Key Topics in Molecular Docking for Drug Design

International Journal of Molecular Sciences

FlorianoP. Silva-Jr¹  Paula Jofily²  PedroH. M. Torres³  AnaC. R. Sodero⁴ 

[1] Federal University of Rio de Janeiro, Rio de Janeiro 21949-900, RJ, Brazil;School of Pharmacy;Department of Biochemistry, University of Cambridge, Cambridge CB2 1GA, UK;Department of Drugs and Medicines;

关键词: computer-aided drug design;    structure-based drug design;    benchmarking sets;    consensus methods;    fragment-based;    machine learning;   

DOI  :  10.3390/ijms20184574

来源: DOAJ

【 摘 要 】

Molecular docking has been widely employed as a fast and inexpensive technique in the past decades, both in academic and industrial settings. Although this discipline has now had enough time to consolidate, many aspects remain challenging and there is still not a straightforward and accurate route to readily pinpoint true ligands among a set of molecules, nor to identify with precision the correct ligand conformation within the binding pocket of a given target molecule. Nevertheless, new approaches continue to be developed and the volume of published works grows at a rapid pace. In this review, we present an overview of the method and attempt to summarise recent developments regarding four main aspects of molecular docking approaches: (i) the available benchmarking sets, highlighting their advantages and caveats, (ii) the advances in consensus methods, (iii) recent algorithms and applications using fragment-based approaches, and (iv) the use of machine learning algorithms in molecular docking. These recent developments incrementally contribute to an increase in accuracy and are expected, given time, and together with advances in computing power and hardware capability, to eventually accomplish the full potential of this area.

【 授权许可】

Unknown