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7QJG

EED in complex with PRC2 allosteric inhibitor compound 6

Summary for 7QJG
Entry DOI10.2210/pdb7qjg/pdb
DescriptorPolycomb protein EED, Histone-lysine N-methyltransferase EZH2, CHLORIDE ION, ... (5 entities in total)
Functional Keywordsinhibitor, complex, transferase
Biological sourceHomo sapiens (human)
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Total number of polymer chains4
Total formula weight92641.23
Authors
Zhao, K.,Zhao, M.,Luo, X.,Zhang, H.,Scheufler, C. (deposition date: 2021-12-16, release date: 2022-04-13, Last modification date: 2024-01-31)
Primary citationHuang, Y.,Sendzik, M.,Zhang, J.,Gao, Z.,Sun, Y.,Wang, L.,Gu, J.,Zhao, K.,Yu, Z.,Zhang, L.,Zhang, Q.,Blanz, J.,Chen, Z.,Dubost, V.,Fang, D.,Feng, L.,Fu, X.,Kiffe, M.,Li, L.,Luo, F.,Luo, X.,Mi, Y.,Mistry, P.,Pearson, D.,Piaia, A.,Scheufler, C.,Terranova, R.,Weiss, A.,Zeng, J.,Zhang, H.,Zhang, J.,Zhao, M.,Dillon, M.P.,Jeay, S.,Qi, W.,Moggs, J.,Pissot-Soldermann, C.,Li, E.,Atadja, P.,Lingel, A.,Oyang, C.
Discovery of the Clinical Candidate MAK683: An EED-Directed, Allosteric, and Selective PRC2 Inhibitor for the Treatment of Advanced Malignancies.
J.Med.Chem., 65:5317-5333, 2022
Cited by
PubMed: 35352560
DOI: 10.1021/acs.jmedchem.1c02148
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

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