Journal Article

FZJ-2017-08384

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Recent advances in dynamic docking for drug discovery

De Vivo, M. (Corresponding author)FZJ* ; Cavalli, A. (Corresponding author)

2017
Wiley-Blackwell Malden, MA

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Please use a persistent id in citations: doi:10.1002/wcms.1320

Abstract: Molecular docking allows the evaluation of ligand-target complementarity. This is the crucial first step in small-molecule drug discovery. Over the last decade, increasing computer power and more efficient molecular dynamics (MD) software have prompted the use of MD for molecular docking. The resulting dynamic docking offers major improvements by (1) taking full account of the structural flexibility of the drug-target system and (2) allowing the computation of the free energy and kinetics associated with drug binding. Here, we examine the recent advances in dynamic docking, while also considering the challenges and limitations that this powerful approach must overcome to impact fast-paced drug discovery.

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Contributing Institute(s):

1. Computational Biomedicine (IAS-5)
2. Computational Biomedicine (INM-9)

Research Program(s):

1. 574 - Theory, modelling and simulation (POF3-574) (POF3-574)

Appears in the scientific report 2017

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Database coverage:
; Current Contents - Physical, Chemical and Earth Sciences ; IF >= 10 ; JCR ; SCOPUS ; Science Citation Index Expanded ; Thomson Reuters Master Journal List ; Web of Science Core Collection

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