ERRα-Predictor: A Framework of Ensemble Models for Prediction of ERRα Binders, Antagonists, and Agonists Using Artificial Intelligence
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| Název: | ERRα-Predictor: A Framework of Ensemble Models for Prediction of ERRα Binders, Antagonists, and Agonists Using Artificial Intelligence |
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| Autoři: | Le Xiong, Jiahao Xu, Hongbo Yu, Weihua Li, Xinmin Li, Wenxiang Song, Jingwei Zhang, Yun Tang, Guixia Liu |
| Rok vydání: | 2025 |
| Témata: | Biophysics, Biochemistry, Molecular Biology, Biotechnology, Computational Biology, Biological Sciences not elsewhere classified, Mathematical Sciences not elsewhere classified, Information Systems not elsewhere classified, representative structural modifications, related receptor α, matthews correlation coefficient, https :// github, various machine learning, substructure extraction techniques, model applicability domains, three datasets using, predict three datasets, comprehensive predictive models, based topological information, constructed ensemble models, three datasets, ensemble models, various databases, analytical techniques, test sets, significant importance, promising target, open source, molecule ligands, model prediction |
| Popis: | Estrogen-related receptor α (ERRα) is considered a promising target for the treatment of cancer and metabolic diseases. The development of comprehensive predictive models for ERRα binders, antagonists, and agonists is of significant importance. In this study, we collected and curated publicly available ERRα ligands from various databases (PubChem, ChEMBL, ExCAPE-DB, BindingDB, and IUPHAR). Based on these data, we first constructed baseline models using different sampling methods and various machine learning and graph neural network approaches. Building upon these results, we then developed the final ERRα-Predictor models, which integrated one-dimensional Simplified Molecular Input Line Entry System (SMILES) sequences and graph-based topological information, to predict three datasets: binders, antagonists, and agonists. Overall, the ERRα-Predictor models achieved promising performance, with the Matthews correlation coefficient (MCC) on the test sets of the three datasets being 0.633, 0.560, and 0.545, respectively. Additionally, we applied the models to challenging external validation sets while considering the definition of the model applicability domains. In addition to the accuracy of the model prediction, we also conducted interpretative explorations using Shapley additive explanations (SHAP) and GNNExplainer, respectively. Furthermore, we studied the representative structural modifications and substructures of the three datasets using the matched molecular pair analysis (MMPA) method and substructure extraction techniques. Based on these findings, the data collated in this study, along with the constructed ensemble models and analytical techniques, provide an effective and reliable framework for the prediction and analysis of ERRα small-molecule ligands. All code for ERRα-Predictor is open source and available at https://github.com/lxiongZ/ERRalpha-Predictor. |
| Druh dokumentu: | article in journal/newspaper |
| Jazyk: | unknown |
| DOI: | 10.1021/acs.jcim.5c01106.s001 |
| Dostupnost: | https://doi.org/10.1021/acs.jcim.5c01106.s001 https://figshare.com/articles/journal_contribution/ERR_-Predictor_A_Framework_of_Ensemble_Models_for_Prediction_of_ERR_Binders_Antagonists_and_Agonists_Using_Artificial_Intelligence/29443292 |
| Rights: | CC BY-NC 4.0 |
| Přístupové číslo: | edsbas.16A853AF |
| Databáze: | BASE |
Nájsť tento článok vo Web of Science | Abstrakt: | Estrogen-related receptor α (ERRα) is considered a promising target for the treatment of cancer and metabolic diseases. The development of comprehensive predictive models for ERRα binders, antagonists, and agonists is of significant importance. In this study, we collected and curated publicly available ERRα ligands from various databases (PubChem, ChEMBL, ExCAPE-DB, BindingDB, and IUPHAR). Based on these data, we first constructed baseline models using different sampling methods and various machine learning and graph neural network approaches. Building upon these results, we then developed the final ERRα-Predictor models, which integrated one-dimensional Simplified Molecular Input Line Entry System (SMILES) sequences and graph-based topological information, to predict three datasets: binders, antagonists, and agonists. Overall, the ERRα-Predictor models achieved promising performance, with the Matthews correlation coefficient (MCC) on the test sets of the three datasets being 0.633, 0.560, and 0.545, respectively. Additionally, we applied the models to challenging external validation sets while considering the definition of the model applicability domains. In addition to the accuracy of the model prediction, we also conducted interpretative explorations using Shapley additive explanations (SHAP) and GNNExplainer, respectively. Furthermore, we studied the representative structural modifications and substructures of the three datasets using the matched molecular pair analysis (MMPA) method and substructure extraction techniques. Based on these findings, the data collated in this study, along with the constructed ensemble models and analytical techniques, provide an effective and reliable framework for the prediction and analysis of ERRα small-molecule ligands. All code for ERRα-Predictor is open source and available at https://github.com/lxiongZ/ERRalpha-Predictor. |
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| DOI: | 10.1021/acs.jcim.5c01106.s001 |