y
Basic Information | |
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Species | Glycine max |
Cazyme ID | Glyma05g33420.1 |
Family | GT47 |
Protein Properties | Length: 417 Molecular Weight: 47132.4 Isoelectric Point: 6.4376 |
Chromosome | Chromosome/Scaffold: 05 Start: 38068343 End: 38071713 |
Description | Exostosin family protein |
View CDS |
External Links |
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NCBI Taxonomy |
Plaza |
CAZyDB |
Signature Domain Download full data set without filtering | |||
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Family | Start | End | Evalue |
GT47 | 49 | 344 | 0 |
RLKVFVYELPSKYNKKILQKDPRCLNHMFAAEIFMHRFLLSSPVRTLNPEEADWFYTPVYTTCDLTPNGLPLPFKSPRMMRSAIQLISSNWPYWNRTEGA DHFFVVPHDFGACFHYQEEKAIERGILTLLRRATLVQTFGQRNHVCLKEGSITIPPYAPPQKMHTHLIPDKTPRSIFVYFRGLFYDVGNDPEGGYYARGA RAAVWENFKDNLLFDISTEHPTTYYEDMQRAVFCLCPLGWAPWSPRLVEAVIFGCIPVIIADDIVLPFADAIPWEEIGVFVDEEDVPKLDTILTSI |
Full Sequence |
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Protein Sequence Length: 417 Download |
MGVSKLGFLG LLFADFLFAV GAVELGRNQP TERISGSAGD VLEDDPVGRL KVFVYELPSK 60 YNKKILQKDP RCLNHMFAAE IFMHRFLLSS PVRTLNPEEA DWFYTPVYTT CDLTPNGLPL 120 PFKSPRMMRS AIQLISSNWP YWNRTEGADH FFVVPHDFGA CFHYQEEKAI ERGILTLLRR 180 ATLVQTFGQR NHVCLKEGSI TIPPYAPPQK MHTHLIPDKT PRSIFVYFRG LFYDVGNDPE 240 GGYYARGARA AVWENFKDNL LFDISTEHPT TYYEDMQRAV FCLCPLGWAP WSPRLVEAVI 300 FGCIPVIIAD DIVLPFADAI PWEEIGVFVD EEDVPKLDTI LTSIPPEVIL RKQRLLANPS 360 MKQAMLFPQP AQPGDAFHQV LNGLARKLPH DNTVFLKPGE KILNWTAGPV GDLKPW* 420 |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 4.0e-81 | 49 | 344 | 304 | + 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 |
GenBank | AAM64940.1 | 0 | 9 | 416 | 8 | 415 | unknown [Arabidopsis thaliana] |
RefSeq | NP_568941.1 | 0 | 9 | 416 | 8 | 415 | GUT1; catalytic/ glucuronoxylan glucuronosyltransferase [Arabidopsis thaliana] |
RefSeq | XP_002284685.1 | 0 | 1 | 416 | 1 | 416 | PREDICTED: hypothetical protein [Vitis vinifera] |
RefSeq | XP_002318180.1 | 0 | 1 | 416 | 1 | 417 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002511079.1 | 0 | 1 | 416 | 1 | 417 | catalytic, putative [Ricinus communis] |
Metabolic Pathways | |||
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Pathway Name | Reaction | EC | Protein Name |
xylogalacturonan biosynthesis | RXN-9589 | EC-2.4.2.41 | xylogalacturonan β-1,3-xylosyltransferase |