| Literature DB >> 18007423 |
Wenxu Zhou1, Zhihong Song, Ragu Kanagasabai, Jialin Liu, Pruthvi Jayasimha, Archana Sinha, Phani Veeramachanemi, Mathew B Miller, W David Nes.
Abstract
Current progress on the mechanism and substrate recognition by sterol methyl transferase (SMT), the role of mechanism-based inactivators, other inhibitors of SMT action to probe catalysis and phytosterol synthesis is reported. SMT is a membrane-bound enzyme which catalyzes the coupled C-methylation-deprotonation reaction of sterol acceptor molecules generating the 24-alkyl sterol side chains of fungal ergosterol and plant sitosterol. This C-methylation step can be rate-limiting in the post-lanosterol (fungal) or post-cycloartenol (plant) pathways. A series of sterol analogs designed to impair SMT activity irreversibly have provided deep insight into the C-methylation reaction and topography of the SMT active site and as reviewed provide leads for the development of antifungal agents.Entities:
Mesh:
Substances:
Year: 2004 PMID: 18007423 PMCID: PMC6147339 DOI: 10.3390/90400185
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411