Identification of a catalytically essential nucleophilic residue in sheep liver cytoplasmic aldehyde dehydrogenase

Biochem J. 1991 Apr 1;275 ( Pt 1)(Pt 1):207-10. doi: 10.1042/bj2750207.

Abstract

Sheep liver cytoplasmic aldehyde dehydrogenase was labelled by reaction with the substrate p-nitrophenyl di[14C]methylcarbamate. After tryptic digestion and peptide fractionation the labelled residue was identified as Cys-302. This is the first unequivocal identification of the essential enzymic nucleophile in the esterase activity of aldehyde dehydrogenase. By implication, Cys-302 is probably also the residue that is acylated by aldehyde substrates and the first residue that is modified by disulfiram.

MeSH terms

  • Aldehyde Dehydrogenase / chemistry*
  • Aldehyde Dehydrogenase / metabolism
  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Carbamates / metabolism
  • Cysteine / chemistry*
  • Cytoplasm / enzymology
  • Liver / enzymology*
  • Molecular Sequence Data
  • Peptide Fragments / chemistry
  • Peptide Fragments / isolation & purification
  • Sheep
  • Trypsin

Substances

  • Carbamates
  • Peptide Fragments
  • 4-nitrophenyl dimethylcarbamate
  • Aldehyde Dehydrogenase
  • Trypsin
  • Cysteine