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7CP3

Crystal Structure of PAK4 in complex with inhibitor 47

Summary for 7CP3
Entry DOI10.2210/pdb7cp3/pdb
DescriptorSerine/threonine-protein kinase PAK 4, [(3R)-3-azanylpiperidin-1-yl]-[1-(2-azanylpyrimidin-4-yl)-6-[2-(1-oxidanylcyclohexyl)ethynyl]indol-3-yl]methanone (2 entities in total)
Functional Keywordsatp binding pocket, transferase
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight33469.93
Authors
Zhao, F.,Li, H. (deposition date: 2020-08-05, release date: 2021-08-11, Last modification date: 2023-11-29)
Primary citationSong, P.,Zhao, F.,Cheng, M.
Discovery of 6-ethynyl-1H-indole-3-carboxamide Derivatives as Highly Potent and Selective p21-Activated Kinase 4 (PAK4) Inhibitors
to be published,
Experimental method
X-RAY DIFFRACTION (2.9 Å)
Structure validation

223166

건을2024-07-31부터공개중

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