Basic Information | |
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Species | Ricinus communis |
Cazyme ID | 30065.m001141 |
Family | GT47 |
Protein Properties | Length: 501 Molecular Weight: 57928.7 Isoelectric Point: 6.5809 |
Chromosome | Chromosome/Scaffold: 30065 Start: 339304 End: 340809 |
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 | 75 | 415 | 0 |
SCSGRYIYVHDLPQRFNDLLVENCTGLYRFYDMCPFLTNSGFGFQVVENPEGIISGRNWFATHQFLLEVIFRTRMNNYECLTNDSSLASAIFVPYYGGLD VARYLWDYNISRDSLGADLVKWLRKKPEWKILWGRDHFFVSGRIGWDFRRHVDNDNGWGSNLMSLPESMNMTMVTIESSAWSNEFAIPYPTHFHPSSETE LIEWQNKMRKRKRHYLFSFAGAPRPFLQDSIRSEIINHCLGSKRLCKLLDCDSGPNKCDNPVEVIKVFQDSVFCLQPPGDSYTRRSAFDSIVAGCIPVFF HPGSAYAQYEWHLPNDYATYSVFIPGNLVKDGNISINETLL |
Full Sequence |
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Protein Sequence Length: 501 Download |
MEKSTIGHNR LWFVIFIAYS FLFLFLCASD YSLFSNDYET NALDSKLKDF ANAFSTQKSN 60 YDSLDDSDPK SYSDSCSGRY IYVHDLPQRF NDLLVENCTG LYRFYDMCPF LTNSGFGFQV 120 VENPEGIISG RNWFATHQFL LEVIFRTRMN NYECLTNDSS LASAIFVPYY GGLDVARYLW 180 DYNISRDSLG ADLVKWLRKK PEWKILWGRD HFFVSGRIGW DFRRHVDNDN GWGSNLMSLP 240 ESMNMTMVTI ESSAWSNEFA IPYPTHFHPS SETELIEWQN KMRKRKRHYL FSFAGAPRPF 300 LQDSIRSEII NHCLGSKRLC KLLDCDSGPN KCDNPVEVIK VFQDSVFCLQ PPGDSYTRRS 360 AFDSIVAGCI PVFFHPGSAY AQYEWHLPND YATYSVFIPG NLVKDGNISI NETLLQVPND 420 KITSMREEVI KLIPKIIYAN PKSKLESFED AFDIAIKGVL ARIEKVRKEI REGKDPGIGF 480 AEPNWRLRFS RMGQKDWSPF F |
Functional Domains Download unfiltered results here | ||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description |
pfam03016 | Exostosin | 8.0e-64 | 75 | 417 | 357 | + 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 |
RefSeq | XP_002321098.1 | 0 | 49 | 500 | 26 | 477 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002518604.1 | 0 | 1 | 501 | 1 | 457 | catalytic, putative [Ricinus communis] |
RefSeq | XP_002518606.1 | 0 | 1 | 501 | 1 | 498 | Xyloglucan galactosyltransferase KATAMARI1, putative [Ricinus communis] |
RefSeq | XP_002518609.1 | 0 | 1 | 501 | 1 | 501 | Xyloglucan galactosyltransferase KATAMARI1, putative [Ricinus communis] |
RefSeq | XP_002532518.1 | 0 | 8 | 482 | 11 | 513 | Xyloglucan galactosyltransferase KATAMARI1, putative [Ricinus communis] |