5ANQ
inhibitors of JumonjiC domain-containing histone demethylases
Summary for 5ANQ
Entry DOI | 10.2210/pdb5anq/pdb |
Descriptor | LYSINE-SPECIFIC DEMETHYLASE 4A, 2-{2-[(pyridin-3-ylmethyl)amino]pyrimidin-4-yl}pyridine-4-carboxylic acid, FE (II) ION, ... (7 entities in total) |
Functional Keywords | oxidoreductase, epigenetics, histone demethylases, inhibitors, jumonjic domain, virtual screening |
Biological source | HOMO SAPIENS (HUMAN) |
Cellular location | Nucleus : O75164 |
Total number of polymer chains | 2 |
Total formula weight | 84918.27 |
Authors | Roatsch, M.,Robaa, D.,Pippel, M.,Nettleship, J.E.,Reddivari, Y.,Bird, L.E.,Hoffmann, I.,Franz, H.,Owens, R.J.,Schuele, R.,Flaig, R.,Sippl, W.,Jung, M. (deposition date: 2015-09-07, release date: 2016-03-23, Last modification date: 2024-01-10) |
Primary citation | Roatsch, M.,Robaa, D.,Pippel, M.,Nettleship, J.E.,Reddivari, Y.,Bird, L.E.,Hoffmann, I.,Franz, H.,Owens, R.J.,Schole, R.,Flaig, R.,Sippl, W.,Jung, M. Substituted 2-(2-Aminopyrimidin-4-Yl)Pyridine-4-Carboxylates as Potent Inhibitors of Jumonjic Domain-Containing Histone Demethylases. Fut.Med.Chem., 8:1553-, 2016 Cited by PubMed: 26971619DOI: 10.4155/FMC.15.188 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2 Å) |
Structure validation
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