3EC0
High Resolution HIV-2 Protease Structure in Complex with Antiviral Inhibitor GRL-06579A
Summary for 3EC0
Entry DOI | 10.2210/pdb3ec0/pdb |
Related | 3EBZ |
Descriptor | Protease, (3AS,5R,6AR)-HEXAHYDRO-2H-CYCLOPENTA[B]FURAN-5-YL (2S,3S)-3-HYDROXY-4-(4-(HYDROXYMETHYL)-N-ISOBUTYLPHENYLSULFONAMIDO)-1-PHENYLBUTAN-2-YLCARBAMATE, IMIDAZOLE, ... (7 entities in total) |
Functional Keywords | hiv-2, aspartic protease, inhibitor, protease-inhibitor complex, hydrolase |
Biological source | Human immunodeficiency virus type 2 (ISOLATE ROD) |
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): P04584 |
Total number of polymer chains | 2 |
Total formula weight | 23392.59 |
Authors | Kovalevsky, A.Y.,Weber, I.T. (deposition date: 2008-08-28, release date: 2008-09-16, Last modification date: 2023-11-01) |
Primary citation | Kovalevsky, A.Y.,Louis, J.M.,Aniana, A.,Ghosh, A.K.,Weber, I.T. Structural evidence for effectiveness of darunavir and two related antiviral inhibitors against HIV-2 protease J.Mol.Biol., 384:178-192, 2008 Cited by PubMed: 18834890DOI: 10.1016/j.jmb.2008.09.031 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.18 Å) |
Structure validation
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