Basic Information | |
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Species | Glycine max |
Cazyme ID | Glyma13g21240.1 |
Family | GT47 |
Protein Properties | Length: 506 Molecular Weight: 58286.8 Isoelectric Point: 9.3541 |
Chromosome | Chromosome/Scaffold: 13 Start: 24743928 End: 24747092 |
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 | 173 | 454 | 0 |
EKQFKVFVYEEGELPVFHEGPCASIYSTEGSFIHAIEMNEHFRTRDPKKAHVFFLPFSVVMMVRYVYIRDSHDFGPIKRTVRDYINVIAARYPYWNRSLG ADHFMLSCHDWGPEASKFSPYLRKNSIRVLCNANTSEGFDPRKDVSFPEINLQRGPIDGLLGGPSASQRSILAFFAGGIHGPIRPILLEHWEKKDEDIQV HQYLPKGVSYYGMLRKSKFCLCPSGYEVASPRVVEAIYTGCVPVLISDHYVPPFSDVLNWKMFSVEVSMKEIPNLKDILMNI |
Full Sequence |
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Protein Sequence Length: 506 Download |
MGSSRWINCC AWRGSEASST MRLFLFMVPL LVLAGFASIK GSTVYNGRDF IAKRYASWSS 60 LITPSNSSSQ TLLDPPSNSS LQTLHQSNET EVFNVSKPGF NLAPANESDE SHPRQKRKRK 120 FSFLDKTEAV LAQARAAIRE AENWNQTQDS DYVPVGPMYW NPKEFHRSYL EMEKQFKVFV 180 YEEGELPVFH EGPCASIYST EGSFIHAIEM NEHFRTRDPK KAHVFFLPFS VVMMVRYVYI 240 RDSHDFGPIK RTVRDYINVI AARYPYWNRS LGADHFMLSC HDWGPEASKF SPYLRKNSIR 300 VLCNANTSEG FDPRKDVSFP EINLQRGPID GLLGGPSASQ RSILAFFAGG IHGPIRPILL 360 EHWEKKDEDI QVHQYLPKGV SYYGMLRKSK FCLCPSGYEV ASPRVVEAIY TGCVPVLISD 420 HYVPPFSDVL NWKMFSVEVS MKEIPNLKDI LMNISPRKYI RMQKRVRQIR RHFEVHSPPK 480 RYDVFHMILH SVWLRRLNFR VLDDQ* |
Functional Domains Download unfiltered results here | ||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description |
pfam03016 | Exostosin | 4.0e-66 | 172 | 454 | 301 | + 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 |
DDBJ | BAB08605.1 | 0 | 106 | 501 | 10 | 405 | unnamed protein product [Arabidopsis thaliana] |
RefSeq | NP_001031828.1 | 0 | 106 | 501 | 120 | 515 | unknown protein [Arabidopsis thaliana] |
RefSeq | XP_002284018.1 | 0 | 172 | 501 | 1 | 330 | PREDICTED: hypothetical protein [Vitis vinifera] |
RefSeq | XP_002326234.1 | 0 | 172 | 498 | 1 | 327 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002528630.1 | 0 | 145 | 505 | 209 | 569 | catalytic, putative [Ricinus communis] |
Metabolic Pathways | |||
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Pathway Name | Reaction | EC | Protein Name |
xylogalacturonan biosynthesis | RXN-9589 | EC-2.4.2.41 | xylogalacturonan β-1,3-xylosyltransferase |