TY - JOUR
T1 - TransPTM
T2 - A transformer-based model for non-histone acetylation site prediction
AU - Meng, Lingkuan
AU - Chen, Xingjian
AU - Cheng, Ke
AU - Chen, Nanjun
AU - Zheng, Zetian
AU - Wang, Fuzhou
AU - Sun, Hongyan
AU - Wong, Ka-Chun
PY - 2024/5
Y1 - 2024/5
N2 - Protein acetylation is one of the extensively studied post-translational modifications (PTMs) due to its significant roles across a myriad of biological processes. Although many computational tools for acetylation site identification have been developed, there is a lack of benchmark dataset and bespoke predictors for non-histone acetylation site prediction.To address these problems,we have contributed to both dataset creation and predictor benchmark in this study. First, we construct a non-histone acetylation site benchmark dataset, namely NHAC, which includes 11 subsets according to the sequence length ranging from 11 to 61 amino acids. There are totally 886 positive samples and 4707 negative samples for each sequence length. Secondly, we propose TransPTM, a transformer-based neural network model for non-histone acetylation site predication. During the data representation phase, per-residue contextualized embeddings are extracted using ProtT5 (an existing pre-trained protein language model). This is followed by the implementation of a graph neural network framework, which consists of three TransformerConv layers for feature extraction and a multilayer perceptron module for classification. The benchmark results reflect that TransPTM has the competitive performance for non-histone acetylation site prediction over three state-of-the-art tools.It improves our comprehension on the PTM mechanism and provides a theoretical basis for developing drug targets for diseases. Moreover, the created PTM datasets fills the gap in non-histone acetylation site datasets and is beneficial to the related communities. The related source code and data utilized by TransPTM are accessible at https://www.github. com/TransPTM/TransPTM.
© The Author(s) 2024. Published by Oxford University Press.
AB - Protein acetylation is one of the extensively studied post-translational modifications (PTMs) due to its significant roles across a myriad of biological processes. Although many computational tools for acetylation site identification have been developed, there is a lack of benchmark dataset and bespoke predictors for non-histone acetylation site prediction.To address these problems,we have contributed to both dataset creation and predictor benchmark in this study. First, we construct a non-histone acetylation site benchmark dataset, namely NHAC, which includes 11 subsets according to the sequence length ranging from 11 to 61 amino acids. There are totally 886 positive samples and 4707 negative samples for each sequence length. Secondly, we propose TransPTM, a transformer-based neural network model for non-histone acetylation site predication. During the data representation phase, per-residue contextualized embeddings are extracted using ProtT5 (an existing pre-trained protein language model). This is followed by the implementation of a graph neural network framework, which consists of three TransformerConv layers for feature extraction and a multilayer perceptron module for classification. The benchmark results reflect that TransPTM has the competitive performance for non-histone acetylation site prediction over three state-of-the-art tools.It improves our comprehension on the PTM mechanism and provides a theoretical basis for developing drug targets for diseases. Moreover, the created PTM datasets fills the gap in non-histone acetylation site datasets and is beneficial to the related communities. The related source code and data utilized by TransPTM are accessible at https://www.github. com/TransPTM/TransPTM.
© The Author(s) 2024. Published by Oxford University Press.
KW - deep learning
KW - Non-histone acetylation
KW - protein language model
KW - transformer
UR - https://www.scopus.com/pages/publications/85192792843
UR - https://www.scopus.com/pages/publications/85192792843#tab=impact
U2 - 10.1093/bib/bbae219
DO - 10.1093/bib/bbae219
M3 - RGC 21 - Publication in refereed journal
C2 - 38725156
SN - 1467-5463
VL - 25
JO - Briefings in Bioinformatics
JF - Briefings in Bioinformatics
IS - 3
M1 - bbae219
ER -