<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pyrih J</submitter><funding>Grantová Agentura České Republiky</funding><funding>Agentúra na Podporu Výskumu a Vývoja</funding><funding>European Research Council</funding><funding>ERD funds</funding><funding>Agentúra Ministerstva Školstva, Vedy, Výskumu a Športu SR</funding><pagination>e0234918</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7314023</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(6)</volume><pubmed_abstract>ZapE/Afg1 is a component of the inner cell membrane of some eubacteria and the inner mitochondrial membrane of eukaryotes. This protein is involved in FtsZ-dependent division of eubacteria. In the yeast and human mitochondrion, ZapE/Afg1 likely interacts with Oxa1 and facilitates the degradation of mitochondrion-encoded subunits of respiratory complexes. Furthermore, the depletion of ZapE increases resistance to apoptosis, decreases oxidative stress tolerance, and impacts mitochondrial protein homeostasis. It remains unclear whether ZapE is a multifunctional protein, or whether some of the described effects are just secondary phenotypes. Here, we have analyzed the functions of ZapE in Trypanosoma brucei, a parasitic protist, and an important model organism. Using a newly developed proximit</pubmed_abstract><journal>PloS one</journal><pubmed_title>ZapE/Afg1 interacts with Oxa1 and its depletion causes a multifaceted phenotype.</pubmed_title><pmcid>PMC7314023</pmcid><funding_grant_id>LL1601</funding_grant_id><funding_grant_id>OPVVV 0000759</funding_grant_id><funding_grant_id>1/0387/17</funding_grant_id><funding_grant_id>18-18699S</funding_grant_id><funding_grant_id>APVV-0286-12</funding_grant_id><funding_grant_id>18-15962S</funding_grant_id><pubmed_authors>Panek T</pubmed_authors><pubmed_authors>Pyrih J</pubmed_authors><pubmed_authors>Raskova V</pubmed_authors><pubmed_authors>Skodova-Sverakova I</pubmed_authors><pubmed_authors>Lukes J</pubmed_authors></additional><is_claimable>false</is_claimable><name>ZapE/Afg1 interacts with Oxa1 and its depletion causes a multifaceted phenotype.</name><description>ZapE/Afg1 is a component of the inner cell membrane of some eubacteria and the inner mitochondrial membrane of eukaryotes. This protein is involved in FtsZ-dependent division of eubacteria. In the yeast and human mitochondrion, ZapE/Afg1 likely interacts with Oxa1 and facilitates the degradation of mitochondrion-encoded subunits of respiratory complexes. Furthermore, the depletion of ZapE increases resistance to apoptosis, decreases oxidative stress tolerance, and impacts mitochondrial protein homeostasis. It remains unclear whether ZapE is a multifunctional protein, or whether some of the described effects are just secondary phenotypes. Here, we have analyzed the functions of ZapE in Trypanosoma brucei, a parasitic protist, and an important model organism. Using a newly developed proximit</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2026-05-02T18:30:22.176Z</modification><creation>2020-07-03T07:05:50Z</creation></dates><accession>S-EPMC7314023</accession><cross_references><pubmed>32579605</pubmed><doi>10.1371/journal.pone.0234918</doi></cross_references></HashMap>