Basic Information | |
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Species | Glycine max |
Cazyme ID | Glyma01g07060.1 |
Family | GT47 |
Protein Properties | Length: 510 Molecular Weight: 58576.3 Isoelectric Point: 9.6554 |
Chromosome | Chromosome/Scaffold: 01 Start: 7606031 End: 7608993 |
Description | exostosin family protein |
View CDS |
External Links |
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NCBI Taxonomy |
Plaza |
CAZyDB |
Signature Domain Download full data set without filtering | |||
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Family | Start | End | Evalue |
GT47 | 119 | 433 | 0 |
LKVFMYDLPPEFHFGLLDWKPSGNSVWPDVRTNIPGYPGGLNLQHSIEFWLTLDILASEFPQASKARTVIRVQNSSEADIIFVPFFSSLSYNRYSKSKPH VKKSKNKILQEKLVTYLMAQEEWKRSGGKDHLILAHHPNSMLDARMKLWPATFILSDFGRYPPNIANVEKDVIAPYKHLISSYVNDNSNFDSRPTLLYFQ GAIYRKDGGLARQELFYLLKDEKDVHFSFGSIGKDGIKKATEGMRASKFCLNIAGDTPSSNRLFDAIASHCVPVIISDKIELPYEDVIDYSEFCIFVRTS DAIKEKFLINFIRGI |
Full Sequence |
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Protein Sequence Length: 510 Download |
MAERIGASSL KVVSRKSLLF FFIMTSVLFI MSWFFVLRST SRPHFIDHNL LPNSKLFSTL 60 DGSKSHMQKQ NVESSFGNRA ILVDSEDVEE ASETKARNGK EKLVKHDGKK CNRNDEVVLK 120 VFMYDLPPEF HFGLLDWKPS GNSVWPDVRT NIPGYPGGLN LQHSIEFWLT LDILASEFPQ 180 ASKARTVIRV QNSSEADIIF VPFFSSLSYN RYSKSKPHVK KSKNKILQEK LVTYLMAQEE 240 WKRSGGKDHL ILAHHPNSML DARMKLWPAT FILSDFGRYP PNIANVEKDV IAPYKHLISS 300 YVNDNSNFDS RPTLLYFQGA IYRKDGGLAR QELFYLLKDE KDVHFSFGSI GKDGIKKATE 360 GMRASKFCLN IAGDTPSSNR LFDAIASHCV PVIISDKIEL PYEDVIDYSE FCIFVRTSDA 420 IKEKFLINFI RGIAKEEWTR MWNKLKEVEH FFEFHFPSKE NDAVQMIWQA VARKVPAMRL 480 KLNRFERFSR SPPSTDEGLR SIPVPKNFW* |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 6.0e-51 | 119 | 433 | 325 | + 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 |
GenBank | AAX33321.1 | 0 | 1 | 509 | 1 | 509 | secondary cell wall-related glycosyltransferase family 47 [Populus tremula x Populus tremuloides] |
EMBL | CAN68950.1 | 0 | 1 | 509 | 1 | 488 | hypothetical protein [Vitis vinifera] |
RefSeq | XP_002268382.1 | 0 | 1 | 509 | 1 | 488 | PREDICTED: hypothetical protein [Vitis vinifera] |
RefSeq | XP_002319201.1 | 0 | 1 | 489 | 3 | 450 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002530948.1 | 0 | 1 | 505 | 1 | 496 | catalytic, putative [Ricinus communis] |