Evidence map›Paper›PMID 40577786›Full record

ArticleBioinformatics (Oxford, England)2025

FusionEncoder: identification of intrinsically disordered regions based on multi-feature fusion.

Sicen Liu, Shutao Chen, Tao Bai, Bin Liu

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 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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1citing papers in PubMed
–field-weighted citation impact
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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Sicen LiuSMBU-MSU-BIT Joint Laboratory on Bioinformatics and Engineering Biology, Shenzhen MSU-BIT University, Shenzhen, Guangdong 518172, China.ORCID 0000-0001-6608-7442
Shutao ChenSchool of Computer Science and Technology, Beijing Institute of Technology, Beijing 100081, China.
Tao BaiSchool of Computer Science and Technology, Beijing Institute of Technology, Beijing 100081, China.
Bin LiuSMBU-MSU-BIT Joint Laboratory on Bioinformatics and Engineering Biology, Shenzhen MSU-BIT University, Shenzhen, Guangdong 518172, China.ORCID 0000-0003-3685-9469

Funding

Beijing Natural Science Foundation L248013National Natural Science Foundation of China U22A2039Zhongguancun Academy 20240101
6 · The paper itself

Abstract

motivationIntrinsic disorder regions (IDRs) play a significant role in diverse biological processes and are widely distributed in proteins. Thus, accurately predicting these regions is essential for analyzing protein structure and function. Amino acid feature extraction servers as a foundational process in the development of computational predictive models. Existing methods typically rely on traditional biological features (e.g. PSSM) or use pre-trained protein language models (PPLMs) to capture sequence semantic information, often resorting to straightforward feature concatenation. However, these approaches fail to capture the multi-semantic interactions between traditional biological features and PPLMs-based features.

resultsIn this study, we propose a method named FusionEncoder designed for the integration of traditional biological and PPLMs-based features of the protein. FusionEncoder is a fusion network built on a variant of long short-term memory (LSTM). We consider traditional biological features and PPLMs-based features to be two types of semantic inputs within a "multi-semantic" space. Traditional features are input into the cell state of the LSTM, while PPLMs-based features are fed into the input part. A fusion cell is then utilized to fuse these two types of features. This strategy leverages the capability of LSTM to encode long sequences, enhancing context-aware semantic learning of amino acid sequences. Finally, a transformer-based encoder layer is employed to predict the IDRs. Evaluation on four independent test datasets indicate that FusionEncoder obviously improves the accuracy of amino acid feature representation and achieves superior performance compared to the other existing methods. AVAILABILITY AND IMPLEMENTATION: To facilitate accessibility for experimental researchers, a user-friendly and publicly available webserver for the FusionEncoder predictor has been deployed at http://bliulab.net/FusionEncoder/. FusionEncoder is expected to serve as a valuable tool for the accurate identification of IDRs.

Indexed as

Computational BiologyIntrinsically Disordered ProteinsSoftwareAlgorithmsDatabases, ProteinSemanticsSequence Analysis, ProteinIntrinsically Disordered Proteins

Identifiers

PMID40577786
PMCPMC12231546

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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 OpenQuestion graph.