Search Count: 20
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Hbx Fused Ddb1 4M Mutant
Organism: Hepatitis b virus, Homo sapiens
Method: ELECTRON MICROSCOPY Release Date: 2025-06-04 Classification: VIRAL PROTEIN |
Organism: Hepatitis b virus, Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2025-06-04
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Hbx Complexed With Ddb1
Organism: Homo sapiens, Hepatitis b virus
Method: ELECTRON MICROSCOPY Release Date: 2025-06-04 Classification: VIRAL PROTEIN |
Organism: Homo sapiens, Hepatitis b virus
Method: ELECTRON MICROSCOPY
Release Date: 2025-06-04
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Sars-Cov-2 Spike Rbd In Complex With Neutralizing Antibody Ut28K
Organism: Severe acute respiratory syndrome coronavirus 2, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.75 Å Release Date: 2022-05-25 Classification: VIRAL PROTEIN |
Organism: Severe acute respiratory syndrome coronavirus 2, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-05-25
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Discovery Of Clinical Candidate N-{(1S)-1-[3-Fluoro-4-(Trifluoromethoxy)Phenyl]-2-Methoxyethyl}-7-Methoxy-2-Oxo-2,3-Dihydropyrido[2,3-B]Pyrazine-4(1H)-Carboxamide (Tak-915), A Highly Potent, Selective, And Brain-Penetrating Phosphodiesterase 2A Inhibitor For The Treatment Of Cognitive Disorders
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2017-08-23 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: ZN, MG, 9GJ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-08-23
Ligands: ZN, MG, 9GJ
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Crystal Structure Of Human Phosphodiesterase 2A In Complex With 6-Methyl-N-(1-(4-(Trifluoromethoxy)Phenyl)Propyl)Pyrazolo[1,5-A]Pyrimidine-3-Carboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.16 Å Release Date: 2017-08-16 Classification: HYDROLASE Ligands: MG, ZN, 87R |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2017-08-16
Ligands: MG, ZN, 87R
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Crystal Structure Of Human K-Ras G12D Mutant In Complex With Gdp And Cyclic Inhibitory Peptide
Organism: Homo sapiens, Enterobacteria phage t7
Method: X-RAY DIFFRACTION Resolution:1.25 Å Release Date: 2017-05-24 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: GDP, EDO |
Organism: Homo sapiens, Enterobacteria phage t7
Method: X-RAY DIFFRACTION
Release Date: 2017-05-24
Ligands: GDP, EDO
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Structure Of Tyk2 With Inhibitor 16: 3-Azanyl-5-[(2~{S})-3-Methylbutan-2-Yl]-7-[1-Methyl-5-(2-Oxidanylpropan-2-Yl)Pyrazol-3-Yl]-1~{H}-Pyrazolo[4,3-C]Pyridin-4-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.65 Å Release Date: 2016-01-13 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 5U3 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-01-13
Ligands: 5U3
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Structure Of Tyk2 With Inhibitor 4: 3-Azanyl-5-(2-Methylphenyl)-7-(1-Methylpyrazol-3-Yl)-1~{H}-Pyrazolo[4,3-C]Pyridin-4-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.91 Å Release Date: 2016-01-13 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 5U4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-01-13
Ligands: 5U4
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Crystal Structure Of S6K1 Kinase Domain In Complex With A Pyrimidine Derivative Pf-4708671 2-{[4-(5-Ethylpyrimidin-4-Yl)Piperazin-1-Yl]Methyl}-5-(Trifluoromethyl)-1H-Benzimidazole
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2014-08-06 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: ZN, 5FI |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-08-06
Ligands: ZN, 5FI
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Crystal Structure Of S6K1 Kinase Domain In Complex With A Pyrazolopyrimidine Derivative 4-[4-(1H-Benzimidazol-2-Yl)Piperidin-1-Yl]-1H-Pyrazolo[3,4-D]Pyrimidine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2014-08-06 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: ZN, FZ8 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-08-06
Ligands: ZN, FZ8
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Crystal Structure Of S6K1 Kinase Domain In Complex With A Pyrazolopyrimidine Derivative 4-[4-(1H-Indol-3-Yl)-3,6-Dihydropyridin-1(2H)-Yl]-1H-Pyrazolo[3,4-D]Pyrimidine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.03 Å Release Date: 2014-08-06 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: ZN, FZ9 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-08-06
Ligands: ZN, FZ9
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Crystal Structure Of S6K1 Kinase Domain In Complex With A Purine Derivative 1-(9H-Purin-6-Yl)-N-[3-(Trifluoromethyl)Phenyl]Piperidine-4-Carboxamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2014-08-06 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: ZN, FS9, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-08-06
Ligands: ZN, FS9, GOL
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Crystal Structure Of S6K1 Kinase Domain In Complex With A Quinoline Derivative 2-Oxo-2-[(4-Sulfamoylphenyl)Amino]Ethyl 7,8,9,10-Tetrahydro-6H-Cyclohepta[B]Quinoline-11-Carboxylate
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.98 Å Release Date: 2014-08-06 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: ZN, F76, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-08-06
Ligands: ZN, F76, GOL
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Crystal Structure Of S6K1 Kinase Domain In Complex With A Quinoline Derivative 1-Oxo-1-[(4-Sulfamoylphenyl)Amino]Propan-2-Yl-2-Methyl-1,2,3,4-Tetrahydroacridine-9-Carboxylate
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.04 Å Release Date: 2014-08-06 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: ZN, FS7, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-08-06
Ligands: ZN, FS7, GOL
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Crystal Structure Of Phosphodiesterase 4B In Complex With Compound 10F
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2013-10-23 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: QPC, ZN, CA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-10-23
Ligands: QPC, ZN, CA
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Crystal Structure Of Phosphodiesterase 4B In Complex With Compound 31E
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2013-05-29 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: NVW, ZN, CA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-05-29
Ligands: NVW, ZN, CA
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Crystal Structure Of Lump Complexed With Riboflavin
Organism: Photobacterium kishitanii
Method: X-RAY DIFFRACTION Resolution:1.42 Å Release Date: 2009-11-10 Classification: LUMINESCENT PROTEIN Ligands: RBF |
Organism: Photobacterium kishitanii
Method: X-RAY DIFFRACTION
Release Date: 2009-11-10
Ligands: RBF
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Crystal Structure Of Lump Complexed With Flavin Mononucleotide
Organism: Photobacterium kishitanii
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2009-11-10 Classification: LUMINESCENT PROTEIN Ligands: FMN, RBF |
Organism: Photobacterium kishitanii
Method: X-RAY DIFFRACTION
Release Date: 2009-11-10
Ligands: FMN, RBF
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Crystal Structure Of Lump Complexed With 6,7-Dimethyl-8-(1'-D-Ribityl) Lumazine
Organism: Photobacterium kishitanii
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2009-11-10 Classification: LUMINESCENT PROTEIN Ligands: DLZ |
Organism: Photobacterium kishitanii
Method: X-RAY DIFFRACTION
Release Date: 2009-11-10
Ligands: DLZ
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Double Layered 2D Crystal Structure Of Aquaporin-4 (Aqp4M23) At 3.2 A Resolution By Electron Crystallography
Organism: Rattus norvegicus
Method: ELECTRON CRYSTALLOGRAPHY Resolution:3.20 Å Release Date: 2006-01-31 Classification: TRANSPORT PROTEIN |
Organism: Rattus norvegicus
Method: ELECTRON CRYSTALLOGRAPHY
Release Date: 2006-01-31