The mechanism of caseinolytic protease (ClpP) inhibition

  • Malte Gersch
  • , Felix Gut
  • , Vadim S. Korotkov
  • , Johannes Lehmann
  • , Thomas Böttcher
  • , Marion Rusch
  • , Christian Hedberg
  • , Herbert Waldmann
  • , Gerhard Klebe
  • , Stephan A. Sieber

Research output: Contribution to journalArticlepeer-review

49 Scopus citations

Abstract

Catch me if you can: The ClpP protease mediates protein homeostasis and can be efficiently inhibited by β-lactones. A combination of molecular docking, mutagenesis, activity-based protein profiling, and kinetics studies now reveals the mechanism of ClpP inhibition. A hydrophobic pocket next to the active site allows binding of long aliphatic and aromatic residues. The preferred stereoisomer binds into the oxyanion hole.

Original languageEnglish
Pages (from-to)3009-3014
Number of pages6
JournalAngewandte Chemie International Edition in English
Volume52
Issue number10
DOIs
StatePublished - 4 Mar 2013

Keywords

  • ClpP
  • enzyme inhibitors
  • lactones
  • molecular docking
  • structure-activity relationship

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