Sequence 1: | XP_016882868.1 | Gene: | FBN3 / 84467 | HGNCID: | 18794 | Length: | 2851 | Species: | Homo sapiens |
---|---|---|---|---|---|---|---|---|---|
Sequence 2: | NP_114013.2 | Gene: | Fbn1 / 83727 | RGDID: | 620908 | Length: | 2872 | Species: | Rattus norvegicus |
Alignment Length: | 2896 | Identity: | 1754/2896 - (60%) |
---|---|---|---|
Similarity: | 2182/2896 - (75%) | Gaps: | 78/2896 - (2%) |
- Green bases have known domain annotations that are detailed below.
Human 8 LARGPLARLLLAWSALLCMAGGQGRWDGALEAAG-----PGRVRRRGSPG--ILQGPNVCGSRFH 65
Human 66 AYCCPGWRTFPGRSQCVVPICRRACGEGFCSQPNLCTCADGTLAPSCGVSRGSGCSVSCMNGGTC 130
Human 131 RGASCLCQKGYTGTVCGQPICDRGCHNGGRCIGPNRCACVYGFMGPQCERDYRTGPCFGQVGPEG 195
Human 196 CQHQLTGLVCTKALCCATVGRAWGLPCELCPAQPHPCRRGFIPNIHTGACQDVDECQAVPGLCQG 260
Human 261 GSCVNMVGSFHCRCPVGHRLSDSSAACEDVNECLSLSGLCSGGDCTNTVGSYVCTCSQGFASSLD 325
Human 326 GTHCLNYRAGACFSVLFGGRCAGDLAGHYTRRQCCCDRGRCWAAG--PVPELCPPRGSNEFQQLC 388
Human 389 AQRLPL-LPGHPGLFPGLL----------GFGSNGMGPPLGPARLNPHGSDARGIPSLGPGNSNI 442
Human 443 GTATLNQTIDICRHFTNLCLNGRCLPTPSSYRCECNVGYTQDVRGECIDVDECTSSPCHHGDCVN 507
Human 508 IPGTYHCRCYPGFQATPTRQACVDVDECIVSGGLCHLGRCVNTEGSFQCVCNAGFELSPDGKNCV 572
Human 573 DHNECATSTMCVNGVCLNEDGSFSCLCKPGFLLAPGGHYCMDIDECQTPGICVNGHCTNTEGSFR 637
Human 638 CQCLGGLAVGTDGRVCVDTHVRSTCYGAIEKGSCARPFPGTVTKSECCCANPDHGFGEPCQLCPA 702
Human 703 KDSAEFQALCSSGLGITTDGRDINECALDPEVCANGVCENLRGSYRCVCNLGYEAGASGKDCTDV 767
Human 768 DECALNSLLCDNGWCQNSPGSYSCSCPPGFHFWQDTEICKDVDECLSSPCVSGVCRNLAGSYTCK 832
Human 833 CGPGSRLDPSGTFCLDSTKGTCWLKIQESRCEVNLQGASLRSECCATLGAAWGSPCERCEIDPAC 897
Human 898 ARGFARMTGVTCDDVNECESFPGVCPNGRCVNTAGSFRCECPEGLMLDASGRLCVDVRLEPCFLR 962
Human 963 WDEDECGVTLPGKYRMDVCCCSIGAVWGV-ECEACPDPESLEFASLCPRGLGFASRDFLSGRPFY 1026
Human 1027 KDVNECKVFPGLCTHGTCRNTVGSFHCACAGGFALDAQERNCTDIDECRISPDLCGQGTCVNTPG 1091
Human 1092 SFECECFPGYESGFMLMKNCMDVDECARDPLLCRGGTCTNTDGSYKCQCPPGHELTAKGTACEDI 1156
Human 1157 DECSLSDGLCPHGQCVNVIGAFQCSCHAGFQSTPDRQGCVDINECRVQNGGCDVHCINTEGSYRC 1221
Human 1222 SCGQGYSLMPDGRACADVDECEENPRVCDQGHCTNMPGGHRCLCYDGFMATPDMRTCVDVDECDL 1286
Human 1287 NPHICLHGDCENTKGSFVCHCQLGYMVRKGATGCSDVDECEVGGHNCDSHASCLNIPGSFSCRCL 1351
Human 1352 PGWVGDGFECHDLDECVSQEHRCSPRGDCLNVPGSYRCTCRQGFAGDGFFCEDRDECAENVDLCD 1416
Human 1417 NGQCLNAPGGYRCECEMGFDPTEDHRACQDVDECAQGNLCAFGSCENLPGMFRCICNGGYELDRG 1481
Human 1482 GGNCTDINECADPVNCINGVCINTPGSYLCSCPQDFELNPSGVGCVDTRAGNCFLETHDRGDSG- 1545
Human 1546 ISCSAEIGVGVTRASCCCSLGRAWGNPCELCPMANTTEYRTLCPGGEGFQPNRITVILEDIDECQ 1610
