scholarly article | Q13442814 |
P2093 | author name string | Suzuki T | |
Sasakawa C | |||
Lett MC | |||
P2860 | cites work | A comprehensive set of sequence analysis programs for the VAX | Q26778432 |
A simple method for displaying the hydropathic character of a protein | Q26778481 | ||
Crystal structures explain functional properties of two E. coli porins | Q27642119 | ||
Characterization of the Neisseria Iga beta-core. The essential unit for outer membrane targeting and extracellular protein secretion | Q30194663 | ||
Molecular Architecture and Electrostatic Properties of a Bacterial Porin | Q30195553 | ||
Models for the structure of outer-membrane proteins of Escherichia coli derived from raman spectroscopy and prediction methods | Q30196253 | ||
Identification of icsA, a plasmid locus of Shigella flexneri that governs bacterial intra- and intercellular spread through interaction with F-actin | Q33859430 | ||
Gene structure and extracellular secretion of Neisseria gonorrhoeae IgA protease | Q34048661 | ||
A Haemophilus influenzae IgA protease-like protein promotes intimate interaction with human epithelial cells | Q34316789 | ||
Selection of functional signal peptide cleavage sites from a library of random sequences | Q36104950 | ||
virG, a plasmid-coded virulence gene of Shigella flexneri: identification of the virG protein and determination of the complete coding sequence | Q36173163 | ||
Mutational alterations affecting the export competence of a truncated but fully functional maltose-binding protein signal peptide | Q36236000 | ||
Export of unprocessed precursor maltose-binding protein to the periplasm of Escherichia coli cells | Q36236066 | ||
Escherichia coli mutants accumulating the precursor of a secreted protein in the cytoplasm | Q38357752 | ||
Cleavage of Shigella surface protein VirG occurs at a specific site, but the secretion is not essential for intracellular spreading | Q39836159 | ||
Unipolar localization and ATPase activity of IcsA, a Shigella flexneri protein involved in intracellular movement | Q39927930 | ||
A comparative genetic study of serologically distinct Haemophilus influenzae type 1 immunoglobulin A1 proteases | Q39933960 | ||
vacB, a novel chromosomal gene required for expression of virulence genes on the large plasmid of Shigella flexneri | Q39940375 | ||
Specific excretion of Serratia marcescens protease through the outer membrane of Escherichia coli | Q39967530 | ||
The secretion pathway of IgA protease-type proteins in gram-negative bacteria | Q40732273 | ||
Extracellular association and cytoplasmic partitioning of the IpaB and IpaC invasins of S. flexneri | Q41497452 | ||
AIDA-I, the adhesin involved in diffuse adherence of the diarrhoeagenic Escherichia coli strain 2787 (O126:H27), is synthesized via a precursor molecule | Q42612193 | ||
The 120 kilodalton outer membrane protein (rOmp B) of Rickettsia rickettsii is encoded by an unusually long open reading frame: evidence for protein processing from a large precursor | Q42617349 | ||
Cloning, expression and sequence analysis of the gene encoding the 120 kD surface-exposed protein of Rickettsia rickettsii | Q42640705 | ||
A genetic determinant required for continuous reinfection of adjacent cells on large plasmid in S. flexneri 2a. | Q44058237 | ||
Genetic analysis of the Helicobacter pylori vacuolating cytotoxin: structural similarities with the IgA protease type of exported protein | Q48083694 | ||
Identification of a protein required for disulfide bond formation in vivo | Q48201805 | ||
Nucleotide sequence of the alkaline phosphatase gene of Escherichia coli | Q48370356 | ||
Intragenic suppressor mutations that restore export of maltose binding protein with a truncated signal peptide | Q48390907 | ||
P433 | issue | 52 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 30874-30880 | |
P577 | publication date | 1995-12-01 | |
P1433 | published in | Journal of Biological Chemistry | Q867727 |
P1476 | title | Extracellular transport of VirG protein in Shigella | |
