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...
保存先:
| 出版年: | Mol Cell Biol |
|---|---|
| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Taylor & Francis
1996
|
| 主題: | |
| オンライン･アクセス: | 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 |
| タグ: |
タグなし, このレコードへの初めてのタグを付けませんか!
|