Sequence 1: | NP_001399.1 | Gene: | CELSR2 / 1952 | HGNCID: | 3231 | Length: | 2923 | Species: | Homo sapiens |
---|---|---|---|---|---|---|---|---|---|
Sequence 2: | NP_506256.3 | Gene: | fmi-1 / 179788 | WormBaseID: | WBGene00001475 | Length: | 2596 | Species: | Caenorhabditis elegans |
Alignment Length: | 2778 | Identity: | 790/2778 - (28%) |
---|---|---|---|
Similarity: | 1229/2778 - (44%) | Gaps: | 354/2778 - (12%) |
- Green bases have known domain annotations that are detailed below.
Human 51 CAPMGWLCPSSASNLWLYTSR--CRDAGTELTGHLVPHHDGLRVWCPESEAHIPLPPAPEGCPWS 113
Human 114 CRLLGIGGHLSPQGKLTLPEEHPCLKAPRLR------CQSCKLAQAPGLRAGER-SPEESLGGR- 170
Human 171 -----RKRNVN-TAPQFQPPSYQATVPENQPAGTPVASLRAIDPDEGEAGRLEYTMDALFDSRSN 229
Human 230 QFFSLDPVTGAVTTAEELDRETKSTHVFRVTAQDHGMPRRSALATLTILVTDTNDHDPVFEQQEY 294
Human 295 KESLRENLEVGYEVLTVRATDGDAPPNANILYRLLEGSGGSPSEVFEIDPRSGVIRTRGPVDREE 359
Human 360 VESYQLTVEASDQGRDPGPRSTTAAVFLSVEDDNDNAPQFSEKRYVVQVREDVTPGAPVLRVTAS 424
Human 425 DRDKGSNAVVHYSIMSGNARGQFYLDAQTGALDVVSPLDYETTKEYTLRVRAQDGGRPPLSNVSG 489
Human 490 LVTVQVLDINDNAPIFVSTPFQATVLESVPLGYLVLHVQAIDADAGDNARLEYRLAGVGHDFPFT 554
Human 555 INNGTGWISVAAELDREEVDFYSFGVEARDHGTPALTASASVSVTVLDVNDNNPTFTQPEYTVRL 619
Human 620 NEDAAVGTSVVTVSAVDRDAHSVITYQITSGNTRNRFSITSQSGGGLVSLALPLDYKLERQ---Y 681
Human 682 VLAVTASD-GTRQDTAQIVVNVTDANTHRPVFQSSHYTVNVNEDRPAGTTVVLISATDEDTGENA 745
Human 746 RITYFMEDSIPQFRIDADTGAVTTQAELDYEDQVSYTLAITARDNGIPQKSDTTYLEILVNDVND 810
Human 811 NAPQFLRDSYQGSVYEDVPPFTSVLQISATDRDSGLNGRVFYTFQGGDDGDGD--FIVESTSGIV 873
Human 874 RTLRRLDRENVAQYVLRAYAVDKGMPPARTPMEVTVTVLDVNDNPPVFEQDEFDVFVEENSPIGL 938
Human 939 AVARVTATDPDEGTNAQIMYQIVEGNIPEVFQLDIFSGELTALV------DLDYEDRP-EYVLVI 996
Human 997 QATSAPLVSRATVHVRLLDRNDNPPVLGNFEILFNNYVTNRSSSFPGGAIGRVPAHDPDISDSLT 1061
Human 1062 YSFERGNELSLVLLNASTGELKLSRALDNNRPLEAIMSVLVSDGVHSVTAQCALRVTIITDEMLT 1126
Human 1127 HSITLRLEDMSPERFLSPLLGLFIQAVAATLAT-PPDHVVVFNVQRDTDAPGGHILNVSLSVGQP 1190
Human 1191 PGPGGGPPFLPSEDLQERLYLNRSLLTAISAQRVLPFDDNICLREPCENYMRCVSVLRFDSSAPF 1255
Human 1256 IASSSVLFRPIHPVGGLRCRCPPGFT-----GDYCETEVDLCYSRPCGPHGRCRSREGGYTCLCR 1315
Human 1316 DGYTGEHCEVSARSGRCTPGVCKNGGTCVNLLVGGFKC-DCP-SGDFEKPYCQVTTRSFPAHSFI 1378
Human 1379 TFRGLRQRFHFTLALSFATKERDGLLLYNGRFNEKHDFVALEVIQEQVQLTFSAG--ESTTTVSP 1441
Human 1442 FVPGGVSDGQWHTVQLKYYNKPLLGQTGLPQGPSEQKVAVVTVDGCDTGVALRFGSVLGNYSCAA 1506
Human 1507 QGTQGGSKKS----------LDLTGPLLLGGVPDLPESFPVRMRQFVGCMRNLQVDSRHIDMADF 1561
Human 1562 --IANNGTV-PGCPAKKNVCDSN--TCHNGGTCVNQWDAFSCECPLGFGGKSCAQEMANPQHFLG 1621
Human 1622 SSLVAWHGLSL----PISQPWYLSLMFRTRQADGVLLQAITRGRSTITLQLREGHVMLSV-EGT- 1680
