8VKZ
Crystal structure of Glucocorticoid Receptor in complex with an inhibitor
This is a non-PDB format compatible entry.
Summary for 8VKZ
Entry DOI | 10.2210/pdb8vkz/pdb |
Descriptor | Glucocorticoid receptor, Nuclear receptor coactivator 2, (4aR,4bS,5R,6aS,6bS,8R,9aR,10aR,10bR)-8-{4-[(3-aminophenyl)methyl]phenyl}-5-hydroxy-6b-(hydroxyacetyl)-4a,6a-dimethyl-4a,4b,5,6,6a,6b,9a,10,10a,10b,11,12-dodecahydro-2H,8H-naphtho[2',1':4,5]indeno[1,2-d][1,3]dioxol-2-one, ... (4 entities in total) |
Functional Keywords | glucocorticord receptor, modulator, transcription, transcription-inhibitor complex, transcription/inhibitor |
Biological source | Homo sapiens (human) More |
Total number of polymer chains | 4 |
Total formula weight | 63143.28 |
Authors | Judge, R.A.,Hobson, A.D. (deposition date: 2024-01-10, release date: 2024-01-24, Last modification date: 2024-05-08) |
Primary citation | Hobson, A.D.,Zhu, H.,Qiu, W.,Judge, R.A.,Longenecker, K. Minimising the payload solvent exposed hydrophobic surface area optimises the antibody-drug conjugate properties. Rsc Med Chem, 15:832-838, 2024 Cited by PubMed: 38516584DOI: 10.1039/d3md00540b PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.133 Å) |
Structure validation
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