scholarly article | Q13442814 |
P356 | DOI | 10.1016/0092-8674(90)90160-G |
P698 | PubMed publication ID | 2170023 |
P50 | author | Franz-Ulrich Hartl | Q91435 |
P2093 | author name string | W Wickner | |
J P Hendrick | |||
E Schiebel | |||
S Lecker | |||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Escherichia coli | Q25419 |
P304 | page(s) | 269-279 | |
P577 | publication date | 1990-10-01 | |
P1433 | published in | Cell | Q655814 |
P1476 | title | The binding cascade of SecB to SecA to SecY/E mediates preprotein targeting to the E. coli plasma membrane | |
P478 | volume | 63 |
Q63359881 | A Single Amino Acid Substitution in SecY Stabilizes the Interaction with SecA |
Q57976571 | A molecular switch in SecA protein couples ATP hydrolysis to protein translocation |
Q39538718 | A mutation in secY that causes enhanced SecA insertion and impaired late functions in protein translocation |
Q36098219 | A mutation of Escherichia coli SecA protein that partially compensates for the absence of SecB. |
Q37187834 | A new twist on an old pathway--accessory Sec [corrected] systems |
Q28284583 | A secY homologue is found in the plastid genome of Cryptomonas phi |
Q54576716 | A significant fraction of functional SecA is permanently embedded in the membrane. SecA cycling on and off the membrane is not essential during protein translocation. |
Q61451642 | ATP-induced asymmetric pre-protein folding as a driver of protein translocation through the Sec machinery |
Q38305697 | Ability of MBP or RBP signal peptides to influence folding and in vitro translocation of wild-type and hybrid precursors |
Q54551221 | Allosteric communication between signal peptides and the SecA protein DEAD motor ATPase domain. |
Q54443615 | Allosteric regulation of SecA: magnesium-mediated control of conformation and activity. |
Q45947385 | An accessory sec locus of Streptococcus gordonii is required for export of the surface protein GspB and for normal levels of binding to human platelets. |
Q40387036 | Anionic phospholipids are involved in membrane association of FtsY and stimulate its GTPase activity |
Q46249070 | Anti-Salmonella Activity Modulation of Mastoparan V1-A Wasp Venom Toxin-Using Protease Inhibitors, and Its Efficient Production via an Escherichia coli Secretion System |
Q44493487 | Antifolding activity of the SecB chaperone is essential for secretion of HasA, a quickly folding ABC pathway substrate |
Q33940324 | Archaeal protein translocation crossing membranes in the third domain of life |
Q37015789 | Assembly of the translocase motor onto the preprotein-conducting channel. |
Q38325245 | Bacillus subtilis histone-like protein, HBsu, is an integral component of a SRP-like particle that can bind the Alu domain of small cytoplasmic RNA. |
Q28073328 | Bacterial Secretion Systems: An Overview |
Q36287480 | Bacterial expression, correct membrane targeting and functional folding of the HIV-1 membrane protein Vpu using a periplasmic signal peptide |
Q36972407 | Bacterial protein secretion through the translocase nanomachine |
Q58798686 | Bacterial secretion chaperones: the mycobacterial type VII case |
Q44727022 | Binding of SecA to the SecYEG complex accelerates the rate of nucleotide exchange on SecA. |
Q39918354 | Binding, activation and dissociation of the dimeric SecA ATPase at the dimeric SecYEG translocase |
Q44845097 | Biochemical analysis of the biogenesis and function of the Escherichia coli export factor SecY. |
Q40764095 | Biochemical characterization of the presecretory protein translocation machinery of Escherichia coli |
Q41657961 | Biogenesis of the gram-negative bacterial envelope |
Q36151146 | Both an N-terminal 65-kDa domain and a C-terminal 30-kDa domain of SecA cycle into the membrane at SecYEG during translocation |
Q52541487 | Both transmembrane domains of SecG contribute to signal sequence recognition by the Escherichia coli protein export machinery. |
Q38065265 | Breaking on through to the other side: protein export through the bacterial Sec system. |
Q36280993 | Calorimetric analyses of the interaction between SecB and its ligands |
Q26786998 | Channel crossing: how are proteins shipped across the bacterial plasma membrane? |
Q54602395 | Chaperone SecB: conformational changes demonstrated by circular dichroism. |
