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The cell cycle inhibitor p21CIP is phosphorylated by cyclin A-CDK2 complexes

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13 de January de 1998/in Casanovas's Lab/by miguel

Biochem Biophys Res Commun. 1997 Dec 18;241(2):434-8. doi: 10.1006/bbrc.1997.7787.

ABSTRACT

We report here experimental evidence indicating that the p21CIP, the universal inhibitor of cyclin-dependent protein kinases, general inhibitor CDKs is a substrate oof cyclin A-cdk2. The evidence comes from phosphorylation experiments in which the endogenous p21CIP present in using the original cyclin A-cdk2 complexes immunoprecipitated from HeLa cells extracts can be phosphorylated by the cdk2 of the same complexes. In vitro experiments showing that reconstituted GSTcyclin A-GSTcdk2 complexes from phosphorylate recombinant GSTp21CIP confirms that p21CIP is a cyclin A-cdk2 substrate.

PMID:9425288 | DOI:10.1006/bbrc.1997.7787

https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg 0 0 miguel https://procure-oncology.com/wp-content/uploads/2023/10/Procure-icoRecurso-1@2x-100.jpg miguel1998-01-13 11:00:001998-01-13 11:00:00The cell cycle inhibitor p21CIP is phosphorylated by cyclin A-CDK2 complexes

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