Search Count: 23
 |
Structure Of Plasmodium Falciparum 20S Proteasome Bound To An Asparagine-Ethylenediamine Based Inhibitor Tdi6245
Organism: Plasmodium falciparum
Method: ELECTRON MICROSCOPY Resolution:2.86 Å Release Date: 2026-07-29 Classification: HYDROLASE Ligands: A1CRS |
Organism: Plasmodium falciparum
Method: ELECTRON MICROSCOPY
Release Date: 2026-07-29
Ligands: A1CRS
 |
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
 |
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
 |
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
 |
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
 |
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
 |
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
 |
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
 |
Crystal Structure Of Hte Cryptosporidium Muris Cytosolic Leucyl-Trna Synthetase Editing Domain Complex With A Post-Transfer Editing Analogue Of Norvaline (Nv2Aa)
Organism: Cryptosporidium muris
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2016-08-03 Classification: LYASE Ligands: VRT, EDO, K |
Organism: Cryptosporidium muris
Method: X-RAY DIFFRACTION
Release Date: 2016-08-03
Ligands: VRT, EDO, K
 |
Crystal Structure Of The Cryptosporidium Muris Cytosolic Leucyl-Trna Synthetase Editing Domain Complex With A Post-Transfer Editing Analogue Of Isoeucine (Ile2Aa)
Organism: Cryptosporidium muris
Method: X-RAY DIFFRACTION Resolution:1.77 Å Release Date: 2016-08-03 Classification: LYASE Ligands: PO4, SO8 |
Organism: Cryptosporidium muris
Method: X-RAY DIFFRACTION
Release Date: 2016-08-03
Ligands: PO4, SO8
 |
Crystal Structure Of The Cryptosporidium Muris Cytosolic Leucyl-Trna Synthetase Editing Domain Complex With The Adduct Amp-An6426
Organism: Cryptosporidium muris
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2016-08-03 Classification: LIGASE Ligands: A2H, PO4 |
Organism: Cryptosporidium muris
Method: X-RAY DIFFRACTION
Release Date: 2016-08-03
Ligands: A2H, PO4
 |
Crystal Structure Of The Cryptosporidium Muris Cytosolic Leucyl-Trna Synthetase Editing Domain (Apo Structure)
Organism: Cryptosporidium muris
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2016-08-03 Classification: LIGASE |
Organism: Cryptosporidium muris
Method: X-RAY DIFFRACTION
Release Date: 2016-08-03
 |
Crystal Structure Of The P.Falciparum Cytosolic Leucyl-Trna Synthetase Editing Domain (Space Group P1)
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2016-06-22 Classification: LIGASE |
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION
Release Date: 2016-06-22
 |
Crystal Structure Of The P.Falciparum Cytosolic Leucyl-Trna Synthetase Editing Domain (Space Group P21)
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2016-06-22 Classification: LIGASE |
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION
Release Date: 2016-06-22
 |
Crystal Structure Of The P.Falciparum Cytosolic Leucyl-Trna Synthetase Editing Domain (Space Group P1) Containing Deletions Of Insertions 1 And 3
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2016-06-22 Classification: LIGASE Ligands: EDO |
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION
Release Date: 2016-06-22
Ligands: EDO
 |
Crystal Structure Of The P.Knowlesi Cytosolic Leucyl-Trna Synthetase Editing Domain
Organism: Plasmodium knowlesi
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2016-06-22 Classification: LIGASE |
Organism: Plasmodium knowlesi
Method: X-RAY DIFFRACTION
Release Date: 2016-06-22
 |
Crystal Structure Of Falcipain-3 With Its Inhibitor, K11017
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION Resolution:2.42 Å Release Date: 2009-01-20 Classification: HYDROLASE Ligands: C1P, SO4 |
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION
Release Date: 2009-01-20
Ligands: C1P, SO4
 |
Crystal Structure Of Falcipain-2 With Its Inhibitor, E64
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION Resolution:2.90 Å Release Date: 2008-12-30 Classification: HYDROLASE Ligands: E64, GOL |
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION
Release Date: 2008-12-30
Ligands: E64, GOL
 |
Crystal Structure Of Falcipain-3 With Its Inhibitor, Leupeptin
Organism: Streptomyces roseus, Plasmodium falciparum
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2008-12-30 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: SO4 |
Organism: Streptomyces roseus, Plasmodium falciparum
Method: X-RAY DIFFRACTION
Release Date: 2008-12-30
Ligands: SO4
 |
The Crystal Structure Of Rhodesain, The Major Cysteine Protease Of T. Brucei Rhodesiense, Bound To Inhibitor K777
Organism: Trypanosoma brucei rhodesiense
Method: X-RAY DIFFRACTION Resolution:1.65 Å Release Date: 2008-03-25 Classification: HYDROLASE Ligands: D1R |
Organism: Trypanosoma brucei rhodesiense
Method: X-RAY DIFFRACTION
Release Date: 2008-03-25
Ligands: D1R