Basic Information
Gene ID
Bpev01.c0974.g0018
Position
Contig974:182979-183989 (-)
1010bp
Gene Type
gene
Gene Description (Protein Product)
Belongs to the UDP-glycosyltransferase family
Organism
Also AS AT2G18560

Gene Structure

upstream:

Domain
Database EntryID E-Value Start end InterPro ID Description

Regulation&Interaction
Protein-protein interaction (PPI)
Bpev01.c2220.g0001 Removal of H(2)O(2), oxidation of toxic reductants, biosynthesis and degradation of lignin, suberization, auxin catabolism, response to environmental stresses such as wounding, pathogen attack and oxidative stress
Bpev01.c1767.g0003 Belongs to the peroxidase family. Classical plant (class III) peroxidase subfamily
Bpev01.c1529.g0006 Belongs to the peroxidase family. Classical plant (class III) peroxidase subfamily

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Annotation

Orthologous Group
Orthologous ID Species Number All hits in PereRegDB Hits of this species Orthologous Detail

Expression Profile
DataSet Number of Samples expressed(TPM>1) Mean Min Max Standard deviation(SD) Coeffcient variation(CV)


Pathway
GO Term Description GO Category
GO:0003674 molecular_function MF
GO:0003824 catalytic activity MF
GO:0005575 cellular_component CC
GO:0005622 intracellular anatomical structure CC
GO:0005623 obsolete cell CC
GO:0008194 UDP-glycosyltransferase activity MF
GO:0016740 transferase activity MF
GO:0016757 glycosyltransferase activity MF
GO:0016758 hexosyltransferase activity MF
GO:0035251 UDP-glucosyltransferase activity MF
GO:0043226 organelle CC
GO:0043227 membrane-bounded organelle CC
GO:0043229 intracellular organelle CC
GO:0043231 intracellular membrane-bounded organelle CC
GO:0044424 obsolete intracellular part CC
GO:0044464 obsolete cell part CC
GO:0046527 glucosyltransferase activity MF
GO:0080043 quercetin 3-O-glucosyltransferase activity MF
GO:0080044 quercetin 7-O-glucosyltransferase activity MF
KEGG Term Name Description
map01110 Biosynthesis of secondary metabolites -
map00940 Phenylpropanoid biosynthesis Phenylpropanoids are a group of plant secondary metabolites derived from phenylalanine and having a wide variety of functions both as structural and signaling molecules. Phenylalanine is first converted to cinnamic acid by deamination. It is followed by hydroxylation and frequent methylation to generate coumaric acid and other acids with a phenylpropane (C6-C3) unit. Reduction of the CoA-activated carboxyl groups of these acids results in the corresponding aldehydes and alcohols. The alcohols are called monolignols, the starting compounds for biosynthesis of lignin.