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Taylor JC , Bock CW , Takusagawa F , Markham GD
Discovery of Novel Types of Inhibitors of S-Adenosylmethionine Synthesis by Virtual Screening
Journal of Medicinal Chemistry. 2009 Oct;52(19) :5967-5973
PMCID: PMC 2869451
AbstractS-Adenosylmethionine (AdoMet) lies at all intersection of nucleotide and amino acid metabolism and performs a Multitude of metabolic functions. AdoMet formation is catalyzed by S-adenosylmethionine synthetase (ATP: L-methionine S-adenosyltransferase (MAT)), which is a target for development of anticancer and antimicrobial agents. High affinity MAT inhibitors have been found through computational docking of more than 200000 compounds for predicted binding to the crystallographically defined nucleotide binding region of the enzyme's active site. Two of the top scoring candidate compounds had IC50 values less than 10 nM, more than 10000-fold lower than the substrates' Km values. The compounds are structurally unrelated to the natural ligands of the enzyme. The enzyme is protected from inhibition by ATP, but not by methionine, consistent with binding at the adenosyl region of the active site. These results validate in silico screening as a robust approach to the discovery of inhibitors of this chemotherapeutically relevant enzyme.
NotesTaylor, John C. Bock, Charles W. Takusagawa, Fusao Markham, George D. Amer chemical soc Washington 501ef