review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Fernando Ruiz-Perez | |
Fernando Navarro-Garcia | |||
Ángel Cataldi | |||
Mariano Larzábal | |||
P2860 | cites work | Vibrio cholerae type 6 secretion system effector trafficking in target bacterial cells | Q46321188 |
The genome sequence of E. coli W (ATCC 9637): comparative genome analysis and an improved genome-scale reconstruction of E. coli | Q21266710 | ||
Identification of a conserved bacterial protein secretion system in Vibrio cholerae using the Dictyostelium host model system | Q24537443 | ||
What is type VI secretion doing in all those bugs? | Q24594338 | ||
The type VI secretion toolkit | Q24644999 | ||
PAAR-Rhs proteins harbor various C-terminal toxins to diversify the antibacterial pathways of type VI secretion systems | Q46456498 | ||
In vivo structures of an intact type VI secretion system revealed by electron cryotomography | Q46764741 | ||
The Role of Type VI Secretion System Effectors in Target Cell Lysis and Subsequent Horizontal Gene Transfer | Q47251475 | ||
Structure-Function Analysis of the C-Terminal Domain of the Type VI Secretion TssB Tail Sheath Subunit | Q47311961 | ||
Identification of a novel gene in ROD9 island of Salmonella Enteritidis involved in the alteration of virulence-associated genes expression | Q47410801 | ||
Dissection of a type VI secretion system in Edwardsiella tarda | Q48076617 | ||
Type VI secretion TssK baseplate protein exhibits structural similarity with phage receptor-binding proteins and evolved to bind the membrane complex | Q48222755 | ||
T6SS intraspecific competition orchestrates Vibrio cholerae genotypic diversity | Q49985263 | ||
Imaging type VI secretion-mediated bacterial killing. | Q50485497 | ||
Adaptor Proteins of Type VI Secretion System Effectors. | Q51322442 | ||
Molecular Dissection of the Interface between the Type VI Secretion TssM Cytoplasmic Domain and the TssG Baseplate Component. | Q51531303 | ||
Structure-Function Analysis of the TssL Cytoplasmic Domain Reveals a New Interaction between the Type VI Secretion Baseplate and Membrane Complexes. | Q51531311 | ||
Diverse toxic effectors are harbored by vgrG islands for interbacterial antagonism in type VI secretion system. | Q52576837 | ||
The type VI secretion system of Vibrio cholerae fosters horizontal gene transfer. | Q53348717 | ||
A phospholipase A1 antibacterial Type VI secretion effector interacts directly with the C-terminal domain of the VgrG spike protein for delivery. | Q54253962 | ||
Heterogeneity of enteroaggregative Escherichia coli virulence demonstrated in volunteers. | Q54617716 | ||
Three Hcp homologs with divergent extended loop regions exhibit different functions in avian pathogenic Escherichia coli. | Q55094311 | ||
In vivo TssA proximity labelling during type VI secretion biogenesis reveals TagA as a protein that stops and holds the sheath | Q57060056 | ||
Biogenesis and structure of a type VI secretion baseplate | Q57464807 | ||
Structure of the type VI secretion system TssK-TssF-TssG baseplate subcomplex revealed by cryo-electron microscopy | Q60300791 | ||
Characterization of multiple type-VI secretion system (T6SS) VgrG proteins in the pathogenicity and antibacterial activity of porcine extra-intestinal pathogenic Escherichia coli | Q61810844 | ||
Bidirectional contraction of a type six secretion system | Q64073432 | ||
and high-resolution cryo-EM structure of a bacterial type VI secretion system membrane complex | Q64086440 | ||
Comparative Genome Analysis of an Extensively Drug-Resistant Isolate of Avian Sequence Type 167 Strain Sanji with Novel Serotype O89b:H9 | Q64102322 | ||
The different roles of hcp and hcp of the type VI secretion system in Escherichia coli strain CE129 | Q64448447 | ||
Comparative Transcriptome Profiling Reveals a Potential Role of Type VI Secretion System and Fimbriae in Virulence of Non-O157 Shiga Toxin-Producing | Q64448554 | ||
Identification of a unique IAHP (IcmF associated homologous proteins) cluster in Vibrio cholerae and other proteobacteria through in silico analysis | Q73897572 | ||
