Search Count: 62
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Crystal Structure Of Human Gpx4-R152H
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2024-08-28 Classification: OXIDOREDUCTASE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-08-28
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Crystal Structure Of Human Gpx4-U46C-I129S-L130S
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2024-08-28 Classification: OXIDOREDUCTASE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-08-28
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Crystal Structure Of Cathepsin K With N-Desmethyl Thalassospiramide C
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2019-06-26 Classification: HYDROLASE Ligands: G4B |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-06-26
Ligands: G4B
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Small Molecule Inhibitor Abs-143 Bound To The Botulinum Neurotoxin Serotype A Light Chain
Organism: Clostridium botulinum
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2017-07-26 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, 90G |
Organism: Clostridium botulinum
Method: X-RAY DIFFRACTION
Release Date: 2017-07-26
Ligands: ZN, 90G
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Small Molecule Inhibitor Abs-143 Bound To The Botulinum Neurotoxin Serotype A Light Chain
Organism: Clostridium botulinum
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2017-07-26 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, 90J |
Organism: Clostridium botulinum
Method: X-RAY DIFFRACTION
Release Date: 2017-07-26
Ligands: ZN, 90J
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Small Molecule Inhibitor Abs-143 Bound To The Botulinum Neurotoxin Serotype A Light Chain
Organism: Clostridium botulinum
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2017-07-26 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, 90M |
Organism: Clostridium botulinum
Method: X-RAY DIFFRACTION
Release Date: 2017-07-26
Ligands: ZN, 90M
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Structure-Guided Dot1L Probe Optimization By Label-Free Ligand Displacement
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.41 Å Release Date: 2014-12-03 Classification: Transferase/Transferase inhibitor Ligands: 3US, SO4, GOL, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-12-03
Ligands: 3US, SO4, GOL, EDO
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Crystal Structure Of The Lin-41 Filamin Domain
Organism: Caenorhabditis elegans
Method: X-RAY DIFFRACTION Resolution:1.68 Å Release Date: 2014-10-01 Classification: STRUCTURAL PROTEIN |
Organism: Caenorhabditis elegans
Method: X-RAY DIFFRACTION
Release Date: 2014-10-01
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Structure Of The Ddb1-Crbn E3 Ubiquitin Ligase Bound To Thalidomide
Organism: Homo sapiens, Gallus gallus
Method: X-RAY DIFFRACTION Resolution:2.98 Å Release Date: 2014-07-16 Classification: DNA BINDING PROTEIN/PROTEIN Ligands: ZN, EF2 |
Organism: Homo sapiens, Gallus gallus
Method: X-RAY DIFFRACTION
Release Date: 2014-07-16
Ligands: ZN, EF2
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Structure Of The Ddb1-Crbn E3 Ubiquitin Ligase Bound To Lenalidomide
Organism: Homo sapiens, Gallus gallus
Method: X-RAY DIFFRACTION Resolution:2.95 Å Release Date: 2014-07-16 Classification: DNA BINDING PROTEIN/PROTEIN BINDING Ligands: ZN, LVY |
Organism: Homo sapiens, Gallus gallus
Method: X-RAY DIFFRACTION
Release Date: 2014-07-16
Ligands: ZN, LVY
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Structure Of The Ddb1-Crbn E3 Ubiquitin Ligase Bound To Pomalidomide
Organism: Homo sapiens, Gallus gallus
Method: X-RAY DIFFRACTION Resolution:3.50 Å Release Date: 2014-07-16 Classification: DNA BINDING PROTEIN Ligands: ZN, Y70 |
Organism: Homo sapiens, Gallus gallus
Method: X-RAY DIFFRACTION
Release Date: 2014-07-16
Ligands: ZN, Y70
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Selective & Brain-Permeable Polo-Like Kinase-2 (Plk-2) Inhibitors That Reduce -Synuclein Phosphorylation In Rat Brain
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2013-12-25 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: R78 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-12-25
Ligands: R78
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Selective & Brain-Permeable Polo-Like Kinase-2 (Plk-2) Inhibitors That Reduce -Synuclein Phosphorylation In Rat Brain
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.74 Å Release Date: 2013-12-25 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 1D1 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-12-25
Ligands: 1D1
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Selective & Brain-Permeable Polo-Like Kinase-2 (Plk-2) Inhibitors That Reduce -Synuclein Phosphorylation In Rat Brain
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2013-11-20 Classification: transferase/transferase inhibitor Ligands: 11G |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-11-20
Ligands: 11G
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Selective & Brain-Permeable Polo-Like Kinase-2 (Plk-2) Inhibitors That Reduce -Synuclein Phosphorylation In Rat Brain
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2013-11-20 Classification: transferase/transferase inhibitor Ligands: 1C7 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-11-20
Ligands: 1C7
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Selective & Brain-Permeable Polo-Like Kinase-2 (Plk-2) Inhibitors That Reduce Alpha-Synuclein Phosphorylation In Rat Brain
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.91 Å Release Date: 2013-08-14 Classification: transferase/transferase inhibitor Ligands: 1C8 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-08-14
Ligands: 1C8
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Design And Synthesis Of Hydroxyethylamine (Hea) Bace-1 Inhibitors: Prime Side Chromane-Containing Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2012-03-28 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: C6A |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-03-28
Ligands: C6A
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Low Molecular Weigth Human Urokinase Type Plasminogen Activator 2-[6-(3'-Aminomethyl-Biphenyl-3-Yloxy)-4-(3-Dimethylamino-Pyrrolidin-1-Yl)-3,5-Difluoro-Pyridin-2-Yloxy]-4-Dimethylamino-Benzoic Acid Complex
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.83 Å Release Date: 2009-10-13 Classification: HYDROLASE Ligands: 438, PO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-10-13
Ligands: 438, PO4
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Human Heat-Shock Protein 90 (Hsp90) In Complex With {4-[3-(2,4-Dihydroxy-5-Isopropyl-Phenyl)-5-Thioxo- 1,5-Dihydro-[1,2,4]Triazol-4-Yl]-Benzyl}-Carbamic Acid Ethyl Ester {Zk 2819}
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.59 Å Release Date: 2009-07-14 Classification: CHAPERONE Ligands: 819 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2009-07-14
Ligands: 819
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Crystal Structure Of Leukotriene A4 Hydrolase In Complex With 2-Amino-N-[4-(Phenylmethoxy)Phenyl]-Acetamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2008-04-22 Classification: HYDROLASE Ligands: ZN, YB, ACT, 4BG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-04-22
Ligands: ZN, YB, ACT, 4BG