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TitleStructure-based design and synthesis of cell active N-pyrazole, N-thiazole urea inhibitors of the MAP kinase p38alpha
Journal, issue, pagesTo be Published
Publish dateOct 29, 2010 (structure data deposition date)
AuthorsGetlik, M. / Gruetter, C. / Simard, J.R. / Van Otterlo, W. / Robubi, A. / Aust, B. / Rauh, D.
External linksSearch PubMed
MethodsX-ray diffraction
Resolution2 Å
Structure data

PDB-3pg3:
Human p38 MAP Kinase in Complex with RL182
Method: X-RAY DIFFRACTION / Resolution: 2 Å

Chemicals

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

ChemComp-DG7:
1-[3-tert-butyl-1-(4-methylphenyl)-1H-pyrazol-5-yl]-3-{4-[2-(pyridin-3-ylmethoxy)ethyl]-1,3-thiazol-2-yl}urea

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE/TRANSFERASE INHIBITOR / DFG-out / SAR / Kinase domain / Thiazole-urea / TRANSFERASE-TRANSFERASE INHIBITOR complex

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