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Structure paper

TitleInhibition of p38 MAP kinase by utilizing a novel allosteric binding site.
Journal, issue, pagesNat. Struct. Biol., Vol. 9, Page 268-272, Year 2002
Publish dateJan 23, 2002 (structure data deposition date)
AuthorsPargellis, C. / Tong, L. / Churchill, L. / Cirillo, P.F. / Gilmore, T. / Graham, A.G. / Grob, P.M. / Hickey, E.R. / Moss, N. / Pav, S. / Regan, J.
External linksNat. Struct. Biol. / PubMed:11896401
MethodsX-ray diffraction
Resolution2.5 - 2.8 Å
Structure data

PDB-1kv1:
p38 MAP Kinase in Complex with Inhibitor 1
Method: X-RAY DIFFRACTION / Resolution: 2.5 Å

PDB-1kv2:
Human p38 MAP Kinase in Complex with BIRB 796
Method: X-RAY DIFFRACTION / Resolution: 2.8 Å

Chemicals

ChemComp-BMU:
1-(5-TERT-BUTYL-2-METHYL-2H-PYRAZOL-3-YL)-3-(4-CHLORO-PHENYL)-UREA

ChemComp-HOH:
WATER

ChemComp-B96:
1-(5-TERT-BUTYL-2-P-TOLYL-2H-PYRAZOL-3-YL)-3-[4-(2-MORPHOLIN-4-YL-ETHOXY)-NAPHTHALEN-1-YL]-UREA

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / protein-inhibitor complex

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