Basic Information | |
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Species | Glycine max |
Cazyme ID | Glyma08g29110.2 |
Family | GT47 |
Protein Properties | Length: 471 Molecular Weight: 54548 Isoelectric Point: 9.4935 |
Chromosome | Chromosome/Scaffold: 08 Start: 23499687 End: 23501099 |
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 | 62 | 404 | 0 |
SCSGQYIYVYDLASRFNEDLLKGCHSLSKSIDMCPYMSNLGLGPKVSKKSNEKVLLKESFYATNQFSLEVIFHNTLKHYKCLTNDSSLASAIYVPYYAGL DVVQYLWGGFNVSIRDASPKELVKWLAQQPEWKRMWGRDHFMVVGRIGSDFRRRTENNDDWGTKLMLLPEARNMSILSIESGSKENEFSIPYPTYFHPSK DKEVFQWQKKMRKVKRPYLFSFAGAPRPYYNYLSSIIRNEIIKECQSSRSCKLLNCNAGHNYCNDPVHVTKVFQSSVFCLQPPGDSFTRRSTFDSILAGC IPVFFHPESAYNQYLWHLPKNGSSYSVYIPERDVIEKRVTINE |
Full Sequence |
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Protein Sequence Length: 471 Download |
MDKLPLRKYF DKIRFVFFTS FIFCLSLLLL NYYMTACDYG VTFLLFNMND AKQAHMPKPS 60 NSCSGQYIYV YDLASRFNED LLKGCHSLSK SIDMCPYMSN LGLGPKVSKK SNEKVLLKES 120 FYATNQFSLE VIFHNTLKHY KCLTNDSSLA SAIYVPYYAG LDVVQYLWGG FNVSIRDASP 180 KELVKWLAQQ PEWKRMWGRD HFMVVGRIGS DFRRRTENND DWGTKLMLLP EARNMSILSI 240 ESGSKENEFS IPYPTYFHPS KDKEVFQWQK KMRKVKRPYL FSFAGAPRPY YNYLSSIIRN 300 EIIKECQSSR SCKLLNCNAG HNYCNDPVHV TKVFQSSVFC LQPPGDSFTR RSTFDSILAG 360 CIPVFFHPES AYNQYLWHLP KNGSSYSVYI PERDVIEKRV TINEKLSKVP KSEVLAMRKE 420 IIRLIPRIIY RYPSSRLESV EDAFDIAVKG ILGRIEAIRR NITNVNYTIS * 480 |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 1.0e-69 | 62 | 397 | 348 | + 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_193135.2 | 0 | 13 | 459 | 31 | 488 | exostosin family protein [Arabidopsis thaliana] |
RefSeq | XP_002280815.1 | 0 | 60 | 462 | 90 | 487 | PREDICTED: hypothetical protein [Vitis vinifera] |
RefSeq | XP_002300146.1 | 0 | 1 | 464 | 7 | 494 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002321098.1 | 0 | 44 | 462 | 31 | 445 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002532518.1 | 0 | 11 | 460 | 12 | 499 | Xyloglucan galactosyltransferase KATAMARI1, putative [Ricinus communis] |