Search Count: 29
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Crystal Structure Of Malt1 In Complex With An Allosteric Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2025-10-29 Classification: HYDROLASE Ligands: CA, A1BM0 |
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Crystal Structure Of Malt1 In Complex With An Allosteric Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.45 Å Release Date: 2025-10-29 Classification: HYDROLASE Ligands: CA, PGE, A1BMX |
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Crystal Structure Of Malt1 In Complex With An Allosteric Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.34 Å Release Date: 2025-10-29 Classification: HYDROLASE Ligands: CA, PGE, EDO, A1BMY |
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Crystal Structure Of Fgfr3 Bound To Indazole Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2025-06-25 Classification: CELL CYCLE Ligands: A1A6M, CL, MG |
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Crystal Structure Of Candida Albicans Calcineurin A, Calcineurin B, Fkbp12 And Fk506 (Tacrolimus)
Organism: Candida albicans (strain wo-1), Candida albicans (strain sc5314 / atcc mya-2876)
Method: X-RAY DIFFRACTION Resolution:2.55 Å Release Date: 2019-09-18 Classification: Hydrolase/Isomerase/Calcium Binding Ligands: PO4, ZN, FE, EDO, CA, FK5 |
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Crystal Structure Of Aspergillus Fumigatus Calcineurin A, Calcineurin B, Fkbp12 And Fk506 (Tacrolimus)
Organism: Neosartorya fumigata (strain atcc mya-4609 / af293 / cbs 101355 / fgsc a1100)
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2019-09-18 Classification: Hydrolase/Isomerase/Calcium Binding Ligands: ZN, FE, PO4, EDO, CA, FK5 |
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Crystal Structure Of Cryptococcus Neoformans Calceineurin A, Calcineurin B, And Fkbp12 With Fk-506
Organism: Cryptococcus neoformans var. grubii serotype a (strain h99 / atcc 208821 / cbs 10515 / fgsc 9487)
Method: X-RAY DIFFRACTION Resolution:3.30 Å Release Date: 2019-09-18 Classification: Hydrolase/Isomerase/Calcium Binding Ligands: SO4, FE, ZN, CA, FK5 |
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Crystal Structure Of Calcineurin A And Calcineurin B In Complex With Fkbp12 And Fk506 From Coccidioides Immitis Rs
Organism: Coccidioides immitis (strain rs)
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2015-05-20 Classification: HYDROLASE Ligands: ZN, FE, MES, EDO, CA, FK5 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |