Search Count: 9
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Erbb4 Kinase Domain Complexed With A Thienopyrimidine Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2008-03-18 Classification: TRANSFERASE Ligands: GW7 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-03-18
Ligands: GW7
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Structure Of The B-Raf Kinase Domain Bound To Sb-590885
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2006-12-12 Classification: TRANSFERASE Ligands: 215 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-12-12
Ligands: 215
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Egfr Kinase Domain Complexed With A Quinazoline Inhibitor- Gw572016
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2004-12-07 Classification: TRANSFERASE Ligands: PO4, FMM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2004-12-07
Ligands: PO4, FMM
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Cdk2 Complexed With N-Methyl-4-{[(2-Oxo-1,2-Dihydro-3H-Indol-3-Ylidene)Methyl]Amino}Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2002-05-14 Classification: TRANSFERASE Ligands: LS1 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2002-05-14
Ligands: LS1
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Cyclin-Dependent Kinase 2 (Cdk2) Complexed With N-Methyl-{4-[2-(7-Oxo-6,7-Dihydro-8H-[1,3]Thiazolo[5,4-E]Indol-8-Ylidene)Hydrazino]Phenyl}Methanesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2002-05-14 Classification: TRANSFERASE Ligands: LS2 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2002-05-14
Ligands: LS2
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Cyclin-Dependent Kinase 2 (Cdk2) Complexed With 3-{[(2,2-Dioxido-1,3-Dihydro-2-Benzothien-5-Yl)Amino]Methylene}-5-(1,3-Oxazol-5-Yl)-1,3-Dihydro-2H-Indol-2-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2002-05-14 Classification: TRANSFERASE Ligands: LS3 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2002-05-14
Ligands: LS3
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Cyclin-Dependent Kinase 2 (Cdk2) Complexed With 4-{[(2-Oxo-1,2-Dihydro-3H-Indol-3-Ylidene)Methyl]Amino}-N-(1,3-Thiazol-2-Yl)Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2002-05-14 Classification: TRANSFERASE Ligands: LS4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2002-05-14
Ligands: LS4
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Cyclin-Dependent Kinase 2 (Cdk2) Complexed With 3-{[4-({[Amino(Imino)Methyl]Aminosulfonyl)Anilino]Methylene}-2-Oxo-2,3-Dihydro-1H-Indole
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2002-05-14 Classification: TRANSFERASE Ligands: LS5 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2002-05-14
Ligands: LS5
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Peptide Inhibitors Of Src Sh3-Sh2-Phosphoprotein Interactions
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 1995-01-26 Classification: COMPLEX(TRANSFERASE/PEPTIDE) |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 1995-01-26