Search Count: 17
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Novel Structural Insights For A Pair Of Monoclonal Antibodies Recognizing Non-Overlapping Epitopes Of The Glucosyltransferase Domain Of Clostridium Difficile Toxin B
Organism: Homo sapiens, Clostridioides difficile r20291
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2022-05-11 Classification: TOXIN/IMMUNE SYSTEM |
Organism: Homo sapiens, Clostridioides difficile r20291
Method: X-RAY DIFFRACTION
Release Date: 2022-05-11
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Novel Structural Insights For A Pair Of Monoclonal Antibodies Recognizing Non-Overlapping Epitopes Of The Glucosyltransferase Domain Of Clostridium Difficile Toxin B
Organism: Clostridioides difficile, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.59 Å Release Date: 2022-05-11 Classification: TOXIN/IMMUNE SYSTEM |
Organism: Clostridioides difficile, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-05-11
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Exploitation Of Hydrogen Bonding Constraints And Flat Hydrophobic Energy Landscapes In Pim-1 Kinase Needle Screening And Inhibitor Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2012-03-21 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0F5 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-03-21
Ligands: 0F5
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Exploitation Of Hydrogen Bonding Constraints And Flat Hydrophobic Energy Landscapes In Pim-1 Kinase Needle Screening And Inhibitor Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.23 Å Release Date: 2012-03-21 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0F9 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-03-21
Ligands: 0F9
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Exploitation Of Hydrogen Bonding Constraints And Flat Hydrophobic Energy Landscapes In Pim-1 Kinase Needle Screening And Inhibitor Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.08 Å Release Date: 2012-03-21 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0FK |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-03-21
Ligands: 0FK
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Exploitation Of Hydrogen Bonding Constraints And Flat Hydrophobic Energy Landscapes In Pim-1 Kinase Needle Screening And Inhibitor Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.48 Å Release Date: 2012-03-21 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0FN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-03-21
Ligands: 0FN
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Exploitation Of Hydrogen Bonding Constraints And Flat Hydrophobic Energy Landscapes In Pim-1 Kinase Needle Screening And Inhibitor Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.03 Å Release Date: 2012-03-21 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0FO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-03-21
Ligands: 0FO
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Exploitation Of Hydrogen Bonding Constraints And Flat Hydrophobic Energy Landscapes In Pim-1 Kinase Needle Screening And Inhibitor Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.27 Å Release Date: 2012-03-21 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 0FR, IMD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-03-21
Ligands: 0FR, IMD
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Exploitation Of Hydrogen Bonding Constraints And Flat Hydrophobic Energy Landscapes In Pim-1 Kinase Needle Screening And Inhibitor Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.23 Å Release Date: 2012-03-21 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: IMD, 0FS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2012-03-21
Ligands: IMD, 0FS
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The Discovery Of Novel Benzofuran-2-Carboxylic Acids As Potent Pim-1 Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.10 Å Release Date: 2011-05-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: IMD, UNJ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-05-11
Ligands: IMD, UNJ
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The Discovery Of Novel Benzofuran-2-Carboxylic Acids As Potent Pim-1 Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2011-05-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: IMD, UNE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-05-11
Ligands: IMD, UNE
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The Discovery Of Novel Benzofuran-2-Carboxylic Acids As Potent Pim-1 Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.95 Å Release Date: 2011-05-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: UNM, IMD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-05-11
Ligands: UNM, IMD
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The Discovery Of Novel Benzofuran-2-Carboxylic Acids As Potent Pim-1 Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2011-05-11 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: UNQ, IMD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2011-05-11
Ligands: UNQ, IMD
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Ligand Binding Domain Of The Wild-Type Aspartate Receptor With Aspartate
Organism: Salmonella typhimurium
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 1997-05-15 Classification: COMPLEX (CHEMOTAXIS/PEPTIDE) Ligands: ASP |
Organism: Salmonella typhimurium
Method: X-RAY DIFFRACTION
Release Date: 1997-05-15
Ligands: ASP
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Ligand Binding Domain Of The Wild-Type Aspartate Receptor
Organism: Salmonella typhimurium
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 1997-04-21 Classification: CHEMOTAXIS |
Organism: Salmonella typhimurium
Method: X-RAY DIFFRACTION
Release Date: 1997-04-21
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The Three-Dimensional Structure Of The Ligand-Binding Domain Of A Wild-Type Bacterial Chemotaxis Receptor
Organism: Salmonella typhimurium
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 1994-12-20 Classification: CHEMOTAXIS |
Organism: Salmonella typhimurium
Method: X-RAY DIFFRACTION
Release Date: 1994-12-20
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The Three-Dimensional Structure Of The Ligand-Binding Domain Of A Wild-Type Bacterial Chemotaxis Receptor
Organism: Salmonella typhimurium
Method: X-RAY DIFFRACTION Resolution:3.00 Å Release Date: 1994-12-20 Classification: CHEMOTAXIS Ligands: ASP |
Organism: Salmonella typhimurium
Method: X-RAY DIFFRACTION
Release Date: 1994-12-20
Ligands: ASP