Title of article
Inactivation of Short-Chain Acyl-Coenzyme A Dehydrogenase from Pig Liver by 2-Pentynoyl-Coenzyme A
Author/Authors
Lundberg، نويسنده , , N.N. and Thorpe، نويسنده , , C.، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 1993
Pages
6
From page
454
To page
459
Abstract
2-Pentynoyl-CoA is a mechanism-based inactivator of the flavoprotein short-chain acyl-CoA dehydrogenase from pig liver. Inactivation is associated with the formation of an intermediate absorbing at 800 nm and results in the incorporation of 0.86 ± 0.13 molecules of radiolabeled inhibitor per subunit. A rapid procedure was devised to isolate the labeled peptide. A glutamate residue was identified as the target of 2-pentynoyl-CoA treatment and proved homologous to the proposed catalytic base, GLU376, in the corresponding medium-chain acyl-CoA dehydrogenase sequence. These results are discussed in terms of the lack of conservation of this glutamate residue in the acyl-CoA dehydrogenase enzyme family.
Journal title
Archives of Biochemistry and Biophysics
Serial Year
1993
Journal title
Archives of Biochemistry and Biophysics
Record number
1450868
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