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.
- 1. Biocenter Oulu, Department of Biochemistry, University of Oulu, Oulu, Finland.
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.