Title
Clustering Molecular Dynamics Trajectories for Optimizing Docking Experiments.
Abstract
Molecular dynamics simulations of protein receptors have become an attractive tool for rational drug discovery. However, the high computational cost of employing molecular dynamics trajectories in virtual screening of large repositories threats the feasibility of this task. Computational intelligence techniques have been applied in this context, with the ultimate goal of reducing the overall computational cost so the task can become feasible. Particularly, clustering algorithms have been widely used as a means to reduce the dimensionality of molecular dynamics trajectories. In this paper, we develop a novel methodology for clustering entire trajectories using structural features from the substrate-binding cavity of the receptor in order to optimize docking experiments on a cloud-based environment. The resulting partition was selected based on three clustering validity criteria, and it was further validated by analyzing the interactions between 20 ligands and a fully flexible receptor (FFR) model containing a 20 ns molecular dynamics simulation trajectory. Our proposed methodology shows that taking into account features of the substrate-binding cavity as input for the k-means algorithm is a promising technique for accurately selecting ensembles of representative structures tailored to a specific ligand.
Year
DOI
Venue
2015
10.1155/2015/916240
COMPUTATIONAL INTELLIGENCE AND NEUROSCIENCE
Keywords
Field
DocType
proteins,artificial intelligence,molecular dynamics simulation,cluster analysis,algorithms,ligands
Computational intelligence,Computer science,Curse of dimensionality,Software,Molecular dynamics,Artificial intelligence,Virtual screening,Cluster analysis,Machine learning,Trajectory,Cloud computing
Journal
Volume
ISSN
Citations 
2015
1687-5265
5
PageRank 
References 
Authors
0.45
15
5