Human 1611 ELPGLCQGGDCVNTFGSFQCECPPGYHLSEHTRICEDIDECSTHSGICGPGTCYNTLGNYTCVCP 1675
Human 1676 AEYLQVNGGNNCMDMRKSVCFRHY---NGTCQNELAFNVTRKMCCCSYNIGQAWNRPCEACPTPI 1737
Human 1738 SPDYQILCGNQAPGFLTDIHTGKPLDIDECGEIPAICANGICINQIGSFRCECPAGFNYNSILLA 1802
Human 1803 CEDVDECGSRESP-CQQNADCINIPGSYRCKCTRGYKLSPGGACVGRNECREIPNVCSHGDCMDT 1866
Human 1867 EGSYMCLCHRGFQASADQTLCMDIDECDRQPCGNGTCKNIIGSYNCLCFPGFVVTHNGDCVDFDE 1931
Human 1932 CTTLVGQVCRFGHCLNTAGSFHCLCQDGFELTADGKNCVDTNECLSLAGTCLPGTCQNLEGSFRC 1996
Human 1997 ICPPGFQVQSDHCIDIDECSEEPNLCLFGTCTNSPGSFQCLCPPGFVLSDNGHRCFDTRQSFCFT 2061
Human 2062 RFEAGKCSVPKAFNTTKTRCCCSKRPGEGWGDPCELCPQEGSAAFQELCPFGHGAVPGPDDSRED 2126
Human 2127 VNECAENPGVCTNGVCVNTDGSFRCECPFGYSLDFTGINCVDTDECSVGHPCGQGTCTNVIGGFE 2191
Human 2192 CACADGFEPGLMMTCEDIDECSLNPLLCAFRCHNTEGSYLCTCPAGYTLREDGAMCRDVDECADG 2256
Human 2257 QQDCHARGMECKNLIGTFACVCPPGMRPLPGSGEGCTDDNECHAQPDLCVNGRCVNTAGSFRCDC 2321
Human 2322 DEGFQPSPTLTECHDIRQGPCFAEVLQTMCRSLSSSSEAVTRAECCCGGGRGWGPRCELCPLPGT 2386
Human 2387 SAYRKLCPHGSGYTAEGRDVDECRMLAHLCAHGECINSLGSFRCHCQAGYTPDATATTCLDMDEC 2451
Human 2452 SQVPKPCTFLCKNTKGSFLCSCPRGYLLEEDGRTCKDLDECTSRQHNCQFLCVNTVGAFTCRCPP 2516
Human 2517 GFTQHHQACFDNDECSAQPGPCGAHGHCHNTPGSFRCECHQGFTLVSSGHGCEDVNECDGPHRCQ 2581
Human 2582 HGCQNQLGGYRCSCPQGFTQHSQWAQCVDENECALSPPTCGSASCRNTLGGFRCVCPSGFDFDQA 2646
Human 2647 LGGCQEVDECAGRRGPCSYSCANTPGGFLCGCPQGYFRAGQGHCVSGLGFSPGPQDTPDKEEL-- 2709
Human 2710 --LSSEACYECKINGLSPRDRPRRSAHR------------DHQVNLATLDSEALLTLGLNLSHLG 2760
Human 2761 RAERILELRPALEGLEGRIRYVIVRGNEQGFFRMHHLRGVSSLQLGRRRPGPGTYRLEVVSHMAG 2825
Human 2826 PWGVQPEGQ-----------PGPWGQALRLKVQLQL 2850 |
Gene | Sequence | Domain | Region | External ID | Identity |
---|---|---|---|---|---|
FBN3 | XP_016882868.1 | None | |||
Fbn1 | NP_114013.2 | Fibrillin_U_N | 48..82 | CDD:408021 | 22/33 (67%) |
TB | 195..>228 | CDD:395554 | 26/32 (81%) | ||
EGF_CA | 246..>276 | CDD:214542 | 23/29 (79%) | ||
EGF_CA | 288..329 | CDD:214542 | 22/40 (55%) | ||
TB | 345..389 | CDD:395554 | 19/43 (44%) | ||
EGF_CA | 491..522 | CDD:214542 | 15/30 (50%) | ||
EGF_CA | 531..572 | CDD:214542 | 25/40 (63%) | ||
EGF_CA | 573..613 | CDD:214542 | 24/39 (62%) | ||
EGF_CA | 614..647 | CDD:214542 | 22/32 (69%) | ||
TB | 671..712 | CDD:395554 | 26/40 (65%) | ||
EGF_CA | 724..764 | CDD:419698 | 27/39 (69%) | ||
EGF_CA | 766..>797 | CDD:214542 | 20/30 (67%) | ||
cEGF | 788..811 | CDD:403760 | 9/22 (41%) | ||
TB | 863..>891 | CDD:395554 | 19/27 (70%) | ||
