Evidence map›Paper›PMID 32938375›Full record

ArticleBMC bioinformatics2020

Computationally identifying hot spots in protein-DNA binding interfaces using an ensemble approach.

Yuliang Pan, Shuigeng Zhou, Jihong Guan

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Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
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  9. Nabe: an energetic database of amino acid mutations in protein-nucleic acid binding interfaces.Database : the journal of biological databases and curation · 2021
    Article
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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Yuliang PanDepartment of Computer Science and Technology, Tongji University, No. 4800 Caoan Road, Shanghai, 201804, China.
Shuigeng ZhouShanghai Key Laboratory of Intelligent Information Processing, and School of Computer Science, Fudan University, No. 220 Handan Road, Shanghai, 200433, China.
Jihong GuanDepartment of Computer Science and Technology, Tongji University, No. 4800 Caoan Road, Shanghai, 201804, China. jhguan@tongji.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProtein-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.

resultsHere, 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.

conclusionsPreHots, 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/ .

Indexed as

AlgorithmsDatabases, ProteinDNA-Binding ProteinsHumansModels, MolecularDNA-Binding ProteinsEnsemble stacking classifierFeature selectionHot spotsProtein-DNA complexes

Identifiers

PMID32938375
PMCPMC7495898

What OpenQuestion holds

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LicenceCC BY
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.