P478 | volume | 270 |
Q44655589 | A Neisserial autotransporter NalP modulating the processing of other autotransporters |
Q45986214 | A novel family of channel-forming, autotransporting, bacterial virulence factors. |
Q48027259 | Actin polymerization and bacterial movement |
Q34315723 | Antigen 43-mediated autotransporter display, a versatile bacterial cell surface presentation system |
Q39499980 | Autodisplay: functional display of active beta-lactamase on the surface of Escherichia coli by the AIDA-I autotransporter. |
Q30176650 | Autodisplay: one-component system for efficient surface display and release of soluble recombinant proteins from Escherichia coli |
Q30155423 | Autotransporter protein secretion. |
Q34819995 | Autotransporter-based cell surface display in Gram-negative bacteria |
Q48037242 | Characterization of the C-terminal propeptide involved in bacterial wall spanning of alpha-amylase from the psychrophile Alteromonas haloplanctis |
Q34000323 | Characterization of the avian pathogenic Escherichia coli hemagglutinin Tsh, a member of the immunoglobulin A protease-type family of autotransporters. |
Q30175313 | Characterization of the essential transport function of the AIDA-I autotransporter and evidence supporting structural predictions |
Q30156048 | Comparative Analysis of the Biochemical and Functional Properties of C-Terminal Domains of Autotransporters |
Q33187539 | Display and release of the Plasmodium falciparum circumsporozoite protein using the autotransporter MisL of Salmonella enterica. |
Q36846784 | Display of heterologous proteins on the surface of microorganisms: from the screening of combinatorial libraries to live recombinant vaccines |
Q31065079 | Display of proteins on bacteria |
Q39509333 | Establishment of unipolar localization of IcsA in Shigella flexneri 2a is not dependent on virulence plasmid determinants |
Q30165457 | Export of autotransported proteins proceeds through an oligomeric ring shaped by C-terminal domains |
Q33183819 | Expression of the Plasmodium falciparum immunodominant epitope (NANP)(4) on the surface of Salmonella enterica using the autotransporter MisL |
Q35892385 | Fibronectin binding to the Salmonella enterica serotype Typhimurium ShdA autotransporter protein is inhibited by a monoclonal antibody recognizing the A3 repeat |
Q71246595 | Functional analysis of Shigella VirG domains essential for interaction with vinculin and actin-based motility |
Q33991131 | Functional analysis of a rickettsial OmpA homology domain of Shigella flexneri icsA. |
Q39230762 | How Do the Virulence Factors of Shigella Work Together to Cause Disease? |
Q30164063 | Hydrophobic residues of the autotransporter EspP linker domain are important for outer membrane translocation of its passenger |
Q35819223 | IcsA autotransporter passenger promotes increased fusion protein expression on the cell surface. |
Q34584116 | Identification of Shigella flexneri IcsA residues affecting interaction with N-WASP, and evidence for IcsA-IcsA co-operative interaction. |
Q39714265 | Identification of secretion determinants of the Bordetella pertussis BrkA autotransporter |
Q33764731 | Identification of two Shigella flexneri chromosomal loci involved in intercellular spreading. |
Q40460000 | Immunogenicity and characterization of WRSF2G11: a second generation live attenuated Shigella flexneri 2a vaccine strain. |
Q73341660 | Lipopolysaccharide O antigen chains mask IcsA (VirG) in Shigella flexneri |
Q31121268 | Microbial cell-surface display |
Q34090958 | Molecular basis of the intracellular spreading of Shigella |
Q57857240 | Motilité intracellulaire et polymérisation de l'actine par Listeria monocytogenes et Shigella flexneri |
Q73341665 | Multicopy icsA is able to suppress the virulence defect caused by the wzz(SF) mutation in Shigella flexneri |
Q35450976 | Multiple driving forces required for efficient secretion of autotransporter virulence proteins |
Q33954566 | Multiple pathways allow protein secretion across the bacterial outer membrane |
