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Results for "glutaryl-CoA": 2 genes, 3 gene sets

Name

GCDH Gene

glutaryl-CoA dehydrogenase

The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family. It catalyzes the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and CO(2) in the degradative pathway of L-lysine, L-hydroxylysine, and L-tryptophan metabolism. It uses electron transfer flavoprotein as its electron acceptor. The enzyme exists in the mitochondrial matrix as a homotetramer of 45-kD subunits. Mutations in this gene result in the metabolic disorder glutaric aciduria type 1, which is also known as glutaric acidemia type I. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been identified on chromosome 12. [provided by RefSeq, Mar 2013]

LOC644203 Gene

glutaryl-CoA dehydrogenase, mitochondrial-like

Glutaryl-CoA Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Glutaryl-CoA metabolite from the curated HMDB Metabolites of Enzymes dataset.

glutaryl-coenzyme A Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical glutaryl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset.

PARA-NITROBENZYL GLUTARYL GLYCINIC ACID Gene Set

From DrugBank Drug Targets

interacting proteins for the PARA-NITROBENZYL GLUTARYL GLYCINIC ACID drug from the curated DrugBank Drug Targets dataset.