3LW0
IGF-1RK in complex with ligand MSC1609119A-1
Summary for 3LW0
Entry DOI | 10.2210/pdb3lw0/pdb |
Descriptor | Insulin-like growth factor 1 receptor, 3-cyano-N-{1-[4-(5-cyano-1H-indol-3-yl)butyl]piperidin-4-yl}-1H-indole-7-carboxamide, GLYCEROL, ... (4 entities in total) |
Functional Keywords | protein kinase, transferase |
Biological source | Homo sapiens (human) |
Total number of polymer chains | 4 |
Total formula weight | 142331.72 |
Authors | Graedler, U.,Heinrich, T.,Boettcher, H.,Blaukat, A.,Shutes, A.,Askew, B. (deposition date: 2010-02-23, release date: 2010-09-29, Last modification date: 2023-11-01) |
Primary citation | Heinrich, T.,Gradler, U.,Bottcher, H.,Blaukat, A.,Shutes, A. Allosteric IGF-1R Inhibitors. Acs Med.Chem.Lett., 1:199-203, 2010 Cited by PubMed Abstract: Targeting allosteric protein sites is a promising approach to interfere selectively with cellular signaling cascades. We have discovered a novel class of allosteric insulin-like growth factor-I receptor (IGF-1R) inhibitors. 3-Cyano-1H-indole-7-carboxylic acid {1-[4-(5-cyano-1H-indol-3-yl)butyl]piperidin-4-yl}amide (10) was found with nanomolar biochemical, micromolar, cellular IGF-1R activity and no relevant interference with cellular insulin receptor signaling up to 30 μM. The allosteric binding site was characterized by X-ray crystallographic studies, and the structural information was used to explain the unique mode of action of this new class of inhibitors. PubMed: 24900194DOI: 10.1021/ml100044h PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.79 Å) |
Structure validation
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