3NDT
HIV-1 Protease Saquinavir:Ritonavir 1:1 complex structure
Summary for 3NDT
Entry DOI | 10.2210/pdb3ndt/pdb |
Related PRD ID | PRD_000454 |
Descriptor | Protease, (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, CHLORIDE ION, ... (6 entities in total) |
Functional Keywords | hydrolase, aids, aspartyl protease, carbamylation, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
Biological source | Human immunodeficiency virus type 1 BH10 (HIV-1) |
Cellular location | Matrix protein p17: Virion (Potential). Capsid protein p24: Virion (Potential). Nucleocapsid protein p7: Virion (Potential). Reverse transcriptase/ribonuclease H: Virion (Potential). Integrase: Virion (Potential): P03366 |
Total number of polymer chains | 4 |
Total formula weight | 45019.17 |
Authors | Geremia, S.,Olajuyigbe, F.M.,Demitri, N. (deposition date: 2010-06-08, release date: 2011-07-20, Last modification date: 2023-09-06) |
Primary citation | Olajuyigbe, F.M.,Demitri, N.,Geremia, S. Investigation of 2-Fold Disorder of Inhibitors and Relative Potency by Crystallizations of HIV-1 Protease in Ritonavir and Saquinavir Mixtures Cryst.Growth Des., 11:4378-4385, 2011 Cited by DOI: 10.1021/cg200514zPDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.72 Å) |
Structure validation
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