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Structure paper

Title2,6-Naphthyridines as potent and selective inhibitors of the novel protein kinase C isozymes.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 21, Page 7367-7372, Year 2011
Publish dateSep 23, 2011 (structure data deposition date)
Authorsvan Eis, M.J. / Evenou, J.P. / Floersheim, P. / Gaul, C. / Cowan-Jacob, S.W. / Monovich, L. / Rummel, G. / Schuler, W. / Stark, W. / Strauss, A. ...van Eis, M.J. / Evenou, J.P. / Floersheim, P. / Gaul, C. / Cowan-Jacob, S.W. / Monovich, L. / Rummel, G. / Schuler, W. / Stark, W. / Strauss, A. / Matt, A. / Vangrevelinghe, E. / Wagner, J. / Soldermann, N.
External linksBioorg. Med. Chem. Lett. / PubMed:22078216
MethodsX-ray diffraction
Resolution2.05 Å
Structure data

PDB-3txo:
PKC eta kinase in complex with a naphthyridine
Method: X-RAY DIFFRACTION / Resolution: 2.05 Å

Chemicals

ChemComp-07U:
2-methyl-N~1~-[3-(pyridin-4-yl)-2,6-naphthyridin-1-yl]propane-1,2-diamine

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / kinase / phosphotransferase / TRANSFERASE-TRANSFERASE INHIBITOR complex

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