Q36069355 | Chaperone-assisted folding of newly synthesized proteins in the cytosol |
Q63359921 | Chapter 32 Translocation of proteins across the bacterial cytoplasmic membrane |
Q44624593 | Characterisation of preYvaY export reveals differences in the substrate specificities of Bacillus subtilis and Escherichia coli leader peptidases |
Q67705495 | Characterization of Escherichia coli SecA protein binding to a site on its mRNA involved in autoregulation |
Q34420063 | Characterization of EssB, a protein required for secretion of ESAT-6 like proteins in Staphylococcus aureus |
Q54659309 | Characterization of a Bacillus subtilis SecA mutant protein deficient in translocation ATPase and release from the membrane. |
Q38355196 | Characterization of a potential catalytic residue, Asp-133, in the high affinity ATP-binding site of Escherichia coli SecA, translocation ATPase |
Q36235650 | Characterization of the secretion pathway of the collagen adhesin EmaA of Aggregatibacter actinomycetemcomitans. |
Q35634531 | Chloroplast SecA and Escherichia coli SecA have distinct lipid and signal peptide preferences |
Q37888902 | Cloning and characterization of a secY homolog from Chlamydia trachomatis |
Q63359939 | Cloning and molecular characterization of the secY genes from Bacillus licheniformis and Staphylococcus carnosus: comparative analysis of nine members of the SecY family |
Q74618502 | Cloning and nucleotide sequencing of the secA gene from coryneform bacteria |
Q63359824 | Co- and post-translational translocation through the protein-conducting channel: analogous mechanisms at work? |
Q35624789 | Comparative characterization of SecA from the alpha-subclass purple bacterium Rhodobacter capsulatus and Escherichia coli reveals differences in membrane and precursor specificity |
Q36382139 | Component specificity for the thylakoidal Sec and Delta pH-dependent protein transport pathways |
Q37541742 | Conformational and membrane-binding properties of a signal sequence are largely unaltered by its adjacent mature region |
Q33607777 | Construction of a model secretion system for oral streptococci |
Q41195302 | Contribution of the alanine-rich region of Streptococcus mutans P1 to antigenicity, surface expression, and interaction with the proline-rich repeat domain |
Q38339746 | Correlation between requirement for SecA during export and folding properties of precursor polypeptides |
Q37875023 | Coupling between codon usage, translation and protein export in Escherichia coli. |
Q46663736 | Covalently dimerized SecA is functional in protein translocation |
Q34309801 | Critical regions of secM that control its translation and secretion and promote secretion-specific secA regulation |
Q42574244 | Cross-linked SecA dimers are not functional in protein translocation |
Q27640590 | Crystal structure of Mycobacterium tuberculosis SecA, a preprotein translocating ATPase |
Q42844869 | Crystallization of the chaperone protein SecB. |
Q41057356 | Customized secretion chaperones in pathogenic bacteria |
Q54473734 | Defining the role of the Escherichia coli chaperone SecB using comparative proteomics. |
Q54592711 | Delta mu H+ dependency of in vitro protein translocation into Escherichia coli inner-membrane vesicles varies with the signal-sequence core-region composition. |
Q77955232 | Delta psi stimulates membrane translocation of the C-terminal part of a signal sequence |
Q35587373 | Demonstration in vivo that interaction of maltose-binding protein with SecB is determined by a kinetic partitioning |
Q36674746 | Determination of the Oligomeric State of SecYEG Protein Secretion Channel Complex Using in Vivo Photo- and Disulfide Cross-linking |
Q41545140 | Determination of the intracellular concentration of the export chaperone SecB in Escherichia coli. |
Q52335057 | Development of simple fitness landscapes for peptides by artificial neural filter systems. |
Q54661918 | Different sec-requirements for signal peptide cleavage and protein translocation in a model E. coli protein. |
Q33991486 | Differential dependence of levansucrase and alpha-amylase secretion on SecA (Div) during the exponential phase of growth of Bacillus subtilis. |
Q36581200 | Differential localization of the streptococcal accessory sec components and implications for substrate export. |
Q33836404 | Dimeric SecA is essential for protein translocation |
