Zhang, Hua2; Neimanis, Sonja2; Lopez-Garcia, Laura A2; Arencibia, José M2; Amon, Sabine3; Stroba, Adriana2; Zeuzem, Stefan2; Proschak, Ewgen2; Stark, Holger2; Bauer, Angelika F2; Busschots, Katrien2; Jørgensen, Thomas J. D.3; Engel, Matthias2; Schulze, Jörg O2; Biondi, Ricardo M2
1 Department of Biochemistry and Molecular Biology, Faculty of Science, SDU2 unknown3 Department of Biochemistry and Molecular Biology, Faculty of Science, SDU
Protein kinases play important regulatory roles in cells and organisms. Therefore, they are subject to specific and tight mechanisms of regulation that ultimately converge on the catalytic domain and allow the kinases to be activated or inhibited only upon the appropriate stimuli. AGC protein kinases have a pocket in the catalytic domain, the PDK1-interacting fragment (PIF)-pocket, which is a key mediator of the activation. We show here that helix αC within the PIF-pocket of atypical protein kinase C (aPKC) is the target of the interaction with its inhibitory N-terminal domains. We also provide structural evidence that the small compound PS315 is an allosteric inhibitor that binds to the PIF-pocket of aPKC. PS315 exploits the physiological dynamics of helix αC for its binding and allosteric inhibition. The results will support research on allosteric mechanisms and selective drug development efforts against PKC isoforms.
Chemistry and Biology, 2014, Vol 21, Issue 6, p. 754-65