Search Count: 5
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Crystal Structure Of The First Bromodomain Of Human Brd4 In Complex With A 3,5-Dimethylisoxazol Ligand
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.72 Å Release Date: 2013-02-13 Classification: SIGNALING PROTEIN Ligands: EDO, 1H2, IOD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: EDO, 1H2, IOD
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Crystal Structure Of The First Bromodomain Of Human Brd4 In Complex With A 3,5-Dimethylisoxazol Ligand
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.84 Å Release Date: 2013-02-13 Classification: SIGNALING PROTEIN Ligands: EDO, 1H3 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: EDO, 1H3
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Crystal Structure Of Thymidylate Kinase From Staphylococcus Aureus Bound To Inhibitor.
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION Resolution:1.71 Å Release Date: 2012-10-24 Classification: Transferase/Transferase inhibitor Ligands: 0Y5 |
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION
Release Date: 2012-10-24
Ligands: 0Y5
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Discovery Of Selective And Potent Inhibitors Of Gram-Positive Bacterial Thymidylate Kinase (Tmk: Compound 41)
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2012-10-24 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 13Y |
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION
Release Date: 2012-10-24
Ligands: 13Y
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Discovery Of Selective And Potent Inhibitors Of Gram-Positive Bacterial Thymidylate Kinase (Tmk): Compund 16
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2012-10-24 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 14D |
Organism: Staphylococcus aureus subsp. aureus
Method: X-RAY DIFFRACTION
Release Date: 2012-10-24
Ligands: 14D