Q36747291 | Mutagenesis of the Shigella flexneri autotransporter IcsA reveals novel functional regions involved in IcsA biogenesis and recruitment of host neural Wiscott-Aldrich syndrome protein |
Q24533240 | Neural Wiskott-Aldrich syndrome protein is implicated in the actin-based motility of Shigella flexneri |
Q28218130 | Neutrophil elastase targets virulence factors of enterobacteria |
Q27011231 | Of linkers and autochaperones: an unambiguous nomenclature to identify common and uncommon themes for autotransporter secretion |
Q30168451 | Periplasmic transit and disulfide bond formation of the autotransported Shigella protein IcsA |
Q33934139 | Polar targeting of Shigella virulence factor IcsA in Enterobacteriacae and Vibrio |
Q34245708 | Polarity in action: asymmetric protein localization in bacteria |
Q42146117 | Probing the applicability of autotransporter based surface display with the EstA autotransporter of Pseudomonas stutzeri A15. |
Q30176806 | Processing of the AIDA-I precursor: removal of AIDAc and evidence for the outer membrane anchoring as a beta-barrel structure |
Q34623327 | Protein-translocating outer membrane porins of Gram-negative bacteria |
Q40469163 | Regulation of IcsP, the outer membrane protease of the Shigella actin tail assembly protein IcsA, by virulence plasmid regulators VirF and VirB. |
Q33597847 | Relationship between the Tsh autotransporter and pathogenicity of avian Escherichia coli and localization and analysis of the Tsh genetic region |
Q30155539 | Residues in a conserved α-helical segment are required for cleavage but not secretion of an Escherichia coli serine protease autotransporter passenger domain |
Q41873543 | Rho family GTPase Cdc42 is essential for the actin-based motility of Shigella in mammalian cells. |
Q30159668 | Role of the alpha-helical linker of the C-terminal translocator in the biogenesis of the serine protease subfamily of autotransporters |
Q40240250 | Scavenger receptor-A mediates gp96/GRP94 and calreticulin internalization by antigen-presenting cells |
Q40195229 | Shigella IpgB1 promotes bacterial entry through the ELMO-Dock180 machinery. |
Q36586060 | Shigella as a foodborne pathogen and current methods for detection in food |
Q44461615 | Structural definition on the surface of Helicobacter pylori type IV secretion apparatus |
Q33247360 | Surface display of proteins by gram-negative bacterial autotransporters |
Q42245186 | Surface display of the HPV L1 capsid protein by the autotransporter Shigella IcsA. |
Q42998832 | Surface-displayed viral antigens on Salmonella carrier vaccine. |
Q39497592 | The C-terminal domain of the Bordetella pertussis autotransporter BrkA forms a pore in lipid bilayer membranes. |
Q30164309 | The Haemophilus influenzae Hia autotransporter contains an unusually short trimeric translocator domain. |
Q39157867 | The Shigella Virulence Factor IcsA Relieves N-WASP Autoinhibition by Displacing the Verprolin Homology/Cofilin/Acidic (VCA) Domain |
Q73669123 | The actin-based motility defect of a Shigella flexneri rmlD rough LPS mutant is not due to loss of IcsA polarity |
Q33308956 | The autodisplay story, from discovery to biotechnical and biomedical applications |
Q30176020 | The great escape: structure and function of the autotransporter proteins |
Q41475084 | The making of a gradient: IcsA (VirG) polarity in Shigella flexneri |
Q41671872 | The periplasmic folding of a cysteineless autotransporter passenger domain interferes with its outer membrane translocation |
Q77410714 | The unipolar Shigella surface protein IcsA is targeted directly to the bacterial old pole: IcsP cleavage of IcsA occurs over the entire bacterial surface |
Q33559645 | Type V protein secretion pathway: the autotransporter story |
Q37701998 | Use of Pseudomonas putida EstA as an anchoring motif for display of a periplasmic enzyme on the surface of Escherichia coli |
Q36254772 | Vinculin proteolysis unmasks an ActA homolog for actin-based Shigella motility |
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