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6TUY

Human LSD1/CoREST bound to the quinazoline inhibitor MC4106

Summary for 6TUY
Entry DOI10.2210/pdb6tuy/pdb
DescriptorLysine-specific histone demethylase 1A, REST corepressor 1, FLAVIN-ADENINE DINUCLEOTIDE, ... (9 entities in total)
Functional Keywordsepigenetics, histone demethylase, epigenetic inhibitor, dual inhibitor, oxidoreductase
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains2
Total formula weight149324.00
Authors
Mattevi, A.,Marrocco, B. (deposition date: 2020-01-08, release date: 2021-07-21, Last modification date: 2024-01-24)
Primary citationMenna, M.,Fiorentino, F.,Marrocco, B.,Lucidi, A.,Tomassi, S.,Cilli, D.,Romanenghi, M.,Cassandri, M.,Pomella, S.,Pezzella, M.,Del Bufalo, D.,Zeya Ansari, M.S.,Tomasevic, N.,Mladenovic, M.,Viviano, M.,Sbardella, G.,Rota, R.,Trisciuoglio, D.,Minucci, S.,Mattevi, A.,Rotili, D.,Mai, A.
Novel non-covalent LSD1 inhibitors endowed with anticancer effects in leukemia and solid tumor cellular models.
Eur.J.Med.Chem., 237:114410-114410, 2022
Cited by
PubMed: 35525212
DOI: 10.1016/j.ejmech.2022.114410
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

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