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3G90

JNK-3 bound to (Z)-5-fluoro-1-((6-fluoro-4H-benzo[d][1,3]dioxin-8-yl)methyl)-3-(hydroxyimino)indolin-2-one

Summary for 3G90
Entry DOI10.2210/pdb3g90/pdb
Related3G9L 3G9N
DescriptorMitogen-activated protein kinase 10, (3E)-5-fluoro-1-[(6-fluoro-4H-1,3-benzodioxin-8-yl)methyl]-1H-indole-2,3-dione 3-oxime (3 entities in total)
Functional Keywordskinase, inhibitor, phosphorylation, atp-binding, epilepsy, nucleotide-binding, phosphoprotein, serine/threonine-protein kinase, transferase
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm: P53779
Total number of polymer chains1
Total formula weight42463.01
Authors
Xie, X.,Jacobs, M.D. (deposition date: 2009-02-12, release date: 2009-02-24, Last modification date: 2024-02-21)
Primary citationCao, 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 (2.4 Å)
Structure validation

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