Wang Chao, Zou Quan
Center for Genomic and Personalized Medicine, Guangxi key Laboratory for Genomic and Personalized Medicine, Guangxi Collaborative Innovation Center for Genomic and Personalized Medicine, Guangxi Medical University, Nanning, Guangxi, China.
Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu, China.
PLoS Comput Biol. 2024 Nov 18;20(11):e1012607. doi: 10.1371/journal.pcbi.1012607. eCollection 2024 Nov.
Protein phosphorylation is essential in various signal transduction and cellular processes. To date, most tools are designed for model organisms, but only a handful of methods are suitable for predicting task in fungal species, and their performance still leaves much to be desired. In this study, a novel tool called MFPSP is developed for phosphorylation site prediction in multi-fungal species. The amino acids sequence features were derived from physicochemical and distributed information, and an offspring competition-based genetic algorithm was applied for choosing the most effective feature subset. The comparison results shown that MFPSP achieves a more advanced and balanced performance to several state-of-the-art available toolkits. Feature contribution and interaction exploration indicating the proposed model is efficient in uncovering concealed patterns within sequence. We anticipate MFPSP to serve as a valuable bioinformatics tool and benefiting practical experiments by pre-screening potential phosphorylation sites and enhancing our functional understanding of phosphorylation modifications in fungi. The source code and datasets are accessible at https://github.com/AI4HKB/MFPSP/.
蛋白质磷酸化在各种信号转导和细胞过程中至关重要。迄今为止,大多数工具是针对模式生物设计的,但只有少数方法适用于真菌物种的预测任务,而且它们的性能仍有很大的提升空间。在本研究中,开发了一种名为MFPSP的新型工具,用于多真菌物种中磷酸化位点的预测。氨基酸序列特征来自物理化学和分布信息,并应用基于后代竞争的遗传算法来选择最有效的特征子集。比较结果表明,MFPSP相对于几种现有的先进工具包实现了更先进和平衡的性能。特征贡献和相互作用探索表明,所提出的模型在揭示序列中的隐藏模式方面是有效的。我们期望MFPSP作为一种有价值的生物信息学工具,通过预筛选潜在的磷酸化位点并增强我们对真菌中磷酸化修饰的功能理解,从而使实际实验受益。源代码和数据集可在https://github.com/AI4HKB/MFPSP/获取。