Computational Prediction of Protein Epsilon Lysine Acetylation Sites Based on a Feature Selection Method.

Abstract:

AIM AND OBJECTIVE:Lysine acetylation, as one type of post-translational modifications (PTM), plays key roles in cellular regulations and can be involved in a variety of human diseases. However, it is often high-cost and time-consuming to use traditional experimental approaches to identify the lysine acetylation sites. Therefore, effective computational methods should be developed to predict the acetylation sites. In this study, we developed a position-specific method for epsilon lysine acetylation site prediction. MATERIAL AND METHODS:Sequences of acetylated proteins were retrieved from the UniProt database. Various kinds of features such as position specific scoring matrix (PSSM), amino acid factors (AAF), and disorders were incorporated. A feature selection method based on mRMR (Maximum Relevance Minimum Redundancy) and IFS (Incremental Feature Selection) was employed. RESULTS:Finally, 319 optimal features were selected from total 541 features. Using the 319 optimal features to encode peptides, a predictor was constructed based on dagging. As a result, an accuracy of 69.56% with MCC of 0.2792 was achieved. We analyzed the optimal features, which suggested some important factors determining the lysine acetylation sites. CONCLUSION:We developed a position-specific method for epsilon lysine acetylation site prediction. A set of optimal features was selected. Analysis of the optimal features provided insights into the mechanism of lysine acetylation sites, providing guidance of experimental validation.

authors

Gao J,Tao XW,Zhao J,Feng YM,Cai YD,Zhang N

doi

10.2174/1386207320666170314093216

subject

Has Abstract

pub_date

2017-01-01 00:00:00

pages

629-637

issue

7

eissn

1386-2073

issn

1875-5402

pii

CCHTS-EPUB-82257

journal_volume

20

pub_type

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