Search Count: 20
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Photosynthetic Lh2-Lh1 Complex From The Purple Bacterium Halorhodospira Halophila
Organism: Halorhodospira halophila
Method: ELECTRON MICROSCOPY Release Date: 2025-02-19 Classification: PHOTOSYNTHESIS Ligands: BCL, LMT, CRT, PGV |
Organism: Halorhodospira halophila
Method: ELECTRON MICROSCOPY
Release Date: 2025-02-19
Ligands: BCL, LMT, CRT, PGV
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Crystal Structure Of Tick Tyrosylprotein Sulfotransferase Reveals The Activation Mechanism Of Tick Anticoagulant Protein Madanin
Organism: Ixodes, Longicornis species complex
Method: X-RAY DIFFRACTION Resolution:1.55 Å Release Date: 2024-04-10 Classification: TRANSFERASE Ligands: A3P, 1PS, TRS, MG |
Organism: Ixodes, Longicornis species complex
Method: X-RAY DIFFRACTION
Release Date: 2024-04-10
Ligands: A3P, 1PS, TRS, MG
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Crystal Structure Of Human C1S In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2023-05-17 Classification: HYDROLASE/INHIBITOR Ligands: ZWK, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2023-05-17
Ligands: ZWK, SO4
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Structure Of Cdk12/Cyck In Complex With A Small Molecule Inhibitor N-(4-(1-Methyl-1H-Pyrazol-4-Yl)Phenyl)-N-((1R,4R)-4-(Quinazolin-2-Ylamino)Cyclohexyl)Acetamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2018-08-29 Classification: TRANSFERASE/INHIBITOR Ligands: MG, 8M1 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-08-29
Ligands: MG, 8M1
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Optimization Of 3,5-Disubstitued Piperidine: Discovery Of Non-Peptide Mimetics As An Orally Active Renin Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2017-10-18 Classification: HYDROLASE/HYDROLASE inhibitor Ligands: NAG, 7EK, PGE, PEG, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-10-18
Ligands: NAG, 7EK, PGE, PEG, DMS
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Optimization Of 3,5-Disubstitued Piperidine: Discovery Of Non-Peptide Mimetics As An Orally Active Renin Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.65 Å Release Date: 2017-10-18 Classification: HYDROLASE/HYDROLASE inhibitor Ligands: NAG, 7EJ, DMS, PEG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-10-18
Ligands: NAG, 7EJ, DMS, PEG
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Discovery Of Tak-272: A Novel, Potent And Orally Active Renin In-Hibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2017-07-05 Classification: HYDROLASE/HYDROLASE inhibitor Ligands: NAG, 6VU, PGE, PEG, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-07-05
Ligands: NAG, 6VU, PGE, PEG, DMS
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Discovery Of Tak-272: A Novel, Potent And Orally Active Renin In-Hibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.41 Å Release Date: 2016-11-16 Classification: HYDROLASE/HYDROLASE inhibitor Ligands: NAG, 6VS, DMS, PEG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-11-16
Ligands: NAG, 6VS, DMS, PEG
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Discovery Of Tak-272: A Novel, Potent And Orally Active Renin In-Hibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2016-11-02 Classification: HYDROLASE/HYDROLASE inhibitor Ligands: NAG, 6VR, PEG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-11-02
Ligands: NAG, 6VR, PEG
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Structure-Based Design Of A New Series Of N-Piperidin-3-Ylpyrimidine-5-Carboxamides As Renin Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2016-11-02 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 74U, PEG, NAG, PGE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-11-02
Ligands: 74U, PEG, NAG, PGE
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Structure-Based Design Of A New Series Of N-Piperidin-3-Ylpyrimidine-5-Carboxamides As Renin Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.25 Å Release Date: 2016-11-02 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: NAG, 74V, PGE, DMS, 1PE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-11-02
Ligands: NAG, 74V, PGE, DMS, 1PE
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Structure-Based Design Of A New Series Of N-Piperidin-3-Ylpyrimidine-5-Carboxamides As Renin Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2016-11-02 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: NAG, 74Z, DMS, PEG, 1PE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-11-02
Ligands: NAG, 74Z, DMS, PEG, 1PE
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Structure-Based Design Of A New Series Of N-Piperidin-3-Ylpyrimidine-5-Carboxamides As Renin Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.85 Å Release Date: 2016-11-02 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: NAG, 74Y, PEG, PGE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-11-02
Ligands: NAG, 74Y, PEG, PGE
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Novel Approach Of Fragment-Based Lead Discovery Applied To Renin Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.64 Å Release Date: 2016-10-26 Classification: HYDROLASE/HYDROLASE inhibitor Ligands: NAG, PG6, DMS, 77O, PGE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-10-26
Ligands: NAG, PG6, DMS, 77O, PGE
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Crystal Structure Of Cdcat-Fn
Organism: Equus caballus
Method: X-RAY DIFFRACTION Resolution:1.67 Å Release Date: 2015-11-18 Classification: METAL BINDING PROTEIN Ligands: 4LF, CD, SO4, GOL |
Organism: Equus caballus
Method: X-RAY DIFFRACTION
Release Date: 2015-11-18
Ligands: 4LF, CD, SO4, GOL
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Crystal Structure Of Fecat-Fn
Organism: Equus caballus
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2015-11-18 Classification: METAL BINDING PROTEIN Ligands: 4LF, SO4, CD, FE, GOL |
Organism: Equus caballus
Method: X-RAY DIFFRACTION
Release Date: 2015-11-18
Ligands: 4LF, SO4, CD, FE, GOL
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Crystal Structure Of The Catalytic Domain Of Pde10A Complexed With 3-(1-Phenyl-1H-Pyrazol-5-Yl)-1-(3-(Trifluoromethyl)Phenyl)Pyridazin-4(1H)-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2014-11-19 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: MG, ZN, 3KG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-11-19
Ligands: MG, ZN, 3KG
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Crystal Structure Of The Catalytic Domain Of Pde10A Complexed With 5-Methoxy-3-(1-Phenyl-1H-Pyrazol-5-Yl)-1-(3-(Trifluoromethyl)Phenyl)Pyridazin-4(1H)-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.68 Å Release Date: 2014-11-19 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, MG, 3KB |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-11-19
Ligands: ZN, MG, 3KB
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Crystal Structure Of The Catalytic Domain Of Pde10A Complexed With 1-(2-Fluoro-4-(1H-Pyrazol-1-Yl)Phenyl)-5-Methoxy-3-(1-Phenyl-1H-Pyrazol-5-Yl)Pyridazin-4(1H)-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2014-11-19 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: MG, ZN, 3K9 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-11-19
Ligands: MG, ZN, 3K9
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Nmr Structure Of [F5Y, F16W] Magainin 2 Bound To Phospholipid Vesicles
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Method: SOLUTION NMR
Release Date: 2001-06-27