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N-Myristoyltransferase Is a Cell Wall Target in Aspergillus fumigatus
Author(s) -
Wenxia Fang,
David A. Robinson,
Olawale G. Raimi,
D.E. Blair,
Justin R. Harrison,
Deborah Lockhart,
Leah S. Torrie,
G.F. Ruda,
Paul G. Wyatt,
Ian H. Gilbert,
Daan M. F. van Aalten
Publication year - 2015
Publication title -
acs chemical biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.899
H-Index - 111
eISSN - 1554-8937
pISSN - 1554-8929
DOI - 10.1021/cb5008647
Subject(s) - aspergillus fumigatus , biology , enzyme , microbiology and biotechnology , biochemistry , effector , active site , mode of action , myristoylation , phosphorylation
Treatment of filamentous fungal infections relies on a limited repertoire of antifungal agents. Compounds possessing novel modes of action are urgently required. N-myristoylation is a ubiquitous modification of eukaryotic proteins. The enzyme N-myristoyltransferase (NMT) has been considered a potential therapeutic target in protozoa and yeasts. Here, we show that the filamentous fungal pathogen Aspergillus fumigatus possesses an active NMT enzyme that is essential for survival. Surprisingly, partial repression of the gene revealed downstream effects of N-myristoylation on cell wall morphology. Screening a library of inhibitors led to the discovery of a pyrazole sulphonamide compound that inhibits the enzyme and is fungicidal under partially repressive nmt conditions. Together with a crystallographic complex showing the inhibitor binding in the peptide substrate pocket, we provide evidence of NMT being a potential drug target in A. fumigatus.

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