Effector⁻Immunity Pairs Provide the T6SS Nanomachine its Offensive and Defensive Capabilities | Q88492164 | ||
The gp27-like Hub of VgrG Serves as Adaptor to Promote Hcp Tube Assembly | Q90385366 | ||
ClpV recycles VipA/VipB tubules and prevents non-productive tubule formation to ensure efficient type VI protein secretion | Q95480308 | ||
Type VI secretion system: secretion by a contractile nanomachine | Q26787001 | ||
Type VI secretion apparatus and phage tail-associated protein complexes share a common evolutionary origin | Q27653977 | ||
Identification, Structure, and Function of a Novel Type VI Secretion Peptidoglycan Glycoside Hydrolase Effector-Immunity Pair | Q27679179 | ||
PAAR-repeat proteins sharpen and diversify the type VI secretion system spike | Q27679451 | ||
Structure and properties of the C-terminal β-helical domain of VgrG protein from Escherichia coli O157 | Q27687827 | ||
Biogenesis and structure of a type VI secretion membrane core complex | Q27701595 | ||
In vivo expression technology identifies a type VI secretion system locus in Burkholderia pseudomallei that is induced upon invasion of macrophages | Q28238270 | ||
Type VI secretion is a major virulence determinant in Burkholderia mallei | Q28305456 | ||
Type VI secretion system translocates a phage tail spike-like protein into target cells where it cross-links actin | Q28485710 | ||
Threonine phosphorylation post-translationally regulates protein secretion in Pseudomonas aeruginosa | Q28492573 | ||
Quorum sensing differentially regulates Pseudomonas aeruginosa type VI secretion locus I and homologous loci II and III, which are required for pathogenesis | Q28492577 | ||
A novel serine/threonine protein kinase homologue of Pseudomonas aeruginosa is specifically inducible within the host infection site and is required for full virulence in neutropenic mice | Q28492582 | ||
Type VI secretion system in Pseudomonas aeruginosa: secretion and multimerization of VgrG proteins | Q28492592 | ||
A type VI secretion system of Pseudomonas aeruginosa targets a toxin to bacteria | Q28492922 | ||
Genetically distinct pathways guide effector export through the type VI secretion system | Q28493007 | ||
VgrG and PAAR Proteins Define Distinct Versions of a Functional Type VI Secretion System | Q28552230 | ||
The Vibrio cholerae type VI secretion system employs diverse effector modules for intraspecific competition. | Q30360835 | ||
Shiga toxin 2a and Enteroaggregative Escherichia coli--a deadly combination | Q30360953 | ||
Type VI secretion requires a dynamic contractile phage tail-like structure | Q30530331 | ||
Secretome analysis of Vibrio cholerae type VI secretion system reveals a new effector-immunity pair | Q30908434 | ||
Intraspecies Competition in Serratia marcescens Is Mediated by Type VI-Secreted Rhs Effectors and a Conserved Effector-Associated Accessory Protein | Q30943932 | ||
Evolutionary diversification of an ancient gene family (rhs) through C-terminal displacement | Q30962327 | ||
The Hcp proteins fused with diverse extended-toxin domains represent a novel pattern of antibacterial effectors in type VI secretion systems | Q31153284 | ||
The Francisella pathogenicity island protein IglA localizes to the bacterial cytoplasm and is needed for intracellular growth | Q33269612 | ||
Identification and functional characterization of gene components of Type VI Secretion system in bacterial genomes | Q33359587 | ||
Dissecting the bacterial type VI secretion system by a genome wide in silico analysis: what can be learned from available microbial genomic resources? | Q33417905 | ||
Large genomic sequence repetitions in bacteria: lessons from rRNA operons and Rhs elements | Q33836575 | ||
Identification of protective and broadly conserved vaccine antigens from the genome of extraintestinal pathogenic Escherichia coli | Q33927393 | ||
Nooks and crannies in type VI secretion regulation. | Q34045539 | ||
Infection of mice by Salmonella enterica serovar Enteritidis involves additional genes that are absent in the genome of serovar Typhimurium | Q34074392 | ||
