Evidence map›Paper›PMID 41212592›Full record

ArticleBriefings in bioinformatics2025

BBATProt: a framework predicting biological function with enhanced feature extraction via interpretable deep learning.

Youqing Wang, Xukai Ye, Yue Feng, Haoqian Wang, Xiaofan Lin, Xin Ma, Yifei Zhang

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Youqing WangState Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, North Third Ring Road 15, 100029 Beijing, China.ORCID 0000-0001-6245-1550
Xukai YeCollege of Information Sciences and Technology, Beijing University of Chemical Technology, North Third Ring Road 15, 100029 Beijing, China.
Yue FengCollege of Life Science and Technology, Beijing University of Chemical Technology, North Third Ring Road 15, 100029 Beijing, China.
Haoqian WangCollege of Information Sciences and Technology, Beijing University of Chemical Technology, North Third Ring Road 15, 100029 Beijing, China.
Xiaofan LinState Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, North Third Ring Road 15, 100029 Beijing, China.
Xin MaCollege of Information Sciences and Technology, Beijing University of Chemical Technology, North Third Ring Road 15, 100029 Beijing, China.ORCID 0000-0003-1291-3977
Yifei ZhangState Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, North Third Ring Road 15, 100029 Beijing, China.ORCID 0000-0002-0014-611X

Funding

Beijing Natural Science Foundation L241014China Postdoctoral Science Foundation 2023M730190China Postdoctoral Science Foundation BX20230034Fundamental Research Funds for the Central Universities buctr20120201Fundamental Research Funds for the Central Universities QNTD2023-01National Natural Science Funds of China 32371325National Natural Science Funds of China 62303039National Natural Science Funds of China 62433004National Science Fund for Distinguished Young Scholars of China 62225303
6 · The paper itself

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.

Indexed as

Computational BiologyDeep LearningProteinsProtein Processing, Post-TranslationalProteinsattention mechanismsBERTfunctional prediction frameworkinterpretable deep learning

Identifiers

PMID41212592
PMCPMC12599320

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.