3G9N

JNK3 bound to (Z)-1-((6-fluoro-4H-benzo[d][1,3]dioxin-8-yl)methyl)-3-(hydroxyimino)-4-phenylindolin-2-one

Summary for 3G9N

Entry DOI	10.2210/pdb3g9n/pdb
Related	3G90 3G9L
Descriptor	Mitogen-activated protein kinase 10, (3Z)-1-[(6-fluoro-4H-1,3-benzodioxin-8-yl)methyl]-4-phenyl-1H-indole-2,3-dione 3-oxime (3 entities in total)
Functional Keywords	kinase, inhibitor, phosphorylation, atp-binding, epilepsy, nucleotide-binding, phosphoprotein, serine/threonine-protein kinase, transferase
Biological source	Homo sapiens (human)
Cellular location	Cytoplasm : P53779
Total number of polymer chains	1
Total formula weight	42521.12
Authors	Jacobs, M.D. (deposition date: 2009-02-13, release date: 2009-02-24, Last modification date: 2024-02-21)
Primary citation	Cao, J.,Gao, H.,Bemis, G.,Salituro, F.,Ledeboer, M.,Harrington, E.,Wilke, S.,Taslimi, P.,Pazhanisamy, S.,Xie, X.,Jacobs, M.,Green, J. Structure-based design and parallel synthesis of N-benzyl isatin oximes as JNK3 MAP kinase inhibitors. Bioorg.Med.Chem.Lett., 19:2891-2895, 2009 Cited by PubMed: 19361991 DOI: 10.1016/j.bmcl.2009.03.043 PDB entries with the same primary citation
Experimental method	X-RAY DIFFRACTION (2.8 Å)

Structure validation