Polymorphic toxin systems: Comprehensive characterization of trafficking modes, processing, mechanisms of action, immunity and ecology using comparative genomics | Q34283923 | ||
Two functional type VI secretion systems in avian pathogenic Escherichia coli are involved in different pathogenic pathways | Q34298499 | ||
Lytic activity of the Vibrio cholerae type VI secretion toxin VgrG-3 is inhibited by the antitoxin TsaB. | Q34323842 | ||
Use of proteomics to identify novel virulence determinants that are required for Edwardsiella tarda pathogenesis | Q34330362 | ||
Haemolysin coregulated protein is an exported receptor and chaperone of type VI secretion substrates | Q34364793 | ||
Type VI secretion system effectors: poisons with a purpose | Q34395319 | ||
Type VI secretion and bacteriophage tail tubes share a common assembly pathway | Q34401628 | ||
DotU expression is highly induced during in vivo infection and responsible for virulence and Hcp1 secretion in avian pathogenic Escherichia coli | Q34471456 | ||
Identification of T6SS-dependent effector and immunity proteins by Tn-seq in Vibrio cholerae | Q34567332 | ||
Type VI secretion: a beginner's guide | Q34752940 | ||
Systematic dissection of the agrobacterium type VI secretion system reveals machinery and secreted components for subcomplex formation | Q34825763 | ||
Remodelling of VipA/VipB tubules by ClpV-mediated threading is crucial for type VI protein secretion | Q34918172 | ||
Dissection of the TssB-TssC interface during type VI secretion sheath complex formation | Q35055208 | ||
Translocation of a Vibrio cholerae type VI secretion effector requires bacterial endocytosis by host cells | Q35125979 | ||
Generation of reactive oxygen species by lethal attacks from competing microbes | Q35128847 | ||
Genome based phylogeny and comparative genomic analysis of intra-mammary pathogenic Escherichia coli | Q35216942 | ||
The Type VI Secretion TssEFGK-VgrG Phage-Like Baseplate Is Recruited to the TssJLM Membrane Complex via Multiple Contacts and Serves As Assembly Platform for Tail Tube/Sheath Polymerization | Q35804578 | ||
Hcp family proteins secreted via the type VI secretion system coordinately regulate Escherichia coli K1 interaction with human brain microvascular endothelial cells | Q35805527 | ||
Structural biology of type VI secretion systems | Q35814718 | ||
A widespread bacterial type VI secretion effector superfamily identified using a heuristic approach | Q35982125 | ||
Type VI secretion system contributes to Enterohemorrhagic Escherichia coli virulence by secreting catalase against host reactive oxygen species (ROS) | Q36306336 | ||
An ABC transporter and an outer membrane lipoprotein participate in posttranslational activation of type VI secretion in Pseudomonas aeruginosa. | Q36306345 | ||
Pathogenesis of enteroaggregative Escherichia coli infection | Q36383861 | ||
Secretome analysis uncovers an Hcp-family protein secreted via a type VI secretion system in Agrobacterium tumefaciens | Q36540557 | ||
Molecular characterization of a functional type VI secretion system from a clinical isolate of Aeromonas hydrophila | Q36724845 | ||
Diverse type VI secretion phospholipases are functionally plastic antibacterial effectors | Q36839898 | ||
Roles of Hcp family proteins in the pathogenesis of the porcine extraintestinal pathogenic Escherichia coli type VI secretion system | Q36941397 | ||
Molecular epidemiology and phylogenetic distribution of the Escherichia coli pks genomic island | Q36994573 | ||
A conserved alpha-helix essential for a type VI secretion-like system of Francisella tularensis | Q37157058 | ||
TssK is a trimeric cytoplasmic protein interacting with components of both phage-like and membrane anchoring complexes of the type VI secretion system | Q37189426 | ||
Genomic islands of uropathogenic Escherichia coli contribute to virulence | Q37191735 | ||
Common themes and variations in serine protease autotransporters | Q37205333 | ||
Proteomic identification of novel secreted antibacterial toxins of the Serratia marcescens type VI secretion system. | Q37214662 | ||
