Search Count: 103
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Plasmodium Falciparum 20S Proteasome Bound To Inhibitor 159
Organism: Plasmodium falciparum 3d7
Method: ELECTRON MICROSCOPY Resolution:2.79 Å Release Date: 2025-11-12 Classification: CYTOSOLIC PROTEIN Ligands: A1B74 |
Organism: Plasmodium falciparum 3d7
Method: ELECTRON MICROSCOPY
Release Date: 2025-11-12
Ligands: A1B74
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Plasmodium Falciparum 20S Proteasome Bound To Inhibitor 296
Organism: Plasmodium falciparum 3d7
Method: ELECTRON MICROSCOPY Resolution:2.28 Å Release Date: 2025-11-12 Classification: CYTOSOLIC PROTEIN Ligands: A1B73 |
Organism: Plasmodium falciparum 3d7
Method: ELECTRON MICROSCOPY
Release Date: 2025-11-12
Ligands: A1B73
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Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm1010 (6-Cyclopropyl-2,4-Dimethyl-3-(4-(Trifluoromethyl)Benzyl)-2,6-Dihydro-7H-Pyrazolo[3,4-C]Pyridin-7-One)
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION Resolution:3.00 Å Release Date: 2025-01-29 Classification: OXIDOREDUCTASE Ligands: A1A5P, FMN, OG6 |
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION
Release Date: 2025-01-29
Ligands: A1A5P, FMN, OG6
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Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm679 (Ethyl 1,4-Dimethyl-5-((6-(Trifluoromethyl)Pyridin-3-Yl)Methyl)-1H-Pyrazole-3-Carboxylate)
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION Resolution:2.41 Å Release Date: 2025-01-01 Classification: OXIDOREDUCTASE/INHIBITOR Ligands: A1A51, FMN, OG6, CIT, LDA |
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION
Release Date: 2025-01-01
Ligands: A1A51, FMN, OG6, CIT, LDA
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Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm681 (N-Cyclopropyl-1,4-Dimethyl-5-((6-(Trifluoromethyl)Pyridin-3-Yl)Methyl)-1H-Pyrazole-3-Carboxamide)
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2025-01-01 Classification: OXIDOREDUCTASE/INHIBITOR Ligands: A1A52, FMN, OG6, NA |
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION
Release Date: 2025-01-01
Ligands: A1A52, FMN, OG6, NA
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Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm959 (6-Cyclopropyl-2,4-Dimethyl-3-((6-(Trifluoromethyl)Pyridin-3-Yl)Methyl)-2,6-Dihydro-7H-Pyrazolo[3,4-C]Pyridin-7-One)
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION Resolution:3.10 Å Release Date: 2025-01-01 Classification: OXIDOREDUCTASE/INHIBITOR Ligands: A1A53, FMN, OG6 |
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION
Release Date: 2025-01-01
Ligands: A1A53, FMN, OG6
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Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm1153 (4,6-Dicyclopropyl-3-(3-Fluoro-4-(Trifluoromethyl)Benzyl)-2-Methyl-2,6-Dihydro-7H-Pyrazolo[3,4-D]Pyridazin-7-One)
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION Resolution:3.15 Å Release Date: 2025-01-01 Classification: OXIDOREDUCTASE Ligands: A1A5Q, FMN, OG6 |
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION
Release Date: 2025-01-01
Ligands: A1A5Q, FMN, OG6
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Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm1174 (3-((7-Azaspiro[3.5]Nonan-7-Yl)Methyl)-4-Cyclopropyl-6-Ethyl-2-Methyl-2,6-Dihydro-7H-Pyrazolo[3,4-C]Pyridin-7-One)
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION Resolution:3.30 Å Release Date: 2025-01-01 Classification: OXIDOREDUCTASE Ligands: A1A59, FMN, OG6 |
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION
Release Date: 2025-01-01
Ligands: A1A59, FMN, OG6
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Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm1398 ((S)-3-(Amino(3-Chloro-4-(Trifluoromethyl)Phenyl)(Cyclopropyl)Methyl)-6-Cyclopropyl-2-Methyl-2,6-Dihydro-7H-Pyrazolo[3,4-D]Pyridazin-7-One)
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2025-01-01 Classification: OXIDOREDUCTASE Ligands: A1A6D, FMN, OG6, ACY |
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION
