Basic Information | |
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Species | Prunus persica |
Cazyme ID | ppa004844m |
Family | GT47 |
Protein Properties | Length: 490 Molecular Weight: 55430.4 Isoelectric Point: 7.0459 |
Chromosome | Chromosome/Scaffold: 1 Start: 13047652 End: 13049409 |
Description | Exostosin family protein |
View CDS |
External Links |
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NCBI Taxonomy |
CAZyDB |
Signature Domain Download full data set without filtering | |||
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Family | Start | End | Evalue |
GT47 | 64 | 409 | 0 |
SCSDRYIYIHDDLPSKFNSDFLINCKSISAGISSSSIPSMCPDLLNLGLGPQIENSDGVLANESWFVTNPYLLEVIFHNKMKKYECLTSNSTLASAIYVP FYTGMDASVHLWDSNLTIRDSSAKNLVKWLSGQPEWKKMWGRDHFFVSGRTSWDFRRVRDNSSEWGSKLRFLPESMNMTMLSMEGSLWKNDIAIPYPTSF HPAKDIEVVQWQNRVRQQERPYLFAFVGAPRPHLQGSIRGKIIDHCQASTTCKFLHCGENNCHNPVNIIRVFQSSVYCLQPRGDSDTRRSAFDAILAGCI PVFFHPATAFSQYLWYLPKNHTKYSVFIPVRDVKDLKEEGIIEKVL |
Full Sequence |
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Protein Sequence Length: 490 Download |
MGKPPPGKCF QELWFGLLVS FLLCLVLLCL NYSTSSGANN GIDLSMSKQV RPIGDMKIND 60 TEDSCSDRYI YIHDDLPSKF NSDFLINCKS ISAGISSSSI PSMCPDLLNL GLGPQIENSD 120 GVLANESWFV TNPYLLEVIF HNKMKKYECL TSNSTLASAI YVPFYTGMDA SVHLWDSNLT 180 IRDSSAKNLV KWLSGQPEWK KMWGRDHFFV SGRTSWDFRR VRDNSSEWGS KLRFLPESMN 240 MTMLSMEGSL WKNDIAIPYP TSFHPAKDIE VVQWQNRVRQ QERPYLFAFV GAPRPHLQGS 300 IRGKIIDHCQ ASTTCKFLHC GENNCHNPVN IIRVFQSSVY CLQPRGDSDT RRSAFDAILA 360 GCIPVFFHPA TAFSQYLWYL PKNHTKYSVF IPVRDVKDLK EEGIIEKVLQ GISKDRELAM 420 REEVIRIIAK LVYADPGSRL DTPDAFDIAV QGILERIENV RKVIREGRDP SIGFAEVDGT 480 KFTFPDTID* |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 1.0e-65 | 64 | 401 | 355 | + 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 | NP_193135.2 | 0 | 13 | 484 | 31 | 511 | exostosin family protein [Arabidopsis thaliana] |
RefSeq | XP_002300146.1 | 0 | 1 | 484 | 7 | 512 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002321098.1 | 0 | 26 | 481 | 21 | 462 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002518609.1 | 0 | 11 | 476 | 9 | 482 | Xyloglucan galactosyltransferase KATAMARI1, putative [Ricinus communis] |
RefSeq | XP_002532518.1 | 0 | 9 | 484 | 10 | 521 | Xyloglucan galactosyltransferase KATAMARI1, putative [Ricinus communis] |