ArticleBriefings in bioinformatics2025
BBATProt: a framework predicting biological function with enhanced feature extraction via interpretable deep learning.
Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Proteoformics-driven new concept of human growth hormone in clinical endocrinology.Frontiers in endocrinology · 2026Review
- Harnessing Machine Learning Approaches for the Identification, Characterization, and Optimization of Novel Antimicrobial Peptides.Antibiotics (Basel, Switzerland) · 2025Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
Abstract
Accurate prediction of protein and peptide functions from amino acid sequences is essential for understanding biological processes and advancing biomolecular engineering. Due to the limitations of experimental methods, computational approaches, particularly machine learning, have gained significant attention. However, many existing tools are task-specific and lack adaptability. Here, we propose a BERT-BiLSTM-Attention-TCN Protein Function Prediction Framework (BBATProt), a versatile framework for predicting protein and peptide functions. BBATProt leverages transfer learning with a pretrained bidirectional encoder representations from transformer model to capture high-dimensional features. The custom network integrates bidirectional long short-term memory and temporal convolutional network to align with proteins' spatial characteristics, combining local and global feature extraction via attention mechanisms to achieve more precise predictions. Evaluations demonstrate that BBATProt consistently outperforms state-of-the-art models in tasks such as hydrolytic catalysis, peptide bioactivity, and post-translational modification (PTM) site prediction. Specifically, BBATProt improves accuracy by 2.96%-41.96% in antimicrobial peptide (AMP) prediction and by 0.64%-23.54% in PTM prediction tasks. In terms of area under the receiver operating characteristic curve, improvements range from 0.71% to 40.51% for AMP prediction and 0.62%-27.82% for PTM prediction. Visualizations of feature evolution and refinement via attention mechanisms validate the framework's interpretability, providing transparency into the feature-extraction process and offering deeper insights into the basis of property prediction.
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What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.