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glutaryl the divalent radical of glutaric acid; as glutaryl CoA, a thioester formed with coenzyme A, it is an intermediate in the catabolism of lysine, hydroxylysine, and tryptophan.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
glutaryl-CoA dehydrogenase [EC 1.3.99.7] an enzyme of the oxidoreductase class that catalyzes the oxidative decarboxylation of glutaryl CoA, with sequential reduction of FAD and then electron transfer flavoprotein; the reaction is a step in the degradation of lysine, hydroxylysine, and tryptophan. Deficiency of the enzyme, an autosomal recessive trait, causes glutaricaciduria, type I.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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