| Basic Information | |
|---|---|
| Species | Glycine max |
| Cazyme ID | Glyma03g32481.1 |
| Family | GT47 |
| Protein Properties | Length: 567 Molecular Weight: 65846.7 Isoelectric Point: 7.5354 |
| Chromosome | Chromosome/Scaffold: 03 Start: 40209296 End: 40211990 |
| Description | Exostosin family protein |
| View CDS | |
| External Links |
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| NCBI Taxonomy |
| Plaza |
| CAZyDB |
| Signature Domain Download full data set without filtering | |||
|---|---|---|---|
| Family | Start | End | Evalue |
| GT47 | 107 | 448 | 0 |
| GGRYIFVHDLPSRFNEDMLKHCRSLSLWTNMCKFTTNAGLGPPLENVNGVFSDTGWYATNQFAVDVIFSNRMKQYQCLTRDPSVAAAFFVPFYAGFDIAR YLWGYNISMRDAASLDLVNWLMNRPEWKIMNGRDHFLVAGRITWDFRRLTEEESDWGKQSFLFFPAWKNMSMLVVESSPWNANDFGIPYPTYFHPAKDDD VFIWQERMRRLERKWLFSFAGAPRPDNLKSIRGQIIEQCRRSKVGKLLECDFGESKCHSPSSIMQMFQGSLFCLQPQGDSYTRRSAFDSMLAGCIPVFFH PGSAYTQYTWHLPKNYTKYSVFIQEDDIRKRNVSIEERLRQI | |||
| Full Sequence |
|---|
| Protein Sequence Length: 567 Download |
| MRRRPVAGVL PDQMEKSNTK NPHSRLCFLA SLSAFFWFLL LYFHFAVLRH QPTAPDPAVP 60 ITFQSQQQHQ QPRKNLGFPE RVSEPKEPTF PFDRALRTAD NKSDPCGGRY IFVHDLPSRF 120 NEDMLKHCRS LSLWTNMCKF TTNAGLGPPL ENVNGVFSDT GWYATNQFAV DVIFSNRMKQ 180 YQCLTRDPSV AAAFFVPFYA GFDIARYLWG YNISMRDAAS LDLVNWLMNR PEWKIMNGRD 240 HFLVAGRITW DFRRLTEEES DWGKQSFLFF PAWKNMSMLV VESSPWNAND FGIPYPTYFH 300 PAKDDDVFIW QERMRRLERK WLFSFAGAPR PDNLKSIRGQ IIEQCRRSKV GKLLECDFGE 360 SKCHSPSSIM QMFQGSLFCL QPQGDSYTRR SAFDSMLAGC IPVFFHPGSA YTQYTWHLPK 420 NYTKYSVFIQ EDDIRKRNVS IEERLRQIPE EEVRIMREEV ISLIPRLVYA DPRSKLETLK 480 DAFDVSVQAV IDKVTNLRKD IIEGHTDENF IEENSWKYAL LDEGQREVGP HEWDPFFSKP 540 KPGGDSDDLS AEAAKNSWKN EQRNQS* 600 |
| Functional Domains Download unfiltered results here | ||||||||
|---|---|---|---|---|---|---|---|---|
| Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
| pfam03016 | Exostosin | 6.0e-68 | 105 | 448 | 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 | |
|---|---|
| GO Term | Description |
| GO:0016020 | membrane |
| Annotations - NR Download unfiltered results here | |||||||
|---|---|---|---|---|---|---|---|
| Source | Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
| GenBank | ACY08857.1 | 0 | 83 | 566 | 134 | 617 | xyloglucan galactosyltransferase [Eucalyptus grandis] |
| GenBank | EEC74507.1 | 0 | 1 | 566 | 4 | 604 | hypothetical protein OsI_09988 [Oryza sativa Indica Group] |
| RefSeq | NP_001048945.1 | 0 | 1 | 566 | 4 | 604 | Os03g0144800 [Oryza sativa (japonica cultivar-group)] |
| RefSeq | XP_002301846.1 | 0 | 45 | 566 | 60 | 585 | glycosyltransferase, CAZy family GT47 [Populus trichocarpa] |
| RefSeq | XP_002468517.1 | 0 | 1 | 566 | 1 | 599 | hypothetical protein SORBIDRAFT_01g047270 [Sorghum bicolor] |
