y
Basic Information | |
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Species | Glycine max |
Cazyme ID | Glyma10g07400.2 |
Family | GT47 |
Protein Properties | Length: 492 Molecular Weight: 56360.8 Isoelectric Point: 9.5065 |
Chromosome | Chromosome/Scaffold: 10 Start: 6085673 End: 6090720 |
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 | 159 | 440 | 0 |
EKQFKVFVYEEGETPVFHNGPCKSIYSMEGNFIHAIEMNDHFRTKDPKKAHVFFLPFSVVMMVRFVYQRDSRDFGPIRKTVIDYINLIAARYSYWNRSLG ADHFMLACHDWGPEASLSLPYLHKNSIRVLCNANTSEGFKPAKDVSFPEINLQTGSINGFIGGPSASKRSILAFFAGGVHGPIRPILLEHWENKDEDIQV HKYLPKGVSYYDKLRNSKFCLCPSGYEVASPRVVEAIYTGCVPVLISEHYVPPFSDVLNWKSFSVELSVKDIPNLKDILMSI |
Full Sequence |
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Protein Sequence Length: 492 Download |
MGSSRWNWWA CWGSEVFSKM KLLLFLVPLV LVAGFASVKG PSLCRWGFIA DCSISFTPLP 60 ASSNSSSQTL HQSNETKVFN VSKPGFNLAA ANESDESHPR QKQKRKLSFI DRNEVVLAQA 120 RAAIREAKNE NQTQDSDYVP IGPMYWNAKT FHRSYLEMEK QFKVFVYEEG ETPVFHNGPC 180 KSIYSMEGNF IHAIEMNDHF RTKDPKKAHV FFLPFSVVMM VRFVYQRDSR DFGPIRKTVI 240 DYINLIAARY SYWNRSLGAD HFMLACHDWG PEASLSLPYL HKNSIRVLCN ANTSEGFKPA 300 KDVSFPEINL QTGSINGFIG GPSASKRSIL AFFAGGVHGP IRPILLEHWE NKDEDIQVHK 360 YLPKGVSYYD KLRNSKFCLC PSGYEVASPR VVEAIYTGCV PVLISEHYVP PFSDVLNWKS 420 FSVELSVKDI PNLKDILMSI SPRQYIRMQR RVIQIQRHFE VHSPPKRFDV FHMILHSVWL 480 RRLNFRMTLN L* 540 |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 1.0e-66 | 158 | 440 | 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 | 89 | 487 | 7 | 405 | unnamed protein product [Arabidopsis thaliana] |
RefSeq | NP_001031828.1 | 0 | 59 | 487 | 87 | 515 | unknown protein [Arabidopsis thaliana] |
RefSeq | XP_002284018.1 | 0 | 158 | 487 | 1 | 330 | PREDICTED: hypothetical protein [Vitis vinifera] |
RefSeq | XP_002326234.1 | 0 | 158 | 484 | 1 | 327 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002528630.1 | 0 | 131 | 487 | 209 | 565 | 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 |