Basic Information | |
---|---|
Species | Ricinus communis |
Cazyme ID | 29637.m000730 |
Family | GT47 |
Protein Properties | Length: 430 Molecular Weight: 49318.8 Isoelectric Point: 5.7697 |
Chromosome | Chromosome/Scaffold: 29637 Start: 75283 End: 76575 |
Description | Exostosin family protein |
View CDS |
External Links |
---|
NCBI Taxonomy |
Plaza |
CAZyDB |
Signature Domain Download full data set without filtering | |||
---|---|---|---|
Family | Start | End | Evalue |
GT47 | 25 | 311 | 0 |
GWYATNQFAVDVIFSNRMKQYECLTNDSSLAAAIFVPFYAGFDIARYLWGYNISTRDAASLDLVNWLMKRPEWGIMGGRDHFLVAGRITWDFRRLTDEEG DWGNKLLFLPAAKNMSMLVVESSPWNANDFGIPYPTYFHPAKDDDVFIWQQRMRNLERKWLFSFAGAPRPDNPKSIRGQIIEQCKKSKVGKLLECDFGES KCHSPSSIMQMFQSSLFCLQPQGDSYTRRSAFDSMLAGCIPVFFHPGSAYTQYTWHLPKDYTTYSVFIPEDDIRKRNVSIEECLSQI |
Full Sequence |
---|
Protein Sequence Length: 430 Download |
MCKFTSNAGM GPPLENVEGV FSNTGWYATN QFAVDVIFSN RMKQYECLTN DSSLAAAIFV 60 PFYAGFDIAR YLWGYNISTR DAASLDLVNW LMKRPEWGIM GGRDHFLVAG RITWDFRRLT 120 DEEGDWGNKL LFLPAAKNMS MLVVESSPWN ANDFGIPYPT YFHPAKDDDV FIWQQRMRNL 180 ERKWLFSFAG APRPDNPKSI RGQIIEQCKK SKVGKLLECD FGESKCHSPS SIMQMFQSSL 240 FCLQPQGDSY TRRSAFDSML AGCIPVFFHP GSAYTQYTWH LPKDYTTYSV FIPEDDIRKR 300 NVSIEECLSQ ISPEQVKIMR ENVINLIPRL IYADPRSKLE TLKDAFDVAV QAVIDKVTRL 360 RRNIIEGRTE YDNFVEENSW KYALLDEGQR EVGGHEWDPF FSKPKDGNVE SGGSSAEAAK 420 NSWKNEQRDQ |
Functional Domains Download unfiltered results here | ||||||||
---|---|---|---|---|---|---|---|---|
Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 3.0e-69 | 10 | 311 | 318 | + 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 | |
---|---|
GO Term | Description |
GO:0016020 | membrane |
Sequence Alignments (This image is cropped. Click for full image.) |
---|