Search Count: 26
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Cryoem Structure Of Nadh:Quinone Oxidoreductases Yjlcd From Bacillus Subtilis
Organism: Bacillus subtilis subsp. subtilis str. 168
Method: ELECTRON MICROSCOPY Release Date: 2026-07-01 Classification: OXIDOREDUCTASE Ligands: FAD, SHV, 6NA, 3PE, LEA, GOL, DKA |
Organism: Bacillus subtilis subsp. subtilis str. 168
Method: ELECTRON MICROSCOPY
Release Date: 2026-07-01
Ligands: FAD, SHV, 6NA, 3PE, LEA, GOL, DKA
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Crystal Structure Of Rhodesain In Complex With A Macrolactam Inhibitor
Organism: Trypanosoma brucei rhodesiense
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2018-04-11 Classification: HYDROLASE Ligands: C2K, EDO |
Organism: Trypanosoma brucei rhodesiense
Method: X-RAY DIFFRACTION
Release Date: 2018-04-11
Ligands: C2K, EDO
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Crystal Structure Of Rhodesain In Complex With A Macrolactam Inhibitor
Organism: Trypanosoma brucei rhodesiense
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2018-04-11 Classification: HYDROLASE Ligands: EDO, C3E |
Organism: Trypanosoma brucei rhodesiense
Method: X-RAY DIFFRACTION
Release Date: 2018-04-11
Ligands: EDO, C3E
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Crystal Structure Of Rhodesain In Complex With A Macrolactam Inhibitor
Organism: Trypanosoma brucei rhodesiense
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2018-04-11 Classification: HYDROLASE Ligands: EDO, C2W |
Organism: Trypanosoma brucei rhodesiense
Method: X-RAY DIFFRACTION
Release Date: 2018-04-11
Ligands: EDO, C2W
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Cathepsin L In Complex With (3S,14E)-19-Chloro-N-(1-Cyanocyclopropyl)-5-Oxo-12,17-Dioxa-4-Azatricyclo[16.2.2.06,11]Docosa-1(21),6(11),7,9,14,18(22),19-Heptaene-3-Carboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.37 Å Release Date: 2018-04-11 Classification: HYDROLASE Ligands: C3E, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-04-11
Ligands: C3E, GOL
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Cathepsin L In Complex With (3S,14E)-19-Chloro-N-(1-Cyanocyclopropyl)-5-Oxo-17-Oxa-4-Azatricyclo[16.2.2.06,11]Docosa-1(21),6,8,10,14,18(22),19-Heptaene-3-Carboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.34 Å Release Date: 2018-04-11 Classification: HYDROLASE Ligands: C7Q |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-04-11
Ligands: C7Q
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Cathepsin L In Complex With (3S,14E)-8-(Azetidin-3-Yl)-19-Chloro-N-(1-Cyanocyclopropyl)-5-Oxo-12,17-Dioxa-4-Azatricyclo[16.2.2.06,11]Docosa-1(21),6,8,10,14,18(22),19-Heptaene-3-Carboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.02 Å Release Date: 2018-04-11 Classification: HYDROLASE Ligands: C7T, ZN, CL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-04-11
Ligands: C7T, ZN, CL
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Structure Of Maf Glycosyltransferase From Magnetospirillum Magneticum Amb-1
Organism: Magnetospirillum magneticum amb-1
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2017-11-15 Classification: TRANSFERASE Ligands: SO4, CL, PGE, PG4, EDO |
Organism: Magnetospirillum magneticum amb-1
Method: X-RAY DIFFRACTION
Release Date: 2017-11-15
Ligands: SO4, CL, PGE, PG4, EDO
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Crystal Structure Of Trypanothione Reductase From Trypanosoma Brucei In Complex With Inhibitor Ep127 (5-{5-[1-(Pyrrolidin-1-Yl)Cyclohexyl]-1,3-Thiazol-2-Yl}-1H-Indole)
Organism: Trypanosoma brucei brucei
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2014-05-14 Classification: Oxidoreductase/Oxidoreductase inhibitor Ligands: FAD, 2JR, SO4, EPE |
Organism: Trypanosoma brucei brucei
Method: X-RAY DIFFRACTION
Release Date: 2014-05-14
Ligands: FAD, 2JR, SO4, EPE
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Crystal Structure Of Trypanothione Reductase From Trypanosoma Cruzi In Complex With Inhibitor Ep127 (5-{5-[1-(Pyrrolidin-1-Yl)Cyclohexyl]-1,3-Thiazol-2-Yl}-1H-Indole)
Organism: Trypanosoma cruzi
