| scholarly article | Q13442814 |
| P2093 | author name string | Eric Larquet | |
| Pascal Roux | |||
| Marie-Christine Prévost | |||
| Rolf Köhler | |||
| Anthony P. Pugsley | |||
| Guillaume Vignon | |||
| Stéphanie Giroux | |||
| P2860 | cites work | Journal of Molecular Biology | Q925779 |
| Proceedings of the National Academy of Sciences of the United States of America | Q1146531 | ||
| BioTechniques | Q4914664 | ||
| Molecular interaction between the Strep-tag affinity peptide and its cognate target, streptavidin | Q27732713 | ||
| Isolation of monoclonal antibodies specific for human c-myc proto-oncogene product | Q27860841 | ||
| Flagellar and twitching motility are necessary for Pseudomonas aeruginosa biofilm development | Q27976516 | ||
| Pilus retraction powers bacterial twitching motility | Q28138923 | ||
| Formation of oligomeric rings by XcpQ and PilQ, which are involved in protein transport across the outer membrane of Pseudomonas aeruginosa | Q28492505 | ||
| A novel type II secretion system in Pseudomonas aeruginosa | Q28492615 | ||
| Cleavage, methylation, and localization of the Pseudomonas aeruginosa export proteins XcpT, -U, -V, and -W | Q28492647 | ||
| Amino acid substitutions in PilD, a bifunctional enzyme of Pseudomonas aeruginosa. Effect on leader peptidase and N-methyltransferase activities in vitro and in vivo | Q28492721 | ||
| Protein secretion in Pseudomonas aeruginosa: characterization of seven xcp genes and processing of secretory apparatus components by prepilin peptidase | Q28493043 | ||
| The secretion apparatus of Pseudomonas aeruginosa: identification of a fifth pseudopilin, XcpX (GspK family) | Q28493060 | ||
| The complete general secretory pathway in gram-negative bacteria | Q29615298 | ||
| Secretin PulD: association with pilot PulS, structure, and ion-conducting channel formation | Q30727915 | ||
| Epitopes fused to F-pilin are incorporated into functional recombinant pili. | Q32059812 | ||
| Bacterial type II protein export and pilus biogenesis: more than just homologies? | Q33730388 | ||
| Cloning and expression in Escherichia coli of the Klebsiella pneumoniae genes for production, surface localization and secretion of the lipoprotein pullulanase. | Q33929884 | ||
| Direct observation of extension and retraction of type IV pili | Q33948884 | ||
| Directed polar secretion of protease from single cells of Vibrio cholerae via the type II secretion pathway | Q33950258 | ||
| Analysis of the PilQ secretin from Neisseria meningitidis by transmission electron microscopy reveals a dodecameric quaternary structure. | Q33996354 | ||
| Polymeric display of immunogenic epitopes from herpes simplex virus and transmissible gastroenteritis virus surface proteins on an enteroadherent fimbria. | Q33997509 | ||
| Type II protein secretion is a subset of the PilD-dependent processes that facilitate intracellular infection by Legionella pneumophila | Q34006686 | ||
| Immunoaffinity purification of FLAG epitope-tagged bacterial alkaline phosphatase using a novel monoclonal antibody and peptide elution. | Q34060035 | ||
| Expression of the endogenous type II secretion pathway in Escherichia coli leads to chitinase secretion. | Q34685284 | ||
| Cell-invasive activity of epitope-tagged adenylate cyclase of Bordetella pertussis allows in vitro presentation of a foreign epitope to CD8+ cytotoxic T cells | Q35441983 | ||
| Characterization and expression of the structural gene for pullulanase, a maltose-inducible secreted protein of Klebsiella pneumoniae | Q36278918 | ||
| Suppression of an absolute defect in type IV pilus biogenesis by loss-of-function mutations in pilT, a twitching motility gene in Neisseria gonorrhoeae | Q36758783 | ||
| Domain structure of secretin PulD revealed by limited proteolysis and electron microscopy. | Q37350291 | ||
| Disulfide bond formation in secreton component PulK provides a possible explanation for the role of DsbA in pullulanase secretion | Q39502502 | ||
| Multiple interactions between pullulanase secreton components involved in stabilization and cytoplasmic membrane association of PulE. | Q39587073 | ||
| Assembly of mutant pilins in Pseudomonas aeruginosa: formation of pili composed of heterologous subunits | Q39948652 | ||
| Steps in the development of a Vibrio cholerae El Tor biofilm | Q40225093 | ||
