Search Count: 23
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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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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 The Grapevine Defensin Vvk1
Organism: Vitis vinifera
Method: X-RAY DIFFRACTION Resolution:1.30 Å Release Date: 2020-09-16 Classification: ANTIMICROBIAL PROTEIN |
Organism: Vitis vinifera
Method: X-RAY DIFFRACTION
Release Date: 2020-09-16
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Structure Of Egk Peptide
Organism: Elaeis guineensis
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2020-09-09 Classification: PROTEIN BINDING |
Organism: Elaeis guineensis
Method: X-RAY DIFFRACTION
Release Date: 2020-09-09
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Nmr Solution Structure Of Wild Type Hfabp1 With Gw7647
Organism: Homo sapiens
Method: SOLUTION NMR Release Date: 2019-01-02 Classification: LIPID BINDING PROTEIN |
Organism: Homo sapiens
Method: SOLUTION NMR
Release Date: 2019-01-02
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Nmr Solution Structure Of Wild Type Apo Hfabp1 At 308 K
Organism: Homo sapiens
Method: SOLUTION NMR Release Date: 2018-12-26 Classification: LIPID BINDING PROTEIN |
Organism: Homo sapiens
Method: SOLUTION NMR
Release Date: 2018-12-26
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Nmr Solution Structure Of Wild Type Hfabp1 With Gw7647
Organism: Homo sapiens
Method: SOLUTION NMR Release Date: 2018-12-26 Classification: LIPID BINDING PROTEIN Ligands: 2VN |
Organism: Homo sapiens
Method: SOLUTION NMR
Release Date: 2018-12-26
Ligands: 2VN