Human 1681 --GLQASSLRLEPGRANDGDWHHAQLALGASGGPGHAILSFDYGQQRAEGNLGPRLHGLHLSNIT 1743
Human 1744 VGGIPGPAGGVARGFRGCLQGVRVSDTPEGVNSLDPSHGESINVEQ------GCSLPDPCD-SNP 1801
Human 1802 CPANSYCSNDWDSYSCSCDPGYYGDNCTNVCDL-NPCEHQSVCTRKPSAPHGYTCECPPNYLGPY 1865
Human 1866 CETRI-DQPCPRGWWG-HPTCGPCNCDVSKGFDPDCNKTSGECHCKENHYRPPGSPTCLLCDCYP 1928
Human 1929 TGSLSRVCDPEDGQCPCKPGVIGRQCDRC---DNPFAEVTTNGCEVNYDSCPRAIEAGIWWPRTR 1990
Human 1991 FGLPAAAPCPKGSFGTAVRHCDEHRGWLPPNLFNCTSITFSELKGFAERLQRNESGLDSGRSQQL 2055
Human 2056 ALLLRNATQHTAGYFGSDVKVAYQLATRLLAHESTQRGFGLSATQDVHFTENLLR-VGSALLDTA 2119
Human 2120 NKRHWELIQQTEGGTAWLLQHYEAYASALAQNMRHTYLSPFTIVTPNIVISVVRLDKGNFAGAKL 2184
Human 2185 PRYEALRGEQPPDLETTVILPESVFRETPPVVRPAGPGEAQEPEELARRQRRHPELSQGEAVASV 2249
Human 2250 IIYRTLAGLLPHNYDPDKRSLRVPKRPIINTPVVSISVHDDEELLPRALDKPVTVQFRLLETEER 2314
Human 2315 TKPICVFWNHSILVSGTGGWSARGCEVVFRNESHVSCQCNHMTSFAVLMDVSRRENGEILPLKTL 2379
Human 2380 TYVAL-GVTLAALLLTFFFLTLLRILRS-NQHGIRRN--LTAALGLAQLVFL--LGINQADLPFA 2438
Human 2439 CTVIAILLHFLYLCTFSWALLEALHLYRALTEVRDVNTGPMRFYYMLGWGVPAFITGLAVG---- 2499
Human 2500 --LDPEGYGNPDFCWLSIYDTLIWSFAGPVAFAVSMSVFLYILAARASCAAQRQGFEKKGPVSGL 2562
Human 2563 QPSFAVLLLLSATWLLALLSVNSDTLLFHYLFATCNCIQGPFIFLSYVVLSKEVRKALKLACSRK 2627
Human 2628 PS----PDPALTTKSTLTSSYNCPSPYADGR----------LYQPYGDSAGSLHSTSRSGKSQP- 2677
Human 2678 --------SYIPFLLREESALNPGQGPPGLGDPGSL--FLEGQDQQHD 2715 |
Gene | Sequence | Domain | Region | External ID | Identity |
---|---|---|---|---|---|
CELSR2 | NP_001399.1 | Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite | 154..198 | 14/51 (27%) | |
Cadherin_repeat | 185..285 | CDD:206637 | 34/99 (34%) | ||
Cadherin_repeat | 293..395 | CDD:206637 | 40/101 (40%) | ||
Cadherin_repeat | 404..501 | CDD:206637 | 35/96 (36%) | ||
Cadherin_repeat | 509..606 | CDD:206637 | 37/96 (39%) | ||
Cadherin_repeat | 614..708 | CDD:206637 | 30/97 (31%) | ||
Cadherin_repeat | 716..811 | CDD:206637 | 33/94 (35%) | ||
Cadherin_repeat | 819..917 | CDD:206637 | 40/99 (40%) | ||
Cadherin_repeat | 925..1019 | CDD:206637 | 31/100 (31%) | ||
Cadherin_repeat | 1042..1120 | CDD:206637 | 20/77 (26%) | ||
EGF_CA | 1289..1324 | CDD:238011 | 12/34 (35%) | ||
EGF_CA | 1333..1366 | CDD:238011 | 9/34 (26%) | ||
LamG | 1369..1552 | CDD:238058 | 45/194 (23%) | ||
EGF_CA | 1578..1609 | CDD:238011 | 9/32 (28%) | ||
LamG | 1618..1767 | CDD:238058 | 36/156 (23%) | ||
EGF_CA | 1795..1829 | CDD:238011 | 11/34 (32%) | ||
EGF | 1832..1865 | CDD:278437 | 10/33 (30%) | ||
EGF_Lam | 1924..1969 | CDD:214543 | 17/47 (36%) | ||
HormR | 1972..2034 | CDD:214468 | 22/61 (36%) | ||
GAIN | 2052..2287 | CDD:293098 | 47/235 (20%) | ||
Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite | 2213..2238 | 5/24 (21%) | |||
GPS | 2315..2368 | CDD:197639 | 15/52 (29%) | ||
7tm_4 | 2402..2605 | CDD:304433 | 47/213 (22%) | ||
Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite | 2688..2838 | 10/30 (33%) | |||
Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite | 2854..2888 | ||||
fmi-1 | NP_506256.3 | Cadherin_repeat | 170..266 | CDD:206637 | 34/98 (35%) |
Cadherin_repeat | 274..371 | CDD:206637 | 40/101 (40%) | ||
Cadherin_repeat | 379..475 | CDD:206637 | 35/97 (36%) | ||
Cadherin_repeat | 486..577 | CDD:206637 | 37/93 (40%) | ||
Cadherin_repeat | 686..780 | CDD:206637 | 33/94 (35%) | ||
Cadherin_repeat | 788..888 | CDD:206637 | 40/99 (40%) | ||
Cadherin_repeat | 896..996 | CDD:206637 | 31/100 (31%) | ||
EGF_CA | 1252..1287 | CDD:238011 | 12/34 (35%) | ||
LamG | 1333..1504 | CDD:238058 | 45/194 (23%) | ||
LamG | 1582..1716 | CDD:238058 | 33/150 (22%) | ||
EGF_CA | 1774..1808 | CDD:238011 | 10/35 (29%) | ||
EGF_Lam | 1865..1911 | CDD:238012 | 17/48 (35%) | ||
HormR | 1917..1974 | CDD:214468 | 22/56 (39%) | ||
GPS | 2170..2218 | CDD:197639 | 15/52 (29%) | ||
7tm_GPCRs | 2237..2455 | CDD:421689 | 55/242 (23%) | ||
TM helix 2 | 2258..2284 | CDD:410628 | 6/25 (24%) | ||
TM helix 3 | 2289..2315 | CDD:410628 | 7/25 (28%) | ||
TM helix 4 | 2326..2346 | CDD:410628 | 4/19 (21%) | ||
TM helix 5 | 2356..2383 | CDD:410628 | 4/26 (15%) | ||
TM helix 6 | 2400..2435 | CDD:410628 | 5/34 (15%) | ||
Blue background indicates that the domain is not in the aligned region. |
Tool | Simple Score | Weighted Score | Original Tool Information | |||
---|---|---|---|---|---|---|
BLAST Result | Score | Score Type | Cluster ID | |||
Compara | 1 | 0.930 | - | - | C161463576 | |
Domainoid | 1 | 1.000 | 94 | 1.000 | Domainoid score | I5169 |
eggNOG | 1 | 0.900 | - | - | E2759_KOG4289 | |
Hieranoid | 1 | 1.000 | - | - | ||
Homologene | 0 | 0.000 | Not matched by this tool. | |||
Inparanoid | 1 | 1.050 | 926 | 1.000 | Inparanoid score | I183 |
Isobase | 0 | 0.000 | Not matched by this tool. | |||
OMA | 1 | 1.010 | - | - | QHG48446 | |
OrthoDB | 1 | 1.010 | - | - | D16905at33208 | |
OrthoFinder | 1 | 1.000 | - | - | FOG0001609 | |
OrthoInspector | 1 | 1.000 | - | - | otm15547 | |
orthoMCL | 1 | 0.900 | - | - | OOG6_103211 | |
Panther | 1 | 1.100 | - | - | O | PTHR24026 |
Phylome | 1 | 0.910 | - | - | ||
RoundUp | 1 | 1.030 | - | avgDist | Average_Evolutionary_Distance | R3194 |
SonicParanoid | 1 | 1.000 | - | - | X912 | |
SwiftOrtho | 0 | 0.000 | Not matched by this tool. | |||
TreeFam | 0 | 0.000 | Not matched by this tool. | |||
14 | 13.840 |