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Receptor pharmacophore ensemble (REPHARMBLE): a probabilistic pharmacophore modeling approach using multiple protein-ligand complexes

  • Sivakumar Prasanth Kumar
Original Paper

Abstract

Ensemble methods are gaining more importance in structure-based approaches as single protein-ligand complexes strongly influence the outcomes of virtual screening. Structure-based pharmacophore modeling based on a single protein-ligand complex with complex feature combinations is often limited to certain chemical classes. The REPHARMBLE (receptor pharmacophore ensemble) approach presented here examines the ability of an ensemble of selected protein-ligand complexes to populate pharmacophore space in the ligand binding site, rigorously assesses the importance of pharmacophore features using Poisson statistic and information theory-based entropy calculations, and generates pharmacophore models with high probabilities. In addition, an ensemble scoring function that combines all the resultant high-scoring pharmacophore models to score molecules is derived. The REPHARMBLE approach was evaluated on ten DUD-E benchmark datasets and afforded good screening performance, as measured by receiver operating characteristic, enrichment factor and Güner-Henry score. Although one of the high-scoring models achieved superior statistical results in each dataset, the ensemble scoring function balanced the shortcomings of each model and passed with close performance measures. This approach offers a reliable way of choosing the best-scoring features to build four-feature pharmacophore queries and customize a target-biased ‘pharmacophore ensemble’ scoring function for subsequent virtual screening.

Keywords

Ensemble Structure-based pharmacophore Probabilistic model Protein-ligand complex Virtual screening Entropy 

Notes

Acknowledgments

SPK acknowledges the National Post-Doctoral Fellowship (PDF/2016/000156) funded by Science and Engineering Research Board (SERB), Government of India. SPK is thankful to Prof. N. Srinivasan for his valuable suggestions. The author is very thankful to anonymous reviewers for their valuable suggestions.

Compliance with ethical standards

The author ensured the compliance of ethical standards for publishing the manuscript in this journal.

Disclosure of potential conflicts of interest

The author declared no conflict of interest exists.

Supplementary material

894_2018_3820_MOESM1_ESM.docx (1.6 mb)
ESM 1 (DOCX 1670 kb)

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Molecular Biophysics UnitIndian Institute of ScienceBangaloreIndia

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