7B3Q
Crystal structure of c-MET bound by compound 1
Summary for 7B3Q
Entry DOI | 10.2210/pdb7b3q/pdb |
Descriptor | Hepatocyte growth factor receptor, 1-(phenylmethyl)-5~{H}-pyrrolo[3,2-c]pyridin-4-one, SULFATE ION, ... (4 entities in total) |
Functional Keywords | c-met, kinase, folded p-loop, inhibitor, transferase |
Biological source | Homo sapiens (Human) |
Total number of polymer chains | 1 |
Total formula weight | 34106.53 |
Authors | Collie, G.W. (deposition date: 2020-12-01, release date: 2020-12-09, Last modification date: 2024-05-01) |
Primary citation | Collie, G.W.,Michaelides, I.N.,Embrey, K.,Stubbs, C.J.,Borjesson, U.,Dale, I.L.,Snijder, A.,Barlind, L.,Song, K.,Khurana, P.,Phillips, C.,Storer, R.I. Structural Basis for Targeting the Folded P-Loop Conformation of c-MET. Acs Med.Chem.Lett., 12:162-167, 2021 Cited by PubMed Abstract: We report here a fragment screen directed toward the c-MET kinase from which we discovered a series of inhibitors able to bind to a rare conformation of the protein in which the P-loop adopts a collapsed, or folded, arrangement. Preliminary SAR exploration led to an inhibitor () with nanomolar biochemical activity against c-MET and promising cell activity and kinase selectivity. These findings increase our structural understanding of the folded P-loop conformation of c-MET and provide a sound structural and chemical basis for further investigation of this underexplored yet potentially therapeutically exploitable conformational state. PubMed: 33488978DOI: 10.1021/acsmedchemlett.0c00392 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.75 Å) |
Structure validation
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