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Structural Characterization of CYP51 from Trypanosoma cruzi and Trypanosoma brucei Bound to the Antifungal Drugs Posaconazole and Fluconazole.
- Published in:
- PLoS Neglected Tropical Diseases, 2010, v. 4, n. 4, p. 1, doi. 10.1371/journal.pntd.0000651
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Structural Characterization of CYP51 from Trypanosoma cruzi and Trypanosoma brucei Bound to the Antifungal Drugs Posaconazole and Fluconazole.
- Published in:
- PLoS Neglected Tropical Diseases, 2010, v. 4, n. 4, p. 1, doi. 10.1371/journal.pntd.0000651
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- Publication type:
- Article
Computational identification of a transiently open L1/S3 pocket for reactivation of mutant p53.
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- Nature Communications, 2013, v. 4, n. 1, p. 1407, doi. 10.1038/ncomms2361
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Structure of the proton-gated urea channel from the gastric pathogen Helicobacter pylori.
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- Nature, 2013, v. 493, n. 7431, p. 255, doi. 10.1038/nature11684
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Diverse Inhibitor Chemotypes Targeting Trypanosoma cruzi CYP51.
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- PLoS Neglected Tropical Diseases, 2012, v. 6, n. 7, p. 1, doi. 10.1371/journal.pntd.0001736
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- Article
Diverse Inhibitor Chemotypes Targeting Trypanosoma cruzi CYP51.
- Published in:
- PLoS Neglected Tropical Diseases, 2012, v. 6, n. 7, p. 1, doi. 10.1371/journal.pntd.0001736
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- Publication type:
- Article
Scanning chimeragenesis: the approach used to change the substrate selectivity of fatty acid monooxygenase CYP102A1 to that of terpene ω-hydroxylase CYP4C7.
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- Journal of Biological Inorganic Chemistry (JBIC), 2010, v. 15, n. 2, p. 159, doi. 10.1007/s00775-009-0580-y
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The effect of mutation of F87 on the properties of CYP102A1-CYP4C7 chimeras: altered regiospecificity and substrate selectivity.
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- Journal of Biological Inorganic Chemistry (JBIC), 2008, v. 13, n. 5, p. 813, doi. 10.1007/s00775-008-0368-5
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- Article