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

Protein 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. In 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. PLysPTM-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.

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Publication Details

Journal
BMC Bioinformatics
Published
2026-01-02
DOI
https://doi.org/10.1186/s12859-025-06356-1
Citations
2
Primary Topic
Machine Learning in Bioinformatics
Type
article
Field-Weighted Citation Impact
44.47
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article

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

L. Chen, Bo Zhou, Jingyu Yang, Yu-Dong Cai
2 citations
BMC Bioinformatics
Machine Learning in Bioinformatics
44.47
article

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

L. Chen, Bo Zhou, Jingyu Yang, Yu-Dong Cai
article en
2 citations

Abstract

Protein 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. In 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. PLysPTM-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.

BMC BioinformaticsVol. 27(1)
Shanghai University (CN), Shanghai University of Medicine and Health Sciences (CN), Shanghai Maritime University (CN)
Openalex Percentile: Top 1%
Machine Learning in Bioinformatics
44.47
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PLysPTM-HGNN: predicting lysine PTM sites of proteins using hybrid graph neural networks — L. Chen, Bo Zhou, et al. · BMC Bioinformatics (2026) | TGRS Research Map | TGRS