Basic Information
Gene ID
Prupe.4G252800.v2.1.g
Position
Pp04:17070079-17073025 (+)
2946bp
Gene Type
gene
Gene Description (Protein Product)
Belongs to the chalcone stilbene synthases family
Organism
Also AS AT5G13930PRUPE_4G252800

Gene Structure

upstream:

Domain
Database EntryID E-Value Start end InterPro ID Description

Regulation&Interaction
Protein-protein interaction (PPI)
Prupe.6G040400.v2.1.g Belongs to the cytochrome P450 family
Prupe.6G364800.v2.1.g Omega-hydroxypalmitate O-feruloyl
Prupe.8G160600.v2.1.g 4-coumarate--CoA ligase-like
Regulatory gene
Prupe.1G338500.v2.1.g Protein BASIC PENTACYSTEINE2-like
Prupe.1G369400.v2.1.g Protein BASIC PENTACYSTEINE6-like
Prupe.8G082900.v2.1.g Protein BASIC PENTACYSTEINE4-like

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Annotation

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


Pathway
KEGG Term Name Description
map04712 Circadian rhythm - plant -
map01110 Biosynthesis of secondary metabolites -
map01100 Metabolic pathways -
map00960 Tropane, piperidine and pyridine alkaloid biosynthesis -
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.