ArticleBMC bioinformatics2010
APIS: accurate prediction of hot spots in protein interfaces by combining protrusion index with solvent accessibility.
Article in BMC bioinformatics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.
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66 citing papers in PubMed, 212 citations in OpenAlex.
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- PPI-hotspoteLife · 2024Article
- Prediction of Protein-DNA Interface Hot Spots Based on Empirical Mode Decomposition and Machine Learning.Genes · 2024Article
- Prediction of hot spots in protein-DNA binding interfaces based on discrete wavelet transform and wavelet packet transform.BMC bioinformatics · 2023Article
- Densest subgraph-based methods for protein-protein interaction hot spot prediction.BMC bioinformatics · 2022Article
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- Identification of Small-Molecule Inhibitors of Fibroblast Growth Factor 23 Signaling via In Silico Hot Spot Prediction and Molecular Docking to α-Klotho.Journal of chemical information and modeling · 2022Article
- Predicting Protein-Protein Interactions Based on Ensemble Learning-Based Model from Protein Sequence.Biology · 2022Article
- Improve hot region prediction by analyzing different machine learning algorithms.BMC bioinformatics · 2021Article
- A novel method to identify gene interaction patterns.BMC genomics · 2021Article
- Predicting transcription factor binding sites using DNA shape features based on shared hybrid deep learning architecture.Molecular therapy. Nucleic acids · 2021Article
- An improved DNA-binding hot spot residues prediction method by exploring interfacial neighbor properties.BMC bioinformatics · 2021Article
- Rapid prediction of crucial hotspot interactions for icosahedral viral capsid self-assembly by energy landscape atlasing validated by mutagenesis.PLoS computational biology · 2020Article
- iPNHOT: a knowledge-based approach for identifying protein-nucleic acid interaction hot spots.BMC bioinformatics · 2020Article
- Article
- PreDBA: A heterogeneous ensemble approach for predicting protein-DNA binding affinity.Scientific reports · 2020Article
- Accurate classification of membrane protein types based on sequence and evolutionary information using deep learning.BMC bioinformatics · 2019Article
- NmSEER V2.0: a prediction tool for 2'-O-methylation sites based on random forest and multi-encoding combination.BMC bioinformatics · 2019Article
- Pushing the accuracy limit of shape complementarity for protein-protein docking.BMC bioinformatics · 2019Article
6 more citing papers are in PubMed but not listed here.
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4 authors at 4 institutions in 3 countries.
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No grant is acknowledged in the PubMed record.
Abstract
backgroundIt is well known that most of the binding free energy of protein interaction is contributed by a few key hot spot residues. These residues are crucial for understanding the function of proteins and studying their interactions. Experimental hot spots detection methods such as alanine scanning mutagenesis are not applicable on a large scale since they are time consuming and expensive. Therefore, reliable and efficient computational methods for identifying hot spots are greatly desired and urgently required.
resultsIn this work, we introduce an efficient approach that uses support vector machine (SVM) to predict hot spot residues in protein interfaces. We systematically investigate a wide variety of 62 features from a combination of protein sequence and structure information. Then, to remove redundant and irrelevant features and improve the prediction performance, feature selection is employed using the F-score method. Based on the selected features, nine individual-feature based predictors are developed to identify hot spots using SVMs. Furthermore, a new ensemble classifier, namely APIS (A combined model based on Protrusion Index and Solvent accessibility), is developed to further improve the prediction accuracy. The results on two benchmark datasets, ASEdb and BID, show that this proposed method yields significantly better prediction accuracy than those previously published in the literature. In addition, we also demonstrate the predictive power of our proposed method by modelling two protein complexes: the calmodulin/myosin light chain kinase complex and the heat shock locus gene products U and V complex, which indicate that our method can identify more hot spots in these two complexes compared with other state-of-the-art methods.
conclusionWe have developed an accurate prediction model for hot spot residues, given the structure of a protein complex. A major contribution of this study is to propose several new features based on the protrusion index of amino acid residues, which has been shown to significantly improve the prediction performance of hot spots. Moreover, we identify a compact and useful feature subset that has an important implication for identifying hot spot residues. Our results indicate that these features are more effective than the conventional evolutionary conservation, pairwise residue potentials and other traditional features considered previously, and that the combination of our and traditional features may support the creation of a discriminative feature set for efficient prediction of hot spot residues. The data and source code are available on web site http://home.ustc.edu.cn/~jfxia/hotspot.html.
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