Crystal structure of hH-PGDS with water displacing inhibitor
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Crystal structure of hH-PGDS with water displacing inhibitor Descriptor: 4-(isoquinolin-1-yl)-N-[2-(morpholin-4-yl)ethyl]benzamide, Hematopoietic prostaglandin D synthase, L-GAMMA-GLUTAMYL-3-SULFINO-L-ALANYLGLYCINE, ... Authors: Day, J.E, Thorarensen, A, Trujillo, J.I. Deposit date: 2012-03-28 Release date: 2012-07-18 Last modified: 2024-02-28 Method: X-RAY DIFFRACTION (1.75 Å) Cite: Investigation of the binding pocket of human hematopoietic prostaglandin (PG) D2 synthase (hH-PGDS): a tale of two waters. Bioorg.Med.Chem.Lett., 22, 2012
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2012-03-28
