Computationally identifying hot spots in protein-DNA binding interfaces using an ensemble approach
Open Access
- 17 September 2020
- journal article
- conference paper
- Published by Springer Nature in BMC Bioinformatics
- Vol. 21 (S13) , 1-16
Abstract
Protein-DNA interaction governs a large number of cellular processes, and it can be altered by a small fraction of interface residues, i.e., the so-called hot spots, which account for most of the interface binding free energy. Accurate prediction of hot spots is critical to understand the principle of protein-DNA interactions. There are already some computational methods that can accurately and efficiently predict a large number of hot residues. However, the insufficiency of experimentally validated hot-spot residues in protein-DNA complexes and the low diversity of the employed features limit the performance of existing methods. Here, we report a new computational method for effectively predicting hot spots in protein-DNA binding interfaces. This method, called PreHots (the abbreviation of Predicting Hotspots), adopts an ensemble stacking classifier that integrates different machine learning classifiers to generate a robust model with 19 features selected by a sequential backward feature selection algorithm. To this end, we constructed two new and reliable datasets (one benchmark for model training and one independent dataset for validation), which totally consist of 123 hot spots and 137 non-hot spots from 89 protein-DNA complexes. The data were manually collected from the literature and existing databases with a strict process of redundancy removal. Our method achieves a sensitivity of 0.813 and an AUC score of 0.868 in 10-fold cross-validation on the benchmark dataset, and a sensitivity of 0.818 and an AUC score of 0.820 on the independent test dataset. The results show that our approach outperforms the existing ones. PreHots, which is based on stack ensemble of boosting algorithms, can reliably predict hot spots at the protein-DNA binding interface on a large scale. Compared with the existing methods, PreHots can achieve better prediction performance. Both the webserver of PreHots and the datasets are freely available at: http://dmb.tongji.edu.cn/tools/PreHots/.Keywords
This publication has 49 references indexed in Scilit:
- Structural features that predict real‐value fluctuations of globular proteinsProteins: Structure, Function, and Bioinformatics, 2012
- Assessing the Performance of the MM/PBSA and MM/GBSA Methods. 1. The Accuracy of Binding Free Energy Calculations Based on Molecular Dynamics SimulationsJournal of Chemical Information and Modeling, 2010
- Prediction of protein-protein interaction sites using an ensemble methodBMC Bioinformatics, 2009
- The role of DNA shape in protein–DNA recognitionNature, 2009
- Consensus scoring for enriching near‐native structures from protein–protein docking decoysProteins: Structure, Function, and Bioinformatics, 2008
- Super LearnerStatistical Applications in Genetics and Molecular Biology, 2007
- The Protein Data BankNucleic Acids Research, 2000
- Satisfying Hydrogen Bonding Potential in ProteinsJournal of Molecular Biology, 1994
- Isothermal titration calorimetryAnalytical Chemistry, 1990
- Dictionary of protein secondary structure: Pattern recognition of hydrogen‐bonded and geometrical featuresBiopolymers, 1983