Quantitative three dimensional structure linear interaction energy model of 5′-O-[N-(salicyl)sulfamoyl]adenosine and the aryl acid adenylating enzyme MbtA

Nicholas P. Labello, Eric M. Bennett, David M. Ferguson, Courtney C. Aldrich

Research output: Contribution to journalArticle

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Abstract

MbtA (a salicyl AMP ligase) is a key target for the design of new antitubercular agents. On the basis of structure-activity relationship (SAR) data generated in our laboratory, a structure-based model is developed to predict the binding affinities of aryl acid-AMP bisubstrate inhibitors of MbtA. The approach described takes advantage of the linear interaction energy (LIE) technique to derive linear equations relating ligand structure to function. With only two parameters derived from molecular dynamics simulations, good correlation (R2 = 0.70) was achieved for a set of 31 inhibitors with binding affinities spanning 6 orders of magnitude. The results were applied to understand the effect of steric and heteroatom substitutions on bisubstrate ligand binding and to predict second generation inhibitors of MbtA. The resulting model was further validated by chemical synthesis of a novel inhibitor with a predicted LIE binding affinity of 1.6 nM and a subsequently determined experimental Kiapp of 0.7 nM.

Original languageEnglish (US)
Pages (from-to)7154-7160
Number of pages7
JournalJournal of medicinal chemistry
Volume51
Issue number22
DOIs
StatePublished - Nov 27 2008

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