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TitleContinued exploration of the triazolopyridine scaffold as a platform for p38 MAP kinase inhibition.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 20, Page 469-473, Year 2010
Publish dateOct 27, 2009 (structure data deposition date)
AuthorsJerome, K.D. / Rucker, P.V. / Xing, L. / Shieh, H.S. / Baldus, J.E. / Selness, S.R. / Letavic, M.A. / Braganza, J.F. / McClure, K.F.
External linksBioorg. Med. Chem. Lett. / PubMed:19969459
MethodsX-ray diffraction
Resolution2 Å
Structure data

PDB-3kf7:
Crystal Structure of Human p38alpha Complexed With a Triazolopyrimidine compound
Method: X-RAY DIFFRACTION / Resolution: 2 Å

Chemicals

ChemComp-L9G:
3-{6-[2-(2,4-difluorophenyl)ethyl][1,2,4]triazolo[4,3-a]pyridin-3-yl}-4-methylbenzamide

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / two lobes / ATP pocket / peptide flip / ATP-binding / Kinase / Nucleotide-binding / Nucleus / Phosphoprotein / Serine/threonine-protein kinase

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