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- Erratum in:
- Nature 1998 Nov 26;396(6709):390.
Crystal structure of the complex of the cyclin D-dependent kinase Cdk6 bound to the cell-cycle inhibitor p19INK4d.
Brotherton DH,
Dhanaraj V,
Wick S,
Brizuela L,
Domaille PJ,
Volyanik E,
Xu X,
Parisini E,
Smith BO,
Archer SJ,
Serrano M,
Brenner SL,
Blundell TL,
Laue ED.
Cambridge Centre for Molecular Recognition, Department of Biochemistry, University of Cambridge, UK.
The crystal structure of the cyclin D-dependent kinase Cdk6 bound to the p19 INK4d protein has been determined at 1.9 A resolution. The results provide the first structural information for a cyclin D-dependent protein kinase and show how the INK4 family of CDK inhibitors bind. The structure indicates that the conformational changes induced by p19INK4d inhibit both productive binding of ATP and the cyclin-induced rearrangement of the kinase from an inactive to an active conformation. The structure also shows how binding of an INK4 inhibitor would prevent binding of p27Kip1, resulting in its redistribution to other CDKs. Identification of the critical residues involved in the interaction explains how mutations in Cdk4 and p16INK4a result in loss of kinase inhibition and cancer.
PMID: 9751051 [PubMed - indexed for MEDLINE]
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Structures reported by this article
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P19ink4dCDK6 COMPLEX
PDB: 1BLX
Source: Homo sapiens, Mus musculus
Method: X-Ray Diffraction | Resolution: 1.9 Å