Search Count: 23
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Structural And Biochemical Rationale For Beta Variant Protein Booster Vaccine Broad Cross-Neutralization Of Sars-Cov-2
Organism: Severe acute respiratory syndrome coronavirus 2
Method: ELECTRON MICROSCOPY Release Date: 2024-02-07 Classification: VIRAL PROTEIN Ligands: NAG |
Organism: Severe acute respiratory syndrome coronavirus 2
Method: ELECTRON MICROSCOPY
Release Date: 2024-02-07
Ligands: NAG
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Structural And Biochemical Rationale For Beta Variant Protein Booster Vaccine Broad Cross-Neutralization Of Sars-Cov-2
Organism: Severe acute respiratory syndrome coronavirus 2
Method: ELECTRON MICROSCOPY Release Date: 2024-02-07 Classification: VIRAL PROTEIN Ligands: NAG |
Organism: Severe acute respiratory syndrome coronavirus 2
Method: ELECTRON MICROSCOPY
Release Date: 2024-02-07
Ligands: NAG
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Trka Jm-Kinase With 1-(9{H}-Fluoren-9-Yl)-3-(2-Methyl-4-Phenyl-Pyrimidin-5-Yl)Urea
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.87 Å Release Date: 2016-12-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 6UE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-12-28
Ligands: 6UE
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Trka Jm-Kinase With {N}-(2-Pyridylmethyl)-2-[2-(2-Thienyl)Indol-1-Yl]Acetamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.04 Å Release Date: 2016-12-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 6UF |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-12-28
Ligands: 6UF
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Trka Jm-Kinase With 2-Fluoro-{N}-[2-(4-Fluorophenyl)-6-Methyl-3-Pyridyl]-4-(Trifluoromethyl)Benzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.24 Å Release Date: 2016-12-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 6UG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-12-28
Ligands: 6UG
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Trka Jm-Kinase With 1-(5-Methyl-3-Phenyl-1,2-Oxazol-4-Yl)-3-[[2-(Trifluoromethyl)Phenyl]Methyl]Urea
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.01 Å Release Date: 2016-12-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 6UH |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-12-28
Ligands: 6UH
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Trka Jm-Kinase With 1-(2-Methyl-4-Phenyl-Pyrimidin-5-Yl)-3-(1-Naphthyl)Urea
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.12 Å Release Date: 2016-12-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 6UJ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-12-28
Ligands: 6UJ
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Trka Jm-Kinase With 1-(2-Methyl-4-Phenyl-Pyrimidin-5-Yl)-3-[[2-(Trifluoromethyl)Phenyl]Methyl]Urea
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.14 Å Release Date: 2016-12-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 6UK |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-12-28
Ligands: 6UK
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Trka Jm-Kinase With 1-(2-Methyl-4-Phenyl-Pyrimidin-5-Yl)-3-(2-Pyridyl)Urea
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.67 Å Release Date: 2016-12-28 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 6UM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-12-28
Ligands: 6UM
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Structure-Activity Relationship Guides Enantiomeric Preference Among Potent Inhibitors Of B. Anthracis Dihydrofolate Reductase
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2013-02-13 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: CA, CL, 34S, 34R |
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: CA, CL, 34S, 34R
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Structure-Activity Relationship Guides Enantiomeric Preference Among Potent Inhibitors Of B. Anthracis Dihydrofolate Reductase
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION Resolution:2.35 Å Release Date: 2013-02-13 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: CA, CL, 31I |
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: CA, CL, 31I
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Structure-Activity Relationship Guides Enantiomeric Preference Among Potent Inhibitors Of B. Anthracis Dihydrofolate Reductase
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2013-02-13 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: CA, CL, 35I |
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: CA, CL, 35I
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Structure-Activity Relationship Guides Enantiomeric Preference Among Potent Inhibitors Of B. Anthracis Dihydrofolate Reductase
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2013-02-13 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: 52J, CA, CL, 52I |
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: 52J, CA, CL, 52I
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Structure-Activity Relationship Guides Enantiomeric Preference Among Potent Inhibitors Of B. Anthracis Dihydrofolate Reductase
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2013-02-13 Classification: OXIDOREDUCTASE/OXIDOREDUCTASE INHIBITOR Ligands: CA, 53I, CL, 53J |
Organism: Bacillus anthracis
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: CA, 53I, CL, 53J
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S. Aureus Dihydrofolate Reductase Co-Crystallized With Propyl-Dap Isobutenyl-Dihydrophthalazine Inhibitor
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2013-01-09 Classification: OXIDOREDUCTASE/INHIBITOR Ligands: 0U5, NAP, GOL |
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION
Release Date: 2013-01-09
Ligands: 0U5, NAP, GOL
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S. Aureus Dihydrofolate Reductase Co-Crystallized With Ethyl-Dap Isobutenyl-Dihydrophthalazine Inhibitor
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2013-01-09 Classification: OXIDOREDUCTASE/INHIBITOR Ligands: NAP, 0U6, GOL |
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION
Release Date: 2013-01-09
Ligands: NAP, 0U6, GOL
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High Resolution Crystal Structure Of Argos Bound To The Egf Domain Of Spitz
Organism: Drosophila melanogaster
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2008-05-20 Classification: HORMONE/SIGNALING PROTEIN Ligands: BR |
Organism: Drosophila melanogaster
Method: X-RAY DIFFRACTION
Release Date: 2008-05-20
Ligands: BR
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High Resolution Crystal Structure Of The Egf Domain Of Spitz
Organism: Drosophila melanogaster
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2008-05-20 Classification: HORMONE/SIGNALING PROTEIN |
Organism: Drosophila melanogaster
Method: X-RAY DIFFRACTION
Release Date: 2008-05-20
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Crystal Structure Of Unliganded Argos
Organism: Drosophila melanogaster
Method: X-RAY DIFFRACTION Resolution:2.51 Å Release Date: 2008-05-20 Classification: HORMONE/SIGNALING PROTEIN |
Organism: Drosophila melanogaster
Method: X-RAY DIFFRACTION
Release Date: 2008-05-20
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Crystal Structure Of Gelsolin Domains G1-G3 Bound To Actin
Organism: Equus caballus, Oryctolagus cuniculus
Method: X-RAY DIFFRACTION Resolution:3.00 Å Release Date: 2004-07-27 Classification: CONTRACTILE PROTEIN Ligands: CA, ATP |
Organism: Equus caballus, Oryctolagus cuniculus
Method: X-RAY DIFFRACTION
Release Date: 2004-07-27
Ligands: CA, ATP
