EMBO Member
Tartu | Estonia
EMBO 2025
We study cell cycle regulation by cyclin-dependent kinases (Cdk), multisite phosphorylation and substrate docking. We have proposed a 'unified model of Cdk substrate phosphorylation'. The timing of Cdk-driven processes is determined by a complex blend of tunable parameters, including the sequence, affinities, and positioning of docking sites. Variations of these parameters allow Cdk switches to be triggered at specific Cdk thresholds.
Keywords: Cell cycle / CDK / short linear motifs (SLiMs) / substrate docking / multisite phosphorylation / cell signalling networks / synthetic biology / bioengineering
Subject area(s): Cell Cycle | Proteins & Biochemistry | Signal Transduction