Search Count: 15
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Crystal Structure Of Human Inositol 1,3,4-Trisphosphate 5/6-Kinase (Itpk1) In Complex With An Inhibitor Ncgc00879727
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2026-07-08 Classification: TRANSFERASE Ligands: A1DHL, SO4 |
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Domains 1 And 2 Of Bacillus Anthracis Sap S-Layer In Complex With Nb694
Organism: Lama glama, Bacillus anthracis
Method: X-RAY DIFFRACTION Resolution:1.99 Å Release Date: 2024-11-20 Classification: STRUCTURAL PROTEIN |
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Domains 1 And 2 Of Bacillus Anthracis Sap S-Layer In Complex With Nb692
Organism: Bacillus anthracis, Lama glama
Method: X-RAY DIFFRACTION Resolution:3.11 Å Release Date: 2024-11-20 Classification: STRUCTURAL PROTEIN |
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Langya Virus F Glycoprotein Ectodomain In Prefusion Form
Organism: Langya virus
Method: ELECTRON MICROSCOPY Release Date: 2023-06-28 Classification: VIRAL PROTEIN Ligands: NAG |
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Mojiang Virus F Ectodomain In Prefusion Form
Organism: Mojiang virus
Method: ELECTRON MICROSCOPY Release Date: 2023-06-28 Classification: VIRAL PROTEIN |
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Structure Of Mitochondrial Bc1 In Complex With Ck-2-68
Organism: Bos taurus
Method: ELECTRON MICROSCOPY Release Date: 2023-02-22 Classification: OXIDOREDUCTASE Ligands: HEM, JHB, HEC, FES |
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Crystal Structure Of The Bromodomain Of Human Crebbp Bound To Pyrazolopiperidine Scaffold
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.38 Å Release Date: 2016-11-02 Classification: TRANSFERASE Ligands: 6XB, DMS |
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Crebbp Bromodomain In Complex With Cpd 44 (3-((5-Acetyl-1-(Cyclopropylmethyl)-4,5,6,7-Tetrahydro-1H-Pyrazolo[4,3-C]Pyridin-3-Yl)Amino)-N-Isopropylbenzamide)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.09 Å Release Date: 2016-11-02 Classification: TRANSFERASE Ligands: 6XG, EDO |
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Crebbp Bromodomain In Complex With Cpd59 ((S)-1-(3-((2-Fluoro-4-(1-Methyl-1H-Pyrazol-4-Yl)Phenyl)Amino)-1-(Tetrahydrofuran-3-Yl)-6,7-Dihydro-1H-Pyrazolo[4,3-C]Pyridin-5(4H)-Yl)Ethanone)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.27 Å Release Date: 2016-11-02 Classification: TRANSFERASE Ligands: 6XH, EDO, DMS |
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Brd4 Bromodomain In Complex With Cpd59 ((S)-1-(3-((2-Fluoro-4-(1-Methyl-1H-Pyrazol-4-Yl)Phenyl)Amino)-1-(Tetrahydrofuran-3-Yl)-6,7-Dihydro-1H-Pyrazolo[4,3-C]Pyridin-5(4H)-Yl)Ethanone)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.14 Å Release Date: 2016-11-02 Classification: TRANSFERASE Ligands: EDO, DMS, GOL, PEG, 6XH |
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Crystal Structure Of Full-Length E. Coli Beta-Glucuronidase
Organism: Escherichia coli
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2010-11-17 Classification: HYDROLASE |
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Crystal Structure Of Selenomethionine Substituted E. Coli Beta-Glucuronidase
Organism: Escherichia coli
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2010-11-17 Classification: HYDROLASE |
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Crystal Structure Of E. Coli Beta-Glucuronidase With The Glucaro-D-Lactam Inhibitor Bound
Organism: Escherichia coli
Method: X-RAY DIFFRACTION Resolution:2.39 Å Release Date: 2010-11-17 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: EVA |
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Structure Of E. Coli Beta-Glucuronidase Bound With A Novel, Potent Inhibitor 1-((6,7-Dimethyl-2-Oxo-1,2-Dihydroquinolin-3-Yl)Methyl)-1-(2-Hydroxyethyl)-3-(3-Methoxyphenyl)Thiourea
Organism: Escherichia coli
Method: X-RAY DIFFRACTION Resolution:2.26 Å Release Date: 2010-11-17 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: Z77 |
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Structure Of E. Coli Beta-Glucuronidase Bound With A Novel, Potent Inhibitor 3-(2-Fluorophenyl)-1-(2-Hydroxyethyl)-1-((6-Methyl-2-Oxo-1,2-Dihydroquinolin-3-Yl)Methyl)Urea
Organism: Escherichia coli
Method: X-RAY DIFFRACTION Resolution:2.43 Å Release Date: 2010-11-17 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: Z78 |