Journal
BIOORGANIC & MEDICINAL CHEMISTRY
Volume 50, Issue -, Pages -Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2021.116477
Keywords
Antibacterial drug discovery; Bacterial cell wall synthesis; RmlA; Structure-based optimization
Funding
- Scottish Universities Life Science Alliance
- China Scholarship Council-University of St Andrews PhD Fellowship
- Wellcome Trust [100209/Z/12/Z]
- Wellcome Trust [100209/Z/12/Z] Funding Source: Wellcome Trust
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The study focused on exploring the allosteric site of RmlA, leading to the discovery of potent inhibitors that could be improved by modifying the C6-NH2 of the pyrimidinedione core structure. X-ray crystallographic analysis of the complexes of P. aeruginosa RmlA with the novel analogues revealed how C6-aminoalkyl substituents can be used to position a modifiable amine just outside the allosteric pocket.
The monosaccharide L-Rhamnose is an important component of bacterial cell walls. The first step in the L-Yrhamnose biosynthetic pathway is catalysed by glucose-1-phosphate thymidylyltransferase (RmlA), which condenses glucose-1-phosphate (Glu-1-P) with deoxythymidine triphosphate (dTTP) to yield dTDP-D-glucose. In addition to the active site where catalysis of this reaction occurs, RmlA has an allosteric site that is important for its function. Building on previous reports, SAR studies have explored further the allosteric site, leading to the identification of very potent P. aeruginosa RmlA inhibitors. Modification at the C6-NH2 of the inhibitor's pyrimidinedione core structure was tolerated. X-ray crystallographic analysis of the complexes of P. aeruginosa RmlA with the novel analogues revealed that C6-aminoalkyl substituents can be used to position a modifiable amine just outside the allosteric pocket. This opens up the possibility of linking a siderophore to this class of inhibitor with the goal of enhancing bacterial cell wall permeability.
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