Basic Information | |
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Species | Phaseolus vulgaris |
Cazyme ID | Phvul.004G074100.1 |
Family | GT47 |
Protein Properties | Length: 509 Molecular Weight: 58692.5 Isoelectric Point: 9.8255 |
Chromosome | Chromosome/Scaffold: 04 Start: 11806891 End: 11809785 |
Description | exostosin family protein |
View CDS |
External Links |
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CAZyDB |
Signature Domain Download full data set without filtering | |||
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Family | Start | End | Evalue |
GT47 | 118 | 432 | 0 |
IKVYMYDLPAEFHFGLLDWKPNGKSVWPDVRNNIPGYPGGLNLQHSIEFWLTLDVLASEFPEAPKARTVIRVQNSSEADIIYVPFFSSLSYNRYSKRRPN EMKNGNMILQEKLVKHLTAQEEWKRSGGKDHLILAHHPNSMLDARMKLWPATFILSDFGRYPPNIANVEKDVIAPYKHLIPSYLNDNSTFDTRPTLLYFQ GAIYRKDGGLARQELFYLLKNEKDVHFSFGSIGKDGIKKATEGMRASKFCLNIAGDTPSSNRLFDAIASHCVPVIISDAIELPYEDVIDYSEFCIFVRTT DAIKENFLINFIRGI |
Full Sequence |
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Protein Sequence Length: 509 Download |
MGERKGVSSS KVVFRKLLLF FFTMTSVLFV LSWFYVMRST YRPHFIEYSL LPNSKHLSTL 60 DGSKYDMQKQ NVDSSFGNRA ILVDSEDLKE GGRRKGPNGK EKVVKHRGKC HQNDELVIKV 120 YMYDLPAEFH FGLLDWKPNG KSVWPDVRNN IPGYPGGLNL QHSIEFWLTL DVLASEFPEA 180 PKARTVIRVQ NSSEADIIYV PFFSSLSYNR YSKRRPNEMK NGNMILQEKL VKHLTAQEEW 240 KRSGGKDHLI LAHHPNSMLD ARMKLWPATF ILSDFGRYPP NIANVEKDVI APYKHLIPSY 300 LNDNSTFDTR PTLLYFQGAI YRKDGGLARQ ELFYLLKNEK DVHFSFGSIG KDGIKKATEG 360 MRASKFCLNI AGDTPSSNRL FDAIASHCVP VIISDAIELP YEDVIDYSEF CIFVRTTDAI 420 KENFLINFIR GISKKEWTRM WNMLKEIEHL FEFHFPSKEN DAVQMIWQAV ARKVPAMRLK 480 LNRHGRFSRS PPSADKELKS IPLPRNFW* |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 3.0e-53 | 118 | 432 | 325 | + 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 | AAX33321.1 | 0 | 1 | 508 | 1 | 509 | secondary cell wall-related glycosyltransferase family 47 [Populus tremula x Populus tremuloides] |
EMBL | CAN68950.1 | 0 | 38 | 508 | 37 | 488 | hypothetical protein [Vitis vinifera] |
RefSeq | XP_002268382.1 | 0 | 38 | 508 | 37 | 488 | PREDICTED: hypothetical protein [Vitis vinifera] |
RefSeq | XP_002319201.1 | 0 | 1 | 488 | 3 | 450 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002530948.1 | 0 | 38 | 504 | 37 | 496 | catalytic, putative [Ricinus communis] |