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5OC8

HDM2 (17-111, WILD TYPE) COMPLEXED WITH NVP-HDM201 AT 1.56A

Summary for 5OC8
Entry DOI10.2210/pdb5oc8/pdb
Related5LN2
DescriptorE3 ubiquitin-protein ligase Mdm2, (4~{S})-5-(5-chloranyl-1-methyl-2-oxidanylidene-pyridin-3-yl)-4-(4-chlorophenyl)-2-(2,4-dimethoxypyrimidin-5-yl)-3-propan-2-yl-4~{H}-pyrrolo[3,4-d]imidazol-6-one, CHLORIDE ION, ... (4 entities in total)
Functional Keywordsppi with p53, inhibitor complex, cell cycle, ligase
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight11746.92
Authors
Kallen, J. (deposition date: 2017-06-29, release date: 2018-08-22, Last modification date: 2024-01-17)
Primary citationJeay, S.,Ferretti, S.,Holzer, P.,Fuchs, J.,Chapeau, E.A.,Wartmann, M.,Sterker, D.,Romanet, V.,Murakami, M.,Kerr, G.,Durand, E.Y.,Gaulis, S.,Cortes-Cros, M.,Ruetz, S.,Stachyra, T.M.,Kallen, J.,Furet, P.,Wurthner, J.,Guerreiro, N.,Halilovic, E.,Jullion, A.,Kauffmann, A.,Kuriakose, E.,Wiesmann, M.,Jensen, M.R.,Hofmann, F.,Sellers, W.R.
Dose and Schedule Determine Distinct Molecular Mechanisms Underlying the Efficacy of the p53-MDM2 Inhibitor HDM201.
Cancer Res., 78:6257-6267, 2018
Cited by
PubMed: 30135191
DOI: 10.1158/0008-5472.CAN-18-0338
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.56 Å)
Structure validation

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