Q44456461 | Direct demonstration of ATP-dependent release of SecA from a translocating preprotein by surface plasmon resonance. |
Q43829882 | Direct interaction of YidC with the Sec-independent Pf3 coat protein during its membrane protein insertion |
Q46874460 | Direct observation of chaperone-induced changes in a protein folding pathway |
Q36390935 | Dissecting structures and functions of SecA-only protein-conducting channels: ATPase, pore structure, ion channel activity, protein translocation, and interaction with SecYEG/SecDF•YajC. |
Q39647998 | Dissociation of the dimeric SecA ATPase during protein translocation across the bacterial membrane |
Q33886664 | Distinct catalytic roles of the SecYE, SecG and SecDFyajC subunits of preprotein translocase holoenzyme |
Q73843659 | Distinct membrane binding properties of N- and C-terminal domains of Escherichia coli SecA ATPase |
Q38291165 | Diverse effects of mutation on the activity of the Escherichia coli export chaperone SecB. |
Q54676319 | DnaK and DnaJ heat shock proteins participate in protein export in Escherichia coli |
Q30155150 | Dominant negative lptE mutation that supports a role for LptE as a plug in the LptD barrel |
Q47734450 | Driving Forces of Translocation Through Bacterial Translocon SecYEG. |
Q27337281 | Dynamic Organization of SecA and SecY Secretion Complexes in the B. subtilis Membrane |
Q55513394 | Dynamic action of the Sec machinery during initiation, protein translocation and termination. |
Q34718169 | Effect of signal peptide on stability and folding of Escherichia coli thioredoxin. |
Q54375188 | Electron microscopic visualization of asymmetric precursor translocation intermediates: SecA functions as a dimer. |
Q54674352 | Electron microscopy of thin-sectioned three-dimensional crystals of SecA protein from Escherichia coli: Structure in projection at 40 Å resolution |
Q67540651 | Elevated cytosolic concentrations of SecA compensate for a protein translocation defect in Escherichia coli cells with reduced levels of negatively charged phospholipids |
Q47682296 | Endogenous SecA catalyzes preprotein translocation at SecYEG. |
Q34761920 | Energetics of SecA dimerization |
Q84468988 | Enhanced extracellular production of heterologous proteins in Bacillus subtilis by deleting the C-terminal region of the SecA secretory machinery |
Q43690465 | Escherichia coli SecA helicase activity is not required in vivo for efficient protein translocation or autogenous regulation |
Q35614280 | Escherichia coli SecB stimulates export without maintaining export competence of ribose-binding protein signal sequence mutants. |
Q39885323 | Escherichia coli SecB, SecA, and SecY proteins are required for expression and membrane insertion of the bacteriocin release protein, a small lipoprotein. |
Q54640347 | Escherichia coli SecY and SecE proteins appear insufficient to constitute the SecA receptor. |
Q41239605 | Escherichia coli preprotein translocase |
Q33994549 | Escherichia coli translocase: the unravelling of a molecular machine |
Q34486443 | Evaluating the oligomeric state of SecYEG in preprotein translocase |
Q59327020 | Evolution of mitochondrial TAT translocases illustrates the loss of bacterial protein transport machines in mitochondria |
Q30451851 | Export of maltose-binding protein species with altered charge distribution surrounding the signal peptide hydrophobic core in Escherichia coli cells harboring prl suppressor mutations |
Q38305914 | Expression of Escherichia coli SecB in Bacillus subtilis facilitates secretion of the SecB-dependent maltose-binding protein of E. coli |
Q91555669 | Free-energy landscapes of membrane co-translocational protein unfolding |
Q41622272 | Full-length Escherichia coli SecA dimerizes in a closed conformation in solution as determined by cryo-electron microscopy. |
Q43560168 | Functional signal peptides bind a soluble N-terminal fragment of SecA and inhibit its ATPase activity |
Q54536175 | Functionally significant mobile regions of Escherichia coli SecA ATPase identified by NMR. |
Q57232629 | Genetic dissection of SecA: suppressor mutations against the secY205 translocase defect |
Q44790621 | Global co-ordination of protein translocation by the SecA IRA1 switch |
