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8AN8

Crystal structure of wild-type c-MET bound by compound 7.

Summary for 8AN8
Entry DOI10.2210/pdb8an8/pdb
DescriptorHepatocyte growth factor receptor, SULFATE ION, 3-[bis(fluoranyl)methyl]-~{N}-methyl-~{N}-[(1~{R})-8-methyl-5-(3-methyl-1~{H}-indazol-6-yl)-1,2,3,4-tetrahydronaphthalen-1-yl]pyridine-2-carboxamide, ... (4 entities in total)
Functional Keywordskinase, inhibitor, ac-helix, cancer, transferase
Biological sourceHomo sapiens (human)
Total number of polymer chains2
Total formula weight68345.08
Authors
Collie, G.W. (deposition date: 2022-08-04, release date: 2022-08-31, Last modification date: 2024-03-27)
Primary citationCollie, G.W.,Barlind, L.,Bazzaz, S.,Borjesson, U.,Dale, I.L.,Disch, J.S.,Habeshian, S.,Jetson, R.,Khurana, P.,Madin, A.,Michaelides, I.N.,Peng, L.,Snijder, A.,Stubbs, C.J.
Discovery of a selective c-MET inhibitor with a novel binding mode.
Bioorg.Med.Chem.Lett., 75:128948-128948, 2022
Cited by
PubMed: 35987508
DOI: 10.1016/j.bmcl.2022.128948
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.394 Å)
Structure validation

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