1di9
THE STRUCTURE OF P38 MITOGEN-ACTIVATED PROTEIN KINASE IN COMPLEX WITH 4-[3-METHYLSULFANYLANILINO]-6,7-DIMETHOXYQUINAZOLINE
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OverviewOverview
4-Anilinoquinazolines represent an important class of protein kinase, inhibitor. Modes of binding for two members of this inhibitor class were, determined by X-ray crystallographic analysis of one inhibitor, (4-[3-hydroxyanilino]-6,7-dimethoxyquinazoline) in complex with, cyclin-dependent kinase 2 (CDK2) and the other, (4-[3-methylsulfanylanilino]-6,7-dimethoxyquinazoline) in complex with p38, kinase. In both inhibitor/kinase structures, the 4-anilinoquinazoline was, bound in the ATP site with the quinazoline ring system oriented along the, peptide strand that links the two domains of the protein and with the, anilino substituent projecting into a hydrophobic pocket within the, protein interior. In each case, the nitrogen at position-1 of the, quinazoline accepted a hydrogen bond from a backbone NH (CDK2, Leu-83;, p38, Met-109) of the domain connector strand, and aromatic hydrogen atoms, at C2 and C8 interacted with backbone carbonyl oxygen atoms of the peptide, strand. The anilino group of the CDK2-bound compound was essentially, coplanar with the quinazoline ring system and occupied a pocket between, Lys-33 and Phe-80. For the p38-bound inhibitor, the anilino group was, angled out of plane and was positioned between Lys-53 and Thr-106 in a, manner similar to that observed for the aryl substituent of the, pyridinylimidazole class of inhibitor.
About this StructureAbout this Structure
1DI9 is a Single protein structure of sequence from Homo sapiens with MSQ as ligand. Full crystallographic information is available from OCA.
ReferenceReference
Binding mode of the 4-anilinoquinazoline class of protein kinase inhibitor: X-ray crystallographic studies of 4-anilinoquinazolines bound to cyclin-dependent kinase 2 and p38 kinase., Shewchuk L, Hassell A, Wisely B, Rocque W, Holmes W, Veal J, Kuyper LF, J Med Chem. 2000 Jan 13;43(1):133-8. PMID:10633045
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