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ProfKin: A comprehensive web server for structure-based kinase profiling

  • Zihao Shen
  • , Yu Hang Yan
  • , Shuo Yang
  • , Sang Zhu
  • , Yuan Yuan
  • , Zhiqiang Qiu
  • , Huan Jia
  • , Ruiqiong Wang
  • , Guo Bo Li*
  • , Honglin Li*
  • *此作品的通讯作者
  • East China University of Science and Technology
  • Key Laboratory of Drug Targeting and Drug Delivery System

科研成果: 期刊稿件文章同行评审

摘要

Protein kinases are central mediators of signal-transduction cascades and attractive drug targets for therapeutic intervention. Since kinases are structurally and mechanistically related to each other, kinase inhibitor selectivity is often investigated by kinase profiling and considered as an important index for drug discovery. We here describe a versatile web server termed ProfKin for structure-based kinase profiling, which is based on a kinase-ligand focused database (KinLigDB). It provides all ready-to-use 3D structure coordinates of 4219 kinase-ligand complex structures covering 297 human kinases and the associated information, particularly including binding site type, binding ligand type, interaction fingerprints, downstream molecules and related human diseases. The web server works via predicting possible binding modes for the query molecule, prioritizing the binding modes guided by an interaction fingerprint analysis method, and giving a list of ranked kinases by a comprehensive index. Users can freely select entire or part of the KinLigDB database, e.g. via subfamily and binding site type, to customize the profiling contents. The superimpositions of the predicted binding poses of the query molecule with reference binding modes can be visually inspected on the website. The additional classification attributes and phylogenetic tree are also given for each top-ranked kinase.

源语言英语
文章编号113772
期刊European Journal of Medicinal Chemistry
225
DOI
出版状态已出版 - 5 12月 2021
已对外发布

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