multi-type neighbors enhanced global topology and pairwise attribute learning for drug-protein interaction prediction.

Journal: Briefings in bioinformatics
Published Date:

Abstract

MOTIVATION: Accurate identification of proteins interacted with drugs helps reduce the time and cost of drug development. Most of previous methods focused on integrating multisource data about drugs and proteins for predicting drug-target interactions (DTIs). There are both similarity connection and interaction connection between two drugs, and these connections reflect their relationships from different perspectives. Similarly, two proteins have various connections from multiple perspectives. However, most of previous methods failed to deeply integrate these connections. In addition, multiple drug-protein heterogeneous networks can be constructed based on multiple kinds of connections. The diverse topological structures of these networks are still not exploited completely.

Authors

  • Ping Xuan
    School of Computer Science and Technology, Heilongjiang University, Harbin 150080, China.
  • Xiaowen Zhang
    Department of Foreign Languages and Literatures, Tsinghua University, Beijing, China.
  • Yu Zhang
    College of Marine Electrical Engineering, Dalian Maritime University, Dalian, China.
  • Kaimiao Hu
    School of Computer Science and Technology, Heilongjiang University, Harbin 150080, China.
  • Toshiya Nakaguchi
  • Tiangang Zhang
    School of Mathematical Science, Heilongjiang University, Harbin 150080, China. zhang@hlju.edu.cn.