Search Count: 21
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Liganded X-Ray Crystal Structure Of Cyclin Dependent Kinase 6 (Cdk6)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.31 Å Release Date: 2013-02-06 Classification: TRANSFERASE Ligands: 4AU |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-02-06
Ligands: 4AU
 |
Cdk6 (Monomeric) In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2013-02-06 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0RS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-02-06
Ligands: 0RS
 |
Structure Of Pka-Pkb Chimera Complexed With (1S)-2-Amino-1-(4- Chlorophenyl)-1-(4-(1H-Pyrazol-4-Yl)Phenyl)Ethan-1-Ol
Organism: Bos taurus, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2012-07-25 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: RKD |
Organism: Bos taurus, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-07-25
Ligands: RKD
 |
Structure Of Hsp90 With An Inhibitor Bound
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2010-08-11 Classification: CHAPERONE Ligands: VHD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-08-11
Ligands: VHD
 |
Structure Of Hsp90 With Small Molecule Inhibitor Bound
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.25 Å Release Date: 2010-08-11 Classification: CHAPERONE Ligands: XJG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-08-11
Ligands: XJG
 |
Structure Of Hsp90 With Small Molecule Inhibitor Bound
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2010-08-11 Classification: CHAPERONE Ligands: GOL, L81 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-08-11
Ligands: GOL, L81
 |
Structure Of Hsp90 With Small Molecule Inhibitor Bound
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.66 Å Release Date: 2010-08-11 Classification: CHAPERONE Ligands: XJX |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-08-11
Ligands: XJX
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: GOL, LZ1 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: GOL, LZ1
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H-Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: GOL, LZ2 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: GOL, LZ2
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ3 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ3
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: GOL, LZ4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: GOL, LZ4
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ5 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ5
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.25 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZM
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ7 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ7
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.19 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ8 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ8
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ9 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ9
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZA
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.89 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZB |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZB
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZC |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZC
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.68 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZD