Citation: Lü Wei, XUE Ying. Prediction of Hepatitis C Virus Non-Structural Proteins 5B Polymerase Inhibitors Using Machine Learning Methods[J]. Acta Physico-Chimica Sinica, ;2011, 27(06): 1407-1416. doi: 10.3866/PKU.WHXB20110608 shu

Prediction of Hepatitis C Virus Non-Structural Proteins 5B Polymerase Inhibitors Using Machine Learning Methods

  • Received Date: 2 March 2011
    Available Online: 21 April 2011

    Fund Project: 国家重点基础研究发展规划项目(2009CB118500) (2009CB118500)教育部留学归国人员科研启动基金(20071108-18-15) (20071108-18-15)

  • Non-structural proteins 5B (NS5B) play an important role in protein maturation and gene replication as an RNA dependent RNA polymerase in the hepatitis C virus (HCV). Inhibiting NS5B polymerase will prevent RNA replication and, therefore, it is significant for the treatment of HCV. It is becoming increasingly important to screen and predict molecules that have NS5B inhibitory activity by computational methods. This work explores several machine learning (ML) methods (support vector machine (SVM), k-nearest neighbor (k-NN), and C4.5 decision tree (C4.5 DT)) for the prediction of NS5B inhibitors (NS5BIs). This prediction system was tested using 1248 compounds (552 NS5BIs and 696 non- NS5BIs), which are significantly more diverse in chemical structure than those used in other studies. A feature selection method was used to improve the prediction accuracy and the selection of molecular descriptors responsible for distinguishing between NS5BIs and non-NS5BIs. The prediction accuracies were 81.4%-91.7% for the NS5BIs, 78.2%-87.2% for the non-NS5BIs, and 84.1%-85.0% overall based on the three kinds of machine learning methods. SVM gave the best accuracy of 91.7% for the NS5BIs, C4.5 gave the best accuracy of 87.2% for the non-NS5BIs, and k-NN gave the best overall accuracy of 85.0% for all the compounds. This work suggests that machine learning methods can facilitate the prediction of the NS5BIs potential for unknown sets of compounds and to determine the molecular descriptors associated with NS5BIs.

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