8D7P

Human Casein kinase 1 delta in complex with phosphorylated Drosophila PERIOD peptide

Summary for 8D7P

• Entry DOI: 10.2210/pdb8d7p/pdb
• Descriptor: Casein kinase I isoform delta, Period circadian protein peptide (3 entities in total)
• Functional Keywords: transferase, circadian clock protein, kinase, complex, transferase-circadian clock protein complex, transferase/circadian clock protein
• Biological source: Homo sapiens (human); More
• Total number of polymer chains: 4
• Total formula weight: 74153.15

Authors

Philpott, J.M.,Freeberg, A.M.,Tripathi, S.M.,Partch, C.L. (deposition date: 2022-06-07, release date: 2023-05-17, Last modification date: 2023-10-25)

Primary citation

Philpott, J.M.,Freeberg, A.M.,Park, J.,Lee, K.,Ricci, C.G.,Hunt, S.R.,Narasimamurthy, R.,Segal, D.H.,Robles, R.,Cai, Y.,Tripathi, S.,McCammon, J.A.,Virshup, D.M.,Chiu, J.C.,Lee, C.,Partch, C.L.
PERIOD phosphorylation leads to feedback inhibition of CK1 activity to control circadian period.
Mol.Cell, 83:1677-1692.e8, 2023

PubMed Abstract: PERIOD (PER) and Casein Kinase 1δ regulate circadian rhythms through a phosphoswitch that controls PER stability and repressive activity in the molecular clock. CK1δ phosphorylation of the familial advanced sleep phase (FASP) serine cluster embedded within the Casein Kinase 1 binding domain (CK1BD) of mammalian PER1/2 inhibits its activity on phosphodegrons to stabilize PER and extend circadian period. Here, we show that the phosphorylated FASP region (pFASP) of PER2 directly interacts with and inhibits CK1δ. Co-crystal structures in conjunction with molecular dynamics simulations reveal how pFASP phosphoserines dock into conserved anion binding sites near the active site of CK1δ. Limiting phosphorylation of the FASP serine cluster reduces product inhibition, decreasing PER2 stability and shortening circadian period in human cells. We found that Drosophila PER also regulates CK1δ via feedback inhibition through the phosphorylated PER-Short domain, revealing a conserved mechanism by which PER phosphorylation near the CK1BD regulates CK1 kinase activity.

PubMed: 37207626
DOI: 10.1016/j.molcel.2023.04.019

Experimental method

X-RAY DIFFRACTION (2.25 Å)