bioRxivBioinformaticsPreprint
UniPTM: Multiple PTM site prediction on full-length protein sequence
Lingkuan MengiD, Jiecong LiniD, Ke ChengiD, Kui Xu, Hongyan SuniD, Ka‐Chun WongiD
Abstract
AbstractPost-translational modifications (PTMs) enrich the functional diversity of proteins by attaching chemical groups to the side chains of amino acids. In recent years, a myr-iad of AI models have been proposed to predict many specific types of PTMs. However, those models typically adopt the sliding window approach to extract short and equal-length protein fragments from full-length proteins for model training. Unfortunately, such a subtle step results in the loss of long-range information from distal amino acids, which may impact the PTM formation process. In this study, we introduce UniPTM, a window-free model designed to train and test on natural and full-length protein sequences, enabling the prediction of multiple types of PTMs in a holistic manner. Moreover, we established PTMseq, the first comprehensive dataset of full-length pro-tein sequences with annotated PTMs, to train and validate our model. UniPTM has undergone extensive validations and significantly outperforms existing models, eluci-dating the influence of protein sequence completeness on PTM. Consequently, UniPTM offers interpretable and biologically meaningful predictions, enhancing our understand-ing of protein functionally and regulation. The source code and PTMseq dataset for UniPTM are available at https://www.github.com/TransPTM/UniPTM.
- assay: protein sequence
- research focus: protein structure prediction
- approach: machine learning (classical)
- Citations
- 3
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