Search Count: 12
 |
Crystal Structure Of Sting In Complex With E7766
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.38 Å Release Date: 2021-02-17 Classification: IMMUNE SYSTEM Ligands: V5V |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-02-17
Ligands: V5V
 |
Crystal Structure Of Sting Ref Variant In Complex With E7766
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.77 Å Release Date: 2021-02-17 Classification: IMMUNE SYSTEM Ligands: V5V, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-02-17
Ligands: V5V, EDO
 |
Estrogen Receptor Alpha Y537S Covalently Bound To Antagonist H3B-5942.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.89 Å Release Date: 2018-03-21 Classification: nuclear protein/antagonist Ligands: F3D, EDO, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-03-21
Ligands: F3D, EDO, DMS
 |
Estrogen Receptor Alpha Y537S Bound To Antagonist H3B-9224.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.68 Å Release Date: 2018-03-21 Classification: nuclear protein/antagonist Ligands: F3D, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-03-21
Ligands: F3D, EDO
 |
Crystal Structure Of Fgfr1-Y563C (Fgfr4 Surrogate) Covalently Bound To H3B-6527
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2017-05-24 Classification: transferase/transferase inhibitor Ligands: 9ES, SO4, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-05-24
Ligands: 9ES, SO4, EDO
 |
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
 |
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
 |
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
 |
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
 |
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
 |
Structure Of Map Kinase P38 In Complex With A 1-O-Tolyl-1,2,3-Triazole-4-Carboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.95 Å Release Date: 2008-05-27 Classification: TRANSFERASE Ligands: 337 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-05-27
Ligands: 337
 |
Dipeptide Nitrile Inhibitor Bound To Cathepsin S.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2003-04-22 Classification: HYDROLASE Ligands: BLN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2003-04-22
Ligands: BLN