Search Count: 25
 |
Parp Complexed With A906894
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2010-12-22 Classification: Transferase/Transferase Inhibitor Ligands: L3L |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-12-22
Ligands: L3L
 |
Parp Complexed With A927929
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2010-06-23 Classification: TRANSFERASE Ligands: A92 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-06-23
Ligands: A92
 |
Parp Complexed With A968427
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2010-03-09 Classification: TRANSFERASE Ligands: GJW |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-03-09
Ligands: GJW
 |
Pka Structures Of Akt, Indazole-Pyridine Inhibitors
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2007-06-05 Classification: TRANSFERASE Ligands: SS3 |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2007-06-05
Ligands: SS3
 |
Pka Structures Of Indazole-Pyridine Series Of Akt Inhibitors
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2007-06-05 Classification: TRANSFERASE Ligands: L20 |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2007-06-05
Ligands: L20
 |
Pka Structures Of Indazole-Pyridine Series Of Akt Inhibitors
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2007-06-05 Classification: TRANSFERASE Ligands: SS5 |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2007-06-05
Ligands: SS5
 |
Pka Structures Of Indazole-Pyridine Series Of Akt Inhibitors
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2007-06-05 Classification: TRANSFERASE Ligands: SS4 |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2007-06-05
Ligands: SS4
 |
H-Chk1 Complexed With A431994
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.50 Å Release Date: 2007-03-27 Classification: TRANSFERASE Ligands: A53 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2007-03-27
Ligands: A53
 |
Crystal Structure Of Protein Kinase A In Complex With Pyridine-Pyrazolopyridine Based Inhibitors
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2007-03-20 Classification: TRANSFERASE Ligands: 2PY |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2007-03-20
Ligands: 2PY
 |
Crystal Structure Of Protein Kinase A In Complex With Pyridine-Pyrazolopyridine Based Inhibitors
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2007-03-20 Classification: TRANSFERASE Ligands: 4PY |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2007-03-20
Ligands: 4PY
 |
Pka Complexed With (S)-2-(1H-Indol-3-Yl)-1-(5-Isoquinolin-6-Yl-Pyridin-3-Yloxymethyl-Etylamine
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2006-06-27 Classification: TRANSFERASE Ligands: 2EA |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2006-06-27
Ligands: 2EA
 |
Protein Kinase A Bound To (S)-2-(1H-Indol-3-Yl)-1-[5-((E)-2-Pyridin-4-Yl-Vinyl)-Pyridin-3-Yloxymethyl]-Ethylamine
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2006-06-27 Classification: TRANSFERASE Ligands: 4EA |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2006-06-27
Ligands: 4EA
 |
Protein Kinase A Bound To (R)-1-(1H-Indol-3-Ylmethyl)-2-(2-Pyridin-4-Yl-[1,7]Naphtyridin-5-Yloxy)-Ehylamine
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:3.00 Å Release Date: 2006-06-27 Classification: TRANSFERASE Ligands: 6EA |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2006-06-27
Ligands: 6EA
 |
Substituted 2-Naphthamadine Inhibitors Of Urokinase
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.02 Å Release Date: 2004-10-19 Classification: HYDROLASE Ligands: 745 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2004-10-19
Ligands: 745
 |
Substituted 2-Naphthamidine Inhibitors Of Urokinase
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2004-04-27 Classification: HYDROLASE Ligands: SO4, UI1 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2004-04-27
Ligands: SO4, UI1
 |
Substituted 2-Naphthamidine Inhibitors Of Urokinase
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.84 Å Release Date: 2004-04-27 Classification: HYDROLASE Ligands: SO4, UI2 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2004-04-27
Ligands: SO4, UI2
 |
Substituted 2-Naphthamidine Inhibitors Of Urokinase
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2004-04-27 Classification: HYDROLASE Ligands: UI3 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2004-04-27
Ligands: UI3
 |
Substituted 2-Naphthamidine Inhibitors Of Urokinase
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.32 Å Release Date: 2003-09-30 Classification: HYDROLASE Ligands: 497 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2003-09-30
Ligands: 497
 |
Substituted 2-Naphthamidine Inhibitors Of Urokinase
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2003-09-30 Classification: HYDROLASE Ligands: SO4, 675 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2003-09-30
Ligands: SO4, 675
 |
Substituted 2-Naphthamidine Inhibitors Of Urokinase
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.61 Å Release Date: 2003-09-30 Classification: HYDROLASE Ligands: SO4, 239 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2003-09-30
Ligands: SO4, 239