| Sequence 1: | NP_003015.2 | Gene: | ITSN1 / 6453 | HGNCID: | 6183 | Length: | 1721 | Species: | Homo sapiens |
|---|---|---|---|---|---|---|---|---|---|
| Sequence 2: | XP_038944174.1 | Gene: | Itsn1 / 29491 | RGDID: | 2935 | Length: | 1718 | Species: | Rattus norvegicus |
| Alignment Length: | 1721 | Identity: | 1628/1721 - (94%) |
|---|---|---|---|
| Similarity: | 1667/1721 - (96%) | Gaps: | 3/1721 - (0%) |
- Green bases have known domain annotations that are detailed below.
|
Human 1 MAQFPTPFGGSLDIWAITVEERAKHDQQFHSLKPISGFITGDQARNFFFQSGLPQPVLAQIWALA 65
Human 66 DMNNDGRMDQVEFSIAMKLIKLKLQGYQLPSALPPVMKQQPVAISSAPAFGMGGIASMPPLTAVA 130
Human 131 PVPMGSIPVVGMSPTLVSSVPTAAVPPLANGAPPVIQPLPAFAHPAATLPKSSSFSRSGPGSQLN 195
Human 196 TKLQKAQSFDVASVPPVAEWAVPQSSRLKYRQLFNSHDKTMSGHLTGPQARTILMQSSLPQAQLA 260
Human 261 SIWNLSDIDQDGKLTAEEFILAMHLIDVAMSGQPLPPVLPPEYIPPSFRRVRSGSGISVISSTSV 325
Human 326 DQRLPEEPVLEDEQQQLEKKLPVTFEDKKRENFERGNLELEKRRQALLEQQRKEQERLAQLERAE 390
Human 391 QERKERERQEQERKRQLELEKQLEKQRELERQREEERRKEIERREAAKRELERQRQLEWERNRRQ 455
Human 456 ELLNQRNKEQEDIVVLKAKKKTLEFELEALNDKKHQLEGKLQDIRCRLTTQRQEIESTNKSRELR 520
Human 521 IAEITHLQQQLQESQQMLGRLIPEKQILNDQLKQVQQNSLHRDSLVTLKRALEAKELARQHLRDQ 585
Human 586 LDEVEKETRSKLQEIDIFNNQLKELREIHNKQQLQKQKSMEAERLKQKEQERKIIELEKQKEEAQ 650
Human 651 RRAQERDKQWLEHVQQEDEHQRPRKLHEEEKLKREESVKKKDGEEKGKQEAQDKLGRLFHQHQEP 715
Human 716 AKPAVQAPWSTAEKGPLTISAQENVKVVYYRALYPFESRSHDEITIQPGDIVMVKGEWVDESQTG 780
Human 781 EPGWLGGELKGKTGWFPANYAEKIPENEVPAPVKPVTDSTSAPAPKLALRETPAPLAVTSSEPST 845
Human 846 TPNNWADFSSTWPTSTNEKPETDNWDAWAAQPSLTVPSAGQLRQRSAFTPATATGSSPSPVLGQG 910
Human 911 EKVEGLQAQALYPWRAKKDNHLNFNKNDVITVLEQQDMWWFGEVQGQKGWFPKSYVKLISGPIRK 975
Human 976 STSMDSGSSESPASLKRVASPAAKPVVSGEEFIAMYTYESSEQGDLTFQQGDVILVTKKDGDWWT 1040
Human 1041 GTVGDKAGVFPSNYVRLKDSEGSGTAGKTGSLGKKPEIAQVIASYTATGPEQLTLAPGQLILIRK 1105
Human 1106 KNPGGWWEGELQARGKKRQIGWFPANYVKLLSPGTSKITPTEPPKSTALAAVCQVIGMYDYTAQN 1170
Human 1171 DDELAFNKGQIINVLNKEDPDWWKGEVNGQVGLFPSNYVKLTTDMDPSQQWCSDLHLLDMLTPTE 1235
Human 1236 RKRQGYIHELIVTEENYVNDLQLVTEIFQKPLMESELLTEKEVAMIFVNWKELIMCNIKLLKALR 1300
Human 1301 VRKKMSGEKMPVKMIGDILSAQLPHMQPYIRFCSRQLNGAALIQQKTDEAPDFKEFVKRLAMDPR 1365
Human 1366 CKGMPLSSFILKPMQRVTRYPLIIKNILENTPENHPDHSHLKHALEKAEELCSQVNEGVREKENS 1430
Human 1431 DRLEWIQAHVQCEGLSEQLVFNSVTNCLGPRKFLHSGKLYKAKSNKELYGFLFNDFLLLTQITKP 1495
Human 1496 LGSSGTDKVFSPKSNLQYKMYKTPIFLNEVLVKLPTDPSGDEPIFHISHIDRVYTLRAESINERT 1560
