Search Count: 92
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.93 Å Release Date: 2026-01-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: A1CKP, SO4 |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.12 Å Release Date: 2026-01-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: A1CKQ, SO4 |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.43 Å Release Date: 2026-01-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: A1CKS, SO4 |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.47 Å Release Date: 2026-01-07 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: A1CMW, MTA |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.36 Å Release Date: 2026-01-07 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: A1CMZ, MTA |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.04 Å Release Date: 2026-01-07 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: MTA, A1CM0, SO4 |
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Methyl-Coenzyme M Reductase Of Anme-2D Candidatus Methanoperedens Vercelli Strain 1 From A Bioreactor Enrichment Culture
Organism: Candidatus methanoperedens sp.
Method: X-RAY DIFFRACTION Resolution:0.98 Å Release Date: 2025-07-23 Classification: TRANSFERASE Ligands: K, F43, EDO, TP7, COM, SHT |
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Krypton-Pressurized Methyl-Coenzyme M Reductase Of An Anme-2C Isolated From A Microbial Enrichment
Organism: Candidatus methanogasteraceae archaeon
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2025-07-16 Classification: TRANSFERASE Ligands: KR, MG, PGE, EDO, CL, TP7, F43, PEG, GOL, COM, NA, K |
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Methyl-Coenzyme M Reductase Of Anme-2D Candidatus Methanoperedens Sp. Blz2 From A Bioreactor Enrichment Culture
Organism: Candidatus methanoperedens sp. blz2
Method: X-RAY DIFFRACTION Resolution:0.98 Å Release Date: 2025-07-16 Classification: TRANSFERASE |
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Organism: Candidatus methanogasteraceae archaeon
Method: X-RAY DIFFRACTION Resolution:1.34 Å Release Date: 2025-07-16 Classification: TRANSFERASE Ligands: K, NA, CL, F43, COM, TP7, GOL, MPD, EDO |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.99 Å Release Date: 2025-05-28 Classification: IMMUNE SYSTEM,TRANSFERASE/INHIBITOR Ligands: A1BW0, DMS |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2025-05-28 Classification: IMMUNE SYSTEM,TRANSFERASE/INHIBITOR Ligands: A1BWX |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.33 Å Release Date: 2025-05-28 Classification: IMMUNE SYSTEM,TRANSFERASE/INHIBITOR Ligands: A1BW1 |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.73 Å Release Date: 2025-05-28 Classification: IMMUNE SYSTEM,TRANSFERASE/INHIBITOR Ligands: A1BWY, SO4 |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.14 Å Release Date: 2025-05-28 Classification: IMMUNE SYSTEM,TRANSFERASE/INHIBITOR Ligands: A1BWZ, SO4 |
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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 |
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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 |
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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 |
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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 |
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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 |