| scholarly article | Q13442814 |
| P2093 | author name string | Minny Bhatty | |
| Jenny A Laverde Gomez | |||
| Peter J Christie | |||
| P2860 | cites work | SMART: a web-based tool for the study of genetically mobile domains | Q24515301 |
| SMART 7: recent updates to the protein domain annotation resource | Q24622634 | ||
| Structure of the outer membrane complex of a type IV secretion system | Q24654218 | ||
| A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding | Q25938984 | ||
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| Structural elucidation of the Cys-His-Glu-Asn proteolytic relay in the secreted CHAP domain enzyme from the human pathogenStaphylococcus saprophyticus | Q27652649 | ||
| Structure of the basal components of a bacterial transporter | Q27678103 | ||
| Structure-function analysis of the LytM domain of EnvC, an activator of cell wall remodelling at theEscherichia colidivision site | Q27678759 | ||
| Protein structure prediction on the Web: a case study using the Phyre server | Q27860664 | ||
| Identification and characterization of novel cell wall hydrolase CwlT: a two-domain autolysin exhibiting n-acetylmuramidase and DL-endopeptidase activities | Q28488983 | ||
| A LytM domain dictates the localization of proteins to the mother cell-forespore interface during bacterial endospore formation | Q28489062 | ||
| Crystal structures of active LytM | Q28904963 | ||
| SignalP 4.0: discriminating signal peptides from transmembrane regions | Q29547202 | ||
| F-pili dynamics by live-cell imaging | Q30440803 | ||
| TraG encoded by the pIP501 type IV secretion system is a two-domain peptidoglycan-degrading enzyme essential for conjugative transfer. | Q42201100 | ||
| AtlA functions as a peptidoglycan lytic transglycosylase in the Neisseria gonorrhoeae type IV secretion system | Q42412512 | ||
| Cloning, sequencing and expression of a Bacillus bacteriolytic enzyme in Escherichia coli | Q42653324 | ||
| Role of a type IV-like secretion system of Streptococcus suis 2 in the development of streptococcal toxic shock syndrome | Q43609220 | ||
| Determination of lysozyme activity by a fluorescence technique in comparison with the classical turbidity assay. | Q46498878 | ||
| A multiresistance megaplasmid pLG1 bearing a hylEfm genomic island in hospital Enterococcus faecium isolates | Q48062305 | ||
| Peptidoglycan degradation by specialized lytic transglycosylases associated with type III and type IV secretion systems. | Q50085803 | ||
| The peptidoglycan hydrolase TcpG is required for efficient conjugative transfer of pCW3 in Clostridium perfringens. | Q54344283 | ||
| Direct stimulation of the transfer of antibiotic resistance by sex pheromones in Streptococcus faecalis. | Q54529244 | ||
| Subcellular localization and processing of the lytic transglycosylase of the conjugative plasmid R1 | Q57260168 | ||
| Detection of bacterial cell wall hydrolases after denaturing polyacrylamide gel electrophoresis | Q69805496 | ||
| Improved vectors for nisin-controlled expression in gram-positive bacteria | Q74241039 | ||
| Systematic mutagenesis of the Helicobacter pylori cag pathogenicity island: essential genes for CagA translocation in host cells and induction of interleukin-8 | Q77748414 | ||
| ExeA binds to peptidoglycan and forms a multimer for assembly of the type II secretion apparatus in Aeromonas hydrophila | Q83931322 | ||
| Biological diversity of prokaryotic type IV secretion systems. | Q30927042 | ||
| Coliphage N4 N-acetylmuramidase defines a new family of murein hydrolases | Q31085904 | ||
| Amidase domains from bacterial and phage autolysins define a family of gamma-D,L-glutamate-specific amidohydrolases | Q33187139 | ||
| CsiA is a bacterial cell wall synthesis inhibitor contributing to DNA translocation through the cell envelope | Q33435985 | ||
| Characterization of the pheromone response of the Enterococcus faecalis conjugative plasmid pCF10: complete sequence and comparative analysis of the transcriptional and phenotypic responses of pCF10-containing cells to pheromone induction | Q33758514 | ||
| Specific control of endogenous cCF10 pheromone by a conserved domain of the pCF10-encoded regulatory protein PrgY in Enterococcus faecalis | Q33885733 | ||
| Use of the Strep-Tag and streptavidin for detection and purification of recombinant proteins | Q33921941 | ||
| Biological roles of two new murein hydrolases of Streptococcus pneumoniae representing examples of module shuffling | Q34015637 | ||
| Development of a method for markerless genetic exchange in Enterococcus faecalis and its use in construction of a srtA mutant | Q34097982 | ||
| The CHAP domain: a large family of amidases including GSP amidase and peptidoglycan hydrolases | Q34199699 | ||
| F factor conjugation is a true type IV secretion system. | Q34213377 | ||
| The versatile bacterial type IV secretion systems | Q34307587 | ||
