 LEU 236 ILE 0.000 0.107 -0.107 0.107
195 LEU 199 ILE 0.627 0.520 0.106 0.106
306 THR 310 ILE 0.348 0.450 -0.102 0.102
99 CYS 177 GLN 0.263 0.162 0.101 0.101
286 LEU 287 PRO 0.864 0.965 -0.101 0.101
50 SER 336 ALA 1.674 1.574 0.100 0.100
137 ILE 138 VAL 0.403 0.502 -0.100 0.100
115 MET 150 VAL 2.619 2.519 0.100 0.100
43 GLY 337 PHE 0.097 0.000 0.097 0.097
239 LYS 464 GLU 0.000 0.096 -0.096 0.096
24 SER 25 LYS 0.257 0.162 0.095 0.095
40 GLY 319 SER 0.000 0.094 -0.094 0.094
89 LEU 93 ALA 0.365 0.458 -0.094 0.094
59 SER 61 THR 1.164 1.256 -0.091 0.091
92 TRP 175 ILE 0.141 0.051 0.091 0.091
91 TYR 174 THR 1.967 2.057 -0.090 0.090
72 ASP 323 PRO 0.090 0.000 0.090 0.090
85 ILE 89 LEU 1.117 1.030 0.087 0.087
47 VAL 69 ALA 1.160 1.076 0.083 0.083
462 ASN 464 GLU 0.000 0.083 -0.083 0.083
57 LEU 336 ALA 0.409 0.492 -0.083 0.083
126 ILE 131 PRO 0.063 0.146 -0.083 0.083
274 LEU 279 GLY 0.082 0.000 0.082 0.082
134 TYR 135 PRO 1.578 1.660 -0.082 0.082
321 ILE 325 ILE 1.564 1.482 0.082 0.082
459 LEU 466 VAL 0.176 0.258 -0.082 0.082
77 SER 78 THR 0.806 0.727 0.079 0.079
80 LEU 313 TRP 0.181 0.261 -0.079 0.079
461 GLU 462 ASN 0.090 0.011 0.079 0.079
66 VAL 70 VAL 0.334 0.256 0.078 0.078
108 LEU 154 SER 3.523 3.600 -0.077 0.077
106 ASP 316 TYR 6.272 6.196 0.077 0.077
377 ILE 378 PRO 0.624 0.547 0.076 0.076
254 LYS 259 VAL 0.000 0.076 -0.076 0.076
44 ASN 322 ASN 0.000 0.076 -0.076 0.076
273 THR 330 SER 0.000 0.075 -0.075 0.075
50 SER 57 LEU 1.177 1.102 0.075 0.075
45 ILE 73 LEU 1.251 1.176 0.075 0.075
79 VAL 80 LEU 0.030 0.105 -0.074 0.074
457 ILE 465 GLU 1.103 1.176 -0.073 0.073
75 LEU 316 TYR 1.203 1.130 0.073 0.073
273 THR 326 TYR 0.000 0.073 -0.073 0.073
61 THR 65 ILE 0.038 0.111 -0.073 0.073
192 SER 193 PHE 0.299 0.372 -0.072 0.072
133 ARG 428 SER 0.000 0.070 -0.070 0.070
326 TYR 327 PRO 0.936 0.868 0.068 0.068
288 PHE 293 PRO 0.191 0.124 0.067 0.067
217 GLY 223 LYS 0.000 0.067 -0.067 0.067
377 ILE 383 GLU 0.000 0.065 -0.065 0.065
386 TYR 400 PHE 0.000 0.065 -0.065 0.065
332 GLU 335 LYS 0.000 0.065 -0.065 0.065
81 PRO 82 PHE 0.000 0.064 -0.064 0.064
86 PHE 174 THR 0.000 0.064 -0.064 0.064
115 MET 196 PRO 0.963 0.898 0.064 0.064
296 SER 297 PHE 0.059 0.000 0.059 0.059
115 MET 191 GLY 0.124 0.183 -0.059 0.059
68 LEU 116 GLY 0.057 0.000 0.057 0.057
281 PHE 286 LEU 0.117 0.060 0.056 0.056
111 THR 115 MET 0.360 0.415 -0.056 0.056
184 TYR 188 SER 2.134 2.079 0.055 0.055
29 LEU 34 GLY 0.000 0.054 -0.054 0.054
291 VAL 311 VAL 0.776 0.829 -0.053 0.053
197 LEU 201 LEU 1.459 1.511 -0.051 0.051
297 PHE 298 PHE 1.189 1.240 -0.051 0.051
48 ILE 69 ALA 1.418 1.468 -0.050 0.050
40 GLY 76 THR 1.727 1.678 0.049 0.049
76 THR 80 LEU 0.729 0.682 0.048 0.048
115 MET 118 CYS 0.000 0.047 -0.047 0.047
322 ASN 323 PRO 0.928 0.975 -0.046 0.046
74 LEU 79 VAL 0.421 0.465 -0.045 0.045
188 SER 193 PHE 0.155 0.200 -0.045 0.045
17 PRO 18 PRO 0.658 0.614 0.044 0.044
267 GLU 270 ALA 0.000 0.044 -0.044 0.044
64 TYR 138 VAL 0.157 0.200 -0.043 0.043
101 ILE 105 VAL 0.418 0.375 0.043 0.043
96 ARG 177 GLN 0.042 0.000 0.042 0.042
443 LEU 444 ASP 0.000 0.041 -0.041 0.041
111 THR 157 ILE 0.673 0.714 -0.041 0.041
275 GLY 280 CYS 0.041 0.000 0.041 0.041
46 LEU 340 VAL 0.667 0.707 -0.040 0.040
