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2FDE

Wild type HIV protease bound with GW0385

Summary for 2FDE
Entry DOI10.2210/pdb2fde/pdb
Related2FDD
DescriptorGag-Pol polyprotein, POTASSIUM ION, (3R,3AS,6AR)-HEXAHYDROFURO[2,3-B]FURAN-3-YL [(1S,2R)-3-[(1,3-BENZODIOXOL-5-YLSULFONYL)(ISOBUTYL)AMINO]-2-HYDROXY-1-{4-[(2-METHYL-1,3-THIAZOL-4-YL)METHOXY]BENZYL}PROPYL]CARBAMATE, ... (4 entities in total)
Functional Keywordshiv protease, inhibitor, gw0385, hydrolase
Biological sourceHuman immunodeficiency virus 1
Total number of polymer chains2
Total formula weight22730.12
Authors
Xu, R.X. (deposition date: 2005-12-13, release date: 2006-02-21, Last modification date: 2024-02-14)
Primary citationMiller, J.F.,Andrews, C.W.,Brieger, M.,Furfine, E.S.,Hale, M.R.,Hanlon, M.H.,Hazen, R.J.,Kaldor, I.,McLean, E.W.,Reynolds, D.,Sammond, D.M.,Spaltenstein, A.,Tung, R.,Turner, E.M.,Xu, R.X.,Sherrill, R.G.
Ultra-potent P1 modified arylsulfonamide HIV protease inhibitors: The discovery of GW0385.
Bioorg.Med.Chem.Lett., 16:1788-1794, 2006
Cited by
PubMed: 16458505
DOI: 10.1016/j.bmcl.2006.01.035
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.7 Å)
Structure validation

218853

數據於2024-04-24公開中

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