Basic Information | |
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Species | Glycine max |
Cazyme ID | Glyma11g36640.1 |
Family | GT47 |
Protein Properties | Length: 475 Molecular Weight: 54970.6 Isoelectric Point: 8.1245 |
Chromosome | Chromosome/Scaffold: 11 Start: 38040977 End: 38042773 |
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 | 52 | 396 | 0 |
SCTGRYVYIHQLPSRFNDYLLQNCQSLTRGTDKPNMCPYMQNNGLGPHITYSQGLFSNNTCYATNQFLLEVIFHNRMTKYGCLTNDSSLASAIFVPFYAG LDVSRFLWLSNLTERDSSGRDLLQWVAKRPEWKQMWGRDHFLVSGRIAWDFRRQYDDASYWGSKFRFIPESMNMSMLAVEASSWNNDYAIPYPTSFHPSE DTHVYRWQRKIRHQKRPYLFTFTGAPRPELEGSIRGKIIDQCRASSVCKFVDCSYGVERCDDPINVIKVFESSVFCLQPPGDSYTRRSIFDSILAGCIPV FFHPGTAYSQYKWHLPKNRTKYSVYIPVKDVKQWNVNVEQVLLGI |
Full Sequence |
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Protein Sequence Length: 475 Download |
MDKSCVISPS CYDNHHLCFA FLFSFLFCSL LLSFHAPNLL RLTSKTKNVT DSCTGRYVYI 60 HQLPSRFNDY LLQNCQSLTR GTDKPNMCPY MQNNGLGPHI TYSQGLFSNN TCYATNQFLL 120 EVIFHNRMTK YGCLTNDSSL ASAIFVPFYA GLDVSRFLWL SNLTERDSSG RDLLQWVAKR 180 PEWKQMWGRD HFLVSGRIAW DFRRQYDDAS YWGSKFRFIP ESMNMSMLAV EASSWNNDYA 240 IPYPTSFHPS EDTHVYRWQR KIRHQKRPYL FTFTGAPRPE LEGSIRGKII DQCRASSVCK 300 FVDCSYGVER CDDPINVIKV FESSVFCLQP PGDSYTRRSI FDSILAGCIP VFFHPGTAYS 360 QYKWHLPKNR TKYSVYIPVK DVKQWNVNVE QVLLGIPEGE VFAMREEVIK LLPNIIYADP 420 RSKLDCFEDA FDLAVKGMLE RIEKVREAMR SGRDPSIGFA DEDHYKYTFS QNYS* 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-64 | 52 | 396 | 360 | + 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 | 17 | 470 | 41 | 512 | exostosin family protein [Arabidopsis thaliana] |
RefSeq | XP_002300146.1 | 0 | 37 | 470 | 92 | 513 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002321098.1 | 0 | 35 | 470 | 27 | 466 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002518609.1 | 0 | 44 | 471 | 67 | 491 | Xyloglucan galactosyltransferase KATAMARI1, putative [Ricinus communis] |
RefSeq | XP_002532518.1 | 0 | 48 | 470 | 97 | 522 | Xyloglucan galactosyltransferase KATAMARI1, putative [Ricinus communis] |