| Components and dynamics of fiber formation define a ubiquitous biogenesis pathway for bacterial pili | Q40388345 | ||
| Common components in the assembly of type 4 fimbriae, DNA transfer systems, filamentous phage and protein-secretion apparatus: a general system for the formation of surface-associated protein complexes | Q40637003 | ||
| Pilus formation and protein secretion by the same machinery in Escherichia coli | Q40749053 | ||
| Cloning of DNA sequences encoding foreign peptides and their expression in the K88 pili | Q41941347 | ||
| Characterisation of a Pseudomonas aeruginosa twitching motility gene and evidence for a specialised protein export system widespread in eubacteria | Q42614584 | ||
| Specific interaction between OutD, an Erwinia chrysanthemi outer membrane protein of the general secretory pathway, and secreted proteins. | Q42619538 | ||
| A gene cluster closely related to type II secretion pathway operons of gram-negative bacteria is located on the large plasmid of enterohemorrhagic Escherichia coli O157 strains | Q42652422 | ||
| The PDZ domain of OutC and the N-terminal region of OutD determine the secretion specificity of the type II out pathway of Erwinia chrysanthemi. | Q43591523 | ||
| Export and secretion of the lipoprotein pullulanase by Klebsiella pneumoniae | Q46948520 | ||
| Five additional genes in the pulC-O operon of the gram-negative bacterium Klebsiella oxytoca UNF5023 which are required for pullulanase secretion | Q48262286 | ||
| Protein secretion by gram-negative bacteria. Characterization of two membrane proteins required for pullulanase secretion by Escherichia coli K-12. | Q48284533 | ||
| Permissible peptide insertions surrounding the signal peptide-mature protein junction of the ClpG prepilin: CS31A fimbriae of Escherichia coli as carriers of foreign sequences | Q54193058 | ||
| Energy requirement for pullulanase secretion by the main terminal branch of the general secretory pathway. | Q54509673 | ||
| A rapid screening procedure to identify mini-Tn10 insertion mutants of Escherichia coli K-12 with altered adhesion properties. | Q54583023 | ||
| An enzyme with type IV prepilin peptidase activity is required to process components of the general extracellular protein secretion pathway of Klebsiella oxytoca | Q54682441 | ||
| The expression of mutant pilins in Pseudomonas aeruginosa: fifth position glutamate affects pilin methylation. | Q54746588 | ||
| Mutations in a new chromosomal gene of Escherichia coli K-12, pcnB, reduce plasmid copy number of pBR322 and its derivatives. | Q54773863 | ||
| Multimers of the precursor of a type IV pilin-like component of the general secretory pathway are unrelated to pili | Q64450065 | ||
| The general secretory pathway of Klebsiella oxytoca: no evidence for relocalization or assembly of pilin-like PulG protein into a multiprotein complex | Q64450302 | ||
| Amino acid substitutions in pilin of Pseudomonas aeruginosa. Effect on leader peptide cleavage, amino-terminal methylation, and pilus assembly | Q64450757 | ||
| Processing and methylation of PuIG, a pilin-like component of the general secretory pathway of Klebsiella oxytoca | Q70511675 | ||
| Complementation of deletion mutations in a cloned functional cluster of Erwinia chrysanthemi out genes with Erwinia carotovora out homologues reveals OutC and OutD as candidate gatekeepers of species-specific secretion of proteins via the type II pa | Q71662127 | ||
| Initial binding of Shiga toxin-producing Escherichia coli to host cells and subsequent induction of actin rearrangements depend on filamentous EspA-containing surface appendages | Q77456473 | ||
| Genetic analysis of Escherichia coli biofilm formation: roles of flagella, motility, chemotaxis and type I pili | Q77472923 | ||
| A gene cluster closely related to type II secretion pathway operons of Gram-negative bacteria is located on the large plasmid of enterohemorrhagic Escherichia coli O157 strains | Q115688640 | ||
| A rapid screening procedure to identify mini-Tn10 insertion mutants ofEscherichia coliK-12 with altered adhesion properties | Q115688840 | ||
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | microbiology | Q7193 |
| P304 | page(s) | 3416-3428 | |
| P577 | publication date | 2003-06-01 | |
| P1433 | published in | Journal of Bacteriology | Q478419 |