TB | 968..1010 | CDD:395554 | 21/41 (51%) | ||
EGF_CA | 1071..1105 | CDD:214542 | 27/33 (82%) | ||
EGF_CA | 1114..1150 | CDD:214542 | 25/35 (71%) | ||
FXa_inhibition | 1202..1237 | CDD:405372 | 19/34 (56%) | ||
EGF_3 | 1327..1362 | CDD:403986 | 21/34 (62%) | ||
EGF_3 | 1368..1403 | CDD:403986 | 18/34 (53%) | ||
EGF_CA | 1447..1487 | CDD:214542 | 25/39 (64%) | ||
EGF_CA | 1488..1519 | CDD:214542 | 20/30 (67%) | ||
TB | 1550..1591 | CDD:395554 | 30/40 (75%) | ||
EGF_CA | 1607..1639 | CDD:214542 | 27/31 (87%) | ||
EGF_CA | 1649..1688 | CDD:214542 | 29/39 (74%) | ||
TB | 1707..1750 | CDD:395554 | 26/42 (62%) | ||
EGF_CA | 1767..>1798 | CDD:214542 | 22/30 (73%) | ||
EGF_CA | 1809..1841 | CDD:214542 | 19/33 (58%) | ||
vWFA | <1848..1887 | CDD:412136 | 25/38 (66%) | ||
EGF_CA | 1931..1972 | CDD:311536 | 21/40 (53%) | ||
EGF_CA | 1974..2009 | CDD:238011 | 22/34 (65%) | ||
EGF_CA | 2014..2054 | CDD:419698 | 25/39 (64%) | ||
TB | 2071..2113 | CDD:395554 | 24/42 (57%) | ||
EGF_CA | 2128..2166 | CDD:214542 | 24/40 (60%) | ||
EGF_CA | 2167..2206 | CDD:214542 | 31/38 (82%) | ||
TB | 2357..2392 | CDD:395554 | 23/34 (68%) | ||
vWFA | <2443..2483 | CDD:412136 | 26/39 (67%) | ||
cEGF | 2466..2489 | CDD:403760 | 16/22 (73%) | ||
EGF_CA | 2486..>2517 | CDD:419698 | 24/30 (80%) | ||
EGF_CA | 2525..2567 | CDD:214542 | 22/41 (54%) | ||
EGF_CA | 2568..>2597 | CDD:214542 | 23/28 (82%) | ||
EGF_CA | 2608..2639 | CDD:214542 | 20/31 (65%) |
Tool | Simple Score | Weighted Score | Original Tool Information | |||
---|---|---|---|---|---|---|
BLAST Result | Score | Score Type | Cluster ID | |||
Compara | 0 | 0.000 | Not matched by this tool. | |||
Domainoid | 0 | 0.000 | Not matched by this tool. | |||
eggNOG | 1 | 0.900 | - | - | E33208_3BA2W | |
HGNC | 0 | 0.000 | Not matched by this tool. | |||
Hieranoid | 0 | 0.000 | Not matched by this tool. | |||
Homologene | 0 | 0.000 | Not matched by this tool. | |||
Inparanoid | 0 | 0.000 | Not matched by this tool. | |||
NCBI | 0 | 0.000 | Not matched by this tool. | |||
OMA | 1 | 1.010 | - | - | QHG45501 | |
OrthoDB | 1 | 1.010 | - | - | D1656at32523 | |
OrthoFinder | 1 | 1.000 | - | - | FOG0005059 | |
OrthoInspector | 0 | 0.000 | Not matched by this tool. | |||
orthoMCL | 1 | 0.900 | - | - | OOG6_100900 | |
Panther | 0 | 0.000 | Not matched by this tool. | |||
Phylome | 1 | 0.910 | - | - | ||
SonicParanoid | 1 | 1.000 | - | - | X1431 | |
SwiftOrtho | 1 | 1.000 | - | - | ||
TreeFam | 0 | 0.000 | Not matched by this tool. | |||
8 | 7.730 |