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 language | English |
|---|---|
| Pages (from-to) | 3009-3014 |
| Number of pages | 6 |
| Journal | Angewandte Chemie International Edition in English |
| Volume | 52 |
| Issue number | 10 |
| DOIs | |
| State | Published - 4 Mar 2013 |
Keywords
- ClpP
- enzyme inhibitors
- lactones
- molecular docking
- structure-activity relationship