Structure-based identification of potential antifungal agents against Aspergillus fumigatus through multiscale...

Fungal infections caused by Aspergillus fumigatus pose a serious clinical challenge, particularly in immunocompromised patients, where limited therapeutic options and increasing resistance reduce treatment success. Chitinase B1 is a key enzyme involved in fungal cell wall remodeling and has emerged as an attractive molecular target for antifungal drug discovery. In this study, an integrated computational workflow was employed to identify and evaluate potential inhibitors of A. fumigatus Chitinase B1. A total of 99288 compounds were screened from MTi open screen web server and these structure -based screening resulted in the selection of three promising compounds (124753220, 26746900, and 17439543) based on their highest binding affinity with a docking score between -11.6 to -9.3 kcal/mol within the enzyme active site. Electronic structure analysis of compound 124753220 revealed a high dipole moment and narrow HOMO-LUMO gap, indicating favorable chemical reactivity. Redocking analysis confirmed stable hydrogen bonding and hydrophobic interactions with key catalytic residues. Molecular dynamics simulations conducted over 500 ns demonstrated stable complex formation, as reflected by consistent RMSD score of 1.5-2.0 Å and RMSF below 2.0 Å for all selected profiles. Binding free-energy analysis identified compound 124753220 as the strongest binder (ΔG_total = -78.54 kcal/mol), exhibiting affinity comparable to the reference inhibitor. Principal component analysis and free energy landscape confirmed the stability of the protein-ligand complexes. while QM/MM calculations indicated favorable electronic interactions within the binding pocket. Machine learning-based bioactivity predictions showed comparable potency among all evaluated compounds (pIC₅₀ = 8.225-8.619). Overall, compound 124753220 demonstrated the most favorable binding and stability characteristics, highlighting its potential as a promising antifungal lead for further experimental validation.