PPGR - Gene Detail

Basic Information

Gene Structure

Domain

Regulation&
Interaction

Annotation

Orthologus Group

Expresssion

Pathway

Basic Information

Gene ID	Pt9G57440 View in Genome Browser
Position	chr9:1937430842-1937433272 (+) 2430bp
Gene Type	gene
Gene Description (Protein Product)	Belongs to the chalcone stilbene synthases family
Organism	Pinus tabuliformis
Also AS	AT5G13930

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Domain

Database	EntryID	E-Value	Start	end	InterPro ID	Description

Regulation&Interaction

Protein-protein interaction (PPI)	PtJG32950 Belongs to the iron ascorbate-dependent oxidoreductase family PtQG28940 Belongs to the iron ascorbate-dependent oxidoreductase family PtQG28950 Belongs to the iron ascorbate-dependent oxidoreductase family
Regulatory gene	Pt1G12460 Protein BASIC PENTACYSTEINE6-like Pt1G12480 Protein BASIC PENTACYSTEINE6-like Pt3G55780

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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)

Select Expression

Pathway

GO Term	Description	GO Category
GO:0003674	molecular_function	MF
GO:0003824	catalytic activity	MF
GO:0008150	biological_process	BP
GO:0008152	metabolic process	BP
GO:0009058	biosynthetic process	BP
GO:0009812	flavonoid metabolic process	BP
GO:0009813	flavonoid biosynthetic process	BP
GO:0016210	naringenin-chalcone synthase activity	MF
GO:0016740	transferase activity	MF
GO:0016746	acyltransferase activity	MF
GO:0016747	acyltransferase activity, transferring groups other than amino-acyl groups	MF
GO:0071704	organic substance metabolic process	BP
GO:1901576	organic substance biosynthetic process	BP

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.