Q83231318 | HDX-MS reveals nucleotide-dependent, anti-correlated opening and closure of SecA and SecY channels of the bacterial translocon |
Q35072436 | Heat shock transcription factor σ32 co-opts the signal recognition particle to regulate protein homeostasis in E. coli |
Q40814129 | Heat-shock proteins as molecular chaperones |
Q40104144 | Helicase Motif III in SecA is essential for coupling preprotein binding to translocation ATPase. |
Q72270160 | High yield fermentation and purification of Tendamistat disulphide analogues secreted by Streptomyces lividans |
Q40609301 | How proteins cross the bacterial cytoplasmic membrane. |
Q54567468 | Identification of a region of interaction between Escherichia coli SecA and SecY proteins. |
Q33726768 | Identification of a sequence motif that confers SecB dependence on a SecB-independent secretory protein in vivo |
Q48071441 | Identification of the magnesium-binding domain of the high-affinity ATP-binding site of the Bacillus subtilis and Escherichia coli SecA protein |
Q42485674 | Identification of the preprotein binding domain of SecA. |
Q40253390 | In silico analysis and experimental validation of lipoprotein and novel Tat signal peptides processing in Anabaena sp. PCC7120. |
Q37479627 | In vitro biochemical studies on translocation of presecretory proteins across the cytoplasmic membrane of Escherichia coli |
Q54560116 | In vitro membrane integration of leader peptidase depends on the Sec machinery and anionic phospholipids and can occur post-translationally. |
Q39847154 | In vivo cross-linking of the SecA and SecY subunits of the Escherichia coli preprotein translocase |
Q54450403 | In vivo membrane topology of Escherichia coli SecA ATPase reveals extensive periplasmic exposure of multiple functionally important domains clustering on one face of SecA. |
Q36108969 | In vivo studies of the role of SecA during protein export in Escherichia coli |
Q39942927 | Incorporation of light-harvesting complex I alpha and beta polypeptides into the intracytoplasmic membrane of Rhodobacter capsulatus |
Q35858391 | Individual chaperones required for Yop secretion by Yersinia |
Q39843192 | Influence of impaired chaperone or secretion function on SecB production in Escherichia coli |
Q38359470 | Integration of SecA protein into the Escherichia coli inner membrane is regulated by its amino-terminal ATP-binding domain |
Q41822778 | Interaction of Bacillus subtilis CsaA with SecA and precursor proteins. |
Q36279244 | Interaction of SecB with intermediates along the folding pathway of maltose-binding protein |
Q63359914 | Interaction of SecB with soluble SecA 1 |
Q30982774 | Interaction of the Bacillus subtilis chaperone CsaA with the secretory protein YvaY. |
Q71056385 | Inversion of the membrane topology of SecG coupled with SecA-dependent preprotein translocation |
Q39935707 | Involvement of SecB, a chaperone, in the export of ribose-binding protein |
Q41063571 | Involvement of stress protein PspA (phage shock protein A) of Escherichia coli in maintenance of the protonmotive force under stress conditions |
Q44133891 | Kinetic analysis of the translocation of fluorescent precursor proteins into Escherichia coli membrane vesicles. |
Q27937087 | LMA1 binds to vacuoles at Sec18p (NSF), transfers upon ATP hydrolysis to a t-SNARE (Vam3p) complex, and is released during fusion |
Q35182130 | Large-scale evolutionary analyses on SecB subunits of bacterial sec system. |
Q34004070 | Lon protease quality control of presecretory proteins in Escherichia coli and its dependence on the SecB and DnaJ (Hsp40) chaperones |
Q40734547 | Mammalian and Escherichia coli signal recognition particles |
Q33773458 | Mapping of the signal peptide-binding domain of Escherichia coli SecA using Förster resonance energy transfer |
Q43668401 | Mapping the sites of interaction between SecY and SecE by cysteine scanning mutagenesis. |
Q36118522 | Membrane binding of the bacterial signal recognition particle receptor involves two distinct binding sites |
Q57381586 | Membrane protein assembly |
Q37198083 | Mistranslation of membrane proteins and two-component system activation trigger antibiotic-mediated cell death. |
Q39936450 | Multicopy suppression: an approach to understanding intracellular functioning of the protein export system |
Q34637739 | Multitasking SecB chaperones in bacteria |
Q54651078 | Nucleotide and negatively charged lipid-dependent vesicle aggregation caused by SecA. Evidence that SecA contains two lipid-binding sites. |
Q73626344 | Nucleotide binding activity of SecA homodimer is conformationally regulated by temperature and altered by prlD and azi mutations |
Q48214586 | Nucleotide sequence of the secY gene from Lactococcus lactis and identification of conserved regions by comparison of four SecY proteins |
Q33991984 | Overproduction of SecA suppresses the export defect caused by a mutation in the gene encoding the Escherichia coli export chaperone secB. |
Q47286801 | Penetration into Membrane of Amino-terminal Region of SecA when Associated with SecYEG in Active Complexes |
Q68208733 | Peptide Binding by Chaperone SecB: Implications for Recognition of Nonnative Structure |
Q57381598 | Positively charged residues influence the degree of SecA dependence in protein translocation across the E. coli inner membrane |
Q90024187 | Posttranslational Targeting of a Recombinant Protein Promotes Its Efficient Secretion into the Escherichia coli Periplasm |
Q41518075 | Precursor protein translocation by the Escherichia coli translocase is directed by the protonmotive force |
Q41454285 | Preparation of a highly translocation-competent proOmpA/SecB complex |
Q37113122 | Preprotein translocase of Escherichia coli: solubilization, purification, and reconstitution of the integral membrane subunits SecY/E. |
Q39497981 | Preprotein translocation by a hybrid translocase composed of Escherichia coli and Bacillus subtilis subunits. |
Q24670723 | Preprotein-controlled catalysis in the helicase motor of SecA |
Q41491565 | Principles of membrane protein assembly and structure |
Q35975083 | PrlA and PrlG suppressors reduce the requirement for signal sequence recognition |
Q34058568 | PrlA suppressor mutations cluster in regions corresponding to three distinct topological domains |
Q33889035 | PrlA4 prevents the rejection of signal sequence defective preproteins by stabilizing the SecA-SecY interaction during the initiation of translocation |
Q54590162 | Pro-OmpA derivatives with a His6 tag in their N-terminal "translocation initiation domains" are arrested by Ni2+ at an early post-targeting stage of translocation. |
Q34977908 | Probing the SecYEG translocation pore size with preproteins conjugated with sizable rigid spherical molecules |
Q37976983 | Protein conducting channels-mechanisms, structures and applications |
Q37191850 | Protein export in prokaryotes and eukaryotes. Theme with variations |
Q39021695 | Protein export through the bacterial Sec pathway. |
Q35814726 | Protein secretion and surface display in Gram-positive bacteria |
Q37058881 | Protein secretion in Bacillus species. |
Q41220629 | Protein targeting and translocation; a comparative survey. |
Q33538949 | Protein targeting to the bacterial cytoplasmic membrane. |
Q34070563 | Protein traffic in bacteria: multiple routes from the ribosome to and across the membrane |
Q36328629 | Protein translocation across biological membranes |
Q34293903 | Protein translocation across membranes |
Q74125263 | Protein translocation functions of Escherichia coli SecY: in vitro characterization of cold-sensitive secY mutants |
Q43650948 | Protein translocation. A bacterium catches up. |
Q40764106 | Protein translocation: common themes from bacteria to man. |
Q26747205 | Protein translocation: what's the problem? |
Q35071390 | Protein translocons: multifunctional mediators of protein translocation across membranes |
Q37895211 | Proteomic methods unravel the protein quality control in Escherichia coli |
Q37445539 | Proton transfer is rate-limiting for translocation of precursor proteins by the Escherichia coli translocase |
Q24799937 | Recognition of secretory proteins in Escherichia coli requires signals in addition to the signal sequence and slow folding |
Q57808271 | Reconstitution of Purified Bacterial Preprotein Translocase in Liposomes |
Q37557649 | Reconstitution of a protein translocation system containing purified SecY, SecE, and SecA from Escherichia coli |
Q34253865 | Reconstruction and modeling protein translocation and compartmentalization in Escherichia coli at the genome-scale |
Q41978114 | Reexamination of the role of the amino terminus of SecA in promoting its dimerization and functional state |
