Results 21 to 30 of about 877 (123)

Phosphorylation of VapB antitoxins affects intermolecular interactions to regulate VapC toxin activity in Mycobacterium tuberculosis. [PDF]

open access: yesJ Bacteriol
ABSTRACT Toxin–antitoxin modules are present in many bacterial pathogens. The VapBC family is particularly abundant in members of the Mycobacterium tuberculosis complex, with 50 modules present in the M. tuberculosis genome.
Malakar B   +4 more
europepmc   +4 more sources

Regulation of Enteric vapBC Transcription: Induction by VapC Toxin Dimer-Breaking

open access: yesNucleic Acids Research, 2012
Toxin-antitoxin (TA) loci encode inhibitors of translation, replication or cell wall synthesis and are common elements of prokaryotic plasmids and chromosomes. Ten TA loci of Escherichia coli K-12 encode mRNases that cumulatively contribute to persistence (multidrug tolerance) of the bacterial cells. The mechanisms underlying induction and reversion of
Kristoffer Skovbo Winther, Kenn Gerdes
exaly   +4 more sources

Bioinformatic and literature assessment of toxicity and allergenicity of a CRISPR-Cas9 engineered gene drive to control Anopheles gambiae the mosquito vector of human malaria [PDF]

open access: yesMalaria Journal, 2023
Background Population suppression gene drive is currently being evaluated, including via environmental risk assessment (ERA), for malaria vector control.
Alima Qureshi, John B. Connolly
doaj   +2 more sources

Generation of a toxin/antitoxin-based counterselection marker for Chlamydia trachomatis [PDF]

open access: yesInfection and Immunity
Chlamydia trachomatis is the leading cause of bacterial sexually transmitted infection in the United States. The high rate of asymptomatic cases and absence of a vaccine often leave infections untreated, increasing the risk of serious complications in ...
Eleanor Steiner   +3 more
doaj   +2 more sources

Understanding the physiological role and cross-interaction network of VapBC35 toxin-antitoxin system from Mycobacterium tuberculosis [PDF]

open access: yesCommunications Biology
The VapBC toxin-antitoxin (TA) system, composed of VapC toxin and VapB antitoxin, has gained attention due to its relative abundance in members of the M. tuberculosis complex.
Neelam Singh   +4 more
doaj   +2 more sources

The N-terminal domain is required for cell surface localisation of VapA, a member of the Vap family of Rhodococcus equi virulence proteins. [PDF]

open access: yesPLoS ONE
Rhodococcus equi pneumonia is an important cause of mortality in foals worldwide. Virulent equine isolates harbour an 80-85kb virulence plasmid encoding six virulence-associated proteins (Vaps).
Raúl Miranda-CasoLuengo   +6 more
doaj   +2 more sources

VapC-1 of Nontypeable Haemophilus influenzae Is a Ribonuclease [PDF]

open access: yesJournal of Bacteriology, 2007
ABSTRACT Nontypeable Haemophilus influenzae (NTHi) organisms are obligate parasites of the human upper respiratory tract that can exist as commensals or pathogens. Toxin-antitoxin (TA) loci are highly conserved gene pairs that encode both a toxin and antitoxin moiety.
Daines, Dayle A   +2 more
openaire   +3 more sources

Correction to: Resonance assignments of a VapC family toxin from Clostridium thermocellum [PDF]

open access: yesBiomolecular NMR Assignments, 2020
In the original publication of the article, the authors found a misquote in the Reference section.
Chen Wang   +3 more
openaire   +1 more source

VapCs of Mycobacterium tuberculosis cleave RNAs essential for translation [PDF]

open access: yesNucleic Acids Research, 2016
The major human pathogen Mycobacterium tuberculosis can survive in the host organism for decades without causing symptoms. A large cohort of Toxin-Antitoxin (TA) modules contribute to this persistence. Of these, 48 TA modules belong to the vapBC (virulence associated protein) gene family. VapC toxins are PIN domain endonucleases that, in enterobacteria,
Winther, K   +3 more
openaire   +4 more sources

Analysis of non-typeable Haemophilous influenzae VapC1 mutations reveals structural features required for toxicity and flexibility in the active site. [PDF]

open access: yesPLoS ONE, 2014
Bacteria have evolved mechanisms that allow them to survive in the face of a variety of stresses including nutrient deprivation, antibiotic challenge and engulfment by predator cells.
Brooke Hamilton   +4 more
doaj   +1 more source

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