Search Count: 9
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Design And Application Of Synthetic 17B-Hsd13 Substrates To Drug Discovery, And To Reveal Preserved Catalytic Activity Of Protective Human Variants
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.09 Å Release Date: 2024-11-27 Classification: HYDROLASE Ligands: NAD, A1AG4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-11-27
Ligands: NAD, A1AG4
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Design And Application Of Synthetic 17B-Hsd13 Substrates To Drug Discovery, And To Reveal Preserved Catalytic Activity Of Protective Human Variants
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.36 Å Release Date: 2024-11-27 Classification: HYDROLASE Ligands: NAD, A1AG5 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-11-27
Ligands: NAD, A1AG5
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Design And Application Of Synthetic 17B-Hsd13 Substrates To Drug Discovery, And To Reveal Preserved Catalytic Activity Of Protective Human Variants
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.59 Å Release Date: 2024-11-27 Classification: HYDROLASE Ligands: NAD, A1AG6 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-11-27
Ligands: NAD, A1AG6
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Rat Branched Chain Ketoacid Dehydrogenase Kinase In Complex With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.16 Å Release Date: 2024-11-27 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: ADP, MG, K, A1A40, PO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-11-27
Ligands: ADP, MG, K, A1A40, PO4
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Crystal Structure Of Moab2 Protein From Mycobacterium Smegmatis
Organism: Mycolicibacterium smegmatis
Method: X-RAY DIFFRACTION Resolution:2.53 Å Release Date: 2024-07-10 Classification: BIOSYNTHETIC PROTEIN |
Organism: Mycolicibacterium smegmatis
Method: X-RAY DIFFRACTION
Release Date: 2024-07-10
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Microsomal P450 2A6 With The Inhibitor N,N-Dimethyl(5-(Pyridin-3-Yl)Furan-2-Yl)Methanamine Bound
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2006-11-28 Classification: OXIDOREDUCTASE Ligands: SO4, HEM, D1G |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-11-28
Ligands: SO4, HEM, D1G
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Microsomal P450 2A6 With The Inhibitor N-Methyl(5-(Pyridin-3-Yl)Furan-2-Yl)Methanamine Bound
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.65 Å Release Date: 2006-11-28 Classification: OXIDOREDUCTASE Ligands: SO4, HEM, D2G, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-11-28
Ligands: SO4, HEM, D2G, EDO
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Crystal Structure Of Human Microsomal P450 2A6 With The Inhibitor (5-(Pyridin-3-Yl)Furan-2-Yl)Methanamine Bound
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2006-11-28 Classification: OXIDOREDUCTASE Ligands: HEM, D3G |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-11-28
Ligands: HEM, D3G
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Microsomal P450 2A6 With The Inhibitor Adrithiol Bound
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.95 Å Release Date: 2006-11-28 Classification: OXIDOREDUCTASE Ligands: SO4, HEM, D4G |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-11-28
Ligands: SO4, HEM, D4G