In Silico Structural Modeling and Analysis of Interactions of Tremellomycetes Cytochrome P450 Monooxygenases CYP51s with Substrates and Azoles

Int J Mol Sci. 2021 Jul 22;22(15):7811. doi: 10.3390/ijms22157811.

Abstract

Cytochrome P450 monooxygenase CYP51 (sterol 14α-demethylase) is a well-known target of the azole drug fluconazole for treating cryptococcosis, a life-threatening fungal infection in immune-compromised patients in poor countries. Studies indicate that mutations in CYP51 confer fluconazole resistance on cryptococcal species. Despite the importance of CYP51 in these species, few studies on the structural analysis of CYP51 and its interactions with different azole drugs have been reported. We therefore performed in silico structural analysis of 11 CYP51s from cryptococcal species and other Tremellomycetes. Interactions of 11 CYP51s with nine ligands (three substrates and six azoles) performed by Rosetta docking using 10,000 combinations for each of the CYP51-ligand complex (11 CYP51s × 9 ligands = 99 complexes) and hierarchical agglomerative clustering were used for selecting the complexes. A web application for visualization of CYP51s' interactions with ligands was developed (http://bioshell.pl/azoledocking/). The study results indicated that Tremellomycetes CYP51s have a high preference for itraconazole, corroborating the in vitro effectiveness of itraconazole compared to fluconazole. Amino acids interacting with different ligands were found to be conserved across CYP51s, indicating that the procedure employed in this study is accurate and can be automated for studying P450-ligand interactions to cater for the growing number of P450s.

Keywords: CYP51; Cryptococcus neoformans; Tremellomycetes; cytochrome P450 monooxygenases; docking; drug-resistance; sterol 14α-demethylase; web-application.

MeSH terms

  • Amino Acids / chemistry
  • Amino Acids / metabolism*
  • Antifungal Agents / chemistry
  • Antifungal Agents / metabolism
  • Azoles / chemistry
  • Azoles / metabolism*
  • Basidiomycota / enzymology*
  • Computer Simulation
  • Cytochrome P-450 Enzyme System / chemistry
  • Cytochrome P-450 Enzyme System / metabolism*
  • Fluconazole / chemistry
  • Fluconazole / metabolism*
  • Fungal Proteins / chemistry
  • Fungal Proteins / metabolism*
  • Itraconazole / chemistry
  • Itraconazole / metabolism*
  • Ligands
  • Models, Molecular
  • Phylogeny
  • Protein Binding
  • Protein Conformation
  • Substrate Specificity

Substances

  • Amino Acids
  • Antifungal Agents
  • Azoles
  • Fungal Proteins
  • Ligands
  • Itraconazole
  • Fluconazole
  • Cytochrome P-450 Enzyme System