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5ISL

Linked KDM5A Jmj Domain Bound to the Inhibitor C49 (2-{[(2-{[(E)-2-(dimethylamino)ethenyl](ethyl)amino}-2-oxoethyl)amino]methyl}pyridine-4-carboxylic acid)

Summary for 5ISL
Entry DOI10.2210/pdb5isl/pdb
Related5IVB 5IVC 5IVE 5IVF 5IVJ 5IVV 5IVY 5IW0 5IWF
DescriptorLysine-specific demethylase 5A, 2-{[(2-{[(E)-2-(dimethylamino)ethenyl](ethyl)amino}-2-oxoethyl)amino]methyl}pyridine-4-carboxylic acid, MANGANESE (II) ION, ... (6 entities in total)
Functional Keywordsdemethylase inhibition, oxidoreductase-oxidoreductase inhibitor complex, oxidoreductase/oxidoreductase inhibitor
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight38460.30
Authors
Horton, J.R.,Cheng, X. (deposition date: 2016-03-15, release date: 2016-07-27, Last modification date: 2023-09-27)
Primary citationHorton, J.R.,Liu, X.,Gale, M.,Wu, L.,Shanks, J.R.,Zhang, X.,Webber, P.J.,Bell, J.S.,Kales, S.C.,Mott, B.T.,Rai, G.,Jansen, D.J.,Henderson, M.J.,Urban, D.J.,Hall, M.D.,Simeonov, A.,Maloney, D.J.,Johns, M.A.,Fu, H.,Jadhav, A.,Vertino, P.M.,Yan, Q.,Cheng, X.
Structural Basis for KDM5A Histone Lysine Demethylase Inhibition by Diverse Compounds.
Cell Chem Biol, 23:769-781, 2016
Cited by
PubMed: 27427228
DOI: 10.1016/j.chembiol.2016.06.006
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.694 Å)
Structure validation

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数据于2024-04-24公开中

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