Search Count: 38
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The Kicstor-Gator1 Complex
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Release Date: 2026-02-18 Classification: CELL CYCLE |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2026-02-18
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The Kicstor-Gator1-Samtor Complex
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Resolution:3.34 Å Release Date: 2026-01-21 Classification: CELL CYCLE |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2026-01-21
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The Dimeric Kicstor-Gator1 Supercomplex
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Resolution:5.00 Å Release Date: 2026-01-21 Classification: CELL CYCLE |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2026-01-21
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Human P2Ry8 Bound To S-Geranylgeranyl-L-Glutathione In Complex With Minig13
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY Release Date: 2025-11-05 Classification: MEMBRANE PROTEIN Ligands: A1BIG |
Organism: Homo sapiens
Method: ELECTRON MICROSCOPY
Release Date: 2025-11-05
Ligands: A1BIG
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Crystal Structure Of Human Monoglyceride Lipase With Compound Lei-515
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.55 Å Release Date: 2023-08-23 Classification: HYDROLASE Ligands: NUX |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2023-08-23
Ligands: NUX
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Crystal Structure Of Disulphide-Linked Human C3D Dimer
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2020-11-18 Classification: IMMUNE SYSTEM Ligands: CL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-11-18
Ligands: CL
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Dyrk1A Kinase Domain In Complex With A 6-Azaindole Derivative, Gnf2133.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:3.70 Å Release Date: 2020-03-04 Classification: TRANSFERASE Ligands: Q8J |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-03-04
Ligands: Q8J
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Structure-Based Design Of New Dihydrofolate Reductase Antibacterial Agents: 7-(Benzimidazol-1-Yl)-2,4-Diaminoquinazolines
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION Resolution:1.69 Å Release Date: 2014-02-19 Classification: Oxidoreductase/Oxidoreductase inhibitor Ligands: NAP, 1VM |
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION
Release Date: 2014-02-19
Ligands: NAP, 1VM
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Structure-Based Design Of New Dihydrofolate Reductase Antibacterial Agents: 7-(Benzimidazol-1-Yl)-2,4-Diaminoquinazolines
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2014-02-19 Classification: Oxidoreductase/Oxidoreductase inhibitor Ligands: NAP, 1VN |
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION
Release Date: 2014-02-19
Ligands: NAP, 1VN
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Structure-Based Design Of New Dihydrofolate Reductase Antibacterial Agents: 7-(Benzimidazol-1-Yl)-2,4-Diaminoquinazolines
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION Resolution:1.88 Å Release Date: 2014-02-19 Classification: Oxidoreductase/Oxidoreductase inhibitor Ligands: 1VO, NAP |
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION
Release Date: 2014-02-19
Ligands: 1VO, NAP
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Structure-Based Design Of New Dihydrofolate Reductase Antibacterial Agents: 7-(Benzimidazol-1-Yl)-2,4-Diaminoquinazolines
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2014-02-19 Classification: Oxidoreductase/Oxidoreductase inhibitor Ligands: NAP, 1DN |
Organism: Staphylococcus aureus
Method: X-RAY DIFFRACTION
Release Date: 2014-02-19
Ligands: NAP, 1DN
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Pyrrolopyrimidine Inhibitors Of Dna Gyrase B And Topoisomerase Iv, Part I: Structure Guided Discovery And Optimization Of Dual Targeting Agents With Potent, Broad-Spectrum Enzymatic Activity.
Organism: Enterococcus faecalis
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2013-02-13 Classification: Isomerase/Isomerase inhibitor Ligands: 0WT, GOL |
Organism: Enterococcus faecalis
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: 0WT, GOL
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Pyrrolopyrimidine Inhibitors Of Dna Gyrase B And Topoisomerase Iv, Part I: Structure Guided Discovery And Optimization Of Dual Targeting Agents With Potent, Broad-Spectrum Enzymatic
Organism: Enterococcus faecalis
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2013-02-13 Classification: Isomerase/Isomerase inhibitor Ligands: SUY, GOL |
Organism: Enterococcus faecalis
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: SUY, GOL
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Pyrrolopyrimidine Inhibitors Of Dna Gyrase B And Topoisomerase Iv, Part I: Structure Guided Discovery And Optimization Of Dual Targeting Agents With Potent, Broad-Spectrum Enzymatic Activity
Organism: Enterococcus faecalis
Method: X-RAY DIFFRACTION Resolution:1.69 Å Release Date: 2013-02-13 Classification: Isomerase/Isomerase inhibitor Ligands: CJC, GOL |
Organism: Enterococcus faecalis
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: CJC, GOL
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Pyrrolopyrimidine Inhibitors Of Dna Gyrase B And Topoisomerase Iv, Part I: Structure Guided Discovery And Optimization Of Dual Targeting Agents With Potent, Broad-Spectrum Enzymatic Activity.
Organism: Enterococcus faecalis
Method: X-RAY DIFFRACTION Resolution:1.69 Å Release Date: 2013-02-13 Classification: Isomerase/Isomerase inhibitor Ligands: 1A0, TBU |
Organism: Enterococcus faecalis
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: 1A0, TBU
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Pyrrolopyrimidine Inhibitors Of Dna Gyrase B And Topoisomerase Iv, Part I: Structure Guided Discovery And Optimization Of Dual Targeting Agents With Potent, Broad-Spectrum Enzymatic Activity.
Organism: Francisella tularensis subsp. holarctica
Method: X-RAY DIFFRACTION Resolution:2.70 Å Release Date: 2013-02-13 Classification: isomerase/isomerase inhibitor Ligands: 19Y |
Organism: Francisella tularensis subsp. holarctica
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: 19Y
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Pyrrolopyrimidine Inhibitors Of Dna Gyrase B And Topoisomerase Iv, Part I: Structure Guided Discovery And Optimization Of Dual Targeting Agents With Potent, Broad-Spectrum Enzymatic Activity.
Organism: Francisella tularensis subsp. holarctica
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2013-02-13 Classification: isomerase/isomerase inhibitor Ligands: 19X |
Organism: Francisella tularensis subsp. holarctica
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: 19X
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Pyrrolopyrimidine Inhibitors Of Dna Gyrase B And Topoisomerase Iv, Part I: Structure Guided Discovery And Optimization Of Dual Targeting Agents With Potent, Broad-Spectrum Enzymatic Activity.
Organism: Francisella tularensis subsp. holarctica lvs
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2013-02-13 Classification: Isomerase/Isomerase inhibitor Ligands: CJC |
Organism: Francisella tularensis subsp. holarctica lvs
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: CJC
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Pyrrolopyrimidine Inhibitors Of Dna Gyrase B And Topoisomerase Iv, Part I: Structure Guided Discovery And Optimization Of Dual Targeting Agents With Potent, Broad-Spectrum Enzymatic Activity.
Organism: Escherichia coli
Method: X-RAY DIFFRACTION Resolution:2.60 Å Release Date: 2013-02-13 Classification: Isomerase/Isomerase inhibitor Ligands: 1A1, MG |
Organism: Escherichia coli
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: 1A1, MG
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Pyrrolopyrimidine Inhibitors Of Dna Gyrase B And Topoisomerase Iv, Part I: Structure Guided Discovery And Optimization Of Dual Targeting Agents With Potent, Broad-Spectrum Enzymatic Activity.
Organism: Escherichia coli
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2013-02-13 Classification: Isomerase/Isomerase inhibitor Ligands: 1AV, MG |
Organism: Escherichia coli
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: 1AV, MG