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Identification of computational hot spots in protein interfaces: combining solvent accessibility and inter-residue potentials improves the accuracy

Open access
Tuncbag, Nurcan, Gursoy, Attila, Keskin, Ozlem·2009·Bioinformatics

Abstract

Motivation:Hot spots are residues comprising only a small fraction of interfaces yet accounting for the majority of the binding energy. These residues are critical in understanding the principles of protein interactions. Experimental studies like alanine scanning mutagenesis require significant effort; therefore, there is a need for computational methods to predict hot spots in protein interfaces. Results:We present a new intuitive efficient method to determine computational hot spots based on conservation (C), solvent accessibility [accessible surface area (ASA)] and statistical pairwise residue potentials (PP) of the interface residues. Combination of these features is examined in a comprehensive way to study their effect in hot spot detection. The predicted hot spots are observed to match with the experimental hot spots with an accuracy of 70% and a precision of 64% in Alanine Scanning Energetics Database (ASEdb), and accuracy of 70% and a precision of 73% in Binding Interface Database (BID). Several machine learning methods are also applied to predict hot spots. Performance of our empirical approach exceeds learning-based methods and other existing hot spot prediction methods. Residue occlusion from solvent in the complexes and pairwise potentials are found to be the main discriminative features in hot spot prediction. Conclusion:Our empirical method is a simple approach in hot spot prediction yet with its high accuracy and computational effectiveness. We believe that this method provides insights for the researchers working on characterization of protein binding sites and design of specific therapeutic agents for protein interactions. Availability:The list of training and test sets are available as Supplementary Data at http://prism.ccbb.ku.edu.tr/hotpoint/supplement.doc Contact: agursoy@ku.edu.tr; okeskin@ku.edu.tr Supplementary information: Supplementary data are available at Bioinformatics online.

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Metadata

Authors
Tuncbag, N., Gursoy, A., & Keskin, O.
Venue
Bioinformatics
Published
2009-04-08
Volume
25
Issue
12
Pages
1513-1520
ISSN
  • 1367-4803 (ISSN-L)
  • 1367-4811
OpenAlex
W2141624700
Cited by
254
References
5
FWCI
8.64
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Identification of computational hot spots in protein interfaces: combining solvent accessibility and inter-residue potentials improves the accuracy. https://app.cochat.ai/papers/10.1093/bioinformatics/btp240
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Tuncbag, N., Gursoy, A., & Keskin, O. (2009). Identification of computational hot spots in protein interfaces: combining solvent accessibility and inter-residue potentials improves the accuracy. Bioinformatics. https://doi.org/10.1093/bioinformatics/btp240

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