MétaCan
← all works

Ribosome-Dependent ATPase Interacts with Conserved Membrane Protein in Escherichia coli to Modulate Protein Synthesis and Oxidative Phosphorylation

2011· article· en· 18 citations· W1974393054 on OpenAlex· 10.1371/journal.pone.0018510

Why is this work in the frame?

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

Canadian affiliationAn author listed a Canadian institution. This is the only route the usual frame has.
Canadian funderA Canadian agency funded it. The work may carry no Canadian affiliation at all.

Post-publication record

Nature
Retraction
Reason
Concerns/Issues about Image;Duplication of/in Image;Euphemisms for Duplication;Objections by Author(s);Original Data and/or Images not Provided and/or not Available;Unreliable Results and/or Conclusions;
Date
6/16/2025 0:00
Flagged by OpenAlex?
Yes

Source: Retraction Watch, joined by DOI. OpenAlex records retraction as is_retracted, a boolean over a state space with at least four values, so it cannot express an expression of concern, a correction or a reinstatement — it reports them as false, which reads as “fine”.

Abstract

Elongation factor RbbA is required for ATP-dependent deacyl-tRNA release presumably after each peptide bond formation; however, there is no information about the cellular role. Proteomic analysis in Escherichia coli revealed that RbbA reciprocally co-purified with a conserved inner membrane protein of unknown function, YhjD. Both proteins are also physically associated with the 30S ribosome and with members of the lipopolysaccharide transport machinery. Genome-wide genetic screens of rbbA and yhjD deletion mutants revealed aggravating genetic interactions with mutants deficient in the electron transport chain. Cells lacking both rbbA and yhjD exhibited reduced cell division, respiration and global protein synthesis as well as increased sensitivity to antibiotics targeting the ETC and the accuracy of protein synthesis. Our results suggest that RbbA appears to function together with YhjD as part of a regulatory network that impacts bacterial oxidative phosphorylation and translation efficiency.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

The record

Venue
PLoS ONE
Topic
RNA and protein synthesis mechanisms
Field
Biochemistry, Genetics and Molecular Biology
Canadian institutions
Carleton UniversityUniversity of Toronto
Funders
Canadian Institutes of Health Research
Keywords
Oxidative phosphorylationBiologyRibosomeProtein biosynthesisEscherichia coliCell biologyBiochemistryMembrane proteinMutantPhosphorylationTransfer RNATranslation (biology)RNAGeneMessenger RNAMembrane
Has abstract in OpenAlex
yes