| Type IV secretion: the Agrobacterium VirB/D4 and related conjugation systems | Q34368266 | ||
| Diversity of Firmicutes peptidoglycan hydrolases and specificities of those involved in daughter cell separation. | Q34656809 | ||
| Structure of a type IV secretion system core complex. | Q34917985 | ||
| GI-type T4SS-mediated horizontal transfer of the 89K pathogenicity island in epidemic Streptococcus suis serotype 2. | Q35094135 | ||
| Lytic transglycosylases in macromolecular transport systems of Gram-negative bacteria | Q35587962 | ||
| Molecular cloning, sequencing, and expression of lytM, a unique autolytic gene of Staphylococcus aureus | Q35623935 | ||
| Development of a host-genotype-independent counterselectable marker and a high-frequency conjugative delivery system and their use in genetic analysis of Enterococcus faecalis | Q35751764 | ||
| Two conjugation systems associated with Streptococcus faecalis plasmid pCF10: identification of a conjugative transposon that transfers between S. faecalis and Bacillus subtilis | Q36237822 | ||
| Neisseria gonorrhoeae uses two lytic transglycosylases to produce cytotoxic peptidoglycan monomers | Q36845577 | ||
| Genetic characterization of the conjugative DNA processing system of enterococcal plasmid pCF10. | Q37126851 | ||
| Shared catalysis in virus entry and bacterial cell wall depolymerization | Q37161434 | ||
| The expanding bacterial type IV secretion lexicon | Q37275377 | ||
| A modular master on the move: the Tn916 family of mobile genetic elements. | Q37493047 | ||
| A family of lysozyme-like virulence factors in bacterial pathogens of plants and animals | Q37502145 | ||
| Induced cell aggregation and mating in Streptococcus faecalis: evidence for a bacterial sex pheromone | Q37591243 | ||
| The catalytic domain of a bacterial lytic transglycosylase defines a novel class of lysozymes | Q38294044 | ||
| A general system for generating unlabelled gene replacements in bacterial chromosomes. | Q38559698 | ||
| Enterococcus faecalis PcfC, a spatially localized substrate receptor for type IV secretion of the pCF10 transfer intermediate | Q38608495 | ||
| Functional and mutational analysis of p19, a DNA transfer protein with muramidase activity | Q39503619 | ||
| Gene 19 of plasmid R1 is required for both efficient conjugative DNA transfer and bacteriophage R17 infection | Q39837719 | ||
| Genetic complementation analysis of the Agrobacterium tumefaciens virB operon: virB2 through virB11 are essential virulence genes | Q39932342 | ||
| Controlled release of protein from viable Lactococcus lactis cells | Q40329031 | ||
| VirB1 orthologs from Brucella suis and pKM101 complement defects of the lytic transglycosylase required for efficient type IV secretion from Agrobacterium tumefaciens | Q40584794 | ||
| A type IV-secretion-like system is required for conjugative DNA transport of broad-host-range plasmid pIP501 in gram-positive bacteria | Q42108962 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 527-539 | |
| P577 | publication date | 2013-11-15 | |
| P1433 | published in | Journal of Bacteriology | Q478419 |
| P1476 | title | PrgK, a multidomain peptidoglycan hydrolase, is essential for conjugative transfer of the pheromone-responsive plasmid pCF10. | |
| P478 | volume | 196 |
| Q35167687 | An intermolecular binding mechanism involving multiple LysM domains mediates carbohydrate recognition by an endopeptidase. |
| Q64082357 | Biological and Structural Diversity of Type IV Secretion Systems |
| Q90162000 | Comparative Genomic Analysis Confirms Five Genetic Populations of the Select Agent, Rathayibacter toxicus |
| Q35899801 | Critical Components of the Conjugation Machinery of the Integrative and Conjugative Element ICEBs1 of Bacillus subtilis |
| Q39769615 | Key components of the eight classes of type IV secretion systems involved in bacterial conjugation or protein secretion |
| Q41019427 | Lactobacillus fermentum 3872 genome sequencing reveals plasmid and chromosomal genes potentially involved in a probiotic activity. |
| Q50167594 | Measure of Peptidoglycan Hydrolase Activity. |
| Q37036006 | Mechanism and Function of Type IV Secretion During Infection of the Human Host |
| Q60960288 | Plastid Genomes from Diverse Glaucophyte Genera Reveal a Largely Conserved Gene Content and Limited Architectural Diversity |
| Q46469955 | PrgU: a suppressor of sex pheromone toxicity in Enterococcus faecalis |
| Q27695577 | Structure of the double-stranded DNA-binding type IV secretion protein TraN from Enterococcus |
| Q37713206 | The bifunctional cell wall hydrolase CwlT is needed for conjugation of the integrative and conjugative element ICEBs1 in Bacillus subtilis and B. anthracis |
| Q47299307 | Type IV secretion in Gram-negative and Gram-positive bacteria |
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