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4I8W

Crystal structure of wild type HIV-1 protease in complex with non-peptidic inhibitor, GRL007

Summary for 4I8W
Entry DOI10.2210/pdb4i8w/pdb
Related4HLA 4I8Z
DescriptorProtease, 4-{[(2R,3S)-3-({[(3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yloxy]carbonyl}amino)-2-hydroxy-4-phenylbutyl](2-methylpropyl)sulfamoyl}benzoic acid (3 entities in total)
Functional Keywordshiv-1 protease, hiv-1 protease-inhibitor complex, hydrolase, grl007, protease inhibitor, non-peptidic protease inhibitor, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHuman immunodeficiency virus type 1 (HIV-1)
Cellular locationMatrix protein p17: Virion (Potential). Capsid protein p24: Virion (Potential). Nucleocapsid protein p7: Virion (Potential). Reverse transcriptase/ribonuclease H: Virion (Potential). Integrase: Virion (Potential): P0C6F2
Total number of polymer chains2
Total formula weight22184.17
Authors
Yedidi, R.S.,Palmer, I.,Das, D.,Wingfield, P.T.,Ghosh, A.K.,Mitsuya, H. (deposition date: 2012-12-04, release date: 2013-07-24, Last modification date: 2024-02-28)
Primary citationYedidi, R.S.,Maeda, K.,Fyvie, W.S.,Steffey, M.,Davis, D.A.,Palmer, I.,Aoki, M.,Kaufman, J.D.,Stahl, S.J.,Garimella, H.,Das, D.,Wingfield, P.T.,Ghosh, A.K.,Mitsuya, H.
P2' benzene carboxylic acid moiety is associated with decrease in cellular uptake: evaluation of novel non-peptidic HIV-1 protease inhibitors containing P2 bis-tetrahydrofuran moiety.
Antimicrob.Agents Chemother., 57:4920-4927, 2013
Cited by
PubMed: 23877703
DOI: 10.1128/AAC.00868-13
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.96 Å)
Structure validation

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