Search Count: 13
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Cryoem Structure Of Prmt5 Bound To Covalent Pbm-Site Inhibitor Brd-6988
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Release Date: 2021-03-17 Classification: TRANSFERASE/INHIBITOR Ligands: YJG |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2021-03-17
Ligands: YJG
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Prmt5 Complex Bound To Covalent Pbm Inhibitor Brd6711
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.88 Å Release Date: 2020-11-25 Classification: SPLICING/TRANSFERASE Ligands: QN4, CL, SFG, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-11-25
Ligands: QN4, CL, SFG, GOL
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Structural Model For The N-Terminal Domain Of Human Cdc37
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Organism: Homo sapiens
Method: SOLUTION NMR
Release Date: 2016-05-04
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Potent And Selective Phosphodiesterase 10A Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2012-09-05 Classification: Hydrolase/Hydrolase inhibitor Ligands: ZN, MG, 0T7 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-09-05
Ligands: ZN, MG, 0T7
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Potent And Selective Phosphodiesterase 10A Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.02 Å Release Date: 2012-09-05 Classification: Hydrolase/Hydrolase inhibitor Ligands: ZN, MG, 0T6 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-09-05
Ligands: ZN, MG, 0T6
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Solution Structure Of The Skeletal Muscle And Neuronal Voltage Gated Sodium Channel Antagonist Mu-Conotoxin Cniiic
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Organism: Conus consors
Method: SOLUTION NMR
Release Date: 2012-02-08
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Crystal Structure Of Jnk3 Complexed With Cc-930, An Orally Active Anti-Fibrotic Jnk Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2012-02-01 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: KBI, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-02-01
Ligands: KBI, GOL
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Crystal Structure Of Jnk3 Complexed With Cc-359, A Jnk Inhibitor For The Prevention Of Ischemia-Reperfusion Injury
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2012-01-25 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: JBI |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-01-25
Ligands: JBI
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Highly Potent, Selective, And Orally Active Phosphodiestarase 10A Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.82 Å Release Date: 2011-10-26 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: CL, 540, ZN, MG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-10-26
Ligands: CL, 540, ZN, MG
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Highly Potent, Selective, And Orally Active Phosphodiestarase 10A Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2011-10-26 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, MG, CL, 546 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-10-26
Ligands: ZN, MG, CL, 546
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Highly Potent, Selective, And Orally Active Phosphodiestarase 10A Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2011-10-26 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, MG, 548 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-10-26
Ligands: ZN, MG, 548
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Conkunitzin-S1 Is The First Member Of A New Kunitz-Type Neurotoxin Family- Structural And Functional Characterization
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Organism: Conus striatus
Method: SOLUTION NMR
Release Date: 2006-01-05
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The Crystal Structure Of Allosteric Chorismate Mutase At 2.2 Angstroms Resolution
Organism: Saccharomyces cerevisiae
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 1995-09-15 Classification: ISOMERASE Ligands: TRP |
Organism: Saccharomyces cerevisiae
Method: X-RAY DIFFRACTION
Release Date: 1995-09-15
Ligands: TRP