1HXW
HIV-1 PROTEASE DIMER COMPLEXED WITH A-84538
1HXW の概要
| エントリーDOI | 10.2210/pdb1hxw/pdb |
| 関連するBIRD辞書のPRD_ID | PRD_001001 |
| 分子名称 | HIV-1 PROTEASE, RITONAVIR (3 entities in total) |
| 機能のキーワード | aspartyl protease, hydrolase, aspartic proteinase, hiv, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
| 由来する生物種 | Human immunodeficiency virus 1 |
| 細胞内の位置 | Matrix protein p17: Virion (Potential). Capsid protein p24: Virion (Potential). Nucleocapsid protein p7: Virion (Potential). Reverse transcriptase/ribonuclease H: Virion (Potential). Integrase: Virion (Potential): P12499 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 22382.51 |
| 構造登録者 | |
| 主引用文献 | Kempf, D.J.,Marsh, K.C.,Denissen, J.F.,McDonald, E.,Vasavanonda, S.,Flentge, C.A.,Green, B.E.,Fino, L.,Park, C.H.,Kong, X.P. ABT-538 is a potent inhibitor of human immunodeficiency virus protease and has high oral bioavailability in humans. Proc.Natl.Acad.Sci.USA, 92:2484-2488, 1995 Cited by PubMed Abstract: Examination of the structural basis for antiviral activity, oral pharmacokinetics, and hepatic metabolism among a series of symmetry-based inhibitors of the human immunodeficiency virus (HIV) protease led to the discovery of ABT-538, a promising experimental drug for the therapeutic intervention in acquired immunodeficiency syndrome (AIDS). ABT-538 exhibited potent in vitro activity against laboratory and clinical strains of HIV-1 [50% effective concentration (EC50) = 0.022-0.13 microM] and HIV-2 (EC50 = 0.16 microM). Following a single 10-mg/kg oral dose, plasma concentrations in rat, dog, and monkey exceeded the in vitro antiviral EC50 for > 12 h. In human trials, a single 400-mg dose of ABT-538 displayed a prolonged absorption profile and achieved a peak plasma concentration in excess of 5 micrograms/ml. These findings demonstrate that high oral bioavailability can be achieved in humans with peptidomimetic inhibitors of HIV protease. PubMed: 7708670DOI: 10.1073/pnas.92.7.2484 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.8 Å) |
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