<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(1)</volume><submitter>Rocha OB</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Paracoccidioidomycosis is a systemic mycosis caused by the inhalation of conidia of the genus &lt;i>Paracoccidioides&lt;/i>. During the infectious process, fungal cells use several carbon sources, leading to the production of propionyl-CoA. The latter is metabolized by the methylcitrate synthase, a key enzyme of the methylcitrate cycle. We identified an inhibitor compound (ZINC08964784) that showed antifungal activity against &lt;i>P. brasiliensis&lt;/i>.&lt;h4>Methods&lt;/h4>This work aimed to understand the fungal metabolic response of &lt;i>P. brasiliensis&lt;/i> cells exposed to ZINC08964784 through a proteomics approach. We used a glucose-free medium supplemented with propionate in order to simulate the environment found by the pathogen during the infection. We performed pyruvate dosage, p</pubmed_abstract><journal>Journal of fungi (Basel, Switzerland)</journal><pagination>108</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9865517</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>New Methylcitrate Synthase Inhibitor Induces Proteolysis, Lipid Degradation and Pyruvate Excretion in &lt;i>Paracoccidioides brasiliensis&lt;/i>.</pubmed_title><pmcid>PMC9865517</pmcid><pubmed_authors>Freitas E Silva KS</pubmed_authors><pubmed_authors>Soares CMA</pubmed_authors><pubmed_authors>Bailao AM</pubmed_authors><pubmed_authors>Assuncao LDP</pubmed_authors><pubmed_authors>Santos TG</pubmed_authors><pubmed_authors>Pereira M</pubmed_authors><pubmed_authors>Rocha OB</pubmed_authors><pubmed_authors>Moraes D</pubmed_authors></additional><is_claimable>false</is_claimable><name>New Methylcitrate Synthase Inhibitor Induces Proteolysis, Lipid Degradation and Pyruvate Excretion in &lt;i>Paracoccidioides brasiliensis&lt;/i>.</name><description>&lt;h4>Background&lt;/h4>Paracoccidioidomycosis is a systemic mycosis caused by the inhalation of conidia of the genus &lt;i>Paracoccidioides&lt;/i>. During the infectious process, fungal cells use several carbon sources, leading to the production of propionyl-CoA. The latter is metabolized by the methylcitrate synthase, a key enzyme of the methylcitrate cycle. We identified an inhibitor compound (ZINC08964784) that showed antifungal activity against &lt;i>P. brasiliensis&lt;/i>.&lt;h4>Methods&lt;/h4>This work aimed to understand the fungal metabolic response of &lt;i>P. brasiliensis&lt;/i> cells exposed to ZINC08964784 through a proteomics approach. We used a glucose-free medium supplemented with propionate in order to simulate the environment found by the pathogen during the infection. We performed pyruvate dosage, p</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-05-31T23:31:07.154Z</modification><creation>2025-05-31T23:31:07.154Z</creation></dates><accession>S-EPMC9865517</accession><cross_references><pubmed>36675929</pubmed><doi>10.3390/jof9010108</doi></cross_references></HashMap>