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6MBO

GLP Methyltransferase with Inhibitor EML741-P212121 Crystal Form

Summary for 6MBO
Entry DOI10.2210/pdb6mbo/pdb
DescriptorHistone-lysine N-methyltransferase EHMT1, 2-cyclohexyl-7-methoxy-N-[1-(propan-2-yl)piperidin-4-yl]-8-[3-(pyrrolidin-1-yl)propoxy]-3H-1,4-benzodiazepin-5-amine, ZINC ION, ... (6 entities in total)
Functional Keywordshistone, h3, methylation inhibition, transferase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight64720.80
Authors
Horton, J.R.,Cheng, X. (deposition date: 2018-08-30, release date: 2019-02-27, Last modification date: 2023-10-11)
Primary citationMilite, C.,Feoli, A.,Horton, J.R.,Rescigno, D.,Cipriano, A.,Pisapia, V.,Viviano, M.,Pepe, G.,Amendola, G.,Novellino, E.,Cosconati, S.,Cheng, X.,Castellano, S.,Sbardella, G.
Discovery of a Novel Chemotype of Histone Lysine Methyltransferase EHMT1/2 (GLP/G9a) Inhibitors: Rational Design, Synthesis, Biological Evaluation, and Co-crystal Structure.
J. Med. Chem., 62:2666-2689, 2019
Cited by
PubMed: 30753076
DOI: 10.1021/acs.jmedchem.8b02008
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.591 Å)
Structure validation

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