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7B3Z

Crystal structure of c-MET bound by compound 5

Summary for 7B3Z
Entry DOI10.2210/pdb7b3z/pdb
DescriptorHepatocyte growth factor receptor, DIMETHYL SULFOXIDE, 3-[3-(phenylmethyl)-1~{H}-pyrrolo[2,3-b]pyridin-5-yl]-4,5-dihydro-1~{H}-pyrrolo[3,4-b]pyrrol-6-one, ... (4 entities in total)
Functional Keywordsc-met, kinase, folded p-loop, inhibitor, transferase
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight34192.71
Authors
Collie, G.W. (deposition date: 2020-12-01, release date: 2020-12-09, Last modification date: 2024-05-01)
Primary citationCollie, 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: 33488978
DOI: 10.1021/acsmedchemlett.0c00392
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.8 Å)
Structure validation

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数据于2025-07-16公开中

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