Search Count: 29
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.48 Å Release Date: 2026-03-25 Classification: NUCLEAR PROTEIN Ligands: A1C14 |
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Organism: Homo sapiens, Mus musculus, Hepatitis b virus
Method: X-RAY DIFFRACTION Resolution:2.35 Å Release Date: 2025-10-01 Classification: VIRAL PROTEIN/IMMUNE SYSTEM |
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Organism: Homo sapiens, Mus musculus, Hepatitis b virus
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2025-10-01 Classification: VIRAL PROTEIN/IMMUNE SYSTEM |
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Organism: Homo sapiens, Mus musculus, Hepatitis b virus
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2025-10-01 Classification: VIRAL PROTEIN/IMMUNE SYSTEM |
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Organism: Homo sapiens, Lama glama, Mus musculus
Method: ELECTRON MICROSCOPY Release Date: 2025-10-01 Classification: PEPTIDE BINDING PROTEIN/IMMUNE SYSTEM |
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Organism: Human herpesvirus 1 (strain 17), Homo sapiens
Method: ELECTRON MICROSCOPY Resolution:2.20 Å Release Date: 2025-08-13 Classification: ANTIVIRAL PROTEIN |
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Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Resolution:2.10 Å Release Date: 2025-08-13 Classification: ANTIVIRAL PROTEIN |
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Organism: Lama glama, Homo sapiens, Human herpesvirus 2
Method: ELECTRON MICROSCOPY Resolution:2.30 Å Release Date: 2025-08-13 Classification: ANTIVIRAL PROTEIN |
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Human Jmjd5 In Complex With Mn And 5-((4-Methoxybenzyl)Amino)Pyridine-2,4-Dicarboxylic Acid.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.62 Å Release Date: 2022-02-02 Classification: OXIDOREDUCTASE Ligands: MN, HR3 |
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Human Jmjd5 In Complex With Mn And 5-((4-Phenylbutyl)Amino)Pyridine-2,4-Dicarboxylic Acid.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.72 Å Release Date: 2022-02-02 Classification: OXIDOREDUCTASE Ligands: TRS, MN, HR9 |
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Human Jmjd5 In Complex With Mn And 5-(Benzylamino)Pyridine-2,4-Dicarboxylic Acid.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.92 Å Release Date: 2022-02-02 Classification: OXIDOREDUCTASE Ligands: MN, HRF |
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Human Jmjd5 In Complex With Mn And 5-((2-Methoxybenzyl)Amino)Pyridine-2,4-Dicarboxylic Acid.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.13 Å Release Date: 2022-02-02 Classification: OXIDOREDUCTASE Ligands: HRL, MN |
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Human Jmjd5 In Complex With Mn And 5-((2-Cyclopropylbenzyl)Amino)Pyridine-2,4-Dicarboxylic Acid.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.27 Å Release Date: 2022-02-02 Classification: OXIDOREDUCTASE Ligands: MN, HRR |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2021-02-03 Classification: IMMUNE SYSTEM Ligands: MAN, NAG, U57 |
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Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.26 Å Release Date: 2018-09-12 Classification: PROTEIN BINDING Ligands: HRY, GOL |
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Triazolopyridine Compounds As Selective Jak1 Inhibitors: From Hit Identification To Glpg0634
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2014-11-19 Classification: TRANSFERASE Ligands: 2HB |
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Structure Of The M1 Alanylaminopeptidase From Malaria Complexed With A Hydroxamic Acid-Based Inhibitor
Organism: Plasmodium falciparum fcb1/columbia
Method: X-RAY DIFFRACTION Resolution:1.98 Å Release Date: 2014-10-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, DMS, GOL, R5T |
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Structure Of The M1 Alanylaminopeptidase From Malaria Complexed With A Hydroxamic Acid-Based Inhibitor
Organism: Plasmodium falciparum fcb1/columbia
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2014-10-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, R5V, GOL |
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Structure Of The M1 Alanylaminopeptidase From Malaria Complexed With A Hydroxamic Acid-Based Inhibitor
Organism: Plasmodium falciparum fcb1/columbia
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2014-10-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, GOL, MG, R5X, DMS |
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Structure Of The M17 Leucyl Aminopeptidase From Malaria Complexed With A Hydroxamic Acid-Based Inhibitor
Organism: Plasmodium falciparum 3d7
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2014-10-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, CO3, SO4, R5T, 1PE, DMS |