| Literature DB >> 29040908 |
Zhe Ju1, Juhe Sun2, Yanjie Li2, Li Wang2.
Abstract
Glycation is a nonenzymatic post-translational modification which has been found to be involved in various biological processes and closely associated with many metabolic diseases. The accurate identification of glycation sites is important to understand the underlying molecular mechanisms of glycation. As the traditional experimental methods are often labor-intensive and time-consuming, it is desired to develop computational methods to predict glycation sites. In this study, a novel predictor named BPB_GlySite is proposed to predict lysine glycation sites by using bi-profile bayes feature extraction and support vector machine algorithm. As illustrated by 10-fold cross-validation, BPB_GlySite achieves a satisfactory performance with a Sensitivity of 63.68%, a Specificity of 72.60%, an Accuracy of 69.63% and a Matthew's correlation coefficient of 0.3499. Experimental results also indicate that BPB_GlySite significantly outperforms three existing glycation sites predictors: NetGlycate, PreGly and Gly-PseAAC. Therefore, BPB_GlySite can be a useful bioinformatics tool for the prediction of glycation sites. A user-friendly web-server for BPB_GlySite is established at 123.206.31.171/BPB_GlySite/.Entities:
Keywords: Bi-profile bayes; Glycation; Post-translational modification; Support vector machine
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Year: 2017 PMID: 29040908 DOI: 10.1016/j.compbiolchem.2017.10.004
Source DB: PubMed Journal: Comput Biol Chem ISSN: 1476-9271 Impact factor: 2.877