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2P3C

Crystal Structure of the subtype F wild type HIV protease complexed with TL-3 inhibitor

Summary for 2P3C
Entry DOI10.2210/pdb2p3c/pdb
Related2P3A 2P3B
Related PRD IDPRD_000434
Descriptorprotease, benzyl [(1S,4S,7S,8R,9R,10S,13S,16S)-7,10-dibenzyl-8,9-dihydroxy-1,16-dimethyl-4,13-bis(1-methylethyl)-2,5,12,15,18-pentaoxo-20-phenyl-19-oxa-3,6,11,14,17-pentaazaicos-1-yl]carbamate, ACETIC ACID, ... (4 entities in total)
Functional Keywordswild type subtype f hiv protease, tl-3 inhibitor, non-b hiv protease, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor
Biological sourceHuman immunodeficiency virus 1
Total number of polymer chains2
Total formula weight22570.71
Authors
Sanches, M.,Krauchenco, S.,Martins, N.H.,Gustchina, A.,Wlodawer, A.,Polikarpov, I. (deposition date: 2007-03-08, release date: 2007-04-24, Last modification date: 2024-04-03)
Primary citationSanches, M.,Krauchenco, S.,Martins, N.H.,Gustchina, A.,Wlodawer, A.,Polikarpov, I.
Structural Characterization of B and non-B Subtypes of HIV-Protease: Insights into the Natural Susceptibility to Drug Resistance Development.
J.Mol.Biol., 369:1029-1040, 2007
Cited by
PubMed: 17467738
DOI: 10.1016/j.jmb.2007.03.049
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

218853

數據於2024-04-24公開中

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