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Identification of a cyclin-cdk2 recognition motif present in substrates and p21-like cyclin-dependent kinase inhibitors.

Understanding how cyclin-cdk complexes recognize their substrates is a central problem in cell cycle biology. We identified an E2F1-derived eight-residue peptide which blocked the binding of cyclin A and E-cdk2 complexes to E2F1 and p21. Short peptides spanning similar sequences in p107, p130, and p...

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Bibliografiske detaljer
Udgivet i:Mol Cell Biol
Principais autores: Adams, P D, Sellers, W R, Sharma, S K, Wu, A D, Nalin, C M, Kaelin, W G
Format: Artigo
Sprog:Inglês
Udgivet: Taylor & Francis 1996
Fag:
Online adgang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC231664/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8943316/
https://ncbi.nlm.nih.govhttps://doi.org/10.1128/mcb.16.12.6623
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