Pim-1 Ligand-bound Structures Reveal the Mechanism of Serine/Threonine Kinase Inhibition by LY294002
Models, Molecular
0301 basic medicine
Adenosine
Binding Sites
Molecular Structure
Protein Conformation
Morpholines
Molecular Sequence Data
Hydrogen Bonding
Protein Serine-Threonine Kinases
Ligands
Cyclic AMP-Dependent Protein Kinases
3. Good health
Phosphatidylinositol 3-Kinases
03 medical and health sciences
Proto-Oncogene Proteins c-pim-1
Chromones
Proto-Oncogene Proteins
Humans
Amino Acid Sequence
Enzyme Inhibitors
Sequence Alignment
Protein Binding
DOI:
10.1074/jbc.m413155200
Publication Date:
2005-01-19T02:57:33Z
AUTHORS (7)
ABSTRACT
Pim-1 is an oncogene-encoded serine/threonine kinase primarily expressed in hematopoietic and germ cell lines. Pim-1 kinase was originally identified in Maloney murine leukemia virus-induced T-cell lymphomas and is associated with multiple cellular functions such as proliferation, survival, differentiation, apoptosis, and tumorigenesis (Wang, Z., Bhattacharya, N., Weaver, M., Petersen, K., Meyer, M., Gapter, L., and Magnuson, N. S. (2001) J. Vet. Sci. 2, 167-179). The crystal structures of Pim-1 complexed with staurosporine and adenosine were determined. Although a typical two-domain serine/threonine protein kinase fold is observed, the inter-domain hinge region is unusual in both sequence and conformation; a two-residue insertion causes the hinge to bulge away from the ATP-binding pocket, and a proline residue in the hinge removes a conserved main chain hydrogen bond donor. Without this hydrogen bond, van der Waals interactions with the hinge serve to position the ligand. The hinge region of Pim-1 resembles that of phosphatidylinositol 3-kinase more closely than it does other protein kinases. Although the phosphatidylinositol 3-kinase inhibitor LY294002 also inhibits Pim-1, the structure of the LY294002.Pim-1 complex reveals a new binding mode that may be general for Ser/Thr kinases.
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