Search Count: 39
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Plasmodium Falciparum M1 Aminopeptidase (Pfa-M1) Bound To Inhibitor 3K (Mips3415)
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2026-01-28 Classification: HYDROLASE Ligands: DMS, A1CTH, GOL, ZN, MG, SO4 |
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION
Release Date: 2026-01-28
Ligands: DMS, A1CTH, GOL, ZN, MG, SO4
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Plasmodium Falciparum M17 Aminopeptidase (Pfa-M17) Bound To Inhibitor 3Ab (Mips3413)
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION Resolution:2.37 Å Release Date: 2026-01-28 Classification: HYDROLASE Ligands: ZN, CO3, PEG, SO4, A1CT4, 1PE, DMS, 2PE, A1CT5 |
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION
Release Date: 2026-01-28
Ligands: ZN, CO3, PEG, SO4, A1CT4, 1PE, DMS, 2PE, A1CT5
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Plasmodium Falciparum M17 Aminopeptidase (Pfa-M17) Bound To Inhibitor 3K (Mips3415)
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION Resolution:2.37 Å Release Date: 2026-01-28 Classification: HYDROLASE Ligands: ZN, CO3, PEG, DMS, SO4, GOL, A1CTH, 1PE |
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION
Release Date: 2026-01-28
Ligands: ZN, CO3, PEG, DMS, SO4, GOL, A1CTH, 1PE
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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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Crystal Structure Of The Mertk Kinase Domain In Complex With Inhibitor Mips15692
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.06 Å Release Date: 2021-10-06 Classification: SIGNALING PROTEIN/INHIBITOR Ligands: YR7 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-10-06
Ligands: YR7
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Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm589 (Ethyl 3-Methyl-4-((4-(Trifluoromethyl)Benzo[D]Oxazol-7-Yl)Methyl)-1H-Pyrrole-2-Carboxylate)
Organism: Plasmodium falciparum (isolate 3d7)
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2021-05-19 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: XAJ, FMN, ORO |
Organism: Plasmodium falciparum (isolate 3d7)
Method: X-RAY DIFFRACTION
Release Date: 2021-05-19
Ligands: XAJ, FMN, ORO
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Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm634 (3-Methyl-N-(1-(5-Methylisoxazol-3-Yl)Ethyl)-4-(4-(Trifluoromethyl)Benzyl)-1H-Pyrrole-2-Carboxamide)
Organism: Plasmodium falciparum (isolate 3d7)
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2021-05-19 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: XBY, FMN, ORO, GOL |
Organism: Plasmodium falciparum (isolate 3d7)
Method: X-RAY DIFFRACTION
Release Date: 2021-05-19
Ligands: XBY, FMN, ORO, GOL
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Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm697 (3-Methyl-N-(1-(5-Methylisoxazol-3-Yl)Ethyl)-4-(6-(Trifluoromethyl)-1H-Indol-3-Yl)-1H-Pyrrole-2-Carboxamide)
Organism: Plasmodium falciparum (isolate 3d7)
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2021-05-19 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: XCD, FMN, ORO |
Organism: Plasmodium falciparum (isolate 3d7)
Method: X-RAY DIFFRACTION
Release Date: 2021-05-19
Ligands: XCD, FMN, ORO
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Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm705 (N-(1-(1H-1,2,4-Triazol-3-Yl)Ethyl)-3-Methyl-4-(1-(6-(Trifluoromethyl)Pyridin-3-Yl)Cyclopropyl)-1H-Pyrrole-2-Carboxamide)
Organism: Plasmodium falciparum (isolate 3d7)
Method: X-RAY DIFFRACTION Resolution:1.75 Å Release Date: 2021-05-19 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: XC7, FMN, ORO, MG |
Organism: Plasmodium falciparum (isolate 3d7)
Method: X-RAY DIFFRACTION
Release Date: 2021-05-19
Ligands: XC7, FMN, ORO, MG
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Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm778 (3-Methyl-N-(1-(5-Methyl-1H-Pyrazol-3-Yl)Ethyl)-4-(1-(6-(Trifluoromethyl)Pyridin-3-Yl)Cyclopropyl)-1H-Pyrrole-2-Carboxamide)
Organism: Plasmodium falciparum (isolate 3d7)
Method: X-RAY DIFFRACTION Resolution:1.75 Å Release Date: 2021-05-19 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: XCM, FMN, ORO |
Organism: Plasmodium falciparum (isolate 3d7)
Method: X-RAY DIFFRACTION
Release Date: 2021-05-19
Ligands: XCM, FMN, ORO