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Search Count: 9

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6TQ2 image
N-Terminal Bromodomain Of Human Brd2 With 5-(4-(4-Fluorophenyl)-1H-Imidazol-5-Yl)-1-Methylpyridin-2(1H)-One

6TPX image
N-Terminal Bromodomain Of Human Brd4 With 1-((1-Acetylpiperidin-4-Yl)Methyl)-2-(4-Hydroxy-3,5-Dimethylphenyl)-N-Methyl-1H-Benzo[D]Imidazole-5-Carboxamide

6TPY image
N-Terminal Bromodomain Of Human Brd4 With 1,3-Dimethyl-5-(1-((Tetrahydro-2H-Pyran-4-Yl)Methyl)-1H-Benzo[D]Imidazol-2-Yl)Pyridin-2(1H)-One

6TPZ image
N-Terminal Bromodomain Of Human Brd4 With 5-(1-(1,3-Dimethoxypropan-2-Yl)-5-Morpholino-1H-Benzo[D]Imidazol-2-Yl)-1,3-Dimethylpyridin-2(1H)-One

6TQ1 image
N-Terminal Bromodomain Of Human Brd4 With 5-(1-(1,3-Dimethoxypropan-2-Yl)-5-Morpholino-1H-Benzo[D]Imidazol-2-Yl)-1,3-Dimethylpyridin-2(1H)-One

5HI7 image
Co-Crystal Structure Of Human Smyd3 With An Aza-Sah Compound

5HQ8 image
Co-Crystal Structure Of Human Smyd3 With A Mekk2 Peptide At 2.13A
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.72 Å Release Date: 2016-03-30
Classification: TRANSFERASE
Ligands: ZN, MG, EDO, SAH, GOL

4A9H image
N-Terminal Bromodomain Of Human Brd2 With 1-(2-Methyl-1,2,3,4-Tetrahydroquinolin-1-Yl)Ethan-1-One

3GWT image
Catalytic Domain Of Human Phosphodiesterase 4B2B In Complex With A Quinoline Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.75 Å Release Date: 2010-04-07
Classification: HYDROLASE
Ligands: 066, ZN, MG, ARS, GOL
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