Evidence map›Paper›PMID 41484842›Full record

ArticleBMC bioinformatics2026

PLysPTM-HGNN: predicting lysine PTM sites of proteins using hybrid graph neural networks.

Lei Chen, Jingyu Yang, Bo Zhou, Yu-Dong Cai

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Article in BMC bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Lei ChenCollege of Information Engineering, Shanghai Maritime University, Shanghai, 201306, People's Republic of China. lchen@shmtu.edu.cn.
Jingyu YangCollege of Information Engineering, Shanghai Maritime University, Shanghai, 201306, People's Republic of China.
Bo ZhouSchool of Basic Medical Sciences, Shanghai University of Medicine and Health Sciences, Shanghai, 201318, People's Republic of China.
Yu-Dong CaiSchool of Life Sciences, Shanghai University, Shanghai, 200444, People's Republic of China. cai_yud@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProtein post-translational modification (PTM) is a critical biological process that occurs after protein synthesis and has key roles in several biological processes. Among these, lysine modifications include multiple types and have received considerable attention. Most existing computational models predict whether a specific lysine site in a protein sequence corresponds to a lysine modification type by extracting features from a short peptide segment centered on that site. Therefore, information from the full protein sequence is not used.

resultsIn this study, we gave a different direction for investigating lysine modifications. A computational model, PLysPTM-HGNN, was designed to identify lysine modification types at the protein level. Full protein sequence information was used to derive three feature types: gene ontology features, large language model features, and position-specific scoring matrix features. These features were refined separately through a linear transformation, a hybrid graph neural network, and a convolutional neural network combiner, after which they were concatenated and passed into a fully connected layer for prediction. Cross-validation results showed that the AUROC and AUPR were approximately 0.84 and 0.68, respectively, indicating strong predictive performance.

conclusionsPLysPTM-HGNN outperformed several existing protein subcellular localization models and models based on traditional multi-label classification algorithms. This model provides a useful tool for studies of lysine modifications.

Indexed as

Computational BiologyGraph Neural NetworksLysineProtein Processing, Post-TranslationalProteinsDatabases, ProteinLysineProteinsGene ontologyHybrid graph neural networkLarge language modelLysine modificationPost-translation modification

Identifiers

PMID41484842
PMCPMC12866139

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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.