Search Count: 14
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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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Crystal Structure Of Human Pi3Ka (P110A Subunit) With Mmv085400 Bound To The Active Site Determined At 2.9 Angstroms Resolution
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.91 Å Release Date: 2022-05-04 Classification: TRANSFERASE/INHIBITOR Ligands: ZHY |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-05-04
Ligands: ZHY
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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
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Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm782 (N-(1-(5-Cyano-1H-Pyrazol-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:1.60 Å Release Date: 2021-05-19 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: XCV, FMN, ORO |
Organism: Plasmodium falciparum (isolate 3d7)
Method: X-RAY DIFFRACTION
Release Date: 2021-05-19
Ligands: XCV, FMN, ORO
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Crystal Structure Of Plasmodium Falciparum Dihydroorotate Dehydrogenase Bound With Inhibitor Dsm784 (3-(1-(3-Methyl-4-((6-(Trifluoromethyl)Pyridin-3-Yl)Methyl)-1H-Pyrrole-2-Carboxamido)Ethyl)-1H-Pyrazole-5-Carboxamide)
Organism: Plasmodium falciparum (isolate 3d7)
Method: X-RAY DIFFRACTION Resolution:1.96 Å Release Date: 2021-05-19 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: XE7, FMN, ORO |
Organism: Plasmodium falciparum (isolate 3d7)
Method: X-RAY DIFFRACTION
Release Date: 2021-05-19
Ligands: XE7, FMN, ORO
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Crystal Structure Of Alpha-Amylase From Geobacillus Thermoleovorans, Gta, Complexed With Acarbose
Organism: Geobacillus thermoleovorans
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2013-03-13 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: CA, ACI |
Organism: Geobacillus thermoleovorans
Method: X-RAY DIFFRACTION
Release Date: 2013-03-13
Ligands: CA, ACI