| P1476 | title | Type IV-like pili formed by the type II secreton: specificity, composition, bundling, polar localization, and surface presentation of peptides | |
| Type IV-Like Pili Formed by the Type II Secreton: Specificity, Composition, Bundling, Polar Localization, and Surface Presentation of Peptides | |||
| P478 | volume | 185 |
| Q41355770 | A Putative Type II Secretion System Is Involved in Cellulose Utilization in Cytophaga hutchisonii |
| Q37310146 | A macromolecular complex formed by a pilin-like protein in competent Bacillus subtilis |
| Q35554916 | A new suite of tnaA mutants suggests that Escherichia coli tryptophanase is regulated by intracellular sequestration and by occlusion of its active site |
| Q33204951 | A type II protein secretory pathway required for levansucrase secretion by Gluconacetobacter diazotrophicus |
| Q34354030 | Active-site residues in the type IV prepilin peptidase homologue PibD from the archaeon Sulfolobus solfataricus. |
| Q28264353 | Archaeal flagella, bacterial flagella and type IV pili: a comparison of genes and posttranslational modifications |
| Q40428846 | Cloning-independent markerless gene editing in Streptococcus sanguinis: novel insights in type IV pilus biology |
| Q47150793 | Complex formation and processing of the minor transformation pilins of Bacillus subtilis |
| Q36539601 | Contribution of type IV pili to the virulence of Aeromonas salmonicida subsp. salmonicida in Atlantic salmon (Salmo salar L.). |
| Q40148455 | Cyclic Di-GMP and VpsR Induce the Expression of Type II Secretion in Vibrio cholerae |
| Q22121988 | DNA uptake during bacterial transformation |
| Q39241148 | Deciphering the Xcp Pseudomonas aeruginosa type II secretion machinery through multiple interactions with substrates. |
| Q30495999 | Detailed structural and assembly model of the type II secretion pilus from sparse data |
| Q51320128 | Discovery of the type VII ESX-1 secretion needle? |
| Q30405338 | Distinct docking and stabilization steps of the Pseudopilus conformational transition path suggest rotational assembly of type IV pilus-like fibers |
| Q37434036 | Diversity of archaeal type IV pilin-like structures |
| Q95695195 | Editorial |
| Q39177060 | EspC forms a filamentous structure in the cell envelope of Mycobacterium tuberculosis and impacts ESX-1 secretion |
| Q26999020 | Exceptionally widespread nanomachines composed of type IV pilins: the prokaryotic Swiss Army knives |
| Q30503117 | Expression of a Clostridium perfringens type IV pilin by Neisseria gonorrhoeae mediates adherence to muscle cells |
| Q37582908 | Expression of type IV pili by Moraxella catarrhalis is essential for natural competence and is affected by iron limitation |
| Q37342508 | Genetic Identification of a PilT Motor in Geobacter sulfurreducens Reveals a Role for Pilus Retraction in Extracellular Electron Transfer |
| Q43127743 | Genetic mapping of secretion and functional determinants of the Vibrio cholerae TcpF colonization factor |
| Q41842429 | Green fluorescent chimeras indicate nonpolar localization of pullulanase secreton components PulL and PulM. |
| Q53830048 | Heterologous assembly of type IV pili by a type II secretion system reveals the role of minor pilins in assembly initiation. |
| Q30425258 | Impact of Francisella tularensis pilin homologs on pilus formation and virulence |
| Q34605983 | In vivo cross-linking of EpsG to EpsL suggests a role for EpsL as an ATPase-pseudopilin coupling protein in the Type II secretion system of Vibrio cholerae |
| Q49102598 | Insights into type IV pilus biogenesis and dynamics from genetic analysis of a C-terminally tagged pilin: a role for O-linked glycosylation. |
| Q53182182 | Isolation and identification of new inner membrane-associated proteins that localize to cell poles in Escherichia coli. |
| Q27939366 | Minor pseudopilin self-assembly primes type II secretion pseudopilus elongation. |
| Q37124947 | Novel archaeal adhesion pilins with a conserved N terminus |
| Q35814702 | On the path to uncover the bacterial type II secretion system |
| Q39427949 | Pilin Processing Follows a Different Temporal Route than That of Archaellins in Methanococcus maripaludis |
| Q54327377 | Prime time for minor subunits of the type II secretion and type IV pilus systems. |
