Search Count: 9
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Crystal Structure Of The Human Brd2 Bd1 Bromodomain In Complex With 9-(Cyclopropylmethyl)-7-[(2R,6S)-2,6-Dimethylmorpholine-4-Carbonyl]-3-(3,5-Dimethyl-1,2-Oxazol-4-Yl)-9H-Carbazole-1-Carboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.49 Å Release Date: 2021-09-29 Classification: CELL CYCLE Ligands: YW1, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-09-29
Ligands: YW1, EDO
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Crystal Structure Of The First Bromodomain Of Human Brd4 In Complex With 9-Benzyl-2-(3,5-Dimethyl-1,2-Oxazol-4-Yl)-7-(2-Hydroxypropan-2-Yl)-9H-Carbazole-4-Carboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2021-09-29 Classification: CELL CYCLE Ligands: YW4, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-09-29
Ligands: YW4, EDO
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Crystal Structure Of The First Bromodomain Of Human Brd4 In Complex With 2-(3,5-Dimethyl-1,2-Oxazol-4-Yl)-7-(2-Hydroxypropan-2-Yl)-9-[(S)-(Oxan-4-Yl)(Phenyl)Methyl]-9H-Carbazole-4-Carboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2021-09-29 Classification: CELL CYCLE Ligands: YW7, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-09-29
Ligands: YW7, EDO
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Crystal Structure Of The First Bromodomain Of Human Brd4 In Complex With Bms-986158, 2-{3-(1,4-Dimethyl-1H-1,2,3-Triazol-5-Yl)-5-[(S)-(Oxan-4-Yl)(Phenyl)Methyl]-5H-Pyrido[3,2-B]Indol-7-Yl}Propan-2-Ol
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2021-09-29 Classification: CELL CYCLE Ligands: YWA, IOD, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-09-29
Ligands: YWA, IOD, EDO
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Crystal Structure Of Cyclin-Dependent Kinase 2 (Cdk2-Wt) Complex With N-[5-[[[5-(1,1-Dimethylethyl)-2-Oxazolyl] Methyl]Thio]-2-Thiazolyl]-4-Piperidinecarboxamide (Bms-387032)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2015-08-12 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 56H |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-08-12
Ligands: 56H
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Crystal Structure Of Cyclin-Dependent Kinase 2 (Cdk2-Wt) Complex With (2S)-N-(5-(((5-Tert-Butyl-1,3-Oxazol-2-Yl)Methyl)Sulfanyl)-1,3-Thiazol-2-Yl)-2-Phenylpropanamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2013-10-02 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 1YG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-10-02
Ligands: 1YG
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Human Alpha-Thrombin Complexed With N-(Methylsulfonyl)-D-Phenylalanyl-N-((1-Carbamimidoyl-4-Piperidinyl)Methyl)-L-Prolinamide (Bms-189664)
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION Resolution:2.49 Å Release Date: 2011-10-12 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 0BM |
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION
Release Date: 2011-10-12
Ligands: 0BM
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Integrin Binding Collagen Peptide
Organism: Artificial gene
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2011-01-12 Classification: DE NOVO PROTEIN |
Organism: Artificial gene
Method: X-RAY DIFFRACTION
Release Date: 2011-01-12
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Structure Of A Retro-Binding Peptide Inhibitor Complexed With Human Alpha-Thrombin
Organism: Hirudo medicinalis, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 1995-10-15 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: 0E7 |
Organism: Hirudo medicinalis, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 1995-10-15
Ligands: 0E7