| Literature DB >> 9857180 |
D Hermand1, A Pihlak, T Westerling, V Damagnez, J Vandenhaute, G Cottarel, T P Mäkelä.
Abstract
Cell cycle progression is dependent on the sequential activity of cyclin-dependent kinases (CDKs). For full activity, CDKs require an activating phosphorylation of a conserved residue (corresponding to Thr160 in human CDK2) carried out by the CDK-activating kinase (CAK). Two distinct CAK kinases have been described: in budding yeast Saccharomyces cerevisiae, the Cak1/Civ1 kinase is responsible for CAK activity. In several other species including human, Xenopus, Drosophila and fission yeast Schizosaccharomyces pombe, CAK has been identified as a complex homologous to CDK7-cyclin H (Mcs6-Mcs2 in fission yeast). Here we identify the fission yeast Csk1 kinase as an in vivo activating kinase of the Mcs6-Mcs2 CAK defining Csk1 as a CAK-activating kinase (CAKAK).Entities:
Mesh:
Substances:
Year: 1998 PMID: 9857180 PMCID: PMC1171069 DOI: 10.1093/emboj/17.24.7230
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598