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• W3118342920 abstract "To the best of our knowledge, this is the first molecular dynamics simulation study on the dimeric form of the LuxS enzyme from Vibrio cholerae to evaluate its structural and dynamical properties including the dynamics of the interface formed by the two monomeric chains of the enzyme. The dynamics of the interfacial region were investigated in terms of inter-residual contacts and the associated interface area of the enzyme in its ligand-free and ligand-bound states which produced characteristics contrast in the interfacial dynamics. Moreover, the binding patterns of the two inhibitors (RHC and KRI) to the enzyme forming two different enzyme-ligand complexes were analyzed which pointed towards a varying inhibition potential of the inhibitors as also revealed by the free energies of ligand binding. It is shown that KRI is a more potent inhibitor than RHC - a substrate analogue, showing correlation with experimental data. Moreover, the role of a loop in chain B of the enzyme was found to facilitate the binding of RHC similar to that of the substrate, while KRI demonstrates a differing binding pattern. The computation of the free energy of binding for the two ligands was also carried out via thermodynamic integration which ultimately served to correlate the dynamical properties with the inhibition potential of two different ligands against the enzyme. Furthermore, this successful study provides a rational to suggest novel LuxS inhibitors which could become promising candidates to treat the diseases caused by a broad variety of bacterial species." @default.
• W3118342920 created "2021-01-18" @default.
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• W3118342920 date "2021-01-01" @default.
• W3118342920 modified "2023-09-27" @default.
• W3118342920 title "Exploring interfacial dynamics in homodimeric <i>S</i>-ribosylhomocysteine lyase (LuxS) from <i>Vibrio cholerae</i> through molecular dynamics simulations" @default.
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• W3118342920 doi "https://doi.org/10.1039/d0ra08809a" @default.
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• W3118342920 hasPublicationYear "2021" @default.
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