Volume 2 Supplement 1

5th German Conference on Cheminformatics: 23. CIC-Workshop

Open Access

Ensemble docking revisited

  • Oliver Korb1,
  • S Bowden1,
  • T Olsson1,
  • D Frenkel1,
  • J Liebeschuetz1 and
  • J Cole1
Journal of Cheminformatics20102(Suppl 1):P25

https://doi.org/10.1186/1758-2946-2-S1-P25

Published: 04 May 2010

In recent years, the importance of considering induced fit effects in molecular docking calculations has been widely recognised in the molecular modelling community. While small-scale protein side-chain movements are now accounted for in many state-of-the-art docking strategies, the explicit modelling of large-scale protein motions such as loop movements in kinase domains is still a challenging task. For this reason ensemble-based methods have been introduced taking into account several discrete protein conformations in the conformational sampling step. Our protein-ligand docking approach GOLD [1, 2] has been extended to search such conformational ensembles time-efficiently. The performance of the approach has been assessed on several protein targets using different scoring functions. A detailed analysis of pose prediction and virtual screening results in dependence of the number of protein structures considered in the conformational ensemble will be presented and limitations of the approach will be highlighted.

Authors’ Affiliations

(1)
Cambridge Crystallographic Data Centre

References

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Copyright

© Oliver et al; licensee BioMed Central Ltd. 2010

This article is published under license to BioMed Central Ltd.