Basic Information
Gene ID
Ciclev10032697m.g.v1.0
Position
scaffold_4:3335945-3338632 (+)
2687bp
Gene Type
gene
Gene Description (Protein Product)
Belongs to the chalcone isomerase family
Organism
Also AS AT3G55120CICLE_v10032697mg

Gene Structure

upstream:

Domain
Database EntryID E-Value Start end InterPro ID Description

Regulation&Interaction
Protein-protein interaction (PPI)
Ciclev10032749m.g.v1.0 Belongs to the chalcone isomerase family
Ciclev10033821m.g.v1.0 leucoanthocyanidin
Ciclev10032704m.g.v1.0 cell division topological specificity factor
Regulatory gene
Ciclev10000065m.g.v1.0 Protein ALWAYS EARLY
Ciclev10000454m.g.v1.0 Trihelix transcription factor
Ciclev10000593m.g.v1.0 Trihelix transcription factor

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Annotation

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


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:0005737 cytoplasm CC
GO:0005783 endoplasmic reticulum CC
GO:0008150 biological_process BP
GO:0008152 metabolic process BP
GO:0009058 biosynthetic process BP
GO:0009628 response to abiotic stimulus BP
GO:0009812 flavonoid metabolic process BP
GO:0009813 flavonoid biosynthetic process BP
GO:0012505 endomembrane system CC
GO:0016853 isomerase activity MF
GO:0016872 intramolecular lyase 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:0044444 obsolete cytoplasmic part CC
GO:0044464 obsolete cell part CC
GO:0045430 chalcone isomerase activity MF
GO:0050896 response to stimulus BP
GO:0071704 organic substance metabolic process BP
GO:0080167 response to karrikin BP
GO:1901576 organic substance biosynthetic process BP
KEGG Term Name Description
map01110 Biosynthesis of secondary metabolites -
map01100 Metabolic pathways -
map00941 Flavonoid biosynthesis Flavonoids are a major class of plant secondary metabolites that serves a multitude of functions including pigments and antioxidant activity. Flavonoids are synthesized from phenylpropanoid derivatives by condensation with malonyl-CoA. For example, condensation of p-coumaroyl-CoA (C6-C3) with three malonyl-CoA (C3) molecules results in naringenin chalcone with a diphenylpropane (C6-C3-C6) unit, which is converted to naringenin with the flavone (2-phenylchromen-4-one) backbone by conjugate ring closure. These and further modifications yield a variety of structural forms including chalcones, flavanones, dihyroflavonols, and flavans, anthocyanins, flavones and flavonols, and isoflavonoids.