ArticleBMC genomics2025
A novel prediction method for protein-DNA binding sites based on protein language model fusion features with SE-connection pyramidal network and ensemble learning.
Article in BMC genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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1 citing paper in PubMed.
- A Novel Weighted Ensemble Framework of Transformer and Deep Q-Network for ATP-Binding Site Prediction Using Protein Language Model Features.International journal of molecular sciences · 2026Article
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4 authors.
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Abstract
Protein-DNA interactions are crucial in life processes such as gene expression and regulation. Therefore, the accurate prediction of DNA-binding sites on proteins is highly important for the advancement of scientific understanding in the field of biological activities. In this work, we propose a protein-DNA binding site prediction framework, termed Evolutionary Scale Modeling-SE-Connection Pyramidal (ESM-SECP), which integrates a sequence-feature-based prediction method with a sequence-homology-based predictor via ensemble learning. The sequence-feature-based prediction method is built on two types of input features: ESM-2 protein language model embeddings and evolutionary conservation information computed by PSI-BLAST. These features are fused by a multi-head attention mechanism and processed through the newly proposed SE-Connection Pyramidal(SECP) network for prediction. The sequence-template method, based on sequence homology, serves as a complementary approach to predict DNA-binding residues. The two predictors are combined via ensemble learning to improve overall model performance. Through the experimental validation of the TE46 and TE129 datasets, ESM-SECP outperforms the traditional methods in several evaluation indices, demonstrating its outstanding performance in Protein-DNA binding site prediction.
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