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The identification of resistance-related proteins as therapeutic targets is pivotal for guiding the rational design of antifungal agents

Acyl-CoA synthetase long-chain family member 4 (ACSL4) preferentially activates polyunsaturated fatty acids such as arachidonic and adrenic acids, forming acyl-CoA derivatives that are incorporated into phosphatidylethanolamine (PE) by membrane-bound O-acyltransferases (MBOATs) [84,85]

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