1JLD
Potent hiv protease inhibitors containing a novel (hydroxyethyl)amide isostere
Summary for 1JLD
Entry DOI | 10.2210/pdb1jld/pdb |
Related PRD ID | PRD_000341 |
Descriptor | Pol polyprotein, (2S)-2-tert-butyl-N~4~-(1-ethylpropyl)-N~1~-[(2R,3S)-2-hydroxy-4-phenyl-3-{[N-(quinolin-2-ylcarbonyl)-L-threonyl]amino}butyl]butanediamide (3 entities in total) |
Functional Keywords | polyprotein, hiv-2 protease, hydrolase-hydrolase inhibitor complex, aids, hydrolase/hydrolase inhibitor |
Biological source | Human immunodeficiency virus 2 |
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): Q7SKJ2 |
Total number of polymer chains | 2 |
Total formula weight | 22118.50 |
Authors | Tong, L. (deposition date: 1997-05-31, release date: 1997-12-03, Last modification date: 2024-02-07) |
Primary citation | Beaulieu, P.L.,Wernic, D.,Abraham, A.,Anderson, P.C.,Bogri, T.,Bousquet, Y.,Croteau, G.,Guse, I.,Lamarre, D.,Liard, F.,Paris, W.,Thibeault, D.,Pav, S.,Tong, L. Potent HIV protease inhibitors containing a novel (hydroxyethyl)amide isostere. J.Med.Chem., 40:2164-2176, 1997 Cited by PubMed: 9216835DOI: 10.1021/jm9606608 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.5 Å) |
Structure validation
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