Search Count: 8
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Ogoga In Complex With Ligand 7
Organism: Oceanicola granulosus htcc2516
Method: X-RAY DIFFRACTION Resolution:2.44 Å Release Date: 2026-07-01 Classification: HYDROLASE/INHIBITOR Ligands: A1DE4 |
Organism: Oceanicola granulosus htcc2516
Method: X-RAY DIFFRACTION
Release Date: 2026-07-01
Ligands: A1DE4
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Ogoga In Complex With Ligand 24
Organism: Oceanicola granulosus
Method: X-RAY DIFFRACTION Resolution:1.53 Å Release Date: 2026-07-01 Classification: HYDROLASE/INHIBITOR Ligands: A1DE3, CL, EDO |
Organism: Oceanicola granulosus
Method: X-RAY DIFFRACTION
Release Date: 2026-07-01
Ligands: A1DE3, CL, EDO
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Human Oga In Complex With Ligand 24
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.33 Å Release Date: 2026-07-01 Classification: HYDROLASE/INHIBITOR Ligands: A1DE3, CA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2026-07-01
Ligands: A1DE3, CA
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Crystal Structure Of Btk Kinase Domain In Complex With Pirtobrutinib
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2023-03-01 Classification: TRANSFERASE/INHIBITOR Ligands: Y7W, SO4, GOL, BTB |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2023-03-01
Ligands: Y7W, SO4, GOL, BTB
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Crystal Structure Of Btk C481S Kinase Domain In Complex With Pirtobrutinib
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.33 Å Release Date: 2023-03-01 Classification: TRANSFERASE/INHIBITOR Ligands: Y7W, SO4, GOL, BTB |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2023-03-01
Ligands: Y7W, SO4, GOL, BTB
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Crystal Structure Of Human Pde1B Catalytic Domain In Complex With Inhibitor 16J (6-(4-Methoxybenzyl)-9-((Tetrahydro-2H-Pyran-4-Yl)Methyl)-8,9,10,11-Tetrahydropyrido[4',3':4,5]Thieno[3,2-E][1,2,4]Triazolo[1,5-C]Pyrimidin-5(6H)-One)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.82 Å Release Date: 2017-04-26 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, MG, 8HM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-04-26
Ligands: ZN, MG, 8HM
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Crystal Structure Of Human Pde1B Catalytic Domain In Complex With Inhibitor 3 (6-(4-Chlorobenzyl)-8,9,10,11-Tetrahydrobenzo[4,5]Thieno[3,2-E][1,2,4]Triazolo[1,5-C]Pyrimidin-5(6H)-One)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.04 Å Release Date: 2017-04-26 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, MG, 8HP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-04-26
Ligands: ZN, MG, 8HP
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Crystal Structure Of Human Pde10A In Complex With Inhibitor 16D
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.87 Å Release Date: 2017-04-26 Classification: Hydrolase/Hydrolase Inhibitor Ligands: 8Q7, ZN, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-04-26
Ligands: 8Q7, ZN, MG