Search Count: 3
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Crystallographic Analysis At 3.0-Angstroms Resolution Of The Binding To Human Thrombin Of Four Active Site-Directed Inhibitors
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION Resolution:3.00 Å Release Date: 1994-01-31 Classification: HYDROLASE/HYROLASE INHIBITOR Ligands: MID |
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION
Release Date: 1994-01-31
Ligands: MID
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Refined 2.3 Angstroms X-Ray Crystal Structure Of Bovine Thrombin Complexes Formed With The Benzamidine And Arginine-Based Thrombin Inhibitors Napap, 4-Tapap And Mqpa: A Starting Point For Improving Antithrombotics
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 1994-01-31 Classification: HYDROLASE/HYDROLASE inhibitor Ligands: MID |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 1994-01-31
Ligands: MID
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Geometry Of Binding Of The Benzamidine-And Arginine-Based Inhibitors N-Alpha-(2-Naphthyl-Sulphonyl-Glycyl)-Dl-P-Amidinophenylalanyl-Piperidine (Napap) And (2R,4R)-4-Methyl-1-[N-Alpha-(3-Methyl-1,2,3,4-Tetrahydro-8-Quinolinesulphonyl)-L-Arginyl]-2-Piperidine Carboxylic Acid (Mqpa) To Human Alpha-Thrombin: X-Ray Crystallographic Determination Of The Napap-Trypsin Complex And Modeling Of Napap-Thrombin And Mqpa-Thrombin
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 1994-01-31 Classification: HYDROLASE/hydrolase inhibitor Ligands: MID, CA |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 1994-01-31
Ligands: MID, CA