Basic Information | |
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Species | Glycine max |
Cazyme ID | Glyma03g00910.1 |
Family | GT47 |
Protein Properties | Length: 506 Molecular Weight: 58333.2 Isoelectric Point: 8.6953 |
Chromosome | Chromosome/Scaffold: 03 Start: 620288 End: 623955 |
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 | 117 | 439 | 0 |
AVLRVFMYDLPPEFHFGLLDWKPEENVNSVWPDIKTKAPHYPGGLNSQHSIEYWLTLDLLASELPEAEAQSNARSVIRVRNSSESDVVFVPFFSSLCYNR FSSKTNPHEKRSMNKVLQEKLVKYVTEQEEWKRSGGKDHVIVAHHPNSMLDARMKLWPGTFILSDFGRYPTNIANVEKDVIAPYKHVVGSYDNDQSSFDS RPTLLYFQGAIYRKDGGHVRHELYYLVKNEKDVHFSFGNVEKGGVRNAAEGMRSSKFCLNIAGDTPSSNRLFDAIASHCVPVIISDEIELPYEDVIDYSQ FCVFVRTRDALKKRYLINFIRSI |
Full Sequence |
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Protein Sequence Length: 506 Download |
MVERTVSAGS TIKVVSKKSL CGFFTMTTLL FMLSWLFVLR STRSEASPNS NLFSSFSNSD 60 FDQSVQQQKH MEEEVEPSNF GNRAILVNNI EATTTHDEKQ QQQQQQLGVK CKAHDKAVLR 120 VFMYDLPPEF HFGLLDWKPE ENVNSVWPDI KTKAPHYPGG LNSQHSIEYW LTLDLLASEL 180 PEAEAQSNAR SVIRVRNSSE SDVVFVPFFS SLCYNRFSSK TNPHEKRSMN KVLQEKLVKY 240 VTEQEEWKRS GGKDHVIVAH HPNSMLDARM KLWPGTFILS DFGRYPTNIA NVEKDVIAPY 300 KHVVGSYDND QSSFDSRPTL LYFQGAIYRK DGGHVRHELY YLVKNEKDVH FSFGNVEKGG 360 VRNAAEGMRS SKFCLNIAGD TPSSNRLFDA IASHCVPVII SDEIELPYED VIDYSQFCVF 420 VRTRDALKKR YLINFIRSIG KEEWTRMWNR LKEVESFFEF QFPSKEGDAV QMIWKAVARK 480 VPFMKLKTNR SRRFLRSLYG NHNFW* |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 1.0e-55 | 119 | 439 | 331 | + 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 | 74 | 505 | 72 | 509 | secondary cell wall-related glycosyltransferase family 47 [Populus tremula x Populus tremuloides] |
RefSeq | XP_002268382.1 | 0 | 88 | 500 | 70 | 473 | PREDICTED: hypothetical protein [Vitis vinifera] |
RefSeq | XP_002319201.1 | 0 | 8 | 494 | 8 | 449 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002325457.1 | 0 | 99 | 505 | 49 | 463 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002530948.1 | 0 | 79 | 504 | 66 | 487 | catalytic, putative [Ricinus communis] |