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-Structure paper
Title | Structure-based design and parallel synthesis of N-benzyl isatin oximes as JNK3 MAP kinase inhibitors. |
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Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 19, Page 2891-2895, Year 2009 |
Publish date | Feb 12, 2009 (structure data deposition date) |
![]() | Cao, J. / Gao, H. / Bemis, G. / Salituro, F. / Ledeboer, M. / Harrington, E. / Wilke, S. / Taslimi, P. / Pazhanisamy, S. / Xie, X. ...Cao, J. / Gao, H. / Bemis, G. / Salituro, F. / Ledeboer, M. / Harrington, E. / Wilke, S. / Taslimi, P. / Pazhanisamy, S. / Xie, X. / Jacobs, M. / Green, J. |
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Methods | X-ray diffraction |
Resolution | 2.2 - 2.8 Å |
Structure data | ![]() PDB-3g90: ![]() PDB-3g9l: ![]() PDB-3g9n: |
Chemicals | ![]() ChemComp-J72: ![]() ChemComp-HOH: ![]() ChemComp-J67: ![]() ChemComp-J88: |
Source |
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![]() | TRANSFERASE / kinase / inhibitor / phosphorylation / ATP-binding / Epilepsy / Nucleotide-binding / Phosphoprotein / Serine/threonine-protein kinase |