Function
AMACR (Alpha-methylacyl-CoA racemase) catalyzes the interconversion of (R)- and (S)-stereoisomers of alpha-methyl-branched-chain fatty acyl-CoA esters. It acts solely on coenzyme A thioesters, not on free fatty acids. AMACR accepts a broad range of alpha-methylacyl-CoAs as substrates, including pristanoyl-CoA, trihydroxycoprostanoyl-CoA (an intermediate in bile acid synthesis), and arylpropionic acids such as the anti-inflammatory drug ibuprofen (2-(4-isobutylphenyl)propionic acid). However, it does not metabolize 3-methyl-branched or linear-chain acyl-CoAs.