Basic Information | |
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Species | Glycine max |
Cazyme ID | Glyma04g33600.2 |
Family | GT47 |
Protein Properties | Length: 485 Molecular Weight: 55452.7 Isoelectric Point: 9.284 |
Chromosome | Chromosome/Scaffold: 04 Start: 39232932 End: 39236740 |
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 | 112 | 426 | 0 |
LKVFMYDLPPEFHFGLLGWKGSVNQTWPEVDNPERIPRYPGGLNLQHSMEYWLTLDLLSSKVGQPCTAIRVQDSSQADVIFVPFFSSLSYNRHSKLNGQE KVSLNKRLQDRLVQFLMGRKEWKRSGGKDHLIVAHHPNSLLDARRRLGAAMLVLADFGRYPVELANIKKDIIAPYRHLVGTIPRAESASFEKRTTLVYFQ GAIYRKDGGAIRQELYYLLKDENDVHFTFGSIGGNGINQASQGMALSKFCLNIAGDTPSSNRLFDAIVSHCVPVIISDEIELPFEDDLDYSDFSIIVHAS DAMKKGYLLNLLRSI |
Full Sequence |
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Protein Sequence Length: 485 Download |
MSEKIMVHSR FIFCVMIISM FLLSLSSIFL LQFSSHSLIP RSALELILVN NASLYFMPNL 60 KREQILLPPS GDSNFQSQKP RESDCHASDL SQKTTSVGQQ MNMASHPTRP LLKVFMYDLP 120 PEFHFGLLGW KGSVNQTWPE VDNPERIPRY PGGLNLQHSM EYWLTLDLLS SKVGQPCTAI 180 RVQDSSQADV IFVPFFSSLS YNRHSKLNGQ EKVSLNKRLQ DRLVQFLMGR KEWKRSGGKD 240 HLIVAHHPNS LLDARRRLGA AMLVLADFGR YPVELANIKK DIIAPYRHLV GTIPRAESAS 300 FEKRTTLVYF QGAIYRKDGG AIRQELYYLL KDENDVHFTF GSIGGNGINQ ASQGMALSKF 360 CLNIAGDTPS SNRLFDAIVS HCVPVIISDE IELPFEDDLD YSDFSIIVHA SDAMKKGYLL 420 NLLRSIKRDE WNKMWERLKQ ITHHFEYQYP SQPGDAVNMI WQQVEHKISS IRFNLHRKNR 480 YQRS* |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 2.0e-57 | 112 | 426 | 324 | + 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 | AAD55303.1 | 0 | 1 | 484 | 1 | 449 | AC008263_34 F25A4.34 [Arabidopsis thaliana] |
RefSeq | XP_002284930.1 | 0 | 1 | 484 | 1 | 448 | PREDICTED: hypothetical protein isoform 1 [Vitis vinifera] |
RefSeq | XP_002284932.1 | 0 | 81 | 484 | 3 | 409 | PREDICTED: hypothetical protein isoform 2 [Vitis vinifera] |
RefSeq | XP_002320639.1 | 0 | 112 | 483 | 3 | 374 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002514760.1 | 0 | 1 | 483 | 1 | 486 | catalytic, putative [Ricinus communis] |