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Basic Information | |
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Species | Chlamydomonas reinhardtii |
Cazyme ID | g9003.t1 |
Family | GT47 |
Protein Properties | Length: 757 Molecular Weight: 79614.8 Isoelectric Point: 8.0467 |
Chromosome | Chromosome/Scaffold: 8 Start: 4492915 End: 4501196 |
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 | 205 | 516 | 1.7e-38 |
SAPRIYVYELPPDLNVYGNLERLDRPLMYMVWQRLLSAGVRVADPAQADFFLVPVRVRLSYDSEKVVQAVSYIRATWPYWDGQPGGAAGERHIFVHTGDW GRDELSEEAQALTRNATWLTHWGLARDHEFAGWKAAHRPGRDIVVPLVLQASLLSSYRITRTTPLHPGSAAGGRQPRPRSRTLFFAGRVCGSRAQPSANG TYPNCPDVLGKEDAYSAATRQVAYYHHHNRTGWKVVTASKSYAIDMLTSKFCLAPSGGGMGKRAVISVLMGCIPVTVTDGLMQPFEPELRWDRFAIDVRE RDIPVMHAVLEG |
Full Sequence |
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Protein Sequence Length: 757 Download |
MNLQRQRWIT CLLVLGILLR LAAASGREQG VSNPGRRLRS ERVLVAGDAA SSDGEEALAA 60 PSRPSRCPGR CTEFGTCNEE LGRCDCPIGR NGTDCSEEVP AGPPLQQLCA RYGHTLASCS 120 RVDAAGCVNG CNGRGRCVGG FCHCRPGYFG ADCSLSLAAD AADGSSTTST TSTSDGSGSS 180 SSASSGSPRP AVEILAGQGY TVRRSAPRIY VYELPPDLNV YGNLERLDRP LMYMVWQRLL 240 SAGVRVADPA QADFFLVPVR VRLSYDSEKV VQAVSYIRAT WPYWDGQPGG AAGERHIFVH 300 TGDWGRDELS EEAQALTRNA TWLTHWGLAR DHEFAGWKAA HRPGRDIVVP LVLQASLLSS 360 YRITRTTPLH PGSAAGGRQP RPRSRTLFFA GRVCGSRAQP SANGTYPNCP DVLGKEDAYS 420 AATRQVAYYH HHNRTGWKVV TASKSYAIDM LTSKFCLAPS GGGMGKRAVI SVLMGCIPVT 480 VTDGLMQPFE PELRWDRFAI DVRERDIPVM HAVLEGLKQG QVSEFQSNLR CAAQHLFWSS 540 LFGSVFGEDG RYDAFETLMQ VLRMRATYPS LGPEEYAYVD AAFAAFMKCE AHLPAGGSAA 600 AAAATAGGAG SSSSSGTGAA VAAAGGLLGG FNGTGAAGGL LDVAKPDLGQ ALAAHRSGAG 660 AGSATAAAAG DAAAGQLLPA PRALLLPAEL AGPGEEGVSR QELCTHSDLP VPPGSGALPA 720 AGSCSRCPRR RGRLLNPGGT ICCNTKDLAR CPRLWD* 780 |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 6.0e-26 | 203 | 514 | 332 | + 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. |
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 | XP_001693540.1 | 0 | 66 | 589 | 4 | 496 | exostosin-like glycosyltransferase [Chlamydomonas reinhardtii] |
RefSeq | XP_001702517.1 | 0 | 70 | 564 | 14 | 479 | exostosin-like glycosyltransferase [Chlamydomonas reinhardtii] |
RefSeq | XP_001702686.1 | 0 | 12 | 590 | 10 | 554 | exostosin-like glycosyltransferase [Chlamydomonas reinhardtii] |
RefSeq | XP_001703124.1 | 0 | 76 | 589 | 3 | 471 | exostosin-like glycosyltransferase [Chlamydomonas reinhardtii] |
RefSeq | XP_001703125.1 | 0 | 65 | 589 | 65 | 507 | exostosin-like glycosyltransferase [Chlamydomonas reinhardtii] |