Characterization of the binding site for nevirapine (BI-RG-587), a nonnucleoside inhibitor of human immunodeficiency virus type-1 reverse transcriptase

J Biol Chem. 1991 Aug 5;266(22):14670-4.

Abstract

Nevirapine (BI-RG-587) is a potent and specific non-nucleoside inhibitor of human immunodeficiency virus type-1 reverse transcriptase. The compound is non-competitive with respect to template, primer, and nucleoside triphosphates indicating that BI-RG-587 does not act directly at the catalytic site. The binding site for this inhibitor was investigated by employing an azido photoaffinity analogue, BI-RJ-70, to covalently label the enzyme. The resulting photoadduct was subjected to enzymatic digestion by trypsin and endoproteinase lys-C and a single, highly labeled peptide was identified as residues 174-199. Sequencing of this peptide identified Tyr-181 and Tyr-188 as labeled residues.

MeSH terms

  • Affinity Labels
  • Amino Acid Sequence
  • Azepines / metabolism*
  • Binding Sites
  • Chromatography, High Pressure Liquid
  • Electrophoresis, Polyacrylamide Gel
  • HIV-1 / enzymology*
  • Molecular Sequence Data
  • Nevirapine
  • Peptide Mapping
  • Pyridines / metabolism*
  • Reverse Transcriptase Inhibitors*
  • Trypsin

Substances

  • Affinity Labels
  • Azepines
  • Pyridines
  • Reverse Transcriptase Inhibitors
  • Nevirapine
  • Trypsin