Dihydrolipoamide is a lipid of Fatty Acyls (FA) class. Dihydrolipoamide is associated with abnormalities such as Wiskott-Aldrich Syndrome. The involved functions are known as Citric Acid Cycle, Electron Transport, NADH oxidation, Oxidation and Oxidants. Dihydrolipoamide often locates in Mitochondria, Mitochondrial matrix and Chloroplasts. The associated genes with Dihydrolipoamide are Mutant Proteins, Recombinant Proteins, mycothione reductase, Genes, Mitochondrial and alanylproline.

References related to functions published in J. Biol. Chem.

PMIDJournalPublished DateAuthorTitle
16093239J. Biol. Chem.2005Rajashankar KR et al.Crystal structure and functional analysis of lipoamide dehydrogenase from Mycobacterium tuberculosis.
15710613J. Biol. Chem.2005Klyachko NL et al.pH-dependent substrate preference of pig heart lipoamide dehydrogenase varies with oligomeric state: response to mitochondrial matrix acidification.
15456792J. Biol. Chem.2004Argyrou A et al.Characterization of a new member of the flavoprotein disulfide reductase family of enzymes from Mycobacterium tuberculosis.
11744691J. Biol. Chem.2002Gazaryan IG et al.Zinc is a potent inhibitor of thiol oxidoreductase activity and stimulates reactive oxygen species production by lipoamide dehydrogenase.