ORIGINAL RESEARCH article
Front. Cell. Infect. Microbiol.
Sec. Fungal Pathogenesis
Volume 15 - 2025 | doi: 10.3389/fcimb.2025.1615443
Fungi-Kcr: A Language Model for Predicting Lysine Crotonylation in Pathogenic Fungal Proteins
Provisionally accepted- 1Tianjin Medical University Cancer Institute and Hospital, Tianjin, China
- 2Shanxi Normal University, Linfen, Shanxi Province, China
- 3Tianjin Medical University, Tianjin, Tianjin Municipality, China
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Lysine crotonylation (Kcr) is an important post-translational modification (PTM) of proteins, playing a key role in regulating various biological processes in pathogenic fungi.However, the experimental identification of Kcr sites remains challenging due to the high cost and time-consuming nature of mass spectrometry-based techniques. To address this limitation, we developed Fungi-Kcr, a deep learning-based model designed to predict Kcr modification sites in fungal proteins. The model integrates convolutional neural networks (CNN), gated recurrent units (GRU), and word embedding to effectively capture both local and long-range sequence dependencies. Comprehensive evaluations, including ten-fold cross-validation and independent testing, demonstrate that Fungi-Kcr achieves superior predictive performance compared to conventional machine learning models. Moreover, our results indicate that a general predictive model performs better than species-specific models. These findings suggest that despite species-specific variations, certain residues near Kcr sites show consistent enrichment or depletion patterns, implying potential shared regulatory features or substrate preferences among the pathogenic fungi studied. The proposed model provides a valuable computational tool for the large-scale identification of Kcr sites, contributing to a deeper understanding of fungal pathogenesis and potential therapeutic targets. The source code and dataset for Fungi-Kcr are available at https://github.com/zayra77/Fungi-Kcr.
Keywords: lysine crotonylation, Fungal Proteins, language model, pathogen, posttranslational modification
Received: 23 Apr 2025; Accepted: 23 Jun 2025.
Copyright: © 2025 Chen, Wang, Wang and Li. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Yong-Zi Chen, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China
Haixin Li, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China
Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.