Comparison of Data Fusion Methods as Consensus Scores for Ensemble Docking
- PMID: 31344902
- PMCID: PMC6695709
- DOI: 10.3390/molecules24152690
Comparison of Data Fusion Methods as Consensus Scores for Ensemble Docking
Abstract
Ensemble docking is a widely applied concept in structure-based virtual screening-to at least partly account for protein flexibility-usually granting a significant performance gain at a modest cost of speed. From the individual, single-structure docking scores, a consensus score needs to be produced by data fusion: this is usually done by taking the best docking score from the available pool (in most cases- and in this study as well-this is the minimum score). Nonetheless, there are a number of other fusion rules that can be applied. We report here the results of a detailed statistical comparison of seven fusion rules for ensemble docking, on five case studies of current drug targets, based on four performance metrics. Sevenfold cross-validation and variance analysis (ANOVA) allowed us to highlight the best fusion rules. The results are presented in bubble plots, to unite the four performance metrics into a single, comprehensive image. Notably, we suggest the use of the geometric and harmonic means as better alternatives to the generally applied minimum fusion rule.
Keywords: AUC; BEDROC; ROC curve; SRD; data fusion; ensemble docking.
Conflict of interest statement
The authors declare no conflict of interest.
Figures





Similar articles
-
Consensus scoring model for the molecular docking study of mTOR kinase inhibitor.J Mol Graph Model. 2018 Jan;79:81-87. doi: 10.1016/j.jmgm.2017.11.003. Epub 2017 Nov 6. J Mol Graph Model. 2018. PMID: 29154212
-
Pharmacophore modeling, multiple docking, and molecular dynamics studies on Wee1 kinase inhibitors.J Biomol Struct Dyn. 2019 Jul;37(10):2703-2715. doi: 10.1080/07391102.2018.1495576. Epub 2018 Dec 24. J Biomol Struct Dyn. 2019. PMID: 30052133
-
Discovery of novel CK2 leads by cross-docking based virtual screening.Med Chem. 2014;10(6):628-39. doi: 10.2174/1573406409666131128143601. Med Chem. 2014. PMID: 24286395
-
Understanding the challenges of protein flexibility in drug design.Expert Opin Drug Discov. 2015 Dec;10(12):1301-13. doi: 10.1517/17460441.2015.1094458. Epub 2015 Sep 28. Expert Opin Drug Discov. 2015. PMID: 26414598 Review.
-
Consensus Analyses in Molecular Docking Studies Applied to Medicinal Chemistry.Mini Rev Med Chem. 2020;20(14):1322-1340. doi: 10.2174/1389557520666200204121129. Mini Rev Med Chem. 2020. PMID: 32013847 Review.
Cited by
-
Consensus Virtual Screening Identified [1,2,4]Triazolo[1,5-b]isoquinolines As MELK Inhibitor Chemotypes.ChemMedChem. 2022 Jan 19;17(2):e202100569. doi: 10.1002/cmdc.202100569. Epub 2021 Oct 19. ChemMedChem. 2022. PMID: 34632716 Free PMC article.
-
Calcium-Alginate-Chitosan Nanoparticle as a Potential Solution for Pesticide Removal, a Computational Approach.Polymers (Basel). 2023 Jul 12;15(14):3020. doi: 10.3390/polym15143020. Polymers (Basel). 2023. PMID: 37514411 Free PMC article.
-
Merging Ligand-Based and Structure-Based Methods in Drug Discovery: An Overview of Combined Virtual Screening Approaches.Molecules. 2020 Oct 15;25(20):4723. doi: 10.3390/molecules25204723. Molecules. 2020. PMID: 33076254 Free PMC article. Review.
-
Homology Modeling of the Human P-glycoprotein (ABCB1) and Insights into Ligand Binding through Molecular Docking Studies.Int J Mol Sci. 2020 Jun 5;21(11):4058. doi: 10.3390/ijms21114058. Int J Mol Sci. 2020. PMID: 32517082 Free PMC article.
-
Extended many-item similarity indices for sets of nucleotide and protein sequences.Comput Struct Biotechnol J. 2021 Jun 16;19:3628-3639. doi: 10.1016/j.csbj.2021.06.021. eCollection 2021. Comput Struct Biotechnol J. 2021. PMID: 34257841 Free PMC article.
References
-
- Sotriffer C. Virtual Screening: Principles, Challenges, and Practical Guidelines. Wiley-VCH Verlag GmbH & Co. KGaA; Weinheim, Germany: 2011.
-
- Cross J.B. Methods for Virtual Screening of GPCR Targets: Approaches and Challenges. In: Heifetz A., editor. Computational Methods for GPCR Drug Discovery. Humana Press; New York, NY, USA: 2018. pp. 233–264. - PubMed
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources