| review article | Q7318358 |
| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1017168674 |
| P356 | DOI | 10.1038/NMICROBIOL.2016.107 |
| P698 | PubMed publication ID | 27573113 |
| P50 | author | Anastassios Economou | Q42580518 |
| Spyridoula Karamanou | Q47434224 | ||
| Jozefien De Geyter | Q88226630 | ||
| P2093 | author name string | Alexandra Tsirigotaki | |
| Georgia Orfanoudaki | |||
| Valentina Zorzini | |||
| P2860 | cites work | SCOP2 prototype: a new approach to protein structure mining | Q22061728 |
| Structural and energetic basis of folded-protein transport by the FimD usher | Q24616003 | ||
| Type V secretion: mechanism(s) of autotransport through the bacterial outer membrane | Q24621416 | ||
| The Escherichia coli peripheral inner membrane proteome | Q36666333 | ||
| Macromolecular crowding and confinement: biochemical, biophysical, and potential physiological consequences | Q24644640 | ||
| What is the total number of protein molecules per cell volume? A call to rethink some published values | Q26782007 | ||
| Disulfide bond formation in the bacterial periplasm: major achievements and challenges ahead | Q26823827 | ||
| Assembly of β-barrel proteins into bacterial outer membranes | Q26998912 | ||
| The Sec-dependent pathway | Q27010633 | ||
| Core structure of the outer membrane lipoprotein from Escherichia coli at 1.9 A resolution | Q27622792 | ||
| Solution structure of Apo Cu,Zn superoxide dismutase: role of metal ions in protein folding | Q27641822 | ||
| Structural and functional studies of FkpA from Escherichia coli, a cis/trans peptidyl-prolyl isomerase with chaperone activity | Q27642778 | ||
| Fiber formation across the bacterial outer membrane by the chaperone/usher pathway | Q27650634 | ||
| Structural basis for the regulated protease and chaperone function of DegP | Q27650659 | ||
| Crystal Structure of Colicin M, a Novel Phosphatase Specifically Imported by Escherichia coli> | Q27651267 | ||
| Protein-folding location can regulate manganese-binding versus copper- or zinc-binding | Q27652637 | ||
| The prolyl isomerase domain of PpiD fromEscherichia colishows a parvulin fold but is devoid of catalytic activity | Q27658010 | ||
| Genetic selection designed to stabilize proteins uncovers a chaperone called Spy | Q27666964 | ||
| Molecular Adaptation of the DegQ Protease to Exert Protein Quality Control in the Bacterial Cell Envelope | Q27670477 | ||
| Assembly of the Type II Secretion System such as Found in Vibrio cholerae Depends on the Novel Pilotin AspS | Q27675923 | ||
| Newly folded substrates inside the molecular cage of the HtrA chaperone DegQ | Q27676751 | ||
| Intrinsically Disordered Protein Threads Through the Bacterial Outer-Membrane Porin OmpF | Q27678845 | ||
| A protein export pathway involving Escherichia coli porins | Q27679435 | ||
| Quality control of disulfide bond formation in pilus subunits by the chaperone FimC | Q27681723 | ||
| The structural basis of autotransporter translocation by TamA | Q27686750 | ||
| Structural basis of outer membrane protein insertion by the BAM complex | Q27704064 | ||
| The structure of glutamine-binding protein complexed with glutamine at 1.94 A resolution: comparisons with other amino acid binding proteins | Q27756774 | ||
| Bacterial amyloid formation: structural insights into curli biogensis | Q28082740 | ||
| Production of Biopharmaceuticals in E. coli: Current Scenario and Future Perspectives | Q28083443 | ||
| From Levinthal to pathways to funnels | Q28300934 | ||
| The SurA periplasmic PPIase lacking its parvulin domains functions in vivo and has chaperone activity | Q28354278 | ||
| Feeling the hidden mechanical forces in lipid bilayer is an original sense | Q28658571 | ||
| Molecular chaperones in protein folding and proteostasis | Q29547715 | ||
| Outer membrane protein biogenesis in Gram-negative bacteria | Q30152824 | ||
| Impact of holdase chaperones Skp and SurA on the folding of β-barrel outer-membrane proteins | Q30152825 | ||
| A novel pathway for outer membrane protein biogenesis in Gram-negative bacteria | Q30152910 | ||
| Assembly of the secretion pores GspD, Wza and CsgG into bacterial outer membranes does not require the Omp85 proteins BamA or TamA. | Q30152931 | ||
| Looks can be deceiving: recent insights into the mechanism of protein secretion by the autotransporter pathway. | Q30152947 | ||
| The β-barrel membrane protein insertase machinery from Gram-negative bacteria | Q30152967 | ||
| Detecting envelope stress by monitoring β-barrel assembly. | Q30153263 | ||
| Structure of the nonameric bacterial amyloid secretion channel | Q30153286 | ||
| Structural and mechanistic insights into the bacterial amyloid secretion channel CsgG | Q30153336 | ||
| Lateral opening and exit pore formation are required for BamA function | Q30153373 | ||
| Outer membrane β-barrel protein folding is physically controlled by periplasmic lipid head groups and BamA. | Q30153415 | ||
| DegP primarily functions as a protease for the biogenesis of β-barrel outer membrane proteins in the Gram-negative bacterium Escherichia coli. | Q30153460 | ||
| Stepwise folding of an autotransporter passenger domain is not essential for its secretion | Q30153486 | ||
| Protease homolog BepA (YfgC) promotes assembly and degradation of β-barrel membrane proteins in Escherichia coli | Q30153518 | ||
| Autotransporter secretion: varying on a theme. | Q30155115 | ||
| The essential β-barrel assembly machinery complex components BamD and BamA are required for autotransporter biogenesis | Q30155532 | ||
| Lipoprotein sorting in bacteria. | Q30155534 | ||
| Reconstitution of outer membrane protein assembly from purified components | Q30156906 | ||
| Interaction of an autotransporter passenger domain with BamA during its translocation across the bacterial outer membrane. | Q30157080 | ||
| Roles of periplasmic chaperone proteins in the biogenesis of serine protease autotransporters of Enterobacteriaceae | Q30157137 | ||
| Predicting weakly stable regions, oligomerization state, and protein-protein interfaces in transmembrane domains of outer membrane proteins | Q30157187 | ||
| Folding and trimerization of signal sequence-less mature TolC in the cytoplasm of Escherichia coli | Q30157290 | ||
| Model of mouth-to-mouth transfer of bacterial lipoproteins through inner membrane LolC, periplasmic LolA, and outer membrane LolB. | Q30157322 | ||
| Beta-barrel proteins that reside in the Escherichia coli outer membrane in vivo demonstrate varied folding behavior in vitro | Q30157632 | ||
| Crystal structure of Skp, a prefoldin-like chaperone that protects soluble and membrane proteins from aggregation | Q30163883 | ||
| Assembly of TolC, a Structurally Unique and Multifunctional Outer Membrane Protein of Escherichia coli K-12 | Q30164429 | ||
| Membrane protein folding on the example of outer membrane protein A of Escherichia coli. | Q30164479 | ||
| The Periplasmic Molecular Chaperone Protein SurA Binds a Peptide Motif That Is Characteristic of Integral Outer Membrane Proteins | Q30164487 | ||
| Folding and membrane insertion of the trimeric beta-barrel protein OmpF. | Q30177043 | ||
| The role of calcium in the conformational dynamics and thermal stability of the D-galactose/D-glucose-binding protein from Escherichia coli. | Q30351181 | ||
| The periplasmic Escherichia coli peptidylprolyl cis,trans-isomerase FkpA. I. Increased functional expression of antibody fragments with and without cis-prolines. | Q30854397 | ||
| Selection for a periplasmic factor improving phage display and functional periplasmic expression | Q32066800 | ||
| Identification of potential substrate proteins for the periplasmic Escherichia coli chaperone Skp. | Q33383997 | ||
| Characterization of the Cpx regulon in Escherichia coli strain MC4100. | Q33395214 | ||
| Global analysis of extracytoplasmic stress signaling in Escherichia coli | Q33504535 | ||
| Protein refolding by pH-triggered chaperone binding and release | Q33577469 | ||
| Signal peptides are allosteric activators of the protein translocase | Q33662560 | ||
| Decorating microbes: surface display of proteins on Escherichia coli | Q33767417 | ||
| The bacterial cell envelope | Q33800394 | ||
| Zinc-dependent protein folding | Q33878311 | ||
| A primary role for disulfide formation in the productive folding of prokaryotic Cu,Zn-superoxide dismutase | Q33931193 | ||
| Secretory and extracellular production of recombinant proteins using Escherichia coli | Q33976034 | ||
| Dynamic interaction of the sec translocon with the chaperone PpiD | Q33985391 | ||
