y
Basic Information | |
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Species | Volvox carteri |
Cazyme ID | Vocar20014463m |
Family | GT47 |
Protein Properties | Length: 766 Molecular Weight: 86256 Isoelectric Point: 6.8474 |
Chromosome | Chromosome/Scaffold: 96 Start: 101675 End: 112001 |
Description | exostosin family protein |
View CDS |
Signature Domain Download full data set without filtering | |||
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Family | Start | End | Evalue |
GT47 | 254 | 546 | 1.6e-29 |
RGPRIYIYEFPPYMHMWGMLWLDRPLNIIVWERIISMGLREVDPARADYFFIPGCGRGCDKWDDKFHFILAHYGQYWTQNQGRDHIMTHPGDWGRCEHSW DAFADKFISNVTMLQHWGMTVDRSSEVEHNLFNTCHKPNQDILVPPMCGDLYPQFEYNIWHPNRKENPITKTNLASVAGSICGWNSVEEPPCRNRYYSLG VRAALWQLRDVPGFHIAKRVAMMGQSMAESEFCFAPTGAGYGKRNVMATTLGCMPVIISDHVAQPYEPFLNWNEFGVWIPESQAKDVEIILRG |
Full Sequence |
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Protein Sequence Length: 766 Download |
MRIVCAVTTV ASPTRMKLIQ RWLSPCIFIL VMLIAYAEGS NHDYFEELWG LEKSANQRNA 60 RRMLTRDLNM DEIFRYWQKM YGHWPTATYE RHVQEYQRRV ASAGRSWGLP KTDEDFLDIY 120 YYLRSKTKVP HAPGWTPELD KCGPTCHMYG TCNQELAICG CPRGREGPNC SSPVATSCHQ 180 YCHHEGQCHR IIREWCINEC NDRGTCVGGV CHCYPGYFGA DCSLSIDYEG TEPGSRGKGS 240 TVVLAGLNYT ANPRGPRIYI YEFPPYMHMW GMLWLDRPLN IIVWERIISM GLREVDPARA 300 DYFFIPGCGR GCDKWDDKFH FILAHYGQYW TQNQGRDHIM THPGDWGRCE HSWDAFADKF 360 ISNVTMLQHW GMTVDRSSEV EHNLFNTCHK PNQDILVPPM CGDLYPQFEY NIWHPNRKEN 420 PITKTNLASV AGSICGWNSV EEPPCRNRYY SLGVRAALWQ LRDVPGFHIA KRVAMMGQSM 480 AESEFCFAPT GAGYGKRNVM ATTLGCMPVI ISDHVAQPYE PFLNWNEFGV WIPESQAKDV 540 EIILRGFTPQ QKAEKMEKLY CAARHLAFTT VYGGLFEGDT GEFDAMATLV HILRARKRHW 600 GVPDHKLIEV DPEFADFMAC KHRDISTEES GFSGSGGGGA PPPAPPLPLA GVTTSRSHTI 660 DDEAFPQRTV TTVDWIRAAN GEAAGRGQGS DGPVEPRLSG LCYFNPQWVH YADHDAADAT 720 DQVIKEHMKA GQCMPKNANR VAGFPPGASV TCPPTGPITK CAQLV* 780 |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam07974 | EGF_2 | 0.0005 | 198 | 222 | 27 | + EGF-like domain. This family contains EGF domains found in a variety of extracellular proteins. | ||
pfam03016 | Exostosin | 2.0e-22 | 253 | 547 | 317 | + Exostosin family. The EXT family is a family of tumour suppressor genes. Mutations of EXT1 on 8q24.1, EXT2 on 11p11-13, and EXT3 on 19p have been associated with the autosomal dominant disorder known as hereditary multiple exostoses (HME). This is the most common known skeletal dysplasia. The chromosomal locations of other EXT genes suggest association with other forms of neoplasia. EXT1 and EXT2 have both been shown to encode a heparan sulphate polymerase with both D-glucuronyl (GlcA) and N-acetyl-D-glucosaminoglycan (GlcNAC) transferase activities. The nature of the defect in heparan sulphate biosynthesis in HME is unclear. |
Gene Ontology | |
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GO Term | Description |
GO:0016020 | membrane |
Annotations - NR Download unfiltered results here | |||||||
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Source | Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
RefSeq | XP_001693540.1 | 0 | 141 | 620 | 4 | 496 | exostosin-like glycosyltransferase [Chlamydomonas reinhardtii] |
RefSeq | XP_001697348.1 | 0 | 101 | 715 | 27 | 599 | exostosin-like glycosyltransferase [Chlamydomonas reinhardtii] |
RefSeq | XP_001702686.1 | 0 | 142 | 621 | 73 | 554 | exostosin-like glycosyltransferase [Chlamydomonas reinhardtii] |
RefSeq | XP_001703124.1 | 0 | 151 | 621 | 3 | 472 | exostosin-like glycosyltransferase [Chlamydomonas reinhardtii] |
RefSeq | XP_001703125.1 | 0 | 135 | 621 | 60 | 508 | exostosin-like glycosyltransferase [Chlamydomonas reinhardtii] |