Search Count: 14
 |
Crystal Structure Of Aldh1A2 In Complex With Kya33
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.40 Å Release Date: 2025-11-19 Classification: OXIDOREDUCTASE Ligands: EDO, A1IDQ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-11-19
Ligands: EDO, A1IDQ
 |
X-Ray Structure Of Mmp-13 In Complex With 4-(1,2,3-Thiadiazol-4-Yl)Pyridine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2021-08-04 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, CA, 9DY, FMT, PGE, PG4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-08-04
Ligands: ZN, CA, 9DY, FMT, PGE, PG4
 |
X-Ray Co-Structure Of Mmp-13 With Ethyl 5-Carbamoyl-1H-Indole-2-Carboxylate
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2015-06-17 Classification: Hydrolase/Hydrolase inhibitor Ligands: 4UM, ZN, CA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-06-17
Ligands: 4UM, ZN, CA
 |
X-Ray Co-Structure Of Mmp-13 With Ethyl 5-(1-Methyl-1H-Imidazol-5-Yl)-1H-Indole-2-Carboxylate
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.03 Å Release Date: 2015-06-17 Classification: Hydrolase/Hydrolase inhibitor Ligands: ZN, CA, 4UE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-06-17
Ligands: ZN, CA, 4UE
 |
X-Ray Co-Structure Of Mmp-13 With 4-[({5-[2-(Ethoxycarbonyl)-1H-Indol-5-Yl]-1-Methyl-1H-Pyrazol-3-Yl}Formamido)Methyl]Benzoate
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.79 Å Release Date: 2015-06-17 Classification: Hydrolase/Hydrolase inhibitor Ligands: ZN, CA, 4UF |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-06-17
Ligands: ZN, CA, 4UF
 |
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
 |
Soluble Epoxide Hydrolase In Complex With Pyrazole Antagonist
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.00 Å Release Date: 2010-10-27 Classification: HYDROLASE Ligands: MZL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-10-27
Ligands: MZL
 |
Mmp-13 In Complex With A Non Zinc-Chelating Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.95 Å Release Date: 2009-09-01 Classification: HYDROLASE Ligands: ZN, CA, FMT, 732 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-09-01
Ligands: ZN, CA, FMT, 732
 |
Mmp-13 In Complex With A Non Zinc-Chelating Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.21 Å Release Date: 2009-09-01 Classification: HYDROLASE Ligands: ZN, CA, 518 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-09-01
Ligands: ZN, CA, 518
 |
P56Lck Sh2 Domain Inhibitor Complex
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 1998-10-21 Classification: TRANSFERASE/TRANSFERASE INHIBITOR |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 1998-10-21
 |
Free P56Lck Sh2 Domain
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 1998-10-21 Classification: SH2 DOMAIN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 1998-10-21