y
Basic Information | |
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Species | Glycine max |
Cazyme ID | Glyma06g20840.2 |
Family | GT47 |
Protein Properties | Length: 494 Molecular Weight: 56746.5 Isoelectric Point: 9.9876 |
Chromosome | Chromosome/Scaffold: 06 Start: 17245459 End: 17249147 |
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 | 114 | 428 | 0 |
LKVFMYDLPPEFHFGLLGWKRSVNQTWPEVNNPKRIPRYPGGLNLQHSMEYWLTLDLLSSKVGQPCTAIRVQDSSQADVIFVPFFSSLSYNRHSKLNGEE KVSLNKMLQDRLVQFLMGQKEWKRSGGKDHLIVAHHPNSLLDARRKLGAAMLVLADFGRYPTELANIKKDIIAPYRHLVSTIPKAKSASFEKRTTLVYFQ GAIYRKDGGAIRQELYYLLKDEKDVHFTFGSIGGNGINQASQGMAMSKFCLNIAGDTPSSNRLFDAIVSHCVPVIISDEIELPFEDVLDYSDFSIFVRAS DSMKKGYLLNLLRSI |
Full Sequence |
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Protein Sequence Length: 494 Download |
MSEKIMVHSR FIFCMMIISL FLLILSSIFL LQFSSHSLIP RSVLELILVN NASLYFMPNL 60 KREQVLHPPY PSGDLKFQSQ NPRESDCQTS NSSQKTTSVG QQMNMVSYPT RPLLKVFMYD 120 LPPEFHFGLL GWKRSVNQTW PEVNNPKRIP RYPGGLNLQH SMEYWLTLDL LSSKVGQPCT 180 AIRVQDSSQA DVIFVPFFSS LSYNRHSKLN GEEKVSLNKM LQDRLVQFLM GQKEWKRSGG 240 KDHLIVAHHP NSLLDARRKL GAAMLVLADF GRYPTELANI KKDIIAPYRH LVSTIPKAKS 300 ASFEKRTTLV YFQGAIYRKD GGAIRQELYY LLKDEKDVHF TFGSIGGNGI NQASQGMAMS 360 KFCLNIAGDT PSSNRLFDAI VSHCVPVIIS DEIELPFEDV LDYSDFSIFV RASDSMKKGY 420 LLNLLRSITQ KEWSKMWERL KQITHHFEYQ YPSQPGDAVN MIWQQVERKI SSIRFNLHRK 480 NRYQRSQLRV KSN* 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-58 | 114 | 428 | 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 |
RefSeq | NP_565089.1 | 0 | 1 | 488 | 4 | 454 | exostosin family protein [Arabidopsis thaliana] |
RefSeq | XP_002284930.1 | 0 | 1 | 493 | 1 | 455 | PREDICTED: hypothetical protein isoform 1 [Vitis vinifera] |
RefSeq | XP_002284932.1 | 0 | 83 | 493 | 3 | 416 | PREDICTED: hypothetical protein isoform 2 [Vitis vinifera] |
RefSeq | XP_002320639.1 | 0 | 114 | 485 | 3 | 374 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002514760.1 | 0 | 34 | 489 | 34 | 490 | catalytic, putative [Ricinus communis] |