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Abstract
Two regions in casein kinase 1a (CK1a) are required for anchoring to frequency (FRQ), with approximately 100 sites targeted for hyperphosphorylation.
- The circadian clock timing in Neurospora relies on the hyperphosphorylation of FRQ, facilitated by CK1a anchoring.
- Mutation of the p1 region in CK1a leads to a non-functional circadian clock, while mutation of the p2 region results in non-viability.
- Both p1 and p2 are suggested to create an interface for the interaction between CK1a and FRQ.
- The anchoring mechanism allows CK1a's active site to remain accessible for phosphorylation at multiple sites on FRQ.
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