Structure and specificity of the Type VI secretion system ClpV-TssC interaction in enteroaggregative Escherichia coli. | Q37307118 | ||
The type VI secretion system: translocation of effectors and effector-domains | Q37375434 | ||
Contractile tail machines of bacteriophages | Q37980623 | ||
Enteroaggregative Escherichia coli pathotype: a genetically heterogeneous emerging foodborne enteropathogen | Q38024836 | ||
Architecture and assembly of the Type VI secretion system. | Q38200408 | ||
VgrG, Tae, Tle, and beyond: the versatile arsenal of Type VI secretion effectors | Q38231827 | ||
Secretion systems in Gram-negative bacteria: structural and mechanistic insights. | Q38482854 | ||
TssA: The cap protein of the Type VI secretion system tail. | Q38620180 | ||
Type VI secretion and anti-host effectors | Q38684791 | ||
The Type VI Secretion System in Escherichia coli and Related Species. | Q38844038 | ||
Interbacterial predation as a strategy for DNA acquisition in naturally competent bacteria | Q39424297 | ||
Characterization of IcmF of the type VI secretion system in an avian pathogenic Escherichia coli (APEC) strain. | Q39502999 | ||
The Legionella pneumophila icmGCDJBF genes are required for killing of human macrophages | Q39571241 | ||
BcsKC is an essential protein for the type VI secretion system activity in Burkholderia cenocepacia that forms an outer membrane complex with BcsLB | Q39664786 | ||
A novel sensor kinase-response regulator hybrid controls biofilm formation and type VI secretion system activity in Burkholderia cenocepacia | Q40006381 | ||
FNR Regulates the Expression of Important Virulence Factors Contributing to the Pathogenicity of Avian Pathogenic Escherichia coli | Q40142217 | ||
The HsiB1C1 (TssB-TssC) complex of the Pseudomonas aeruginosa type VI secretion system forms a bacteriophage tail sheathlike structure | Q41116566 | ||
Horizontal Gene Transfer of Functional Type VI Killing Genes by Natural Transformation. | Q41126951 | ||
Internalization of Pseudomonas aeruginosa Strain PAO1 into Epithelial Cells Is Promoted by Interaction of a T6SS Effector with the Microtubule Network | Q41189092 | ||
Biochemical analysis of TssK, a core component of the bacterial Type VI secretion system, reveals distinct oligomeric states of TssK and identifies a TssK-TssFG subcomplex | Q41253912 | ||
The Salmonella enterica subspecies I specific centisome 7 genomic island encodes novel protein families present in bacteria living in close contact with eukaryotic cells | Q41469984 | ||
Genomic comparison of Escherichia coli K1 strains isolated from the cerebrospinal fluid of patients with meningitis | Q41957733 | ||
Quorum sensing and silencing in Vibrio parahaemolyticus | Q42150850 | ||
Sequential displacement of Type VI Secretion System effector genes leads to evolution of diverse immunity gene arrays in Vibrio cholerae | Q42314845 | ||
The Type VI Secretion System Plays a Role in Type 1 Fimbria Expression and Pathogenesis of an Avian Pathogenic Escherichia coli Strain | Q42363502 | ||
Proteomic and microarray characterization of the AggR regulon identifies a pheU pathogenicity island in enteroaggregative Escherichia coli | Q42596037 | ||
The Citrobacter rodentium genome sequence reveals convergent evolution with human pathogenic Escherichia coli | Q42938903 | ||
Genetic diversity and features analysis of type VI secretion systems loci in avian pathogenic Escherichia coli by wide genomic scanning | Q44599095 | ||
Inter-species population dynamics enhance microbial horizontal gene transfer and spread of antibiotic resistance | Q46179212 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P921 | main subject | Escherichia coli | Q25419 |
P304 | page(s) | 1965 | |
P577 | publication date | 2019-08-30 | |
P1433 | published in | Frontiers in Microbiology | Q27723481 |
P1476 | title | Type VI Secretion System in Pathogenic Escherichia coli: Structure, Role in Virulence, and Acquisition | |
P478 | volume | 10 |
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