<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>19(1)</volume><submitter>Oliveira MP</submitter><pubmed_abstract>In a proteomics approach conducted with Leishmania amazonensis, parasite proteins showed either an increase or a decrease in their expression content during extensive in vitro cultivation, and were related to the survival and the infectivity of the parasites, respectively. In the current study, a computational screening was performed to predict virulence factors among these molecules. Three proteins were selected, one of which presented no homology to human proteins. This candidate, namely small myristoylated protein-3 (SMP-3), was cloned, and its recombinant version (rSMP-3) was used to stimulate peripheral blood mononuclear cells (PBMCs) from healthy subjects living in an endemic area of leishmaniasis and from visceral leishmaniasis patients. Results showed high interferon-γ (IFN-γ) prod</pubmed_abstract><journal>International journal of molecular sciences</journal><pagination>E129</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5796078</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Small Myristoylated Protein-3, Identified as a Potential Virulence Factor in Leishmania amazonensis, Proves to be a Protective Antigen against Visceral Leishmaniasis.</pubmed_title><pmcid>PMC5796078</pmcid><pubmed_authors>Lage DP</pubmed_authors><pubmed_authors>Teixeira AL</pubmed_authors><pubmed_authors>Coelho EAF</pubmed_authors><pubmed_authors>Oliveira MP</pubmed_authors><pubmed_authors>Santos TTO</pubmed_authors><pubmed_authors>Chavez-Fumagalli MA</pubmed_authors><pubmed_authors>Martins VT</pubmed_authors><pubmed_authors>Costa LE</pubmed_authors><pubmed_authors>Ribeiro PAF</pubmed_authors><pubmed_authors>Machado-de-Avila RA</pubmed_authors><pubmed_authors>Ramos FF</pubmed_authors><pubmed_authors>Salles BCS</pubmed_authors><pubmed_authors>Dias DS</pubmed_authors><pubmed_authors>Schneider MS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Small Myristoylated Protein-3, Identified as a Potential Virulence Factor in Leishmania amazonensis, Proves to be a Protective Antigen against Visceral Leishmaniasis.</name><description>In a proteomics approach conducted with Leishmania amazonensis, parasite proteins showed either an increase or a decrease in their expression content during extensive in vitro cultivation, and were related to the survival and the infectivity of the parasites, respectively. In the current study, a computational screening was performed to predict virulence factors among these molecules. Three proteins were selected, one of which presented no homology to human proteins. This candidate, namely small myristoylated protein-3 (SMP-3), was cloned, and its recombinant version (rSMP-3) was used to stimulate peripheral blood mononuclear cells (PBMCs) from healthy subjects living in an endemic area of leishmaniasis and from visceral leishmaniasis patients. Results showed high interferon-γ (IFN-γ) prod</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jan</publication><modification>2025-06-01T03:28:06.167Z</modification><creation>2025-06-01T03:28:06.167Z</creation></dates><accession>S-EPMC5796078</accession><cross_references><pubmed>29301342</pubmed><doi>10.3390/ijms19010129</doi></cross_references></HashMap>