Refinement of homology-based protein structures by molecular dynamics simulation techniques

Fan, H. and Mark, A. E. (2004) Refinement of homology-based protein structures by molecular dynamics simulation techniques. Protein Science, 13 1: 211-220. doi:10.1110/ps.03381404

Author Fan, H.
Mark, A. E.
Title Refinement of homology-based protein structures by molecular dynamics simulation techniques
Journal name Protein Science   Check publisher's open access policy
ISSN 0961-8368
Publication date 2004-01-01
Year available 2004
Sub-type Article (original research)
DOI 10.1110/ps.03381404
Open Access Status DOI
Volume 13
Issue 1
Start page 211
End page 220
Total pages 10
Place of publication Woodbury
Publisher Cold Spring Harbor Lab Press, Publications Dept
Language eng
Abstract The use of classical molecular dynamics simulations, performed in explicit water, for the refinement of structural models of proteins generated ab initio or based on homology has been investigated. The study involved a test set of 15 proteins that were previously used by Baker and coworkers to assess the efficiency of the ROSETTA method for ab initio protein structure prediction. For each protein, four models generated using the ROSETTA procedure were simulated for periods of between 5 and 400 nsec in explicit solvent, under identical conditions. In addition, the experimentally determined structure and the experimentally derived structure in which the side chains of all residues had been deleted and then regenerated using the WHATIF program were simulated and used as controls. A significant improvement in the deviation of the model structures from the experimentally determined structures was observed in several cases. In addition, it was found that in certain cases in which the experimental structure deviated rapidly from the initial structure in the simulations, indicating internal strain, the structures were more stable after regenerating the side-chain positions. Overall, the results indicate that molecular dynamics simulations on a tens to hundreds of nanoseconds time scale are useful for the refinement of homology or ab initio models of small to medium-size proteins.
Keyword Biochemistry & Molecular Biology
protein structure prediction
homology modeling
molecular dynamics
structure refinement
Dna-binding Domain
Structure Prediction
Secondary Structure
Q-Index Code C1
Institutional Status Non-UQ

Document type: Journal Article
Sub-type: Article (original research)
Collections: Excellence in Research Australia (ERA) - Collection
School of Chemistry and Molecular Biosciences
Version Filter Type
Citation counts: TR Web of Science Citation Count  Cited 117 times in Thomson Reuters Web of Science Article | Citations
Scopus Citation Count Cited 124 times in Scopus Article | Citations
Google Scholar Search Google Scholar
Created: Thu, 20 Sep 2007, 04:07:56 EST