Results 21 to 30 of about 18,051 (202)

Toxin-antitoxin systems in bacterial pathogenesis. [PDF]

open access: yesHeliyon, 2023
Toxin-Antitoxin (TA) systems are abundant in prokaryotes and play an important role in various biological processes such as plasmid maintenance, phage inhibition, stress response, biofilm formation, and dormant persister cell generation. TA loci are abundant in pathogenic intracellular micro-organisms and help in their adaptation to the harsh host ...
Sonika S, Singh S, Mishra S, Verma S.
europepmc   +4 more sources

Intracellular Localization of the Proteins Encoded by Some Type II Toxin-Antitoxin Systems in Escherichia coli

open access: yesmBio, 2021
Bacterial toxin-antitoxin (TA) systems encode a toxin and an antitoxin that counteracts the toxin. Such TA systems are found abundantly on bacterial chromosomes and on extrachromosomal genetic elements. The toxin is always a protein.
Alexander Mager   +2 more
doaj   +1 more source

Bacterial retrons encode phage-defending tripartite toxin-antitoxin systems. [PDF]

open access: yesNature, 2022
Bobonis J   +19 more
europepmc   +2 more sources

Bacterial toxin-antitoxin systems [PDF]

open access: yesMobile Genetic Elements, 2011
Toxin-antitoxin (TA) systems are composed of two elements: a toxic protein and an antitoxin which is either an RNA (type I and III) or a protein (type II). Type II systems are abundant in bacterial genomes in which they move via horizontal gene transfer.
Guglielmini, Julien   +1 more
openaire   +3 more sources

Toxin-Antitoxin Systems in Clinical Pathogens [PDF]

open access: yesToxins, 2016
Toxin-antitoxin (TA) systems are prevalent in bacteria and archaea. Although not essential for normal cell growth, TA systems are implicated in multiple cellular functions associated with survival under stress conditions. Clinical strains of bacteria are currently causing major human health problems as a result of their multidrug resistance ...
Laura Fernández-García   +6 more
openaire   +4 more sources

MenT nucleotidyltransferase toxins extend tRNA acceptor stems and can be inhibited by asymmetrical antitoxin binding

open access: yesNature Communications, 2023
Mycobacterium tuberculosis, the bacterium responsible for human tuberculosis, has a genome encoding a remarkably high number of toxin-antitoxin systems of largely unknown function. We have recently shown that the M.
Xibing Xu   +9 more
doaj   +1 more source

Rapid Identification of Secondary Structure and Binding Site Residues in an Intrinsically Disordered Protein Segment

open access: yesFrontiers in Genetics, 2021
Mycobacterium tuberculosis harbours nine toxin-antitoxin (TA) systems of the MazEF family. MazEF TA modules are of immense importance due to the perceived role of the MazF toxin in M. tuberculosis persistence and disease.
Soumyanetra Chandra   +2 more
doaj   +1 more source

Toxin–antitoxin systems: reversible toxicity

open access: yesCurrent Opinion in Microbiology, 2017
Toxin-antitoxin (TA) systems encoded on the plasmids and chromosomes of bacteria are emerging as key players in stress adaptation. In particular, they have been implicated in the induction of persisters non-growing cells that can evade antibiotic exposure.
Hall, A, Gollan, B, Helaine, S
openaire   +4 more sources

The vapB-vapC operon of Acidovorax citrulli functions as a bona-fide toxin-antitoxin module

open access: yesFrontiers in Microbiology, 2016
Toxin–antitoxin systems are commonly found on plasmids and chromosomes of bacteria and archaea. These systems appear as biscystronic genes encoding a stable toxin and a labile antitoxin, which protects the cells from the toxin’s activity. Under specific,
Reut eShavit   +4 more
doaj   +1 more source

The coevolution of toxin and antitoxin genes drives the dynamics of bacterial addiction complexes and intragenomic conflict [PDF]

open access: yes, 2012
Bacterial genomes commonly contain ‘addiction’ gene complexes that code for both a toxin and a corresponding antitoxin. As long as both genes are expressed, cells carrying the complex can remain healthy.
Brown, Sam P.   +3 more
core   +1 more source

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