79 VAL 316 TYR 1.263 1.303 -0.040 0.040
139 THR 141 ARG 0.295 0.256 0.039 0.039
78 THR 79 VAL 0.618 0.579 0.039 0.039
84 ALA 313 TRP 2.208 2.170 0.038 0.038
170 PRO 175 ILE 0.000 0.037 -0.037 0.037
98 PHE 102 TRP 0.000 0.036 -0.036 0.036
276 ILE 280 CYS 0.326 0.290 0.036 0.036
184 TYR 189 ALA 0.013 0.049 -0.036 0.036
30 GLY 35 GLY 0.000 0.036 -0.036 0.036
167 GLN 168 PRO 0.845 0.880 -0.035 0.035
64 TYR 120 ILE 2.110 2.145 -0.035 0.035
80 LEU 320 CYS 0.034 0.000 0.034 0.034
47 VAL 65 ILE 0.709 0.676 0.033 0.033
386 TYR 396 GLU 0.000 0.033 -0.033 0.033
110 CYS 316 TYR 0.097 0.065 0.032 0.032
67 ASN 150 VAL 0.021 0.053 -0.032 0.032
307 VAL 311 VAL 0.076 0.108 -0.031 0.031
85 ILE 90 GLY 0.031 0.000 0.031 0.031
298 PHE 301 PHE 0.763 0.732 0.031 0.031
123 ASP 138 VAL 1.160 1.130 0.031 0.031
227 SER 427 LYS 0.000 0.030 -0.030 0.030
54 HIS 335 LYS 0.000 0.030 -0.030 0.030
165 TRP 179 ASN 2.479 2.509 -0.029 0.029
190 LEU 194 TYR 0.893 0.863 0.029 0.029
239 LYS 460 SER 0.000 0.028 -0.028 0.028
107 VAL 111 THR 0.481 0.509 -0.028 0.028
457 ILE 459 LEU 0.000 0.027 -0.027 0.027
73 LEU 76 THR 0.252 0.278 -0.026 0.026
403 MET 404 PRO 1.308 1.333 -0.025 0.025
97 VAL 101 ILE 0.341 0.366 -0.025 0.025
309 LYS 313 TRP 0.000 0.024 -0.024 0.024
79 VAL 105 VAL 1.532 1.508 0.024 0.024
80 LEU 81 PRO 0.768 0.746 0.022 0.022
248 MET 252 LYS 0.020 0.000 0.020 0.020
114 ILE 289 PHE 0.966 0.986 -0.020 0.020
102 TRP 103 ALA 0.679 0.659 0.020 0.020
16 GLN 17 PRO 0.472 0.453 0.019 0.019
99 CYS 166 ARG 0.214 0.196 0.018 0.018
325 ILE 330 SER 0.000 0.018 -0.018 0.018
132 LEU 263 LYS 0.000 0.017 -0.017 0.017
174 THR 175 ILE 0.463 0.446 0.017 0.017
27 ILE 31 VAL 0.153 0.137 0.016 0.016
298 PHE 299 PRO 0.170 0.155 0.015 0.015
19 ALA 20 PRO 0.565 0.579 -0.014 0.014
111 THR 116 GLY 0.000 0.013 -0.013 0.013
195 LEU 196 PRO 1.351 1.338 0.012 0.012
75 LEU 81 PRO 0.000 0.011 -0.011 0.011
79 VAL 83 SER 0.600 0.590 0.011 0.011
250 SER 254 LYS 0.010 0.000 0.010 0.010
38 LEU 43 GLY 0.000 0.010 -0.010 0.010
75 LEU 285 TRP 0.000 0.010 -0.010 0.010
37 ILE 84 ALA 0.534 0.543 -0.010 0.010
274 LEU 277 VAL 0.000 0.009 -0.009 0.009
105 VAL 109 CYS 0.513 0.521 -0.008 0.008
204 TYR 207 VAL 0.058 0.050 0.008 0.008
208 TYR 267 GLU 0.008 0.000 0.008 0.008
37 ILE 41 VAL 0.202 0.194 0.008 0.008
82 PHE 92 TRP 0.767 0.774 -0.007 0.007
49 LEU 53 CYS 0.007 0.000 0.007 0.007
293 PRO 298 PHE 0.065 0.058 0.007 0.007
39 PHE 44 ASN 0.000 0.006 -0.006 0.006
130 TYR 131 PRO 0.094 0.099 -0.005 0.005
375 VAL 377 ILE 0.103 0.099 0.004 0.004
23 ILE 27 ILE 0.964 0.960 0.004 0.004
72 ASP 318 ASN 0.000 0.004 -0.004 0.004
2 VAL 4 LEU 0.004 0.000 0.004 0.004
169 ALA 170 PRO 0.586 0.582 0.004 0.004
355 ALA 356 LEU 0.004 0.000 0.004 0.004
392 ASP 394 VAL 0.003 0.000 0.003 0.003
73 LEU 78 THR 0.002 0.000 0.002 0.002
128 VAL 268 LYS 0.000 0.001 -0.001 0.001
178 ILE 288 PHE 0.000 0.001 -0.001 0.001
294 ILE 299 PRO 0.073 0.073 0.000 0.000
432 VAL 434 CYS 0.551 0.551 -0.000 0.000

RRCS change distribution

-0.16
Mean ΔRRCS
1.57
Std Dev
-0.04
Median

Magnitude classification

17
High (|Δ| ≥ 5.0)
72
Medium (2.2 ≤ |Δ| < 5.0)
694
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| ≥ 2.19, 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