Search Count: 15
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Crystal Structure Of Human Cathepsin S Bound To A Non-Covalent Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2014-10-29 Classification: hydrolase/hydrolase inhibitor Ligands: SO4, 2FC |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-10-29
Ligands: SO4, 2FC
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Crystal Structure Of Human Cathepsin S Bound To A Non-Covalent Inhibitor.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.58 Å Release Date: 2014-10-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 2FZ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-10-29
Ligands: 2FZ
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Porcine Factor Ixa Complexed To 1-{3-[Amino(Imino)Methyl]Phenyl}-N-[4-(1H-Benzimidazol-1-Yl)-2-Fluorophenyl]-3-(Trifluoromethyl)-1H-Pyrazole-5-Carboxamide
Organism: Sus scrofa
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2005-08-16 Classification: blood clotting,hydrolase Ligands: 187 |
Organism: Sus scrofa
Method: X-RAY DIFFRACTION
Release Date: 2005-08-16
Ligands: 187
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Molecular Recognition Of Cyclic Urea Hiv Protease Inhibitors
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 1999-03-23 Classification: ASPARTYL PROTEASE Ligands: 216 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1999-03-23
Ligands: 216
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Nonpeptide Cyclic Cyanoguanidines As Hiv Protease Inhibitors
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 1998-12-30 Classification: ACID PROTEASE Ligands: Q82 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1998-12-30
Ligands: Q82
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Hiv-1 Protease (V82F/I84V) Double Mutant Complexed With Xv638 Of Dupont Pharmaceuticals
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 1998-10-30 Classification: HYDROLASE Ligands: XV6 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1998-10-30
Ligands: XV6
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Counteracting Hiv-1 Protease Drug Resistance: Structural Analysis Of Mutant Proteases Complexed With Xv638 And Sd146, Cyclic Urea Amides With Broad Specificities
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 1998-09-30 Classification: HYDROLASE Ligands: XV6 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1998-09-30
Ligands: XV6
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Hiv-1 Protease (I84V) Complexed With Xv638 Of Dupont Pharmaceuticals
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 1998-09-30 Classification: HYDROLASE Ligands: XV6 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1998-09-30
Ligands: XV6
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Hiv-1 Protease (V82F/I84V) Double Mutant Complexed With Sd146 Of Dupont Pharmaceuticals
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 1998-09-30 Classification: HYDROLASE Ligands: 146 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1998-09-30
Ligands: 146
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Structure Of Hiv-1 Protease Complex
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 1997-11-12 Classification: ASPARTYL PROTEINASE Ligands: DMQ |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1997-11-12
Ligands: DMQ
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Hiv-1 Protease Inhibitors Wiih Low Nanomolar Potency
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 1997-10-15 Classification: ASPARTYL PROTEASE Ligands: XV6 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1997-10-15
Ligands: XV6
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Hiv-1 Protease Inhibitors Wiih Low Nanomolar Potency
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 1997-10-15 Classification: ASPARTYL PROTEASE Ligands: DMP |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1997-10-15
Ligands: DMP
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Hiv-1 Protease Inhibitors Wiih Low Nanomolar Potency
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 1997-10-15 Classification: ASPARTYL PROTEASE Ligands: 146 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1997-10-15
Ligands: 146
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Hiv-1 Protease Inhibitors Wiih Low Nanomolar Potency
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 1997-10-15 Classification: ASPARTYL PROTEASE Ligands: 846 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1997-10-15
Ligands: 846
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Rational Design Of Potent, Bioavailable, Nonpeptide Cyclic Ureas As Hiv Protease Inhibitors
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 1995-01-26 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: XK2 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1995-01-26
Ligands: XK2