Inferring Chemogenomic Features from Drug-Target Interaction Networks

被引:6
|
作者
Yamanishi, Yoshihiro [1 ,2 ]
机构
[1] Kyushu Univ, Med Inst Bioregulat, Multiscale Res Ctr Med Sci, Div Syst Cohort,Higashi Ku, Fukuoka 8128582, Japan
[2] Kyushu Univ, Inst Adv Study, Higashi Ku, Fukuoka 8128581, Japan
关键词
Chemogenomics; Drug-target interactions; Chemical substructures; Protein domains; Feature extraction; PROTEIN-BINDING POCKET; IN-VITRO; PREDICTION; DISCOVERY;
D O I
10.1002/minf.201300079
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Drug effects are mainly caused by the interactions between drug molecules and target proteins including primary targets and off-targets. Understanding of the molecular mechanisms behind overall drugtarget interactions is crucial in the drug design process. In this paper we review recently developed methods to infer chemogenomic features (the underlying associations between drug chemical substructures and protein domains) which are strongly involved in drug-target interaction networks. We show the usefulness of the methods to detect ligand chemical fragments specific for each protein domain and ligand core substructures important for a wide range of protein families. We also discuss how to use the chemogenomic features for predicting unknown drug-target interactions on a large scale.
引用
收藏
页码:991 / 999
页数:9
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