| Novel proteomic tools reveal essential roles of SRP and importance of proper membrane protein biogenesis | Q34059311 | ||
| Periplasmic peptidyl prolyl cis-trans isomerases are not essential for viability, but SurA is required for pilus biogenesis in Escherichia coli | Q34124391 | ||
| Role of cofactors in protein folding | Q34602512 | ||
| Proteome-wide subcellular topologies of E. coli polypeptides database (STEPdb). | Q34635044 | ||
| Expression of the endogenous type II secretion pathway in Escherichia coli leads to chitinase secretion. | Q34685284 | ||
| Covalent attachment of proteins to peptidoglycan. | Q34749060 | ||
| Detecting folding intermediates of a protein as it passes through the bacterial translocation channel | Q35004080 | ||
| How Co-translational Folding of Multi-domain Protein Is Affected by Elongation Schedule: Molecular Simulations | Q35686986 | ||
| Sequence analysis of bacterial redox enzyme maturation proteins (REMPs). | Q35815031 | ||
| Protein misfolding occurs by slow diffusion across multiple barriers in a rough energy landscape | Q35845795 | ||
| The E. coli CsgB nucleator of curli assembles to β-sheet oligomers that alter the CsgA fibrillization mechanism | Q35922016 | ||
| pH of the cytoplasm and periplasm of Escherichia coli: rapid measurement by green fluorescent protein fluorimetry | Q35949254 | ||
| Control of DegP-dependent degradation of c-type cytochromes by heme and the cytochrome c maturation system in Escherichia coli | Q35949562 | ||
| Type I secretion in gram-negative bacteria. | Q35951967 | ||
| Beyond transcription--new mechanisms for the regulation of molecular chaperones | Q36069364 | ||
| Cloning, purification, crystallization and preliminary X-ray diffraction studies of Escherichia coli PapD-like protein (EcpD). | Q36143563 | ||
| Proteomic study and marker protein identification of Caenorhabditis elegans lipid droplets | Q36144142 | ||
| Lipids assist the membrane insertion of a BAM-independent outer membrane protein | Q36158729 | ||
| Reconstitution of a nanomachine driving the assembly of proteins into bacterial outer membranes | Q36248731 | ||
| Solving the membrane protein folding problem | Q36327794 | ||
| Curli biogenesis and function | Q36480477 | ||
| Membrane protein thermodynamic stability may serve as the energy sink for sorting in the periplasm | Q36692899 | ||
| Substrate protein folds while it is bound to the ATP-independent chaperone Spy | Q36843657 | ||
| Autotransporters: The Cellular Environment Reshapes a Folding Mechanism to Promote Protein Transport | Q36846535 | ||
| Deuterium Labeling Together with Contrast Variation Small-Angle Neutron Scattering Suggests How Skp Captures and Releases Unfolded Outer Membrane Proteins | Q37019529 | ||
| Use of folding modulators to improve heterologous protein production in Escherichia coli. | Q37097393 | ||
| Role for Skp in LptD assembly in Escherichia coli | Q37124929 | ||
| Structural plasticity of an acid-activated chaperone allows promiscuous substrate binding | Q37138591 | ||
| The perspectives of studying multi-domain protein folding. | Q37381955 | ||
| Outer-membrane vesicles from Gram-negative bacteria: biogenesis and functions | Q37641231 | ||
| Managing membrane stress: the phage shock protein (Psp) response, from molecular mechanisms to physiology. | Q37773394 | ||
| Type IV secretion systems: versatility and diversity in function | Q37774038 | ||
| Swimming against the tide: progress and challenges in our understanding of colicin translocation | Q37808099 | ||
| Bacterial outer membrane vesicles in disease and preventive medicine | Q37820396 | ||
| Protein quality control in the bacterial periplasm | Q37884601 | ||
| Intrinsically disordered proteins undergo and assist folding transitions in the proteome. | Q38059042 | ||
| Breaking on through to the other side: protein export through the bacterial Sec system. | Q38065265 | ||
| Unusual biophysics of intrinsically disordered proteins | Q38069936 | ||
| Biocatalysis with immobilized Escherichia coli | Q38072332 | ||
| Protein translocation across the inner membrane of Gram-negative bacteria: the Sec and Tat dependent protein transport pathways. | Q38097261 | ||
| The molecular dissection of the chaperone-usher pathway | Q38154006 | ||
