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Probing the ligand preferences of the three types of bacterial pantothenate kinase
Authors:Jinming Guan  Leanne Barnard  Jeanne Cresson  Annabelle Hoegl  Justin H. Chang  Erick Strauss  Karine Auclair
Affiliation:1. Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montreal, Quebec H3A 0B8, Canada;2. Department of Biochemistry, Stellenbosch University, Stellenbosch 7600, South Africa
Abstract:Pantothenate kinase (PanK) catalyzes the transformation of pantothenate to 4′-phosphopantothenate, the first committed step in coenzyme A biosynthesis. While numerous pantothenate antimetabolites and PanK inhibitors have been reported for bacterial type I and type II PanKs, only a few weak inhibitors are known for bacterial type III PanK enzymes. Here, a series of pantothenate analogues were synthesized using convenient synthetic methodology. The compounds were exploited as small organic probes to compare the ligand preferences of the three different types of bacterial PanK. Overall, several new inhibitors and substrates were identified for each type of PanK.
Keywords:Antimetabolites  Pantothenate kinase inhibitors  PanK  Pantothenate kinase  Coenzyme A
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