Search Count: 5
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Crystal Structure Of Human Chymase In Complex With Fragment Inhibitor 6-Chloro-1,3-Dihydro-2H-Indol-2-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2013-05-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, NAG, ES2 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-05-29
Ligands: ZN, NAG, ES2
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Crystal Structure Of Human Chymase In Complex With Fragment Inhibitor 6-Chloro-2,3-Dihydro-1H-Isoindol-1-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2013-05-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: NAG, ZN, 1P7 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-05-29
Ligands: NAG, ZN, 1P7
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Crystal Structure Of Human Chymase In Complex With Fragment 6-Bromo-1,3-Dihydro-2H-Indol-2-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2013-05-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: NAG, ZN, 1P8 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-05-29
Ligands: NAG, ZN, 1P8
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Crystal Structure Of Human Chymase In Complex With Fragment Linked Benzimidazolone Inhibitor: (3S)-3-{3-[(6-Bromo-2-Oxo-2,3-Dihydro-1H-Indol-4-Yl)Methyl]-2-Oxo-2,3-Dihydro-1H-Benzimidazol-1-Yl}Hexanoic Acid
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2013-05-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, NAG, 1P9 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-05-29
Ligands: ZN, NAG, 1P9
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Crystal Structure Of Human Chymase With Benzimidazolone Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.95 Å Release Date: 2011-07-20 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: NAG, ZN, 0BB |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-07-20
Ligands: NAG, ZN, 0BB