| Everything old is new again: an update on current research on the Cpx envelope stress response | Q38159109 | ||
| Folding mechanisms of periplasmic proteins | Q38163277 | ||
| Mechanism and structure of the bacterial type IV secretion systems | Q38175753 | ||
| Type II secretion system: a magic beanstalk or a protein escalator | Q38175754 | ||
| The membrane insertase YidC. | Q38177989 | ||
| Co-translational protein targeting to the bacterial membrane | Q38186912 | ||
| Antibiotic targeting of the bacterial secretory pathway. | Q38188773 | ||
| Protein transport by the bacterial Tat pathway | Q38192369 | ||
| SecA-mediated targeting and translocation of secretory proteins. | Q38192370 | ||
| Mechanistic studies of the biogenesis and folding of outer membrane proteins in vitro and in vivo: what have we learned to date? | Q38194733 | ||
| Bacterial whole-cell biocatalysts by surface display of enzymes: toward industrial application. | Q38237971 | ||
| Molecular simulations of metal-coupled protein folding | Q38293694 | ||
| SecD is involved in the release of translocated secretory proteins from the cytoplasmic membrane of Escherichia coli | Q38322783 | ||
| Macromolecular crowding: Macromolecules friend or foe. | Q38470900 | ||
| Secretion systems in Gram-negative bacteria: structural and mechanistic insights. | Q38482854 | ||
| Type III secretion systems: the bacterial flagellum and the injectisome | Q38586932 | ||
| Type III Secretion: Building and Operating a Remarkable Nanomachine. | Q38621246 | ||
| Aim, Load, Fire: The Type VI Secretion System, a Bacterial Nanoweapon. | Q38628417 | ||
| Type VI secretion and anti-host effectors | Q38684791 | ||
| Discovery of an archetypal protein transport system in bacterial outer membranes. | Q39370957 | ||
| Secretion of curli fibre subunits is mediated by the outer membrane-localized CsgG protein | Q39620322 | ||
| Escherichia coli K-12 possesses multiple cryptic but functional chaperone-usher fimbriae with distinct surface specificities. | Q39722282 | ||
| Rapid label-free quantitative analysis of the E. coli BL21(DE3) inner membrane proteome | Q40432637 | ||
| Effect of crowding by Ficolls on OmpA and OmpT refolding and membrane insertion | Q41583523 | ||
| The periplasmic folding of a cysteineless autotransporter passenger domain interferes with its outer membrane translocation | Q41671872 | ||
| Cofactor effects on the protein folding reaction: acceleration of alpha-lactalbumin refolding by metal ions | Q41837248 | ||
| Identification of putative substrates for the periplasmic chaperone YfgM in Escherichia coli using quantitative proteomics | Q41883371 | ||
| Bacterial surface proteins and vaccines | Q42100644 | ||
| The Salmonella FlgA protein, a putativeve periplasmic chaperone essential for flagellar P ring formation | Q42488636 | ||
| Use of thioredoxin as a reporter to identify a subset of Escherichia coli signal sequences that promote signal recognition particle-dependent translocation | Q42723141 | ||
| A non-classical assembly pathway of Escherichia coli pore-forming toxin cytolysin A. | Q42905558 | ||
| Periplasmic chaperone FkpA is essential for imported colicin M toxicity | Q43211287 | ||
| The periplasmic chaperone Skp facilitates targeting, insertion, and folding of OmpA into lipid membranes with a negative membrane surface potential | Q43271459 | ||
| Solubilization of protein aggregates by the acid stress chaperones HdeA and HdeB. | Q46687850 | ||
| Equilibrium folding of pro-HlyA from Escherichia coli reveals a stable calcium ion dependent folding intermediate | Q46889399 | ||
| A temperature-dependent switch from chaperone to protease in a widely conserved heat shock protein. | Q47348771 | ||
| Type VII secretion--mycobacteria show the way. | Q48689947 | ||
| Vesicle-mediated export and assembly of pore-forming oligomers of the enterobacterial ClyA cytotoxin | Q50102555 | ||
| Immunization with Escherichia coli outer membrane vesicles protects bacteria-induced lethality via Th1 and Th17 cell responses. | Q53115452 | ||
| Global proteomic profiling of native outer membrane vesicles derived from Escherichia coli. | Q53530186 | ||
| Folding and assembly of bacterial alkaline phosphatase in vitro and in vivo. | Q54242630 | ||
