Search Count: 11
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Sars-Cov-2 Main Protease With Inhibitor
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2025-10-22 Classification: VIRAL PROTEIN, HYDROLASE Ligands: A1B3B, BTB, EDO |
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION
Release Date: 2025-10-22
Ligands: A1B3B, BTB, EDO
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Sars-Cov-2 Main Protease With Inhibitor
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION Resolution:1.55 Å Release Date: 2025-09-10 Classification: VIRAL PROTEIN Ligands: A1A3N |
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION
Release Date: 2025-09-10
Ligands: A1A3N
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Sars-Cov-2 Main Protease With Inhibitor
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION Resolution:1.40 Å Release Date: 2025-09-10 Classification: VIRAL PROTEIN Ligands: A1A3O |
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION
Release Date: 2025-09-10
Ligands: A1A3O
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Structure Of Sars-Cov-2 Main Protease With Potent Peptide Aldehyde Inhibitor
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION Resolution:1.35 Å Release Date: 2024-08-07 Classification: HYDROLASE/INHIBITOR Ligands: A1ADM, NA, EDO, PEG |
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION
Release Date: 2024-08-07
Ligands: A1ADM, NA, EDO, PEG
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Sars-Cov-2 Main Protease With Covalent Inhibitor
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION Resolution:2.07 Å Release Date: 2024-04-03 Classification: VIRAL PROTEIN Ligands: BTB, A1AD0, DMS, EDO |
Organism: Severe acute respiratory syndrome coronavirus 2
Method: X-RAY DIFFRACTION
Release Date: 2024-04-03
Ligands: BTB, A1AD0, DMS, EDO
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Potent, Reversible Metap2 Inhibitors Via Fragment Based Drug Discovery
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2016-05-25 Classification: Hydrolase/Hydrolase Inhibitor Ligands: MN, DMS, EDO, 6KP |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-05-25
Ligands: MN, DMS, EDO, 6KP
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Potent, Reversible Metap2 Inhibitors Via Fbdd
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2016-05-25 Classification: Hydrolase/Hydrolase Inhibitor Ligands: MN, GOL, DMS, 6KO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-05-25
Ligands: MN, GOL, DMS, 6KO
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Potent, Reversible Metap2 Inhibitors Via Fbdd
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2016-05-25 Classification: Hydrolase4/Hydrolase Inhibitor Ligands: MN, SO4, 6KN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2016-05-25
Ligands: MN, SO4, 6KN
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Fragment-Based Discovery Of A Small Molecule Reversible Inhibitor Of Bruton'S Tyrosine Kinase
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2015-07-01 Classification: TRANSFERASE Ligands: IMD, IPA, EDO, 4L6 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-07-01
Ligands: IMD, IPA, EDO, 4L6
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Crystal Structure Of Bruton'S Tyrosine Kinase Bound To A Cinnoline Fragment
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.65 Å Release Date: 2015-07-01 Classification: Transferase/Transferase Inhibitor Ligands: IMD, IPA, DMS, 4RU |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-07-01
Ligands: IMD, IPA, DMS, 4RU
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Crystal Structure Of Bruton'S Tyrosine Kinase In Complex With A Substituted Cinnoline
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2015-07-01 Classification: Transferase/Transferase Inhibitor Ligands: IMD, IPA, DMS, 4RV |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2015-07-01
Ligands: IMD, IPA, DMS, 4RV