Search Count: 9
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Human Tlr8 Bound To The Potent Agonist, Gs-9688 (Selgantolimod)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2021-02-03 Classification: IMMUNE SYSTEM Ligands: MAN, NAG, U57 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-02-03
Ligands: MAN, NAG, U57
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Crystal Structure Of Hcv Ns3/4A Protease In Complex With Voxilaprevir
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:1.40 Å Release Date: 2019-07-10 Classification: viral protein/inhibitor Ligands: L9P, ZN, SO4 |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2019-07-10
Ligands: L9P, ZN, SO4
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Crystal Structure Of Hcv Ns3/4A Protease In Complex With Compound 12
Organism: Hepatitis c virus subtype 1a
Method: X-RAY DIFFRACTION Resolution:1.55 Å Release Date: 2019-07-10 Classification: viral protein/inhibitor Ligands: L9J, ZN, SO4 |
Organism: Hepatitis c virus subtype 1a
Method: X-RAY DIFFRACTION
Release Date: 2019-07-10
Ligands: L9J, ZN, SO4
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N-Terminal Bromodomain Of Human Brd2 With N-((4-(3-(N-Cyclopentylsulfamoyl)-4-Methylphenyl)-3-Methylisoxazol-5-Yl)Methyl)Acetamide Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2019-01-23 Classification: transcription/transcription inhibitor Ligands: JWA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-01-23
Ligands: JWA
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N-Terminal Bromodomain Of Human Brd2 In Complex With 4,4'-(Quinoline-5,7-Diyl)Bis(3,5-Dimethylisoxazole) Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2019-01-23 Classification: transcription/transcription inhibitor Ligands: JWD, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-01-23
Ligands: JWD, SO4
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N-Terminal Bromodomain Of Human Brd2 In Complex With N-Cyclopentyl-7-(3,5-Dimethylisoxazol-4-Yl)Quinoline-5-Sulfonamide Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2019-01-23 Classification: transcription/transcription inhibitor Ligands: JVY |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-01-23
Ligands: JVY
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C-Terminal Bromodomain Of Human Brd2 In Complex With 4-(2-Cyclopropyl-7-(6-Methylquinolin-5-Yl)-1H-Benzo[D]Imidazol-5-Yl)-3,5-Dimethylisoxazole Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.27 Å Release Date: 2019-01-23 Classification: transcription/transcription inhibitor Ligands: JW4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-01-23
Ligands: JW4, GOL
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Selectivity Switch Between Fak And Pyk2: Macrocyclization Of Fak Inhibitors Improves Pyk2 Potency
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.12 Å Release Date: 2017-11-29 Classification: Transferase/Transferase Inhibitor Ligands: YAM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-11-29
Ligands: YAM
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Selectivity Switch Between Fak And Pyk2: Macrocyclization Of Fak Inhibitors Improves Pyk2 Potency
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.98 Å Release Date: 2016-12-21 Classification: Transferase/Transferase Inhibitor Ligands: 7FM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-12-21
Ligands: 7FM