MTNA: A deep learning based predictor for identifying multiple types of N-terminal protein acetylated sites

Author:

Chen Yongbing1,Qin Wenyuan1,Liu Tong1,Li Ruikun1,He Fei1,Han Ye2,Ma Zhiqiang3,Ren Zilin4

Affiliation:

1. School of Information Science and Technology, Northeast Normal University, Changchun 130117, China

2. School of Information Technology, Jilin Agricultural University, Changchun 130118, China

3. Department of Computer Science, College of Humanities & Sciences of Northeast Normal University, Changchun 130119, China

4. Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun 130122, China

Abstract

<abstract> <p>N-terminal acetylation is a specific protein modification that occurs only at the N-terminus but plays a significant role in protein stability, folding, subcellular localization and protein-protein interactions. Computational methods enable finding N-terminal acetylated sites from large-scale proteins efficiently. However, limited by the number of the labeled proteins, existing tools only focus on certain subtypes of N-terminal acetylated sites on frequently detected amino acids. For example, NetAcet focuses on alanine, glycine, serine and threonine only, and N-Ace predicts on alanine, glycine, methionine, serine and threonine. With the growth of experimental N-terminal acetylated site data, it is observed that N-terminal protein acetylation occurs on nearly ten types of amino acids. To facilitate comprehensive analysis, we have developed MTNA (Multiple Types of N-terminal Acetylation), a deep learning network capable of accurately predicting N-terminal protein acetylation sites for various amino acids at the N-terminus. MTNA not only outperforms existing tools but also has the capability to identify rare types of N-terminal protein acetylated sites occurring on less studied amino acids.</p> </abstract>

Publisher

American Institute of Mathematical Sciences (AIMS)

Subject

General Mathematics

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