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9FWG

LSD1/CoREST bound to bomedemstat

This is a non-PDB format compatible entry.
Summary for 9FWG
Entry DOI10.2210/pdb9fwg/pdb
DescriptorLysine-specific histone demethylase 1A, REST corepressor 1, Bomedemstat FAD adduct (3 entities in total)
Functional Keywordsbomedemstat, epigenetics, histone demethylase, oxidoreductase
Biological sourceHomo sapiens (human)
More
Total number of polymer chains2
Total formula weight147350.52
Authors
Speranzini, V.,Mattevi, A. (deposition date: 2024-06-30, release date: 2024-07-10)
Primary citationJasmine, S.,Mandl, A.,Krueger, T.E.G.,Dalrymple, S.L.,Antony, L.,Dias, J.,Celatka, C.A.,Tapper, A.E.,Kleppe, M.,Kanayama, M.,Jing, Y.,Speranzini, V.,Wang, Y.Z.,Luo, J.,Trock, B.J.,Denmeade, S.R.,Carducci, M.A.,Mattevi, A.,Rienhoff, H.Y.,Isaacs, J.T.,Brennen, W.N.
Characterization of structural, biochemical, pharmacokinetic, and pharmacodynamic properties of the LSD1 inhibitor bomedemstat in preclinical models.
Prostate, 84:909-921, 2024
Cited by
PubMed: 38619005
DOI: 10.1158/1078-0432.CCR-20-2380
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.2 Å)
Structure validation

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