y
Basic Information | |
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Species | Glycine max |
Cazyme ID | Glyma12g08530.2 |
Family | GT47 |
Protein Properties | Length: 462 Molecular Weight: 53103.6 Isoelectric Point: 9.7917 |
Chromosome | Chromosome/Scaffold: 12 Start: 6282058 End: 6286089 |
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 | 101 | 400 | 0 |
KNLKVFVYDLPQKYNTDWLSNERCSKHLFASEVAIHRALLTSEVRTFDPYDADFFFVPVYVSCNFSTVNGFPAIGHARSLIASAVSLVSSEYPFWNRSRG SDHVFVASHDFGSCFHTLEDVAMADGVPEIMRNSIVLQTFGVVYDHPCQSVEHVVIPPYVSPESVRDTMENFPVNGRRDIWAFFRGKMELHPKNVSGRFY SKKVRTVIWRKFNGDRRFYLQRQRFAGYQSEIARSVFCLCPLGWAPWSPRLVESVALGCVPVIIADGIRLPFISAVKWPEISITVAEKDVGRLAEILERV |
Full Sequence |
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Protein Sequence Length: 462 Download |
MAQKRPPNSR GYYVKMKLLH KHGRPHHHHQ QQQEKNCLYR YYKWVLWLSL SLYFFTSYLI 60 SNNNNNNHHS KQPSHVSRAL MESNHTTPPQ QQALNSLGSL KNLKVFVYDL PQKYNTDWLS 120 NERCSKHLFA SEVAIHRALL TSEVRTFDPY DADFFFVPVY VSCNFSTVNG FPAIGHARSL 180 IASAVSLVSS EYPFWNRSRG SDHVFVASHD FGSCFHTLED VAMADGVPEI MRNSIVLQTF 240 GVVYDHPCQS VEHVVIPPYV SPESVRDTME NFPVNGRRDI WAFFRGKMEL HPKNVSGRFY 300 SKKVRTVIWR KFNGDRRFYL QRQRFAGYQS EIARSVFCLC PLGWAPWSPR LVESVALGCV 360 PVIIADGIRL PFISAVKWPE ISITVAEKDV GRLAEILERV AATNLSTIQR NLWDPVTRSA 420 LLFNSQVQKG DATWQILRAL SEKLDRSFRS SRVSRQLDFD T* 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-72 | 99 | 400 | 310 | + 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 |
GenBank | AAX33322.1 | 0 | 16 | 454 | 1 | 440 | secondary cell wall-related glycosyltransferase family 47 [Populus tremula x Populus tremuloides] |
GenBank | ABI64067.1 | 0 | 16 | 456 | 1 | 442 | glycosyltransferase GT47C [Populus tremula x Populus alba] |
RefSeq | XP_002275679.1 | 0 | 5 | 445 | 6 | 441 | PREDICTED: hypothetical protein [Vitis vinifera] |
RefSeq | XP_002314302.1 | 0 | 4 | 456 | 6 | 462 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002523710.1 | 0 | 1 | 456 | 1 | 461 | transferase, putative [Ricinus communis] |