Basic Information | |
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Species | Picea abies |
Cazyme ID | MA_100374g0010 |
Family | GT47 |
Protein Properties | Length: 525 Molecular Weight: 60046.2 Isoelectric Point: 9.7224 |
View CDS |
Signature Domain Download full data set without filtering | |||
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Family | Start | End | Evalue |
GT47 | 100 | 446 | 0 |
CNGRYVYMYNLPAKFNDLLLRECRELSGWTNMCPHIANSGFGQPLLQQGLLGGPEAAGSSWFDTNQFTAEVIFHERMKRYRCLTPHPTKATAFYVPFYAG FDMSRHVRDHNLTARDRAGIELVQFLRSKPQWKKRGGRDHFMVIGRIARDFMRGQDSPRAWGNKFLLHPEIMNMSSLLIEAQPRDKNQHGIPYPSYFHPR NRSEIDRWQKRMRSKRRQILFSFAGAPRPRLERASIRGQILEQCSSSPRCELLRCQKGLSICNEPSEVMRLFSDSVFCLQPQGDSFTRRSIFDSMLAGCI PVFFTEHSAYTQYKWHLPRNRSSYSVYIPEKSVQRSGNRSIEQHLQS |
Full Sequence |
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Protein Sequence Length: 525 Download |
MGKQNFHKIL CWILLCSSVL WFILLAPTFT DFAGTDPFRS ALQTTRQISL LTDGYASTEV 60 INRQSADKDS AVLLSASQQL GSGSNEFKGI KHENSIADDC NGRYVYMYNL PAKFNDLLLR 120 ECRELSGWTN MCPHIANSGF GQPLLQQGLL GGPEAAGSSW FDTNQFTAEV IFHERMKRYR 180 CLTPHPTKAT AFYVPFYAGF DMSRHVRDHN LTARDRAGIE LVQFLRSKPQ WKKRGGRDHF 240 MVIGRIARDF MRGQDSPRAW GNKFLLHPEI MNMSSLLIEA QPRDKNQHGI PYPSYFHPRN 300 RSEIDRWQKR MRSKRRQILF SFAGAPRPRL ERASIRGQIL EQCSSSPRCE LLRCQKGLSI 360 CNEPSEVMRL FSDSVFCLQP QGDSFTRRSI FDSMLAGCIP VFFTEHSAYT QYKWHLPRNR 420 SSYSVYIPEK SVQRSGNRSI EQHLQSLSAD QVESMRREVI GLIPSLTYAD PRHSNVDFTD 480 SFDLTLQGLV NKITQGEDEN SLVQPSTNSR GHGSNVRRKS RHVLT |
Functional Domains Download unfiltered results here | ||||||||
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Cdd ID | Domain | E-Value | Start | End | Length | Domain Description | ||
pfam03016 | Exostosin | 2.0e-63 | 100 | 434 | 347 | + 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 |
GenBank | EEC74507.1 | 0 | 44 | 495 | 102 | 533 | hypothetical protein OsI_09988 [Oryza sativa Indica Group] |
RefSeq | NP_001048945.1 | 0 | 44 | 495 | 102 | 533 | Os03g0144800 [Oryza sativa (japonica cultivar-group)] |
RefSeq | NP_001147481.1 | 0 | 88 | 495 | 131 | 532 | xyloglucan galactosyltransferase KATAMARI 1 [Zea mays] |
Swiss-Prot | Q8H038 | 0 | 44 | 495 | 86 | 517 | KATAM_ORYSJ RecName: Full=Xyloglucan galactosyltransferase KATAMARI1 homolog |
RefSeq | XP_002468517.1 | 0 | 88 | 495 | 127 | 528 | hypothetical protein SORBIDRAFT_01g047270 [Sorghum bicolor] |