Fungal Lanosterol 14α-demethylase: A target for next-generation antifungal design
Autor: | Rajni K. Wilson, Parham Hosseini, Mikhail V. Keniya, Brian C. Monk, Alia A. Sagatova, Yasmeen N. Ruma |
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Rok vydání: | 2018 |
Předmět: |
Azoles
Antifungal Agents Stereochemistry Biophysics Triazole Biochemistry Analytical Chemistry Food Supply 03 medical and health sciences chemistry.chemical_compound Mice Sterol 14-Demethylase Drug Discovery Imidazole Animals Humans Molecular Biology Ecosystem 030304 developmental biology chemistry.chemical_classification 0303 health sciences biology 030306 microbiology Lanosterol Active site Ligand (biochemistry) chemistry Mycoses 14-alpha Demethylase Inhibitors biology.protein Azole Demethylase Efflux Agrochemicals |
Zdroj: | Biochimica et biophysica acta. Proteins and proteomics. 1868(3) |
ISSN: | 1878-1454 |
Popis: | The cytochrome P450 enzyme lanosterol 14α-demethylase (LDM) is the target of the azole antifungals used widely in medicine and agriculture as prophylaxis or treatments of infections or diseases caused by fungal pathogens. These drugs and agrochemicals contain an imidazole, triazole or tetrazole substituent, with one of the nitrogens in the azole ring coordinating as the sixth axial ligand to the LDM heme iron. Structural studies show that this membrane bound enzyme contains a relatively rigid ligand binding pocket comprised of a deeply buried heme-containing active site together with a substrate entry channel and putative product exit channel that reach to the membrane. Within the ligand binding pocket the azole antifungals have additional affinity determining interactions with hydrophobic side-chains, the polypeptide backbone and via water-mediated hydrogen bond networks. This review will describe the tools that can be used to identify and characterise the next generation of antifungals targeting LDM, with the goal of obtaining highly potent broad-spectrum fungicides that will be able to avoid target and drug efflux mediated antifungal resistance. |
Databáze: | OpenAIRE |
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