9BJC
Crystal structure of CDK2/Cyclin E1 in complex with XC208
This is a non-PDB format compatible entry.
Summary for 9BJC
| Entry DOI | 10.2210/pdb9bjc/pdb |
| Related | 9BJB 9BJD |
| Descriptor | Cyclin-dependent kinase 2, G1/S-specific cyclin-E1, (5aS,6S,7S)-3,7-dihydroxy-6-methoxy-1,4,6,9-tetramethyl-6,7-dihydrodibenzo[b,f][1,4]oxazepine-8,11(5aH,10H)-dione, ... (4 entities in total) |
| Functional Keywords | cyclin-dependent kinase 2 g1/s-specific cyclin-e1 inhibitor, cell cycle, transferase-inhibitor complex, transferase/inhibitor |
| Biological source | Homo sapiens (human) More |
| Total number of polymer chains | 2 |
| Total formula weight | 67487.36 |
| Authors | Hosford, C.J.,Yano, J.,Thevakumaran, N.,Davison, J.,Romeril, S.,Choi, Y.,Hadjithomas, M.,Verdine, G.L. (deposition date: 2024-04-25, release date: 2025-08-27) |
| Primary citation | Verdine, G.L. Nature-guided discovery of a tunable kinase inhibitor scaffold To Be Published, |
| Experimental method | X-RAY DIFFRACTION (2.22 Å) |
Structure validation
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