Antitubercular nucleosides that inhibit siderophore biosynthesis: SAR of the glycosyl domain |
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Authors: | Somu Ravindranadh V Wilson Daniel J Bennett Eric M Boshoff Helena I Celia Laura Beck Brian J Barry Clifton E Aldrich Courtney C |
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Affiliation: | Center for Drug Design, Academic Health Center, University of Minnesota, Minneapolis, MN 55455, USA. |
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Abstract: | Tuberculosis is the leading cause of infectious disease mortality in the world by a bacterial pathogen. We previously demonstrated that a bisubstrate inhibitor of the adenylation enzyme MbtA, which is responsible for the second step of mycobactin biosynthesis, exhibited potent antitubercular activity. Here we systematically investigate the structure-activity relationships of the bisubstrate inhibitor glycosyl domain resulting in the identification of a carbocyclic analogue that possesses a KIapp value of 2.3 nM and MIC99 values of 1.56 microM against M. tuberculosis H37Rv. The SAR data suggest the intriguing possibility that the bisubstrate inhibitors utilize a transporter for entry across the mycobacterial cell envelope. Additionally, we report improved conditions for the expression of MbtA and biochemical analysis, demonstrating that MbtA follows a random sequential enzyme mechanism for the adenylation half-reaction. |
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