Search Count: 36
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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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Co-Crystal Structure Of Toxoplasma Gondii Prolyl Trna Synthetase (Tgprs) In Complex With L96 And L-Pro
Organism: Toxoplasma gondii
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2023-02-08 Classification: TRANSLATION/INHIBITOR Ligands: 1UI, PRO, MES, FMT, ACT |
Organism: Toxoplasma gondii
Method: X-RAY DIFFRACTION
Release Date: 2023-02-08
Ligands: 1UI, PRO, MES, FMT, ACT
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Plasmodium Falciparum Prolyl-Trna Synthetase (Pfprs) In Complex With L-Proline And Compound L95
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION Resolution:2.58 Å Release Date: 2023-01-04 Classification: LIGASE Ligands: JE6, PRO |
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION
Release Date: 2023-01-04
Ligands: JE6, PRO
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Plasmodium Falciparum Prolyl-Trna Synthetase (Pfprs) In Complex With L-Proline And Compound L97
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION Resolution:2.39 Å Release Date: 2023-01-04 Classification: LIGASE/LIGASE INHIBITOR Ligands: PRO, 1XK, BU1, CL, HEZ |
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION
Release Date: 2023-01-04
Ligands: PRO, 1XK, BU1, CL, HEZ
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Structure Of Plasmepsin X (Pm10, Pmx) From Plasmodium Falciparum 3D7 In Complex With Ucb7362
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION Resolution:2.85 Å Release Date: 2022-10-19 Classification: HYDROLASE Ligands: TWU |
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION
Release Date: 2022-10-19
Ligands: TWU
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Homo Sapiens Prolyl-Trna Synthetase (Hsprs) In Complex With L-Proline And Compound L95
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2022-10-05 Classification: LIGASE Ligands: JE6, ZN, CA, PRO, CL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-10-05
Ligands: JE6, ZN, CA, PRO, CL
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Homo Sapiens Prolyl-Trna Synthetase (Hsprs) In Complex With L-Proline And Compound L97
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2022-10-05 Classification: LIGASE/LIGASE INHIBITOR Ligands: 1XK, ZN, CA, CL, PRO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-10-05
Ligands: 1XK, ZN, CA, CL, PRO
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Homo Sapiens Prolyl-Trna Synthetase (Hsprs) In Complex With L-Proline And Compound L95
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2022-10-05 Classification: LIGASE/LIGASE INHIBITOR Ligands: JE6, ZN, CA, CL, PRO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-10-05
Ligands: JE6, ZN, CA, CL, PRO
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Homo Sapiens Prolyl-Trna Synthetase (Hsprs) In Complex With L-Proline And Compound L96
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2022-10-05 Classification: LIGASE/LIGASE INHIBITOR Ligands: 1UI, ZN, CA, CL, PRO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-10-05
Ligands: 1UI, ZN, CA, CL, PRO
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Co-Crystal Structure Of Toxoplasma Gondii Prolyl Trna Synthetase (Tgprs) In Complex With L97 And L-Pro
Organism: Toxoplasma gondii
Method: X-RAY DIFFRACTION Resolution:2.42 Å Release Date: 2022-09-28 Classification: TRANSLATION Ligands: 1XK, PRO |
Organism: Toxoplasma gondii
Method: X-RAY DIFFRACTION
Release Date: 2022-09-28
Ligands: 1XK, PRO