PPGR - Gene Detail

Gene ID	AALBA5B911649
Position	aalba5_s00081843:1560-3056 (-) 1496bp
Gene Type	gene
Gene Description (Protein Product)	Belongs to the chalcone isomerase family
Organism	Abies alba
Also AS	AT3G55120

upstream:

Database	EntryID	E-Value	Start	end	InterPro ID	Description

Protein-protein interaction (PPI)	AALBA5B993274 Cytochrome P450 AALBA5B929211 Vacuolar-sorting receptor AALBA5B916520 Belongs to the cytochrome P450 family
Regulatory gene	AALBA5B008339 Dehydration-responsive element-binding protein 3-like AALBA5B016053 DNA-binding domain in plant proteins such as APETALA2 and EREBPs AALBA5B016397 ethylene-responsive transcription factor

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

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.