iLMS, Computational Identification of Lysine-Malonylation Sites by Combining Multiple Sequence Features

被引:10
作者
Hasan, Md Mehedi [1 ]
Kurata, Hiroyuki [1 ,2 ]
机构
[1] Kyushu Inst Technol, Dept Biosci & Bioinformat, 680-4 Kawazu, Iizuka, Fukuoka 8208502, Japan
[2] Kyushu Inst Technol, Biomed Informat R&D Ctr, 680-4 Kawazu, Iizuka, Fukuoka 8208502, Japan
来源
PROCEEDINGS 2018 IEEE 18TH INTERNATIONAL CONFERENCE ON BIOINFORMATICS AND BIOENGINEERING (BIBE) | 2018年
关键词
Lysine malonylation; feature encoding; feature; selection; support vector machine; SUCCINYLATION; PREDICTION;
D O I
10.1109/BIBE.2018.00077
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Lysine malonylation is a newly discovered post translational modification of proteins, which plays an important role in regulating many cellular functions. Several approaches are available to identify malonylation proteins and its malonylation sites, however; experimental identification of malonylation sites is often laborious and costly. Therefore, computational schemes are needed to identify potential malonylation sites prior to in vitro experimentation. In this paper, a novel computational scheme iLMS (Identification of Lysine-Malonylation Sites) has been developed by combining primary sequences and evolutionary features via a support vector machine classifier. The final iLMS scheme achieved a robust performance in cross-validation test in both human and mouse datasets. For the mouse data, the iLMS predictor outperformed other existing implementations. The iLMS is a promising computational scheme for the prediction of malonylation sites.
引用
收藏
页码:356 / 359
页数:4
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