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Basic Information | |
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Species | Glycine max |
Cazyme ID | Glyma20g31360.1 |
Family | GT47 |
Protein Properties | Length: 482 Molecular Weight: 54025.1 Isoelectric Point: 8.6311 |
Chromosome | Chromosome/Scaffold: 20 Start: 39981751 End: 39985464 |
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 | 58 | 405 | 0 |
STINVYVADLPRSLNYALLHTYWSSFSDSRLPTDADHTTPPSSLHQTAKIPPYPENPLIKQYSAEYWITGDLMTPPQHRATSFAKRVLDPLLADVVFVPF FATLSAEMQLGANKGAFRKKHDNDDYKRQRQVMDAVKNTHAWNRSGGRDHVFVLTDPVAMWHVKDEIAPAVLLVVDFGGWYRLDSRGGSNCSESDVIPHT QVSVIKDVIVPYTHLLPRLDLSDNKERHQLLYFKGAKHRHRGGIIREKLWDLLVSEPGVIMEEGFPNATGREQSIKGMQTSEFCLHPAGDTPTSCRLFDA IQSLCIPVIVSDNIELPFEGMVDYAEFSVFAAVSDALKPSWLVSHLQS |
Full Sequence |
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Protein Sequence Length: 482 Download |
MPVIAAKPNK NPSLYVPKLF LLCTLFSILS LALFLFLIFP TATTTTTLHP SLSPFSSSTI 60 NVYVADLPRS LNYALLHTYW SSFSDSRLPT DADHTTPPSS LHQTAKIPPY PENPLIKQYS 120 AEYWITGDLM TPPQHRATSF AKRVLDPLLA DVVFVPFFAT LSAEMQLGAN KGAFRKKHDN 180 DDYKRQRQVM DAVKNTHAWN RSGGRDHVFV LTDPVAMWHV KDEIAPAVLL VVDFGGWYRL 240 DSRGGSNCSE SDVIPHTQVS VIKDVIVPYT HLLPRLDLSD NKERHQLLYF KGAKHRHRGG 300 IIREKLWDLL VSEPGVIMEE GFPNATGREQ SIKGMQTSEF CLHPAGDTPT SCRLFDAIQS 360 LCIPVIVSDN IELPFEGMVD YAEFSVFAAV SDALKPSWLV SHLQSFSKEQ KDRFRQNMAR 420 VQPIFVYDNG HPGGIGPIPA DGAVNHIWKK VHQKLPMIKE AIIRERRKPP GVSVPRRCHC 480 T* 540 |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 1.0e-52 | 62 | 406 | 357 | + 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_564443.1 | 0 | 60 | 480 | 57 | 476 | exostosin family protein [Arabidopsis thaliana] |
RefSeq | XP_002270238.1 | 0 | 11 | 481 | 13 | 440 | PREDICTED: hypothetical protein [Vitis vinifera] |
RefSeq | XP_002325567.1 | 0 | 16 | 481 | 15 | 476 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002327326.1 | 0 | 31 | 481 | 1 | 449 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002533317.1 | 0 | 56 | 481 | 51 | 478 | catalytic, putative [Ricinus communis] |