1JSU
P27(KIP1)/CYCLIN A/CDK2 COMPLEX
Summary for 1JSU
Entry DOI | 10.2210/pdb1jsu/pdb |
Descriptor | CYCLIN-DEPENDENT KINASE-2, CYCLIN A, P27, ... (5 entities in total) |
Functional Keywords | complex (transferase-cyclin-inhibitor), kinase, cell cycle, cell division, cdk, cyclin, inhibitor, complex (transferase-cyclin-inhibitor) complex, complex (transferase/cyclin/inhibitor) |
Biological source | Homo sapiens (human) More |
Cellular location | Nucleus: P20248 P46527 |
Total number of polymer chains | 3 |
Total formula weight | 73990.20 |
Authors | Russo, A.A.,Jeffrey, P.D.,Pavletich, N.P. (deposition date: 1996-07-03, release date: 1997-07-29, Last modification date: 2024-10-16) |
Primary citation | Russo, A.A.,Jeffrey, P.D.,Patten, A.K.,Massague, J.,Pavletich, N.P. Crystal structure of the p27Kip1 cyclin-dependent-kinase inhibitor bound to the cyclin A-Cdk2 complex. Nature, 382:325-331, 1996 Cited by PubMed Abstract: The crystal structure of the human p27Kip1 kinase inhibitory domain bound to the phosphorylated cyclin A-cyclin-dependent kinase 2 (Cdk2) complex has been determined at 2.3 angstrom. p27Kip1 binds the complex as an extended structure interacting with both cyclin A and Cdk2. On cyclin A, it binds in a groove formed by conserved cyclin box residues. On Cdk2, it binds and rearranges the amino-terminal lobe and also inserts into the catalytic cleft, mimicking ATP. PubMed: 8684460DOI: 10.1038/382325a0 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.3 Å) |
Structure validation
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