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2014-05-14 Classification: Oxidoreductase/Oxidoreductase inhibitor Ligands: FAD, 2JR |
Organism: Trypanosoma cruzi
Method: X-RAY DIFFRACTION
Release Date: 2014-05-14
Ligands: FAD, 2JR
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Crystal Structure Of Plasmodium Falciparum Fabi Complexed With Nad And Inhibitor 7-(4-Chloro-2-Hydroxyphenoxy)-4-Methyl-2H-Chromen-2-One
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2013-11-06 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: CHJ, NAD, GOL, SO4 |
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION
Release Date: 2013-11-06
Ligands: CHJ, NAD, GOL, SO4
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Crystal Structure Of Plasmodium Falciparum Fabi Complexed With Nad And Inhibitor 3-(4-Chloro-2-Hydroxyphenoxy)-7-Hydroxy-2H-Chromen-2-One
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2013-11-06 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: CHV, NAD, GOL, SO4 |
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION
Release Date: 2013-11-06
Ligands: CHV, NAD, GOL, SO4
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5'-Diphenyl Nucleoside Inhibitors Of Plasmodium Falciparum Dutpase
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2012-08-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: DUA, GOL |
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION
Release Date: 2012-08-29
Ligands: DUA, GOL
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5'-Diphenyl Nucleoside Inhibitors Of Plasmodium Falciparum Dutpase
Organism: Plasmodium falciparum 3d7, Escherichia coli
Method: X-RAY DIFFRACTION Resolution:1.65 Å Release Date: 2012-08-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: DU3, SO4 |
Organism: Plasmodium falciparum 3d7, Escherichia coli
Method: X-RAY DIFFRACTION
Release Date: 2012-08-29
Ligands: DU3, SO4
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5'-Diphenyl Nucleoside Inhibitors Of Plasmodium Falciparum Dutpase
Organism: Plasmodium falciparum, Synthetic construct
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2012-08-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: DU2, SO4 |
Organism: Plasmodium falciparum, Synthetic construct
Method: X-RAY DIFFRACTION
Release Date: 2012-08-29
Ligands: DU2, SO4
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5'-Diphenyl Nucleoside Inhibitors Of Plasmodium Falciparum Dutpase
Organism: Plasmodium falciparum, Synthetic construct
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2012-08-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: DU4, SO4 |
Organism: Plasmodium falciparum, Synthetic construct
Method: X-RAY DIFFRACTION
Release Date: 2012-08-29
Ligands: DU4, SO4
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Plasmodium Falciparum Dutpase In Complex With A Trityl Ligand
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2012-03-07 Classification: HYDROLASE Ligands: DUQ, SO4 |
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION
Release Date: 2012-03-07
Ligands: DUQ, SO4
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Quadruple Mutant(N51I+C59R+S108N+I164L) Plasmodium Falciparum Dihydrofolate Reductase-Thymidylate Synthase(Pfdhfr-Ts) Complexed With Qn254, Nadph, And Dump
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2010-07-28 Classification: OXIDOREDUCTASE, TRANSFERASE Ligands: KA5, NDP, UMP |
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION
Release Date: 2010-07-28
Ligands: KA5, NDP, UMP
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Novel Inhibitors Of Plasmodium Falciparum Dutpase Provide A Platform For Anti-Malarial Drug Design
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2005-05-26 Classification: HYDROLASE Ligands: DUX |
Organism: Plasmodium falciparum
Method: X-RAY DIFFRACTION
Release Date: 2005-05-26
Ligands: DUX
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Strong Binding In The Dna Minor Groove By An Aromatic Diamidine With A Shape That Does Not Match The Curvature Of The Groove
Method: X-RAY DIFFRACTION
Resolution:1.78 Å Release Date: 2002-11-15 Classification: DNA Ligands: MG, CGQ |
Method: X-RAY DIFFRACTION
Release Date: 2002-11-15
Ligands: MG, CGQ