5JFU
HIV-1 wild Type protease with GRL-007-14A (a Adamantane P1-Ligand with bis-THF in P2 and benzylamine in P1')
Summary for 5JFU
Entry DOI | 10.2210/pdb5jfu/pdb |
Related | 2IEN 5JFP 5JG1 |
Descriptor | Protease, CHLORIDE ION, (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl {(2S,3R)-4-{benzyl[(4-methoxyphenyl)sulfonyl]amino}-3-hydroxy-1-[(3R,5R,7R)-tricyclo[3.3.1.1~3,7~]decan-1-yl]butan-2-yl}carbamate, ... (4 entities in total) |
Functional Keywords | adamantane, hiv-1 protease inhibitor grl-007-14a, darunavir, multidrug-resistant, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
Biological source | Human immunodeficiency virus 1 |
Total number of polymer chains | 2 |
Total formula weight | 22207.07 |
Authors | Wang, Y.-F.,Agniswamy, J.,Weber, I.T. (deposition date: 2016-04-19, release date: 2016-09-21, Last modification date: 2023-09-27) |
Primary citation | Ghosh, A.K.,Osswald, H.L.,Glauninger, K.,Agniswamy, J.,Wang, Y.F.,Hayashi, H.,Aoki, M.,Weber, I.T.,Mitsuya, H. Probing Lipophilic Adamantyl Group as the P1-Ligand for HIV-1 Protease Inhibitors: Design, Synthesis, Protein X-ray Structural Studies, and Biological Evaluation. J.Med.Chem., 59:6826-6837, 2016 Cited by PubMed: 27389367DOI: 10.1021/acs.jmedchem.6b00639 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.7 Å) |
Structure validation
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