Search Count: 142
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Cryoem Structure Of Human Mata2 In Complex With Mat2B Isoform V1 At 2.6 A Resolution
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Resolution:2.90 Å Release Date: 2026-05-13 Classification: TRANSFERASE |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2026-05-13
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Cryoem Structure Of Human Mata2 In Complex With Mat2B Isoform V1 At 2.6 A Resolution
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Resolution:3.10 Å Release Date: 2026-05-13 Classification: TRANSFERASE |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2026-05-13
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Cryoem Structure Of Human Mata2 In Complex With Matbv2 At 2.6 A Resolution
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Resolution:2.60 Å Release Date: 2026-04-08 Classification: TRANSFERASE |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2026-04-08
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Cryoem Structure Of Human Mata2 In Complex With Mat2B Isoform V1 At 2.6 A Resolution
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Resolution:2.60 Å Release Date: 2026-04-08 Classification: TRANSFERASE |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2026-04-08
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Vitamin D Receptor Complex With A Vitamin D Receptor Agonist/Histone Deacetylase Inhibitor Hybrid Molecule
Organism: Danio rerio, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2025-10-01 Classification: TRANSCRIPTION Ligands: A1JD5 |
Organism: Danio rerio, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2025-10-01
Ligands: A1JD5
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Cryo-Em Structure Of The Autoinhibitory Cd163 Trimer
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Resolution:3.00 Å Release Date: 2025-06-18 Classification: ENDOCYTOSIS Ligands: CA, NAG |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2025-06-18
Ligands: CA, NAG
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Cryo-Em Structure Of The Cd163/Hp(1-1)Hb Complex
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Resolution:3.30 Å Release Date: 2025-06-18 Classification: ENDOCYTOSIS Ligands: NAG, CA, HEM, OXY |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2025-06-18
Ligands: NAG, CA, HEM, OXY
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Cryo-Em Structure Of The Cd163/Hpsphb Complex
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Resolution:4.00 Å Release Date: 2025-06-18 Classification: ENDOCYTOSIS Ligands: CA, HEM, OXY |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2025-06-18
Ligands: CA, HEM, OXY
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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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Cryoem Structure Of The Hendra Henipavirus Nucleocapsid Sauronoid Assembly Multimer
Organism: Hendra henipavirus, Escherichia coli bl21(de3)
Method: ELECTRON MICROSCOPY Release Date: 2024-06-26 Classification: VIRAL PROTEIN |
Organism: Hendra henipavirus, Escherichia coli bl21(de3)
Method: ELECTRON MICROSCOPY
Release Date: 2024-06-26
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Cryoem Structure Of The Hendra Henipavirus Nucleocapsid Sauronoid Assembly Monomer
Organism: Hendra henipavirus, Escherichia coli bl21(de3)
Method: ELECTRON MICROSCOPY Release Date: 2024-06-26 Classification: VIRAL PROTEIN |
Organism: Hendra henipavirus, Escherichia coli bl21(de3)
Method: ELECTRON MICROSCOPY
Release Date: 2024-06-26
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Inactive D62N Mutant Of Bt1760 Endo-Acting Levanase From Bacteroides Thetaiotaomicron Vpi-5482
Organism: Bacteroides thetaiotaomicron
Method: X-RAY DIFFRACTION Resolution:2.65 Å Release Date: 2023-06-21 Classification: HYDROLASE Ligands: SO4 |
Organism: Bacteroides thetaiotaomicron
Method: X-RAY DIFFRACTION
Release Date: 2023-06-21
Ligands: SO4
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Inactive D62N Mutant Of Bt1760 Endo-Acting Levanase From Bacteroides Thetaiotaomicron Vpi-5482
Organism: Bacteroides thetaiotaomicron vpi-5482
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2023-06-21 Classification: HYDROLASE Ligands: SO4 |
Organism: Bacteroides thetaiotaomicron vpi-5482
Method: X-RAY DIFFRACTION
Release Date: 2023-06-21
Ligands: SO4