1D4Y
HIV-1 PROTEASE TRIPLE MUTANT/TIPRANAVIR COMPLEX
Summary for 1D4Y
Entry DOI | 10.2210/pdb1d4y/pdb |
Related | 1D4S |
Descriptor | PROTEIN (HIV-1 PROTEASE), N-(3-{(1R)-1-[(6R)-4-HYDROXY-2-OXO-6-PHENETHYL-6-PROPYL-5,6-DIHYDRO-2H-PYRAN-3-YL]PROPYL}PHENYL)-5-(TRIFLUOROMETHYL)-2-PYRIDINESULFONAMIDE (3 entities in total) |
Functional Keywords | hydrolase, acid protease, aspartyl protease |
Biological source | Human immunodeficiency virus 1 |
Cellular location | Gag-Pol polyprotein: Host cell membrane ; Lipid-anchor. Matrix protein p17: Virion membrane; Lipid- anchor . Capsid protein p24: Virion . Nucleocapsid protein p7: Virion . Reverse transcriptase/ribonuclease H: Virion . Integrase: Virion : P03367 |
Total number of polymer chains | 2 |
Total formula weight | 22212.28 |
Authors | Watenpaugh, K.D.,Janakiraman, M.N. (deposition date: 1999-10-06, release date: 1999-10-13, Last modification date: 2024-02-07) |
Primary citation | Thaisrivongs, S.,Skulnick, H.I.,Turner, S.R.,Strohbach, J.W.,Tommasi, R.A.,Johnson, P.D.,Aristoff, P.A.,Judge, T.M.,Gammill, R.B.,Morris, J.K.,Romines, K.R.,Chrusciel, R.A.,Hinshaw, R.R.,Chong, K.T.,Tarpley, W.G.,Poppe, S.M.,Slade, D.E.,Lynn, J.C.,Horng, M.M.,Tomich, P.K.,Seest, E.P.,Dolak, L.A.,Howe, W.J.,Howard, G.M.,Watenpaugh, K.D. Structure-based design of HIV protease inhibitors: sulfonamide-containing 5,6-dihydro-4-hydroxy-2-pyrones as non-peptidic inhibitors. J.Med.Chem., 39:4349-4353, 1996 Cited by PubMed: 8893827DOI: 10.1021/jm960541s PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.97 Å) |
Structure validation
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