Enzymatic activity with an incomplete catalytic spine - insights from a comparative structural analysis of human CK2alpha and its paralogous isoform CK2alpha'
Bischoff, N., Raaf, J., Olsen, B., Bretner, M., Issinger, O.G., Niefind, K.(2011) Mol Cell Biochem 356: 57-65
- PubMed: 21739153 
- DOI: https://doi.org/10.1007/s11010-011-0948-5
- Primary Citation of Related Structures:  
3RPS - PubMed Abstract: 
Eukaryotic protein kinases are fundamental factors for cellular regulation and therefore subject of strict control mechanisms. For full activity a kinase molecule must be penetrated by two stacks of hydrophobic residues, the regulatory and the catalytic spine that are normally well conserved among active protein kinases. We apply this novel spine concept here on CK2¦Á, the catalytic subunit of protein kinase CK2. Homo sapiens disposes of two paralog isoforms of CK2¦Á (hsCK2¦Á and hsCK2¦Á'). We describe two new structures of hsCK2¦Á constructs one of which in complex with the ATP-analog adenylyl imidodiphosphate and the other with the ATP-competitive inhibitor 3-(4,5,6,7-tetrabromo-1H-benzotriazol-1-yl)propan-1-ol. The former is the first hsCK2¦Á structure with a well defined cosubstrate/magnesium complex and the second with an open ¦Â4/¦Â5-loop. Comparisons of these structures with existing CK2¦Á/CK2¦Á' and cAMP-dependent protein kinase (PKA) structures reveal: in hsCK2¦Á' an open conformation of the interdomain hinge/helix ¦ÁD region that is critical for ATP-binding is found corresponding to an incomplete catalytic spine. In contrast hsCK2¦Á often adopts the canonical, PKA-like version of the catalytic spine which correlates with a closed conformation of the hinge region. HsCK2¦Á can switch to the incomplete, non-canonical, hsCK2¦Á'-like state of the catalytic spine, but this transition apparently depends on binding of either ATP or of the regulatory subunit CK2¦Â. Thus, ATP looks like an activator of hsCK2¦Á rather than a pure cosubstrate.
Organizational Affiliation: 
Universit?t zu K?ln, Institut f¨¹r Biochemie, Z¨¹lpicher Stra?e 47, 50674 K?ln, Germany.