Search Count: 13
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B. Fragilis Cysteine Protease
Organism: Bacteroides fragilis
Method: X-RAY DIFFRACTION Resolution:2.48 Å Release Date: 2016-03-30 Classification: HYDROLASE |
Organism: Bacteroides fragilis
Method: X-RAY DIFFRACTION
Release Date: 2016-03-30
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Structure-Based Design Of Orally Bioavailable Pyrrolopyridine Inhibitors Of The Mitotic Kinase Mps1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2013-12-04 Classification: TRANSFERASE Ligands: 4T9, 1PE, 7PE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-12-04
Ligands: 4T9, 1PE, 7PE
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Structure-Based Design Of Orally Bioavailable Pyrrolopyridine Inhibitors Of The Mitotic Kinase Mps1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.36 Å Release Date: 2013-12-04 Classification: TRANSFERASE Ligands: 7PE, 7CE, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-12-04
Ligands: 7PE, 7CE, EDO
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Structure-Based Design Of Orally Bioavailable Pyrrolopyridine Inhibitors Of The Mitotic Kinase Mps1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.65 Å Release Date: 2013-12-04 Classification: TRANSFERASE Ligands: 7RO, 7PE, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-12-04
Ligands: 7RO, 7PE, EDO
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Structure-Based Design Of Orally Bioavailable Pyrrolopyridine Inhibitors Of The Mitotic Kinase Mps1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2013-12-04 Classification: TRANSFERASE Ligands: 7RO, 7PE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-12-04
Ligands: 7RO, 7PE
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Structure-Based Design Of Orally Bioavailable Pyrrolopyridine Inhibitors Of The Mitotic Kinase Mps1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.65 Å Release Date: 2013-12-04 Classification: TRANSFERASE Ligands: X20, 7PE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-12-04
Ligands: X20, 7PE
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Structure-Based Design Of Orally Bioavailable Pyrrolopyridine Inhibitors Of The Mitotic Kinase Mps1
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2013-12-04 Classification: TRANSFERASE Ligands: X21 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-12-04
Ligands: X21
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Crystal Structure Of Human Chk2 In Complex With Benzimidazole Carboxamide Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.85 Å Release Date: 2012-10-10 Classification: TRANSFERASE Ligands: NO3, RU5, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-10-10
Ligands: NO3, RU5, EDO
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Crystal Structure Of Human Chk2 In Complex With Benzimidazole Carboxamide Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.66 Å Release Date: 2012-10-10 Classification: TRANSFERASE Ligands: NO3, RU9 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-10-10
Ligands: NO3, RU9
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Crystal Structure Of Human Chk2 In Complex With Benzimidazole Carboxamide Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2012-10-10 Classification: TRANSFERASE Ligands: A9T, NO3, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-10-10
Ligands: A9T, NO3, EDO
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Crystal Structure Of Human Chk2 In Complex With Benzimidazole Carboxamide Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.48 Å Release Date: 2012-10-10 Classification: TRANSFERASE Ligands: NO3, EDO, A9U, CL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-10-10
Ligands: NO3, EDO, A9U, CL
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Disulfide Crosslinked Cytochrome P450 Reductase Inactive
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2011-02-23 Classification: OXIDOREDUCTASE Ligands: FMN, FAD |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2011-02-23
Ligands: FMN, FAD
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Disulfide Crosslinked Cytochrome P450 Reductase Inactive
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2011-02-23 Classification: OXIDOREDUCTASE Ligands: FMN, FAD, NAP |
Organism: Rattus norvegicus
Method: X-RAY DIFFRACTION
Release Date: 2011-02-23
Ligands: FMN, FAD, NAP