Search Count: 26
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Structure Of The Human Frataxin-Bound Iron-Sulfur Cluster Assembly Complex
Organism: Homo sapiens, Escherichia coli
Method: ELECTRON MICROSCOPY Release Date: 2019-05-22 Classification: TRANSFERASE, OXIDOREDUCTASE Ligands: PLP, 8Q1, ZN |
Organism: Homo sapiens, Escherichia coli
Method: ELECTRON MICROSCOPY
Release Date: 2019-05-22
Ligands: PLP, 8Q1, ZN
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Engineering Inhibitors Highly Selective For The S1 Sites Of Ser190 Trypsin-Like Serine Protease Drug Targets
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.75 Å Release Date: 2002-05-03 Classification: BLOOD CLOTTING, hydrolase Ligands: CIT, 136 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2002-05-03
Ligands: CIT, 136
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Selectivity At S1, H2O Displacement, Upa, Tpa, Ser190/Ala190 Protease, Structure-Based Drug Design
Organism: Hirudo medicinalis, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.81 Å Release Date: 2002-04-27 Classification: HYDROLASE/HYDROLASE INHIBITOR |
Organism: Hirudo medicinalis, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2002-04-27
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Selectivity At S1, H2O Displacement, Upa, Tpa, Ser190/Ala190 Protease, Structure-Based Drug Design
Organism: Hirudo medicinalis, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.73 Å Release Date: 2002-04-27 Classification: BLOOD CLOTTING,HYDROLASE/INHIBITOR |
Organism: Hirudo medicinalis, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2002-04-27
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Engineering Inhibitors Highly Selective For The S1 Sites Of Ser190 Trypsin-Like Serine Protease Drug Targets
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2002-04-27 Classification: HYDROLASE Ligands: CA, 132 |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2002-04-27
Ligands: CA, 132
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Engineering Inhibitors Highly Selective For The S1 Sites Of Ser190 Trypsin-Like Serine Protease Drug Targets
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2002-04-27 Classification: BLOOD CLOTTING, hydrolase Ligands: CIT, 132 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2002-04-27
Ligands: CIT, 132
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Engineering Inhibitors Highly Selective For The S1 Sites Of Ser190 Trypsin-Like Serine Protease Drug Targets
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.64 Å Release Date: 2002-04-27 Classification: BLOOD CLOTTING, hydrolase Ligands: CIT, 133 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2002-04-27
Ligands: CIT, 133
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Engineering Inhibitors Highly Selective For The S1 Sites Of Ser190 Trypsin-Like Serine Protease Drug Targets
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2002-04-27 Classification: BLOOD CLOTTING, hydrolase Ligands: CIT, 134 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2002-04-27
Ligands: CIT, 134
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Engineering Inhibitors Highly Selective For The S1 Sites Of Ser190 Trypsin-Like Serine Protease Drug Targets
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.56 Å Release Date: 2002-04-27 Classification: BLOOD CLOTTING, hydrolase Ligands: CIT, 135 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2002-04-27
Ligands: CIT, 135
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Engineering Inhibitors Highly Selective For The S1 Sites Of Ser190 Trypsin-Like Serine Protease Drug Targets
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2002-04-27 Classification: BLOOD CLOTTING, hydrolase Ligands: CIT, 130 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2002-04-27
Ligands: CIT, 130
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Engineering Inhibitors Highly Selective For The S1 Sites Of Ser190 Trypsin-Like Serine Protease Drug Targets
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.73 Å Release Date: 2002-04-27 Classification: BLOOD CLOTTING, hydrolase Ligands: CIT, 130 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2002-04-27
Ligands: CIT, 130
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Structural Basis For Selectivity Of A Small Molecule, S1-Binding, Sub-Micromolar Inhibitor Of Urokinase Type Plasminogen Activator
Organism: Hirudo medicinalis, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.47 Å Release Date: 2000-12-22 Classification: BLOOD CLOTTING/HYDROLASE INHIBITOR |
Organism: Hirudo medicinalis, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2000-12-22
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Structural Basis For Selectivity Of A Small Molecule, S1-Binding, Sub-Micromolar Inhibitor Of Urokinase Type Plasminogen Activator
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.95 Å Release Date: 2000-12-22 Classification: BLOOD CLOTTING |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2000-12-22
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Structural Basis For Selectivity Of A Small Molecule, S1-Binding, Sub-Micromolar Inhibitor Of Urokinase Type Plasminogen Activator
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2000-12-22 Classification: HYDROLASE/HYDROLASE INHIBITOR |
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION
Release Date: 2000-12-22
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Structural Basis For Selectivity Of A Small Molecule, S1-Binding, Sub-Micromolar Inhibitor Of Urokinase Type Plasminogen Activator
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2000-12-22 Classification: BLOOD CLOTTING/HYDROLASE INHIBITOR |
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION
Release Date: 2000-12-22
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Structural Basis For Selectivity Of A Small Molecule, S1-Binding, Sub-Micromolar Inhibitor Of Urokinase Type Plasminogen Activator
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:1.43 Å Release Date: 2000-12-22 Classification: HYDROLASE Ligands: CA, MG, SO4, BEN |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2000-12-22
Ligands: CA, MG, SO4, BEN
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Structural Basis For Selectivity Of A Small Molecule, S1-Binding, Sub-Micromolar Inhibitor Of Urokinase Type Plasminogen Activator
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:1.43 Å Release Date: 2000-12-22 Classification: HYDROLASE Ligands: CA, CL, ESI |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2000-12-22
Ligands: CA, CL, ESI
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Structural Basis For Selectivity Of A Small Molecule, S1-Binding, Sub-Micromolar Inhibitor Of Urokinase Type Plasminogen Activator
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:1.47 Å Release Date: 2000-12-22 Classification: HYDROLASE Ligands: FLC, CA, SO4, ESI |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2000-12-22
Ligands: FLC, CA, SO4, ESI
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Structural Basis For Selectivity Of A Small Molecule, S1-Binding, Sub-Micromolar Inhibitor Of Urokinase Type Plasminogen Activator
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:1.36 Å Release Date: 2000-12-22 Classification: HYDROLASE Ligands: CA, SO4, ESX |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2000-12-22
Ligands: CA, SO4, ESX
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Structural Basis For Selectivity Of A Small Molecule, S1-Binding, Sub-Micromolar Inhibitor Of Urokinase Type Plasminogen Activator
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:1.37 Å Release Date: 2000-12-22 Classification: HYDROLASE Ligands: CA, ESP |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2000-12-22
Ligands: CA, ESP