Search Count: 5
 |
B-Raf Wild-Type Kinase Domain In Complex With A Purinylpyridinylamino-Based Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.89 Å Release Date: 2016-05-04 Classification: Transferase/Transferase Inhibitor Ligands: 5XJ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-05-04
Ligands: 5XJ
 |
Crystal Structure Of C-Met In Complex With Naphthyridinone Inhibitor 5
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2016-02-10 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 5SZ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-02-10
Ligands: 5SZ
 |
Crystal Structure Of C-Met In Complex With Amg 337
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2016-02-10 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 5T1 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-02-10
Ligands: 5T1
 |
Crystal Structure Of C-Met In Complex With (R)-5-(8-Fluoro-3-(1-Fluoro-1-(3-Methoxyquinolin-6-Yl)Ethyl)-[1,2,4]Triazolo[4,3-A]Pyridin-6-Yl)-3-Methylisoxazole
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.75 Å Release Date: 2015-03-11 Classification: Transferase/transferase inhibitor Ligands: 46G |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-03-11
Ligands: 46G
 |
Crystal Structure Of C-Met In Complex With (S)-5-(8-Fluoro-3-(1-(3-(2-Methoxyethoxy)Quinolin-6-Yl)Ethyl)-[1,2,4]Triazolo[4,3-A]Pyridin-6-Yl)-3-Methylisoxazole
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2015-03-11 Classification: TRANSFERASE/TRANSFERASE Inhibitor Ligands: 44X |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-03-11
Ligands: 44X