Search Count: 11
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X-Ray Crystal Structure Of Staphylococcus Aureus Fema
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2002-09-04 Classification: ANTIBIOTIC INHIBITOR |
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION
Release Date: 2002-09-04
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Crystal Structure Of S. Aureus Peptide Deformylase
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2002-06-12 Classification: HYDROLASE Ligands: ZN |
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION
Release Date: 2002-06-12
Ligands: ZN
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Mac-1 I Domain Magnesium Complex
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 1998-11-04 Classification: CELL ADHESION Ligands: MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 1998-11-04
Ligands: MG
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Mac-1 I Domain Cadmium Complex
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 1998-11-04 Classification: CELL ADHESION Ligands: CD, ACE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 1998-11-04
Ligands: CD, ACE
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Mac-1 I Domain Metal Free
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 1998-11-04 Classification: CELL ADHESION |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 1998-11-04
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Hiv-1 Protease Complex With U095438 [3-[1-(4-Bromophenyl) Isobutyl]-4-Hydroxycoumarin
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:2.22 Å Release Date: 1996-10-14 Classification: HYDROLASE (ACID PROTEASE) Ligands: U01 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1996-10-14
Ligands: U01
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Hiv-1 Protease Complex With U100313 ([3-[[3-[Cyclopropyl [4-Hydroxy-2Oxo-6-[1-(Phenylmethyl)Propyl]-2H-Pyran-3-Yl] Methyl]Phenyl]Amino]-3-Oxo-Propyl]Carbamic Acid Tert-Butyl Ester)
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:3.00 Å Release Date: 1996-10-14 Classification: HYDROLASE (ACID PROTEASE) Ligands: U02 |
Organism: Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 1996-10-14
Ligands: U02
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Human Immunodeficiency Virus Type 2 Protease Mutant With Lys 57 Replaced By Leu (K57L) Complex With U096333 [4-Hydroxy-3-[1-(Phenyl)Propyl]-7-Methoxycoumarin]
Organism: Human immunodeficiency virus 2
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 1996-10-14 Classification: HYDROLASE (ACID PROTEASE) Ligands: U03 |
Organism: Human immunodeficiency virus 2
Method: X-RAY DIFFRACTION
Release Date: 1996-10-14
Ligands: U03
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Human Immunodeficiency Virus Type 2 Protease Mutant With Lys 57 Replaced By Leu (K57L) Complex With U097410 [4-Hydroxy-3-[1-[3-[[[[(Tert-Butyloxycarbonyl) Aminomethyl]Carbonyl]Amino]Phenyl]Propyl]Coumarin
Organism: Human immunodeficiency virus 2
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 1996-10-14 Classification: HYDROLASE (ACID PROTEASE) Ligands: U04 |
Organism: Human immunodeficiency virus 2
Method: X-RAY DIFFRACTION
Release Date: 1996-10-14
Ligands: U04
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The Crystallographic Structure Of The Protease From Human Immunodeficiency Virus Type 2 With Two Synthetic Peptidic Transition State Analog Inhibitors
Organism: Human immunodeficiency virus 2
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 1993-07-15 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 1ZK |
Organism: Human immunodeficiency virus 2
Method: X-RAY DIFFRACTION
Release Date: 1993-07-15
Ligands: 1ZK
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The Crystallographic Structure Of The Protease From Human Immunodeficiency Virus Type 2 With Two Synthetic Peptidic Transition State Analog Inhibitors
Organism: Human immunodeficiency virus 2
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 1993-07-15 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 0PX |
Organism: Human immunodeficiency virus 2
Method: X-RAY DIFFRACTION
Release Date: 1993-07-15
Ligands: 0PX