3LBK
Structure of human MDM2 protein in complex with a small molecule inhibitor
Summary for 3LBK
Entry DOI | 10.2210/pdb3lbk/pdb |
Related | 1YCR 3LBJ 3LBL |
Descriptor | E3 ubiquitin-protein ligase Mdm2, 6-chloro-3-[1-(4-chlorobenzyl)-4-phenyl-1H-imidazol-5-yl]-1H-indole-2-carboxylic acid, SULFATE ION, ... (4 entities in total) |
Functional Keywords | mdmx, mdm2, p53, inhibitor, alternative splicing, cytoplasm, ligase, nucleus, phosphoprotein, proto-oncogene, ubl conjugation, ubl conjugation pathway, zinc-finger |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 1 |
Total formula weight | 11717.46 |
Authors | Popowicz, G.M.,Czarna, A.,Wolf, S.,Holak, T.A. (deposition date: 2010-01-08, release date: 2010-03-16, Last modification date: 2023-11-01) |
Primary citation | Popowicz, G.M.,Czarna, A.,Wolf, S.,Wang, K.,Wang, W.,Domling, A.,Holak, T.A. Structures of low molecular weight inhibitors bound to MDMX and MDM2 reveal new approaches for p53-MDMX/MDM2 antagonist drug discovery Cell Cycle, 9:1104-1111, 2010 Cited by PubMed: 20237429DOI: 10.4161/cc.9.6.10956 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.3 Å) |
Structure validation
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