Investigation of potential inhibitors of chorismate-utilizing enzymes
Language English Country United Arab Emirates Media print
Document type Journal Article, Research Support, Non-U.S. Gov't, Review
PubMed
25666801
DOI
10.2174/0929867322666150209152446
PII: CMC-EPUB-65087
Knihovny.cz E-resources
- MeSH
- Biocatalysis drug effects MeSH
- Enzyme Inhibitors chemical synthesis chemistry pharmacology MeSH
- Intramolecular Transferases antagonists & inhibitors metabolism MeSH
- Chorismic Acid metabolism MeSH
- Humans MeSH
- Oxo-Acid-Lyases antagonists & inhibitors metabolism MeSH
- Drug Design MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
- Names of Substances
- Enzyme Inhibitors MeSH
- Intramolecular Transferases MeSH
- Chorismic Acid MeSH
- Oxo-Acid-Lyases MeSH
Chorismate-utilizing enzymes (CUE) such as chorismate mutase, anthranilate synthase, chorismate pyruvate-lyase, 4-amino-4-deoxychorismate synthase, isochorismate synthase and salicylate synthase are responsible for converting chorismate into various products necessary for the survival of bacteria. The absence of these enzymes in humans and their importance in the virulence and survival of bacteria make them suitable targets for potential antimicrobial compounds. Furthermore, the CUE have significant structural homology and similar catalytic mechanisms, enabling the strategy of affecting multiple enzymes with one single inhibitor. This review follows up the investigation of mechanisms of CUE-catalysed reactions and the concurrent development of CUE inhibitors. Many active compounds were found amongst the structures mimicking the transition state of chorismate during the reaction. Most recently, high nanomolar and low micromolar inhibitors against isochorismate-pyruvate lyase were identified, which were also effective against chorismate mutase and salicylate synthase and belong to the most active inhibitors reported up to date.
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