Search Count: 22
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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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Crystal Structure Of E. Coli Threonyl-Trna Synthetase Bound To A Novel Inhibitor
Organism: Escherichia coli
Method: X-RAY DIFFRACTION Resolution:1.91 Å Release Date: 2013-09-18 Classification: Ligase/Ligase Inhibitor Ligands: ZN, 409 |
Organism: Escherichia coli
Method: X-RAY DIFFRACTION
Release Date: 2013-09-18
Ligands: ZN, 409
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Crystal Structure Of E. Coli Threonyl-Trna Synthetase Bound To A Novel Inhibitor
Organism: Escherichia coli
Method: X-RAY DIFFRACTION Resolution:1.81 Å Release Date: 2013-09-18 Classification: Ligase/Ligase Inhibitor Ligands: ZN, X16 |
Organism: Escherichia coli
Method: X-RAY DIFFRACTION
Release Date: 2013-09-18
Ligands: ZN, X16
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Crystal Structure Of E. Coli Threonyl-Trna Synthetase Bound To A Novel Inhibitor
Organism: Escherichia coli
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2013-09-18 Classification: Ligase/Ligase Inhibitor Ligands: ZN, 1B2 |
Organism: Escherichia coli
Method: X-RAY DIFFRACTION
Release Date: 2013-09-18
Ligands: ZN, 1B2
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Crystal Structure Of E. Coli Threonyl-Trna Synthetase Bound To A Novel Inhibitor
Organism: Escherichia coli
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2013-09-18 Classification: Ligase/Ligase Inhibitor Ligands: ZN, 1B3 |
Organism: Escherichia coli
Method: X-RAY DIFFRACTION
Release Date: 2013-09-18
Ligands: ZN, 1B3
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Crystal Structure Of Human Threonyl-Trna Synthetase Bound To A Novel Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2013-09-18 Classification: Ligase/Ligase Inhibitor Ligands: ZN, 1B2 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-09-18
Ligands: ZN, 1B2
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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
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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:2.70 Å Release Date: 2013-02-13 Classification: Isomerase/Isomerase inhibitor Ligands: 19Y |
Organism: Enterococcus faecalis
Method: X-RAY DIFFRACTION
Release Date: 2013-02-13
Ligands: 19Y
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Structure Of Mura (Udp-N-Acetylglucosamine Enolpyruvyl Transferase), From Vibrio Fischeri In Complex With Substrate Udp-N-Acetylglucosamine And The Drug Fosfomycin.
Organism: Vibrio fischeri
Method: X-RAY DIFFRACTION Resolution:1.93 Å Release Date: 2012-04-11 Classification: TRANSFERASE/ANTIBIOTIC Ligands: FFQ, UD1, PO4, GOL |
Organism: Vibrio fischeri
Method: X-RAY DIFFRACTION
Release Date: 2012-04-11
Ligands: FFQ, UD1, PO4, GOL