Basic Information | |
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Species | Phaseolus vulgaris |
Cazyme ID | Phvul.001G266100.1 |
Family | GT47 |
Protein Properties | Length: 478 Molecular Weight: 55231.1 Isoelectric Point: 7.9522 |
Chromosome | Chromosome/Scaffold: 01 Start: 51904798 End: 51906231 |
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 | 56 | 399 | 0 |
CTGRYVYIHQLPSRFNTDLLHNCHSLTRGTNKPNMCPYMQNMGLGPQIATSQGVLTNNTWYATNQFLLEVIFHNRMTKYSCLTNDSSLASAIFVPFYAGL DVSRFLWLSNLTDRDSSARDLLQWLADRPEWNKMWGRDHFLISGRIAWDFRRQRDEESYWGSKFRFLPESMNMSMLAVEASSWNNDYAIPYPTSFHPSKD TQVLQWQRKIKFCKRPYLFTFTGAPRPELEGSIRGKIIEQCRASSVCKFVDCSYGVERCDDPVNVMKVFESSVFCLQPPGDSYTRRSIFDSMVAGCIPVF FHPGTAYSQYKWHLPKNRSRYSVYIPVKDVKEWNANVEEVLLKI |
Full Sequence |
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Protein Sequence Length: 478 Download |
MEKSVLISRV CYENHHFCLA ILFSFLFCSL FLSFRAPNHA LTFKPLTKNL TTTHPCTGRY 60 VYIHQLPSRF NTDLLHNCHS LTRGTNKPNM CPYMQNMGLG PQIATSQGVL TNNTWYATNQ 120 FLLEVIFHNR MTKYSCLTND SSLASAIFVP FYAGLDVSRF LWLSNLTDRD SSARDLLQWL 180 ADRPEWNKMW GRDHFLISGR IAWDFRRQRD EESYWGSKFR FLPESMNMSM LAVEASSWNN 240 DYAIPYPTSF HPSKDTQVLQ WQRKIKFCKR PYLFTFTGAP RPELEGSIRG KIIEQCRASS 300 VCKFVDCSYG VERCDDPVNV MKVFESSVFC LQPPGDSYTR RSIFDSMVAG CIPVFFHPGT 360 AYSQYKWHLP KNRSRYSVYI PVKDVKEWNA NVEEVLLKIP EGEVSAMREE VIKVIPNIIY 420 ADPASELDSF EDAFDLAVKG MVERIEKVRE AMRRGIDPSI GFADEDHYKY TFSQNFS* 480 |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 7.0e-67 | 55 | 399 | 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 |
EMBL | CAB10178.1 | 0 | 56 | 473 | 87 | 473 | hypothetical protein [Arabidopsis thaliana] |
RefSeq | NP_193135.2 | 0 | 56 | 473 | 95 | 512 | exostosin family protein [Arabidopsis thaliana] |
RefSeq | XP_002300146.1 | 0 | 56 | 473 | 108 | 513 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002321098.1 | 0 | 27 | 473 | 18 | 466 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002532518.1 | 0 | 1 | 473 | 1 | 522 | Xyloglucan galactosyltransferase KATAMARI1, putative [Ricinus communis] |