Open Biology (Apr 2019)

Crystal structure of human RIOK2 bound to a specific inhibitor

  • Jing Wang,
  • Thibault Varin,
  • Michal Vieth,
  • Jonathan M. Elkins

DOI
https://doi.org/10.1098/rsob.190037
Journal volume & issue
Vol. 9, no. 4

Abstract

Read online

The RIO kinases (RIOKs) are a universal family of atypical kinases that are essential for assembly of the pre-40S ribosome complex. Here, we present the crystal structure of human RIO kinase 2 (RIOK2) bound to a specific inhibitor. This first crystal structure of an inhibitor-bound RIO kinase reveals the binding mode of the inhibitor and explains the structure–activity relationship of the inhibitor series. The inhibitor binds in the ATP-binding site and forms extensive hydrophobic interactions with residues at the entrance to the ATP-binding site. Analysis of the conservation of active site residues reveals the reasons for the specificity of the inhibitor for RIOK2 over RIOK1 and RIOK3, and it provides a template for inhibitor design against the human RIOK family.

Keywords