Q36123480 | Regions of maltose-binding protein that influence SecB-dependent and SecA-dependent export in Escherichia coli |
Q33737540 | Regulation of Escherichia coli secA by cellular protein secretion proficiency requires an intact gene X signal sequence and an active translocon |
Q74567485 | Requirements for the translocation of elongation-arrested, ribosome-associated OmpA across the plasma membrane of Escherichia coli |
Q35122486 | Residues essential for the function of SecE, a membrane component of the Escherichia coli secretion apparatus, are located in a conserved cytoplasmic region |
Q33787527 | Revised translation start site for secM defines an atypical signal peptide that regulates Escherichia coli secA expression |
Q34923130 | Ring-like pore structures of SecA: implication for bacterial protein-conducting channels |
Q33893908 | Role of lipids in the translocation of proteins across membranes |
Q36793326 | Roles of SecG in ATP- and SecA-dependent protein translocation. |
Q63359819 | Sec Protein-Conducting Channel and SecA |
Q34043693 | Sec dependent and sec independent assembly of E. coli inner membrane proteins: the topological rules depend on chain length |
Q57976568 | Sec, drugs and rock’n’roll: antibiotic targeting of bacterial protein translocation |
Q34068950 | Sec-dependent protein export and the involvement of the molecular chaperone SecB. |
Q36224492 | Sec-dependent protein translocation across biological membranes: evolutionary conservation of an essential protein transport pathway (review). |
Q26852214 | Sec-secretion and sortase-mediated anchoring of proteins in Gram-positive bacteria |
Q45975576 | Sec61p and BiP directly facilitate polypeptide translocation into the ER. |
Q63359672 | SecA Is Not Required for Signal Recognition Particle-mediated Targeting and Initial Membrane Insertion of a Nascent Inner Membrane Protein |
Q74620468 | SecA is required for the insertion of inner membrane proteins targeted by the Escherichia coli signal recognition particle |
Q46316930 | SecA mediates cotranslational targeting and translocation of an inner membrane protein |
Q52513940 | SecA promotes preprotein translocation by undergoing ATP-driven cycles of membrane insertion and deinsertion. |
Q54627502 | SecA protein is exposed to the periplasmic surface of the E. coli inner membrane in its active state. |
Q36567392 | SecA protein is required for translocation of a model precursor protein into inverted vesicles of Escherichia coli plasma membrane |
Q44608604 | SecA protein needs both acidic phospholipids and SecY/E protein for functional high-affinity binding to the Escherichia coli plasma membrane |
Q40882511 | SecA protein: autoregulated ATPase catalysing preprotein insertion and translocation across the Escherichia coli inner membrane |
Q35600064 | SecA proteins of Bacillus subtilis and Escherichia coli possess homologous amino-terminal ATP-binding domains regulating integration into the plasma membrane |
Q24631210 | SecA, a remarkable nanomachine |
Q30485740 | SecA, the motor of the secretion machine, binds diverse partners on one interactive surface |
Q40259224 | SecA-a New Twist in the Tale |
Q33807313 | SecA: the ubiquitous component of preprotein translocase in prokaryotes. |
Q39500325 | SecB dependence of an exported protein is a continuum influenced by the characteristics of the signal peptide or early mature region |
Q34336036 | SecB is a bona fide generalized chaperone in Escherichia coli |
Q37710987 | SecB--a chaperone dedicated to protein translocation. |
Q54683049 | SecB-binding does not maintain the translocation-competent state of prePhoE |
Q35003009 | SecB-like chaperone controls a toxin-antitoxin stress-responsive system in Mycobacterium tuberculosis |
Q24596484 | SecD and SecF are required for the proton electrochemical gradient stimulation of preprotein translocation |
Q54565652 | SecE-depleted membranes of Escherichia coli are active. SecE is not obligatorily required for the in vitro translocation of certain protein precursors. |
Q33848928 | SecM facilitates translocase function of SecA by localizing its biosynthesis |
Q41850974 | SecY and SecA interact to allow SecA insertion and protein translocation across the Escherichia coli plasma membrane |
