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Molecular Dynamics Simulations of Protein Targets Identified in Mycobacterium tuberculosis

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Abstract:

Application of molecular dynamics simulation technique has become a conventional computational methodology to calculate significant processes at the molecular level. This computational methodology is particularly useful for analyzing the dynamics of proteinligand systems. Several uses of molecular dynamics simulation makes possible evaluation of important structural features found at interface between a ligand and a protein, such as intermolecular hydrogen bonds, contact area and binding energy. Considering structurebased virtual screening, molecular dynamics simulations play a pivotal role in understanding the features that are important for ligandbinding affinity. This information could be employed to select higher-affinity ligands obtained in screening processes. Many protein targets such as enoyl-[acyl-carrier-protein] reductase (InhA), purine nucleoside phosphorylase (PNP), and shikimate kinase have been submitted to these simulations and will be analyzed here. All command files used in this review are available for download at http://azevedolab.net/md_75.html.





Keywords: GROMACS; Molecular dynamics; Mycobacterium tuberculosis; Protein Targets; computer simulations; enoyl-[acyl-carrier-protein] reductase (InhA); hydrogen bonds; purine nucleoside phosphorylase (PNP); shikimate kinase; structure-based virtual screening

Document Type: Research Article

DOI: http://dx.doi.org/10.2174/092986711795029519

Publication date: March 1, 2011

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  • Current Medicinal Chemistry covers all the latest and outstanding developments in medicinal chemistry and rational drug design. Each issue contains a series of timely in-depth reviews written by leaders in the field covering a range of the current topics in medicinal chemistry. Current Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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