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Search Count: 14

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5HI3 image
Binding Site Elucidation And Structure Guided Design Of Macrocyclic Il-17A Antagonists

5HI4 image
Binding Site Elucidation And Structure Guided Design Of Macrocyclic Il-17A Antagonists

5HI5 image
Binding Site Elucidation And Structure Guided Design Of Macrocyclic Il-17A Antagonists

4JLG image
Setd7 In Complex With Inhibitor (R)-Pfi-2 And S-Adenosyl-Methionine

4HBV image
Crystal Structure Of The First Bromodomain Of Human Brd4 In Complex With A Quinazolin Ligand

4HBW image
Crystal Structure Of The First Bromodomain Of Human Brd4 In Complex With A Quinazoline Ligand

4HBX image
Crystal Structure Of The First Bromodomain Of Human Brd4 In Complex With A Quinazolin Ligand

4HBY image
Crystal Structure Of The First Bromodomain Of Human Brd4 In Complex With A Quinazolin Ligand

4E96 image
Crystal Structure Of The First Bromodomain Of Human Brd4 In Complex With The Inhibitor Pfi-1

2YIS image
Triazolopyridine Inhibitors Of P38 Kinase.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.00 Å Release Date: 2011-11-30
Classification: TRANSFERASE
Ligands: YIS, I46

2YIW image
Triazolopyridine Inhibitors Of P38 Kinase
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.00 Å Release Date: 2011-11-30
Classification: TRANSFERASE
Ligands: YIW, I46

2YIX image
Triazolopyridine Inhibitors Of P38
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.30 Å Release Date: 2011-11-30
Classification: TRANSFERASE
Ligands: YIX

2JEW image
Crystal Structure Of ((2S)-5-Amino-2-((1-N-Propyl-1H-Imidazol-4-Yl) Methyl)Pentanoic Acid) Uk396,082 A Tafia Inhibitor, Bound To Activated Porcine Pancreatic Carboxypeptidaseb
Organism: Sus scrofa
Method: X-RAY DIFFRACTION
Resolution:1.40 Å Release Date: 2007-11-20
Classification: HYDROLASE
Ligands: ZN, 720

1BX6 image
Crystal Structure Of The Potent Natural Product Inhibitor Balanol In Complex With The Catalytic Subunit Of Camp-Dependent Protein Kinase
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