Release Date: 2025-01-01
Ligands: A1A6D, FMN, OG6, ACY
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Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm1211 ((R)-3-(Amino(6-(Trifluoromethyl)Pyridin-3-Yl)Methyl)-4-Cyclopropyl-6-Ethyl-2-Methyl-2,6-Dihydro-7H-Pyrazolo[3,4-C]Pyridin-7-One)
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION Resolution:3.10 Å Release Date: 2025-01-01 Classification: OXIDOREDUCTASE Ligands: A1A6E, FMN, OG6 |
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION
Release Date: 2025-01-01
Ligands: A1A6E, FMN, OG6
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Plasmodium Falciparum 20S Proteasome Bound To An Inhibitor
Organism: Plasmodium falciparum 3d7
Method: ELECTRON MICROSCOPY Release Date: 2024-07-31 Classification: CYTOSOLIC PROTEIN/INHIBITOR Ligands: A1AE6 |
Organism: Plasmodium falciparum 3d7
Method: ELECTRON MICROSCOPY
Release Date: 2024-07-31
Ligands: A1AE6
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Atad2 Bromodomain In Complex With "Oncohistone" Mutation H4S1Ck5Ac (Res 1-15) Ligand
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.01 Å Release Date: 2024-06-05 Classification: PROTEIN BINDING |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-06-05
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Atad2 Bromodomain In Complex With H4S1Phk5Ac (Res 1-15) Ligand
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2024-06-05 Classification: PROTEIN BINDING |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-06-05
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Atad2B Bromodomain In Complex With Histone H4 Acetylated At Lysine 5 With Serine 1 Mutation To Cysteine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.69 Å Release Date: 2024-06-05 Classification: NUCLEAR PROTEIN Ligands: SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-06-05
Ligands: SO4
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Atad2B Bromodomain In Complex With Histone H4 Acetylated At Lysine 12
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.92 Å Release Date: 2024-06-05 Classification: NUCLEAR PROTEIN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-06-05
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Crystal Structure Of The Bromodomain Of Human Atad2B In Complex With Histone H4S1(Ph)K5Ac
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.40 Å Release Date: 2024-06-05 Classification: PEPTIDE BINDING PROTEIN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-06-05
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Acinetobacter Baumannii Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm186
Organism: Acinetobacter baumannii
Method: X-RAY DIFFRACTION Resolution:1.40 Å Release Date: 2022-12-28 Classification: OXIDOREDUCTASE/INHIBITOR Ligands: OBR, FMN, ORO, GOL |
Organism: Acinetobacter baumannii
Method: X-RAY DIFFRACTION
Release Date: 2022-12-28
Ligands: OBR, FMN, ORO, GOL
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Crystal Structure Of Taga With Udp-Glcnac
Organism: Thermoanaerobacter italicus (strain dsm 9252 / ab9)
Method: X-RAY DIFFRACTION Resolution:2.99 Å Release Date: 2021-12-29 Classification: TRANSFERASE Ligands: UD1 |
Organism: Thermoanaerobacter italicus (strain dsm 9252 / ab9)
Method: X-RAY DIFFRACTION
Release Date: 2021-12-29
Ligands: UD1
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Crystal Structure Of Taga With Udp-Mannac
Organism: Thermoanaerobacter italicus (strain dsm 9252 / ab9)
Method: X-RAY DIFFRACTION Resolution:3.30 Å Release Date: 2021-12-29 Classification: TRANSFERASE Ligands: UD9 |
Organism: Thermoanaerobacter italicus (strain dsm 9252 / ab9)
Method: X-RAY DIFFRACTION
Release Date: 2021-12-29
Ligands: UD9
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Crystal Structure Of The Human Cytochrome P450 2C9*8 (Cyp2C9*8) Genetic Variant In Complex With The Drug Losartan
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.23 Å Release Date: 2021-10-06 Classification: OXIDOREDUCTASE Ligands: HEM, LSN, K, PO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-10-06
Ligands: HEM, LSN, K, PO4