Basic Information | |
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Species | Oryza sativa |
Cazyme ID | LOC_Os01g59630.1 |
Family | GT47 |
Protein Properties | Length: 500 Molecular Weight: 55721.1 Isoelectric Point: 9.8405 |
Chromosome | Chromosome/Scaffold: 1 Start: 34485206 End: 34489811 |
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 | 112 | 423 | 0 |
PLRVYVYEMPSRFTYDLLRLFRDSYRETSNLTSNGSPVHRLVEQHSIDYWLWADLIAPESQRLLKNVIRVRRQEEADIFYVPFFTTISYFLLEKQECKAL YREALKWVTDQPAWQRSEGRDHVIPVHHPWSFKSVRRFVKKAIWLLPDMDSTGNWYKPGQVYLEKDVILPYVPNVDLCDSKCVSETQSRRSTLLFFRGRL RRNAGGKIRSKLVTELKDAEGIIIEEGTAGADGKAAAQNGMRKSLFCLNPAGDTPSSARLFDAIVSGCIPVIVSDELELPFEGILDYRKIALFVSSNDAV QPGWLVKYLRSI |
Full Sequence |
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Protein Sequence Length: 500 Download |
MAGKQLPSSL ARARAASPRG LLAAAALLLL LLLAASYSLL LSPSSPGGLA SPSSGPGSAA 60 DTAFLASLDR FLASPRRSAA PAAAPGDLDA AIRAEEEERL YGGGAWPAAP APLRVYVYEM 120 PSRFTYDLLR LFRDSYRETS NLTSNGSPVH RLVEQHSIDY WLWADLIAPE SQRLLKNVIR 180 VRRQEEADIF YVPFFTTISY FLLEKQECKA LYREALKWVT DQPAWQRSEG RDHVIPVHHP 240 WSFKSVRRFV KKAIWLLPDM DSTGNWYKPG QVYLEKDVIL PYVPNVDLCD SKCVSETQSR 300 RSTLLFFRGR LRRNAGGKIR SKLVTELKDA EGIIIEEGTA GADGKAAAQN GMRKSLFCLN 360 PAGDTPSSAR LFDAIVSGCI PVIVSDELEL PFEGILDYRK IALFVSSNDA VQPGWLVKYL 420 RSIDAKRIRQ MQSNLLKYSR HFLYSSPARP LGPEDLTWRM IAGKLVNIKL HIRRSQRVVR 480 ESRSVCTCDC RVGNSTKMF* |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 7.0e-74 | 113 | 423 | 319 | + 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:0003824 | catalytic activity |
GO:0008150 | biological_process |
GO:0008152 | metabolic process |
GO:0009536 | plastid |
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 |
DDBJ | BAF06505.2 | 0 | 1 | 484 | 1 | 484 | Os01g0811400 [Oryza sativa Japonica Group] |
GenBank | EAY76230.1 | 0 | 1 | 487 | 1 | 488 | hypothetical protein OsI_04166 [Oryza sativa Indica Group] |
GenBank | EAZ13904.1 | 0 | 1 | 488 | 1 | 480 | hypothetical protein OsJ_03829 [Oryza sativa Japonica Group] |
RefSeq | NP_001044591.1 | 0 | 1 | 487 | 1 | 487 | Os01g0811400 [Oryza sativa (japonica cultivar-group)] |
RefSeq | NP_001141657.1 | 0 | 1 | 499 | 1 | 497 | hypothetical protein LOC100273782 [Zea mays] |