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8E3W

BRD4-D1 in complex with BET inhibitor

Summary for 8E3W
Entry DOI10.2210/pdb8e3w/pdb
Related8DYR 8E17
DescriptorBromodomain-containing protein 4, (4P)-4-[2-(cyclopropylmethoxy)-5-(methanesulfonyl)phenyl]-2-methylisoquinolin-1(2H)-one, 1,2-ETHANEDIOL, ... (4 entities in total)
Functional Keywordsbromodomain, bet inhibitor, brd4, pet radiotracer, solid tumor imaging, gene regulation-inhibitor complex, gene regulation/inhibitor
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight15544.91
Authors
Gorman, M.A.,Fitzgerald, C.G.D.,White, J.M.,Parker, M.W. (deposition date: 2022-08-17, release date: 2023-03-29, Last modification date: 2023-10-25)
Primary citationDickmann, C.G.F.,McDonald, A.F.,Huynh, N.,Rigopoulos, A.,Liu, Z.,Guo, N.,Osellame, L.D.,Gorman, M.A.,Parker, M.W.,Gan, H.K.,Scott, A.M.,Ackermann, U.,Burvenich, I.J.G.,White, J.M.
Bromodomain and extraterminal protein-targeted probe enables tumour visualisation in vivo using positron emission tomography.
Chem.Commun.(Camb.), 59:3126-3129, 2023
Cited by
PubMed Abstract: Bromodomain and extraterminal (BET) proteins, a family of epigenetic regulators, have emerged as important oncology drug targets. BET proteins have not been targeted for molecular imaging of cancer. Here, we report the development of a novel molecule radiolabelled with positron emitting fluorine-18, [F]BiPET-2, and its and preclinical evaluation in glioblastoma models.
PubMed: 36809538
DOI: 10.1039/d2cc04813b
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.47 Å)
Structure validation

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