Q36618916 | SecYEG activates GTPases to drive the completion of cotranslational protein targeting |
Q38292412 | SecYEG and SecA are the stoichiometric components of preprotein translocase |
Q30843286 | SecYEG assembles into a tetramer to form the active protein translocation channel |
Q41526927 | Selective extracellular release of cholera toxin B subunit by Escherichia coli: dissection of Neisseria Iga beta-mediated outer membrane transport |
Q57976575 | Separable ATPase and Membrane Insertion Domains of the SecA Subunit of Preprotein Translocase |
Q56228657 | Signal Recognition Particle (SRP), a Ubiquitous Initiator of Protein Translocation |
Q67989974 | Signal peptidase I overproduction results in increased efficiencies of export and maturation of hybrid secretory proteins in Escherichia coli |
Q24548495 | Signal peptide-dependent protein transport in Bacillus subtilis: a genome-based survey of the secretome |
Q33662560 | Signal peptides are allosteric activators of the protein translocase |
Q34309758 | Signal recognition particle (SRP), a ubiquitous initiator of protein translocation |
Q43095210 | Sites of interaction between SecA and the chaperone SecB, two proteins involved in export |
Q34435795 | Specific cross-linking of the proline isomerase cyclophilin to a non-proline-containing peptide. |
Q27726706 | Structural basis for the antifolding activity of a molecular chaperone |
Q34442682 | Structural characterization of the complex of SecB and metallothionein-labeled proOmpA by cryo-electron microscopy. |
Q34005867 | Structure and function of the bacterial Sec translocon. |
Q27652526 | Structure of a complex of the ATPase SecA and the protein-translocation channel |
Q57463329 | Substrate Proteins Take Shape at an Improved Bacterial Translocon |
Q30815173 | Substrate specificity of the SecB chaperone |
Q48565780 | Substrate-specific binding of hook-associated proteins by FlgN and FliT, putative chaperones for flagellum assembly. |
Q39837250 | Suppression of signal sequence defects and azide resistance in Escherichia coli commonly result from the same mutations in secA |
Q31000722 | Suppression of the growth and export defects of an Escherichia coli secA(Ts) mutant by a gene cloned from Bacillus subtilis |
Q41013122 | Suppressor analysis suggests a multistep, cyclic mechanism for protein secretion in Escherichia coli |
Q33538951 | Surface proteins of gram-positive bacteria and mechanisms of their targeting to the cell wall envelope |
Q36783256 | SycE, a chaperone-like protein of Yersinia enterocolitica involved in Ohe secretion of YopE. |
Q47828537 | Syd, a SecY-interacting protein, excludes SecA from the SecYE complex with an altered SecY24 subunit. |
Q74495019 | Synthetic signal peptides specifically recognize SecA and stimulate ATPase activity in the absence of preprotein |
Q35738230 | Targeting of GroEL to SecA on the cytoplasmic membrane of Escherichia coli |
Q57830682 | The Bacterial SRP Receptor, SecA and the Ribosome Use Overlapping Binding Sites on the SecY Translocon |
Q54614038 | The C terminus of SecA is involved in both lipid binding and SecB binding. |
Q38827839 | The Canonical and Accessory Sec System of Gram-positive Bacteria. |
Q91638430 | The Dynamic ATP-Driven Mechanism of Bacterial Protein Translocation and the Critical Role of Phospholipids |
Q63359855 | The F286Y mutation of PrlA4 tempers the signal sequence suppressor phenotype by reducing the SecA binding affinity |
Q38294961 | The N terminus of the HasA protein and the SecB chaperone cooperate in the efficient targeting and secretion of HasA via the ATP-binding cassette transporter |
Q47374398 | The Sec System: Protein Export in Escherichia coli |
Q33538582 | The Sec system |
Q40871781 | The SecA and SecY subunits of translocase are the nearest neighbors of a translocating preprotein, shielding it from phospholipids |
Q47684820 | The SecA protein deeply penetrates into the SecYEG channel during insertion, contacting most channel transmembrane helices and periplasmic regions |
Q39568449 | The SecA subunit of Escherichia coli preprotein translocase is exposed to the periplasm |
Q33888292 | The SecB chaperone is involved in the secretion of the Serratia marcescens HasA protein through an ABC transporter. |
Q34086060 | The SecYEG preprotein translocation channel is a conformationally dynamic and dimeric structure |
