MIBPred: Ensemble Learning-Based Metal Ion-Binding Protein Classifier

In biological organisms, metal ion-binding proteins participate in numerous metabolic activities and are closely associated with various diseases. To accurately predict whether a protein binds to metal ions and the type of metal ion-binding protein, this study proposed a classifier named MIBPred. Th...

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Veröffentlicht in:ACS omega 2024-02, Vol.9 (7), p.8439-8447
Hauptverfasser: Zhang, Hong-Qi, Liu, Shang-Hua, Li, Rui, Yu, Jun-Wen, Ye, Dong-Xin, Yuan, Shi-Shi, Lin, Hao, Huang, Cheng-Bing, Tang, Hua
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Sprache:eng
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Zusammenfassung:In biological organisms, metal ion-binding proteins participate in numerous metabolic activities and are closely associated with various diseases. To accurately predict whether a protein binds to metal ions and the type of metal ion-binding protein, this study proposed a classifier named MIBPred. The classifier incorporated advanced Word2Vec technology from the field of natural language processing to extract semantic features of the protein sequence language and combined them with position-specific score matrix (PSSM) features. Furthermore, an ensemble learning model was employed for the metal ion-binding protein classification task. In the model, we independently trained XGBoost, LightGBM, and CatBoost algorithms and integrated the output results through an SVM voting mechanism. This innovative combination has led to a significant breakthrough in the predictive performance of our model. As a result, we achieved accuracies of 95.13% and 85.19%, respectively, in predicting metal ion-binding proteins and their types. Our research not only confirms the effectiveness of Word2Vec technology in extracting semantic information from protein sequences but also highlights the outstanding performance of the MIBPred classifier in the problem of metal ion-binding protein types. This study provides a reliable tool and method for the in-depth exploration of the structure and function of metal ion-binding proteins.
ISSN:2470-1343
2470-1343
DOI:10.1021/acsomega.3c09587