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3OXC

Wild Type HIV-1 Protease with Antiviral Drug Saquinavir

Replaces:  2NMW
Summary for 3OXC
Entry DOI10.2210/pdb3oxc/pdb
Related2IEN 2NMY 2NMZ 2NNK 2NNP 3CYX 3D1X 3D1Y 3MWS 3NU3
Related PRD IDPRD_000454
DescriptorProtease, (2S)-N-[(2S,3R)-4-[(2S,3S,4aS,8aS)-3-(tert-butylcarbamoyl)-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]-3-hydroxy-1 -phenyl-butan-2-yl]-2-(quinolin-2-ylcarbonylamino)butanediamide, FORMIC ACID, ... (5 entities in total)
Functional Keywordsenzyme inhibition, aspartic protease, hiv/aids, saquinavir, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHuman immunodeficiency virus 1
Total number of polymer chains2
Total formula weight22436.37
Authors
Kovalevsky, A.Y.,Wang, Y.-F.,Tie, Y.,Weber, I.T. (deposition date: 2010-09-21, release date: 2010-11-10, Last modification date: 2023-09-06)
Primary citationKovalevsky, A.Y.,Wang, Y.-F.,Tie, Y.,Weber, I.T.
Atomic resolution crystal structures of HIV-1 protease and mutants V82A and I84V with saquinavir
Proteins, 67:232-242, 2007
Cited by
PubMed: 17243183
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.16 Å)
Structure validation

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