Q39750212 | The YSIRK-G/S motif of staphylococcal protein A and its role in efficiency of signal peptide processing |
Q54436247 | The active protein-conducting channel of Escherichia coli contains an apolar patch. |
Q35814696 | The bacterial Sec-translocase: structure and mechanism. |
Q47704872 | The biosynthesis of bacterial and plastidic c-type cytochromes |
Q38339927 | The catalytic cycle of the escherichia coli SecA ATPase comprises two distinct preprotein translocation events |
Q29615298 | The complete general secretory pathway in gram-negative bacteria |
Q28263794 | The conformation of a signal peptide bound by Escherichia coli preprotein translocase SecA |
Q44077345 | The core of the bacterial translocase harbors a tilted transmembrane segment 3 of SecE. |
Q41491050 | The cytosolic SycE and SycH chaperones of Yersinia protect the region of YopE and YopH involved in translocation across eukaryotic cell membranes |
Q72428581 | The delta pH-driven, ATP-independent protein translocation mechanism in the chloroplast thylakoid membrane. Kinetics and energetics |
Q42093934 | The dispensability and requirement of SecA N-terminal aminoacyl residues for complementation, membrane binding, lipid-specific domains and channel activities |
Q37257359 | The lateral gate of SecYEG opens during protein translocation |
Q41006640 | The molecular chaperone SecB is released from the carboxy-terminus of SecA during initiation of precursor protein translocation. |
Q90391222 | The molecular mechanism of cotranslational membrane protein recognition and targeting by SecA |
Q37173155 | The primary pathway of protein export in E. coli |
Q41944218 | The protease-protected 30 kDa domain of SecA is largely inaccessible to the membrane lipid phase |
Q41197368 | The rate of folding dictates substrate secretion by the Escherichia coli hemolysin type 1 secretion system |
Q27939104 | The signal recognition particle in S. cerevisiae |
Q34455348 | The structural view of bacterial translocation-specific chaperone SecB: implications for function |
Q36640900 | The structure of the Sec complex and the problem of protein translocation |
Q42152267 | The variable subdomain of Escherichia coli SecA functions to regulate SecA ATPase activity and ADP release |
Q54201374 | The way is the goal: how SecA transports proteins across the cytoplasmic membrane in bacteria. |
Q54436102 | Topology inversion of SecG is essential for cytosolic SecA-dependent stimulation of protein translocation. |
Q54559159 | Topology of the integral membrane form of Escherichia coli SecA protein reveals multiple periplasmically exposed regions and modulation by ATP binding. |
Q40173948 | Translocated Intimin Receptor and Its Chaperone Interact with ATPase of the Type III Secretion Apparatus of EnteropathogenicEscherichia coli |
Q34041521 | Translocation can drive the unfolding of a preprotein domain. |
Q40630832 | Translocation gets a push |
Q35652456 | Trigger Factor can antagonize both SecB and DnaK/DnaJ chaperone functions in Escherichia coli. |
Q38314889 | Two distinct ATP-binding domains are needed to promote protein export by Escherichia coli SecA ATPase |
Q44542398 | Two-stage binding of SecA to the bacterial translocon regulates ribosome-translocon interaction |
Q42576947 | Two-way communication between SecY and SecA suggests a Brownian ratchet mechanism for protein translocation |
Q39923654 | Unlocking the Bacterial SecY Translocon |
Q37097393 | Use of folding modulators to improve heterologous protein production in Escherichia coli. |
Q34314497 | Yop fusions to tightly folded protein domains and their effects on Yersinia enterocolitica type III secretion. |
Q36105907 | YscN, the putative energizer of the Yersinia Yop secretion machinery |
Q80047274 | [Insertional polymorphism of the CYP2E1 gene in infiltrative pulmonary tuberculosis in populations of Bashkortostan Republic] |
Q36102357 | prlA suppression of defective export of maltose-binding protein in secB mutants of Escherichia coli |
Q33743886 | secG and temperature modulate expression of azide-resistant and signal sequence suppressor phenotypes of Escherichia coli secA mutants |
Q46481993 | ΔμH+ and ATP function at different steps of the catalytic cycle of preprotein translocase |
Search more.