Human 1561 AWVQKIKAASELYIETEKKKREKAYLVRSQRATGIGRLMVNVVEGIELKPCRSHGKSNPYCEVTM 1625
Human 1626 GSQCHITKTIQDTLNPKWNSNCQFFIRDLEQEVLCITVFERDQFSPDDFLGRTEIRVADIKKDQG 1690
Human 1691 SKGPVTKCLLLHEVPTGEIVVRLDLQLFDEP 1721 |
| Gene | Sequence | Domain | Region | External ID | Identity |
|---|---|---|---|---|---|
| ITSN1 | NP_003015.2 | EH | 14..108 | CDD:197477 | 90/93 (97%) |
| EH | 214..309 | CDD:197477 | 94/94 (100%) | ||
| Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite | 322..348 | 19/25 (76%) | |||
| KLERQ | 326..702 | 342/375 (91%) | |||
| Smc | <363..>684 | CDD:440809 | 297/320 (93%) | ||
| Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite | 650..701 | 38/50 (76%) | |||
| SH3_Intersectin1_1 | 744..803 | CDD:212920 | 58/58 (100%) | ||
| INTAP | 803..917 | CDD:435467 | 106/113 (94%) | ||
| Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite | 836..868 | 29/31 (94%) | |||
| SH3_Intersectin1_2 | 917..968 | CDD:212922 | 49/50 (98%) | ||
| SH3_Intersectin1_3 | 1006..1057 | CDD:212924 | 44/50 (88%) | ||
| SH3_Intersectin1_4 | 1074..1138 | CDD:212926 | 63/63 (100%) | ||
| Required for interaction with FCHSD2. /evidence=ECO:0000269|PubMed:29887380 | 1074..1138 | 63/63 (100%) | |||
| Bipartite nuclear localization signal, in isoform 2. /evidence=ECO:0000269|PubMed:29599122 | 1104..1127 | 22/22 (100%) | |||
| SH3_Intersectin1_5 | 1158..1211 | CDD:212928 | 49/52 (94%) | ||
| RhoGEF | 1238..1421 | CDD:238091 | 180/182 (99%) | ||
| PH_13 | 1440..1582 | CDD:465218 | 140/141 (99%) | ||
| C2_Intersectin | 1582..1716 | CDD:176021 | 133/133 (100%) | ||
| Itsn1 | XP_038944174.1 | EH | 14..106 | CDD:197477 | 88/91 (97%) |
| Atrophin-1 | <85..>194 | CDD:460830 | 101/108 (94%) | ||
| EH | 217..309 | CDD:197477 | 91/91 (100%) | ||
| Smc | <362..>655 | CDD:440809 | 274/292 (94%) | ||
| MAP7 | 605..714 | CDD:461709 | 87/109 (80%) | ||
| SH3 | 741..800 | CDD:473055 | 58/58 (100%) | ||
| INTAP | 800..914 | CDD:435467 | 106/113 (94%) | ||
| SH3_Intersectin1_2 | 914..965 | CDD:212922 | 49/50 (98%) | ||
| SH3 | 1003..1054 | CDD:473055 | 44/50 (88%) | ||
| SH3_Intersectin1_4 | 1071..1135 | CDD:212926 | 63/63 (100%) | ||
| SH3_Intersectin1_5 | 1155..1208 | CDD:212928 | 49/52 (94%) | ||
| RhoGEF | 1235..1418 | CDD:238091 | 180/182 (99%) | ||
| PH_13 | 1437..1579 | CDD:465218 | 140/141 (99%) | ||
| C2_Intersectin | 1579..1713 | CDD:176021 | 133/133 (100%) |