y
Basic Information | |
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Species | Zea mays |
Cazyme ID | GRMZM2G075436_T01 |
Family | GT47 |
Protein Properties | Length: 485 Molecular Weight: 54077.8 Isoelectric Point: 8.8004 |
Chromosome | Chromosome/Scaffold: 1 Start: 234910601 End: 234912540 |
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 | 86 | 427 | 0 |
CAGRYIYVYRLPPRFNDDIARGCRTLRPWMDMCPYMPNCGLGRLLGDEGGVFPGRGWYATDQFMLDVIFRCRMRRYECLTGDPARAAAVFVPAYASLDGG RYLWNSTATRDALALDLVAWLARRPEWRATGGRDHFLVAGRTAWDFLRKTDGDDDWGTKLLSIPAVRNMTALVLEIDPWTRSNNLAVPYPTNFHPATAAD LRAWQEKARALDRRWLFSFAGAARPGSNKTVRAQIFQQCGASSRCGMFRCKKGSECEASPGAMMRLFESSTFCLQPRGDTTTRRSTFDAVVAGCIPVFFH PDSAYTQYADHIPADPERWSVLIMHTDVTDRNVSIEEALAKI |
Full Sequence |
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Protein Sequence Length: 485 Download |
MKPMKPSFQK DGADKVDGGT GGVLWPSRIC YLVVLATTLW AVASILFPPS AFPHPLVSSV 60 TVSHHPAPHD SASEDNRTAT ETADRCAGRY IYVYRLPPRF NDDIARGCRT LRPWMDMCPY 120 MPNCGLGRLL GDEGGVFPGR GWYATDQFML DVIFRCRMRR YECLTGDPAR AAAVFVPAYA 180 SLDGGRYLWN STATRDALAL DLVAWLARRP EWRATGGRDH FLVAGRTAWD FLRKTDGDDD 240 WGTKLLSIPA VRNMTALVLE IDPWTRSNNL AVPYPTNFHP ATAADLRAWQ EKARALDRRW 300 LFSFAGAARP GSNKTVRAQI FQQCGASSRC GMFRCKKGSE CEASPGAMMR LFESSTFCLQ 360 PRGDTTTRRS TFDAVVAGCI PVFFHPDSAY TQYADHIPAD PERWSVLIMH TDVTDRNVSI 420 EEALAKIPPA AVKAMREEVI RLIPRLVYAD ARSARADFKD AFDIALDVVL DRVAKRRRRD 480 VDGR* 540 |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 8.0e-49 | 85 | 427 | 351 | + 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_001048945.1 | 0 | 62 | 478 | 118 | 536 | Os03g0144800 [Oryza sativa (japonica cultivar-group)] |
RefSeq | NP_001150032.1 | 0 | 83 | 478 | 55 | 455 | xyloglucan galactosyltransferase KATAMARI 1 [Zea mays] |
Swiss-Prot | Q8H038 | 0 | 62 | 482 | 102 | 524 | KATAM_ORYSJ RecName: Full=Xyloglucan galactosyltransferase KATAMARI1 homolog |
RefSeq | XP_002464524.1 | 0 | 1 | 484 | 1 | 489 | hypothetical protein SORBIDRAFT_01g020080 [Sorghum bicolor] |
RefSeq | XP_002468517.1 | 0 | 77 | 484 | 130 | 537 | hypothetical protein SORBIDRAFT_01g047270 [Sorghum bicolor] |