1. Academic Validation
  2. Structural basis and selectivity of tankyrase inhibition by a Wnt signaling inhibitor WIKI4

Structural basis and selectivity of tankyrase inhibition by a Wnt signaling inhibitor WIKI4

  • PLoS One. 2013 Jun 6;8(6):e65404. doi: 10.1371/journal.pone.0065404.
Teemu Haikarainen 1 Harikanth Venkannagari Mohit Narwal Ezeogo Obaji Hao-Wei Lee Yves Nkizinkiko Lari Lehtiö
Affiliations

Affiliation

  • 1 Biocenter Oulu, Department of Biochemistry, University of Oulu, Oulu, Finland.
Abstract

Recently a novel inhibitor of Wnt signaling was discovered. The compound, WIKI4, was found to act through tankyrase inhibition and regulate β-catenin levels in many Cancer cell lines and human embryonic stem cells. Here we confirm that WIKI4 is a high potency tankyrase inhibitor and that it selectively inhibits tankyrases over other ARTD Enzymes tested. The binding mode of the compound to tankyrase 2 was determined by protein X-ray crystallography to 2.4 Å resolution. The structure revealed a novel binding mode to the adenosine subsite of the donor NAD(+) binding groove of the catalytic domain. Our results form a structural basis for further development of potent and selective tankyrase inhibitors based on the WIKI4 scaffold.

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