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7NQ8

C-TERMINAL BROMODOMAIN OF HUMAN BRD2 WITH N-ethyl-3-(1-methyl-1H-1,2,3-triazol-4-yl)-4-(pyridin-2-ylmethoxy)benzamide

Summary for 7NQ8
Entry DOI10.2210/pdb7nq8/pdb
Related7NQ5 7NQ7
DescriptorBromodomain-containing protein 2, 1,2-ETHANEDIOL, N-ethyl-3-(1-methyl-1H-1,2,3-triazol-4-yl)-4-(pyridin-2-ylmethoxy)benzamide, ... (4 entities in total)
Functional Keywordsinhibitor, histone, epigenetic reader, bromodomain, brd2, bromodomain containing protein 2, antagonist, nuclear protein
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight13956.04
Authors
Chung, C.W. (deposition date: 2021-03-01, release date: 2021-03-24, Last modification date: 2021-04-07)
Primary citationAylott, H.E.,Atkinson, S.J.,Bamborough, P.,Bassil, A.,Chung, C.W.,Gordon, L.,Grandi, P.,Gray, J.R.J.,Harrison, L.A.,Hayhow, T.G.,Messenger, C.,Mitchell, D.,Phillipou, A.,Preston, A.,Prinjha, R.K.,Rianjongdee, F.,Rioja, I.,Seal, J.T.,Wall, I.D.,Watson, R.J.,Woolven, J.M.,Demont, E.H.
Template-Hopping Approach Leads to Potent, Selective, and Highly Soluble Bromo and Extraterminal Domain (BET) Second Bromodomain (BD2) Inhibitors.
J.Med.Chem., 64:3249-3281, 2021
Cited by
PubMed: 33662213
DOI: 10.1021/acs.jmedchem.0c02156
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.602 Å)
Structure validation

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