y
Basic Information | |
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Species | Glycine max |
Cazyme ID | Glyma20g02340.1 |
Family | GT47 |
Protein Properties | Length: 507 Molecular Weight: 57033.5 Isoelectric Point: 9.7174 |
Chromosome | Chromosome/Scaffold: 20 Start: 1985925 End: 1989795 |
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 | 107 | 432 | 0 |
VKVFLYDLPRRFTSGVIHHHTLARGSGGVGGSASRATPDDVADALKYPGHQHMAEWYLFADLSRAESERAGSGSPVVRVADPEEADLFFVPFFSSLSLIV NPVRPPGSNSGLEKPVYSDEENQEALVEWLEKQEYWKRNNGRDHVIVASDPNAMYRVIDRVRNAVLLVSDFGRLRPDQGSLVKDVVVPYSHRIRTYPGDV GVEDRKTLLFFMGNRYRKEGGKIRDLLFQILENEKDVIIKHGAQSRESRRAASHGMHTSKFCLHPAGDTPSACRLFDAIVSLCIPVIVSDNIELPFEDTI DYRKIAVFVETSSAIKPGHLLSKLRA |
Full Sequence |
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Protein Sequence Length: 507 Download |
MRTFNKLKKV AMMPYPKNTN EEAKANKARK PKPPPSFVSR FTTTFSSMAR KPLLKQTLAT 60 LFLFFVLYAI FNAFFHPTDS SAFDAAATFS SASSVLLSAG TTKSLYVKVF LYDLPRRFTS 120 GVIHHHTLAR GSGGVGGSAS RATPDDVADA LKYPGHQHMA EWYLFADLSR AESERAGSGS 180 PVVRVADPEE ADLFFVPFFS SLSLIVNPVR PPGSNSGLEK PVYSDEENQE ALVEWLEKQE 240 YWKRNNGRDH VIVASDPNAM YRVIDRVRNA VLLVSDFGRL RPDQGSLVKD VVVPYSHRIR 300 TYPGDVGVED RKTLLFFMGN RYRKEGGKIR DLLFQILENE KDVIIKHGAQ SRESRRAASH 360 GMHTSKFCLH PAGDTPSACR LFDAIVSLCI PVIVSDNIEL PFEDTIDYRK IAVFVETSSA 420 IKPGHLLSKL RAVTPDRVLE YQKKLKEVKR YFEYEEPDGT INEIWRQVSK KLPLIKLMIN 480 REKRLFGKEV ECSCVCTNQT AVIRTL* 540 |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 2.0e-68 | 107 | 433 | 338 | + 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 |
EMBL | CAN68074.1 | 0 | 48 | 506 | 1 | 460 | hypothetical protein [Vitis vinifera] |
RefSeq | XP_002276440.1 | 0 | 27 | 502 | 8 | 490 | PREDICTED: hypothetical protein [Vitis vinifera] |
RefSeq | XP_002318294.1 | 0 | 111 | 506 | 1 | 382 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002322391.1 | 0 | 48 | 506 | 1 | 457 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002523645.1 | 0 | 48 | 506 | 1 | 452 | catalytic, putative [Ricinus communis] |