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TitleTargeting the Hinge Glycine Flip and the Activation Loop: Novel Approach to Potent p38 alpha Inhibitors.
Journal, issue, pagesJ. Med. Chem., Vol. 55, Page 7862-7874, Year 2012
Publish dateNov 30, 2011 (structure data deposition date)
AuthorsMartz, K.E. / Dorn, A. / Baur, B. / Schattel, V. / Goettert, M.I. / Mayer-Wrangowski, S.C. / Rauh, D. / Laufer, S.A.
External linksJ. Med. Chem. / PubMed:22897496
MethodsX-ray diffraction
Resolution2.4 Å
Structure data

PDB-3uvp:
Human p38 MAP Kinase in Complex with a Benzamide Substituted Benzosuberone
Method: X-RAY DIFFRACTION / Resolution: 2.4 Å

Chemicals

ChemComp-048:
N-{2-fluoro-5-[(5-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)amino]phenyl}benzamide

ChemComp-BOG:
octyl beta-D-glucopyranoside / detergent*YM

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / protein kinase / selective p38 inhibitor / SAR / benzosuberon derivative / TRANSFERASE-TRANSFERASE INHIBITOR complex

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