Evidence map›Paper›PMID 38830995›Full record

ArticleCommunications biology2024

SOFB is a comprehensive ensemble deep learning approach for elucidating and characterizing protein-nucleic-acid-binding residues.

Bin Zhang, Zilong Hou, Yuning Yang, Ka-Chun Wong, Haoran Zhu, Xiangtao Li

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Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
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5 citing papers in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Bin ZhangSchool of Artificial Intelligence, Jilin University, Changchun, China.
Zilong HouSchool of Artificial Intelligence, Jilin University, Changchun, China.
Yuning YangDonnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Canada.
Ka-Chun WongDepartment of Computer Science, City University of Hong Kong, Hong Kong, Hong Kong SAR.ORCID 0000-0001-6062-733X
Haoran ZhuSchool of Artificial Intelligence, Jilin University, Changchun, China. zhuhr20@mails.jlu.edu.cn.ORCID 0000-0002-7240-2696
Xiangtao LiSchool of Artificial Intelligence, Jilin University, Changchun, China. lixt314@jlu.edu.cn.ORCID 0000-0002-8716-9823

Funding

National Natural Science Foundation of China (National Science Foundation of China) Grant No. 62076109
6 · The paper itself

Abstract

Proteins and nucleic-acids are essential components of living organisms that interact in critical cellular processes. Accurate prediction of nucleic acid-binding residues in proteins can contribute to a better understanding of protein function. However, the discrepancy between protein sequence information and obtained structural and functional data renders most current computational models ineffective. Therefore, it is vital to design computational models based on protein sequence information to identify nucleic acid binding sites in proteins. Here, we implement an ensemble deep learning model-based nucleic-acid-binding residues on proteins identification method, called SOFB, which characterizes protein sequences by learning the semantics of biological dynamics contexts, and then develop an ensemble deep learning-based sequence network to learn feature representation and classification by explicitly modeling dynamic semantic information. Among them, the language learning model, which is constructed from natural language to biological language, captures the underlying relationships of protein sequences, and the ensemble deep learning-based sequence network consisting of different convolutional layers together with Bi-LSTM refines various features for optimal performance. Meanwhile, to address the imbalanced issue, we adopt ensemble learning to train multiple models and then incorporate them. Our experimental results on several DNA/RNA nucleic-acid-binding residue datasets demonstrate that our proposed model outperforms other state-of-the-art methods. In addition, we conduct an interpretability analysis of the identified nucleic acid binding residue sequences based on the attention weights of the language learning model, revealing novel insights into the dynamic semantic information that supports the identified nucleic acid binding residues. SOFB is available at https://github.com/Encryptional/SOFB and https://figshare.com/articles/online_resource/SOFB_figshare_rar/25499452 .

Indexed as

Deep LearningBinding SitesComputational BiologyNucleic AcidsProtein BindingProteinsNucleic AcidsProteins

Identifiers

PMID38830995
PMCPMC11148103

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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.