Search Count: 137
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Cpkrs In Complex With Inhibitor Ddd01038762
Organism: Cryptosporidium parvum iowa ii
Method: X-RAY DIFFRACTION Resolution:1.84 Å Release Date: 2026-06-10 Classification: LIGASE Ligands: LYS, A1JCS, SO4, TRS |
Organism: Cryptosporidium parvum iowa ii
Method: X-RAY DIFFRACTION
Release Date: 2026-06-10
Ligands: LYS, A1JCS, SO4, TRS
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Crystal Structure Of Lysyl-Trna Synthetase From Cryptosporidium Parvum Complexed With L-Lysine And Inhibitor Ddd01887015
Organism: Cryptosporidium parvum iowa ii
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2026-06-10 Classification: LIGASE Ligands: A1JCT, EDO, TRS, GOL, LYS, SO4 |
Organism: Cryptosporidium parvum iowa ii
Method: X-RAY DIFFRACTION
Release Date: 2026-06-10
Ligands: A1JCT, EDO, TRS, GOL, LYS, SO4
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Crystal Structure Of Lysyl-Trna Synthetase From Cryptosporidium Parvum Complexed With L-Lysine And Inhibitor Ddd01932549
Organism: Cryptosporidium parvum iowa ii
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2026-06-10 Classification: LIGASE Ligands: LYS, A1JC7, SO4 |
Organism: Cryptosporidium parvum iowa ii
Method: X-RAY DIFFRACTION
Release Date: 2026-06-10
Ligands: LYS, A1JC7, SO4
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Crystal Structure Of Lysyl-Trna Synthetase From Cryptosporidium Parvum / Plasmodium Falciparum Chimera Complexed With L-Lysine And Inhibitor Ddd02174286
Organism: Cryptosporidium parvum iowa ii
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2026-06-10 Classification: LIGASE Ligands: LYS, A1JC4, GOL, SO4, TRS |
Organism: Cryptosporidium parvum iowa ii
Method: X-RAY DIFFRACTION
Release Date: 2026-06-10
Ligands: LYS, A1JC4, GOL, SO4, TRS
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Crystal Structure Of Lysyl-Trna Synthetase From Cryptosporidium Parvum Complexed With L-Lysine And Inhibitor Ddd01827593
Organism: Cryptosporidium parvum iowa ii
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2026-06-10 Classification: LIGASE Ligands: LYS, A1JC9, SO4 |
Organism: Cryptosporidium parvum iowa ii
Method: X-RAY DIFFRACTION
Release Date: 2026-06-10
Ligands: LYS, A1JC9, SO4
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Glucocorticoid Receptor Ligand Binding Domain In Complex With Dexamethasone
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.78 Å Release Date: 2025-11-12 Classification: DNA BINDING PROTEIN Ligands: DEX, CAC, EPE, GOL, SO4, CL, PG4, IMD, PEG, PGE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-11-12
Ligands: DEX, CAC, EPE, GOL, SO4, CL, PG4, IMD, PEG, PGE
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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 Apo Human Glutathione Synthetase Y270E
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.59 Å Release Date: 2024-05-08 Classification: BIOSYNTHETIC PROTEIN Ligands: SO4, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2024-05-08
Ligands: SO4, GOL
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Crystal Structure Of Bg505 Sosip.V4.1-Gt1.2 Trimer In Complex With Gl-Pgv20 And Pgt124 Fabs
Organism: Homo sapiens, Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION Resolution:3.82 Å Release Date: 2023-06-21 Classification: VIRAL PROTEIN/IMMUNE SYSTEM Ligands: NAG |
Organism: Homo sapiens, Human immunodeficiency virus 1
Method: X-RAY DIFFRACTION
Release Date: 2023-06-21
Ligands: NAG
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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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Complex Cyp33-Rrmdelta Alpha : Uaaugucg Rna
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Organism: Homo sapiens
Method: SOLUTION NMR
Release Date: 2022-05-04
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Free Form Of Extended Cyp33-Rrm
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Organism: Homo sapiens
Method: SOLUTION NMR
Release Date: 2022-04-13