Basic Information | |
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Species | Picea abies |
Cazyme ID | MA_372623g0010 |
Family | GT47 |
Protein Properties | Length: 601 Molecular Weight: 68697.8 Isoelectric Point: 7.2194 |
View CDS |
Signature Domain Download full data set without filtering | |||
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Family | Start | End | Evalue |
GT47 | 207 | 542 | 0 |
QCRGRQIYVYDLPKKFNSELLEQCNSLIPWFDLCDYFTNGGMGKPIENFHQHWYQTHQYALEIAFHSRILKHPCLVSNPEEATLFYIPFYGGLDVMRWNL RENISSEKRDELGKDLANWLQGQPWWRRHGGRDHVLVLGKISWDFRRLKDTDQWGNRLLNLPEMQLVTKLLIERHPWDMNEIGVPHPTFFHPRSDKDIWQ WQWRINTVQRPHLISFAGAARPNSSESIRSILIEQCLSRPESCNFLNCTDDVCLSPESTVNLFLESEFCLQPTGDSPTRRSLFDSLIAGCIPVLFNPFTA YYQYPWHLPANESSYSVYIPEETVRQSKINVVEALL |
Full Sequence |
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Protein Sequence Length: 601 Download |
MVNLGYNKRG GVGFAGIGVS AMGKQRKRAK KVEGSVLGMV KCMGTVVQRT LLLPPLFLTL 60 VICFWVMTSL LPVSVLHVCL SSRRLNMYCV SASTTRFPFD DEKISLGSDK ENQGLSVATH 120 DLKIASPLLN ESVNPLGASL KPEIPTTHVE ISSLQKYENV SNELAIIGNK SIDEENVTFA 180 HDVAKMHMEA IRSASMPAGM KDPSQKQCRG RQIYVYDLPK KFNSELLEQC NSLIPWFDLC 240 DYFTNGGMGK PIENFHQHWY QTHQYALEIA FHSRILKHPC LVSNPEEATL FYIPFYGGLD 300 VMRWNLRENI SSEKRDELGK DLANWLQGQP WWRRHGGRDH VLVLGKISWD FRRLKDTDQW 360 GNRLLNLPEM QLVTKLLIER HPWDMNEIGV PHPTFFHPRS DKDIWQWQWR INTVQRPHLI 420 SFAGAARPNS SESIRSILIE QCLSRPESCN FLNCTDDVCL SPESTVNLFL ESEFCLQPTG 480 DSPTRRSLFD SLIAGCIPVL FNPFTAYYQY PWHLPANESS YSVYIPEETV RQSKINVVEA 540 LLKIPEEQRK EMRRTINQEI MPGLVYGDPD SRFDEFQDAF MISLNNILWR IQKAGISTNS 600 P |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 3.0e-64 | 207 | 544 | 353 | + 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 |
EMBL | CBI34680.1 | 0 | 74 | 593 | 513 | 991 | unnamed protein product [Vitis vinifera] |
RefSeq | NP_176534.2 | 0 | 53 | 594 | 74 | 663 | catalytic [Arabidopsis thaliana] |
RefSeq | XP_002269913.1 | 0 | 74 | 593 | 58 | 536 | PREDICTED: hypothetical protein [Vitis vinifera] |
RefSeq | XP_002299537.1 | 0 | 75 | 593 | 59 | 571 | predicted protein [Populus trichocarpa] |
RefSeq | XP_002509789.1 | 0 | 74 | 593 | 58 | 565 | Xyloglucan galactosyltransferase KATAMARI1, putative [Ricinus communis] |