| Conformation and dynamics of the periplasmic membrane-protein-chaperone complexes OmpX-Skp and tOmpA-Skp. | Q54303131 | ||
| Pathways of colicin import: utilization of BtuB, OmpF porin and the TolC drug-export protein. | Q54322880 | ||
| A genetically incorporated crosslinker reveals chaperone cooperation in acid resistance. | Q54353719 | ||
| The periplasmic chaperone PpiD interacts with secretory proteins exiting from the SecYEG translocon. | Q54423305 | ||
| Characterization of the chaperone-like activity of HtrA (DegP) protein from Escherichia coli under the conditions of heat shock. | Q54441860 | ||
| A system for concomitant overexpression of four periplasmic folding catalysts to improve secretory protein production in Escherichia coli. | Q54464752 | ||
| A third envelope stress signal transduction pathway in Escherichia coli. | Q54537447 | ||
| A periplasmic protein (Skp) of Escherichia coli selectively binds a class of outer membrane proteins. | Q54592701 | ||
| The periplasmic Escherichia coli peptidylprolyl cis,trans-isomerase FkpA. II. Isomerase-independent chaperone activity in vitro | Q56896185 | ||
| Periplasmic space and the concept of the periplasm | Q68055318 | ||
| Biopharmaceutical benchmarks 2014 | Q70909584 | ||
| Characterization of the Escherichia coli sigma E regulon | Q73684799 | ||
| Electrostatic contribution to the thermodynamic and kinetic stability of the homotrimeric coiled coil Lpp-56: A computational study | Q80867942 | ||
| Sorting of an integral outer membrane protein via the lipoprotein-specific Lol pathway and a dedicated lipoprotein pilotin | Q83454751 | ||
| P433 | issue | 8 | |
| P921 | main subject | protein folding | Q847556 |
| Escherichia coli | Q25419 | ||
| P304 | page(s) | 16107 | |
| P577 | publication date | 2016-07-26 | |
| P1433 | published in | Nature Microbiology | Q23022567 |
| P1476 | title | Protein folding in the cell envelope of Escherichia coli | |
| P478 | volume | 1 |
| Q57788607 | Breaching the wall |
| Q38989842 | Comprehensive assessment and performance improvement of effector protein predictors for bacterial secretion systems III, IV and VI. |
| Q45944000 | Effective prediction of bacterial type IV secreted effectors by combined features of both C-termini and N-termini. |
| Q92510993 | Enhancing Recombinant Protein Yields in the E. coli Periplasm by Combining Signal Peptide and Production Rate Screening |
| Q89737499 | Escherichia coli Can Adapt Its Protein Translocation Machinery for Enhanced Periplasmic Recombinant Protein Production |
| Q54242376 | Heterologous Complementation Studies With the YscX and YscY Protein Families Reveals a Specificity for Yersinia pseudotuberculosis Type III Secretion. |
| Q47434181 | Hierarchical protein targeting and secretion is controlled by an affinity switch in the type III secretion system of enteropathogenic Escherichia coli. |
| Q38670395 | Identification of a Large Family of Slam-Dependent Surface Lipoproteins in Gram-Negative Bacteria |
| Q42290713 | Identification of specific posttranslational O-mycoloylations mediating protein targeting to the mycomembrane |
| Q92867260 | Inner Membrane Translocases and Insertases |
| Q38728723 | MatureP: prediction of secreted proteins with exclusive information from their mature regions. |
| Q47133897 | Outer membrane protein folding from an energy landscape perspective |
| Q42580446 | Preprotein mature domains contain translocase targeting signals that are essential for secretion |
| Q39021695 | Protein export through the bacterial Sec pathway. |
| Q92565853 | Structural Basis of the Subcellular Topology Landscape of Escherichia coli |
| Q40115920 | Structural basis for substrate selection by the translocation and assembly module of the β-barrel assembly machinery |
| Q39371081 | Super-Resolution Imaging of Protein Secretion Systems and the Cell Surface of Gram-Negative Bacteria |
| Q52720128 | Surface display for metabolic engineering of industrially important acetic acid bacteria. |
| Q92867221 | The Periplasmic Chaperones Skp and SurA |
| Q30152728 | The modular nature of the β-barrel assembly machinery, illustrated in Borrelia burgdorferi |
| Q30152662 | The β-barrel assembly machinery in motion |
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