<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mechoud MA</submitter><funding>European Commission</funding><funding>Spanish Government</funding><pagination>e00221-20</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7357468</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>86(14)</volume><pubmed_abstract>The human monothiol glutaredoxin Glrx3 (PICOT) is ubiquitously distributed in cytoplasm and nuclei in mammalian cells. Its overexpression has been associated with the development of several types of tumors, whereas its deficiency might cause retardation in embryogenesis. Its exact biological role has not been well resolved, although a function as a chaperone distributing iron/sulfur clusters is currently accepted. Yeast humanization and the use of a mouse library have allowed us to find a new partner for PICOT: the human GMP synthase (hGMPs). Both proteins carry out collaborative functions regarding the downregulation of the Saccharomyces cerevisiae Gcn2 pathway under conditions of nutritional stress. Glrx3/hGMPs interact through conserved residues that bridge iron/sulfur clusters and glut</pubmed_abstract><journal>Applied and environmental microbiology</journal><pubmed_title>Interactions of GMP with Human Glrx3 and with Saccharomyces cerevisiae Grx3 and Grx4 Converge in the Regulation of the Gcn2 Pathway.</pubmed_title><pmcid>PMC7357468</pmcid><funding_grant_id>COFUND 2014-51501</funding_grant_id><funding_grant_id>BIO2017-87828-C2-2-P</funding_grant_id><pubmed_authors>Pujol-Carrion N</pubmed_authors><pubmed_authors>Mechoud MA</pubmed_authors><pubmed_authors>de la Torre-Ruiz MA</pubmed_authors><pubmed_authors>Montella-Manuel S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Interactions of GMP with Human Glrx3 and with Saccharomyces cerevisiae Grx3 and Grx4 Converge in the Regulation of the Gcn2 Pathway.</name><description>The human monothiol glutaredoxin Glrx3 (PICOT) is ubiquitously distributed in cytoplasm and nuclei in mammalian cells. Its overexpression has been associated with the development of several types of tumors, whereas its deficiency might cause retardation in embryogenesis. Its exact biological role has not been well resolved, although a function as a chaperone distributing iron/sulfur clusters is currently accepted. Yeast humanization and the use of a mouse library have allowed us to find a new partner for PICOT: the human GMP synthase (hGMPs). Both proteins carry out collaborative functions regarding the downregulation of the Saccharomyces cerevisiae Gcn2 pathway under conditions of nutritional stress. Glrx3/hGMPs interact through conserved residues that bridge iron/sulfur clusters and glut</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2025-06-01T12:00:21.556Z</modification><creation>2021-02-20T17:22:37Z</creation></dates><accession>S-EPMC7357468</accession><cross_references><pubmed>32414791</pubmed><doi>10.1128/AEM.00221-20</doi><doi>10.1128/aem.00221-20</doi></cross_references></HashMap>