Search Count: 15
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.93 Å Release Date: 2026-01-07 Classification: LIGASE Ligands: ZN |
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Organism: Squalus acanthias, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.43 Å Release Date: 2025-09-10 Classification: TOXIN Ligands: GOL, SO4, CL |
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Crystal Structure Of The Sars-Cov-2 Receptor Binding Domain In Complex With Vnar 3B4
Organism: Severe acute respiratory syndrome coronavirus 2, Squalus acanthias
Method: X-RAY DIFFRACTION Resolution:1.92 Å Release Date: 2022-01-05 Classification: VIRAL PROTEIN/IMMUNE SYSTEM Ligands: EDO |
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Crystal Structure Of The Sars-Cov-2 Receptor Binding Domain In Complex With Vnar 2C02
Organism: Severe acute respiratory syndrome coronavirus 2, Squalus acanthias
Method: X-RAY DIFFRACTION Resolution:1.96 Å Release Date: 2022-01-05 Classification: VIRAL PROTEIN/IMMUNE SYSTEM Ligands: EDO, NAG, CL |
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Crystal Structure Of 2-(3-Alkoxy-1-Azetidinyl) Quinolines As Pde10A Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.77 Å Release Date: 2014-12-17 Classification: Hydrolase/Hydrolase Inhibitor Ligands: SO4, GOL, 35E, ZN |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.65 Å Release Date: 2014-12-17 Classification: Hydrolase/Hydrolase Inhibitor Ligands: ZN, SO4, GOL, 35D |
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Crystal Structure Of Pde10A With 1H-Benzimidazol-2-Yl(4-((3-(Tetrahydro-2H-Pyran-4-Yl)-2-Pyridinyl)Oxy)Phenyl)Methanone
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2014-08-06 Classification: Hydrolase/Hydrolase Inhibitor Ligands: ZN, SO4, 2W1 |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.64 Å Release Date: 2013-10-23 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, SO4, GOL, 2F4 |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2013-10-23 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, SO4, 2F5 |
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Crystal Structure Of Pde10A With A Biaryl Ether Inhibitor ((1-(3-(4-((1H-Benzo[D]Imidazol-2-Yl)Amino)Phenoxy)Pyridin-2-Yl)Piperidin-4-Yl)Methanol)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2012-12-12 Classification: hydrolase/hydrolase inhibitor Ligands: ZN, SO4, 15J |
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Crystal Structure Of Pde10A With A Biaryl Ether Inhibitor (1-(1-(3-(4-(Benzo[D]Thiazol-2-Ylamino)Phenoxy)Pyrazin-2-Yl)Piperidin-4-Yl)Ethanol)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2012-12-12 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, SO4, GOL, 15H |
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Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2011-04-27 Classification: HYDROLASE |
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Crystal Structure Of Fatty Acid Amide Hydrolase With Small Molecule Inhibitor
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2011-04-27 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: QJ9, EDO, GOL, PGE |
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Crystal Structure Of Fatty Acid Amide Hydrolase With Small Molecule Compound
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:3.10 Å Release Date: 2011-04-27 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: QKV |
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Crystal Structure Of Fatty Acid Amide Hydrolase With Small Molecule Inhibitor
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2011-04-06 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: QK5, EDO, GOL |