| Q37332326 | Protein secretion and membrane insertion systems in bacteria and eukaryotic organelles |
| Q36839222 | Protein secretion and membrane insertion systems in gram-negative bacteria |
| Q36498040 | Protein secretion in the Archaea: multiple paths towards a unique cell surface |
| Q36098354 | Pseudomonas aeruginosa Type IV pilus expression in Neisseria gonorrhoeae: effects of pilin subunit composition on function and organelle dynamics. |
| Q34801714 | Pseudomonas aeruginosa minor pilins prime type IVa pilus assembly and promote surface display of the PilY1 adhesin |
| Q40645960 | Pseudopilin residue E5 is essential for recruitment by the type 2 secretion system assembly platform |
| Q35788087 | Recent advances in the structure and assembly of the archaeal flagellum |
| Q33415985 | Roles of putative type II secretion and type IV pilus systems in the virulence of uropathogenic Escherichia coli |
| Q37599953 | Secretion of a pneumococcal type II secretion system pilus correlates with DNA uptake during transformation. |
| Q27324610 | Steered molecular dynamics simulations of a type IV pilus probe initial stages of a force-induced conformational transition |
| Q41626918 | Structural insights into the secretin PulD and its trypsin-resistant core |
| Q64448236 | Structure of Microbial Nanowires Reveals Stacked Hemes that Transport Electrons over Micrometers |
| Q27650459 | Structure of the GspK-GspI-GspJ complex from the enterotoxigenic Escherichia coli type 2 secretion system |
| Q27649752 | Structure of the Minor Pseudopilin EpsH from the Type 2 Secretion System of Vibrio cholerae |
| Q45069622 | Structure of the calcium-dependent type 2 secretion pseudopilus |
| Q34180072 | Structure of the cholera toxin secretion channel in its closed state |
| Q37365275 | Surface colonization by marine roseobacters: integrating genotype and phenotype |
| Q27649091 | The Crystal Structure of a Binary Complex of two Pseudopilins: EpsI and EpsJ from the Type 2 Secretion System of Vibrio vulnificus |
| Q35075685 | The TadV protein of Actinobacillus actinomycetemcomitans is a novel aspartic acid prepilin peptidase required for maturation of the Flp1 pilin and TadE and TadF pseudopilins |
| Q36228737 | The Vibrio cholerae Minor Pilin TcpB Initiates Assembly and Retraction of the Toxin-Coregulated Pilus |
| Q41890924 | The XcpV/GspI pseudopilin has a central role in the assembly of a quaternary complex within the T2SS pseudopilus. |
| Q28492892 | The assembly mode of the pseudopilus: a hallmark to distinguish a novel secretion system subtype |
| Q21266650 | The complete genome of Burkholderia phenoliruptrix strain BR3459a, a symbiont of Mimosa flocculosa: highlighting the coexistence of symbiotic and pathogenic genes |
| Q24669928 | The selective value of bacterial shape |
| Q36792557 | The tad locus: postcards from the widespread colonization island |
| Q39293921 | The trans-envelope architecture and function of the type 2 secretion system: new insights raising new questions. |
| Q81227715 | The type II secretion arrowhead: the structure of GspI-GspJ-GspK |
| Q36018127 | The type II secretion system and its ubiquitous lipoprotein substrate, SslE, are required for biofilm formation and virulence of enteropathogenic Escherichia coli |
| Q36995073 | The type II secretion system: biogenesis, molecular architecture and mechanism. |
| Q41995987 | Towards the identification of type II secretion signals in a nonacylated variant of pullulanase from Klebsiella oxytoca |
| Q41842956 | Type II secretion system secretin PulD localizes in clusters in the Escherichia coli outer membrane |
| Q24678451 | Type III pilus of corynebacteria: Pilus length is determined by the level of its major pilin subunit |
| Q36747234 | Type IV pili in Francisella tularensis: roles of pilF and pilT in fiber assembly, host cell adherence, and virulence |
| Q37264187 | Type IV pili in Gram-positive bacteria. |
| Q27024174 | Type IV pilin proteins: versatile molecular modules |
| Q36597261 | Type IV pilin structures: insights on shared architecture, fiber assembly, receptor binding and type II secretion |
| Q35752406 | Type IV pilus structure and bacterial pathogenicity |
| Q39839466 | Uptake of extracellular DNA: competence induced pili in natural transformation of Streptococcus pneumoniae |
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