scholarly article | Q13442814 |
P2093 | author name string | Hironori Niki | |
Piet A J de Boer | |||
Nicole D Pecora | |||
Matthew A Gerding | |||
Yasuyuki Ogata | |||
P2860 | cites work | Proton motive force drives the interaction of the inner membrane TolA and outer membrane pal proteins in Escherichia coli | Q73293362 |
FtsN, a late recruit to the septum in Escherichia coli | Q73663897 | ||
FtsQ, FtsL and FtsI require FtsK, but not FtsN, for co-localization with FtsZ during Escherichia coli cell division | Q77155405 | ||
The TolQ-TolR proteins energize TolA and share homologies with the flagellar motor proteins MotA-MotB | Q77291463 | ||
Recruitment of ZipA to the division site by interaction with FtsZ | Q77345061 | ||
Impairment of cell division in tolA mutants of Escherichia coli at low and high medium osmolarities | Q77731994 | ||
In vitro characterization of peptidoglycan-associated lipoprotein (PAL)-peptidoglycan and PAL-TolB interactions | Q24516911 | ||
CTXphi infection of Vibrio cholerae requires the tolQRA gene products | Q24548978 | ||
Crystal structure of the SOS cell division inhibitor SulA and in complex with FtsZ | Q24670060 | ||
Filamentous phage infection: crystal structure of g3p in complex with its coreceptor, the C-terminal domain of TolA | Q27619054 | ||
One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products | Q27860842 | ||
Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein | Q27861056 | ||
A monomeric red fluorescent protein | Q28131782 | ||
Mechanisms of colicin binding and transport through outer membrane porins | Q28214399 | ||
FtsZ ring structure associated with division in Escherichia coli | Q28245159 | ||
FACS-optimized mutants of the green fluorescent protein (GFP) | Q29547322 | ||
An efficient recombination system for chromosome engineering in Escherichia coli | Q29615038 | ||
Complete set of ORF clones of Escherichia coli ASKA library (a complete set of E. coli K-12 ORF archive): unique resources for biological research | Q29619122 | ||
Distinct constrictive processes, separated in time and space, divide caulobacter inner and outer membranes | Q30799567 | ||
Morphological analysis of nuclear separation and cell division during the life cycle of Escherichia coli | Q30959228 | ||
Macromolecular import into Escherichia coli: the TolA C-terminal domain changes conformation when interacting with the colicin A toxin. | Q31039136 | ||
Translocation of jellyfish green fluorescent protein via the Tat system of Escherichia coli and change of its periplasmic localization in response to osmotic up-shock | Q31636146 | ||
Export of active green fluorescent protein to the periplasm by the twin-arginine translocase (Tat) pathway in Escherichia coli. | Q31727465 | ||
Role of penicillin-binding protein PBP 2B in assembly and functioning of the division machinery of Bacillus subtilis | Q33179603 | ||
Cytokinesis in bacteria | Q33186319 | ||
Role of TolR N-terminal, central, and C-terminal domains in dimerization and interaction with TolA and tolQ. | Q33635245 | ||
The Tol proteins of Escherichia coli and their involvement in the uptake of biomolecules and outer membrane stability | Q33726872 | ||
The TolQRA proteins are required for membrane insertion of the major capsid protein of the filamentous phage f1 during infection | Q33727468 | ||
Bacterial SOS checkpoint protein SulA inhibits polymerization of purified FtsZ cell division protein. | Q33734943 | ||
Mutations in each of the tol genes of Pseudomonas putida reveal that they are critical for maintenance of outer membrane stability | Q33791027 | ||
Green fluorescent protein functions as a reporter for protein localization in Escherichia coli | Q33994417 | ||
Tol-dependent macromolecule import through the Escherichia coli cell envelope requires the presence of an exposed TolA binding motif. | Q34110000 | ||
Pleiotropic Properties and Genetic Organization of the tolA, B Locus of Escherichia coli K-12 | Q34215321 | ||
The Tol-Pal proteins of the Escherichia coli cell envelope: an energized system required for outer membrane integrity? | Q34334962 | ||
FtsZ and the division of prokaryotic cells and organelles | Q34460019 | ||
A division inhibitor and a topological specificity factor coded for by the minicell locus determine proper placement of the division septum in E. coli | Q34497481 | ||
The tubulin ancestor, FtsZ, draughtsman, designer and driving force for bacterial cytokinesis | Q34672738 | ||
Genetic analysis of the cell division protein FtsI (PBP3): amino acid substitutions that impair septal localization of FtsI and recruitment of FtsN. | Q34675381 | ||
Killing of E coli cells by E group nuclease colicins | Q34992673 | ||
The Tol proteins of Escherichia coli and their involvement in the translocation of group A colicins | Q34992676 | ||
Analysis of the Escherichia coli Tol-Pal and TonB systems by periplasmic production of Tol, TonB, colicin, or phage capsid soluble domains. | Q34992680 | ||
Morphogenesis of the bacterial division septum: a new class of septation-defective mutants | Q35004953 | ||
Temporal and spatial regulation in prokaryotic cell cycle progression and development | Q35090187 | ||
A predicted ABC transporter, FtsEX, is needed for cell division in Escherichia coli | Q35546037 | ||
Characterization of the tol-pal region of Escherichia coli K-12: translational control of tolR expression by TolQ and identification of a new open reading frame downstream of pal encoding a periplasmic protein | Q35609184 | ||
Filamentous phage infection: required interactions with the TolA protein | Q35631483 | ||
Bacterial cell division and the septal ring. | Q35921495 | ||
Protein import into Escherichia coli: colicins A and E1 interact with a component of their translocation system | Q35927451 | ||
Inhibition of FtsZ polymerization by SulA, an inhibitor of septation in Escherichia coli | Q35974127 | ||
Diverse paths to midcell: assembly of the bacterial cell division machinery | Q36187570 | ||
Membrane-murein attachment at the leading edge of the division septum: a second membrane-murein structure associated with morphogenesis of the gram-negative bacterial division septum | Q36264040 | ||
Septum enlightenment: assembly of bacterial division proteins | Q36341266 | ||
Physiological characterization of an Escherichia coli mutant altered in the structure of murein lipoprotein | Q36418954 | ||
Role of murein lipoprotein in morphogenesis of the bacterial division septum: phenotypic similarity of lkyD and lpo mutants | Q36419016 | ||
Genetics and physiology of colicin-tolerant mutants of Escherichia coli. | Q37400181 | ||
Identification by genetic suppression of Escherichia coli TolB residues important for TolB-Pal interaction | Q39498889 | ||
Energy-dependent conformational change in the TolA protein of Escherichia coli involves its N-terminal domain, TolQ, and TolR. | Q39504085 | ||
Recruitment of ZipA to the septal ring of Escherichia coli is dependent on FtsZ and independent of FtsA. | Q39547179 | ||
Escherichia coli tol-pal mutants form outer membrane vesicles | Q39567746 | ||
Colicin import into Escherichia coli cells | Q39567863 | ||
Mutational analysis of the Escherichia coli K-12 TolA N-terminal region and characterization of its TolQ-interacting domain by genetic suppression. | Q39568912 | ||
Murein-lipoprotein of Escherichia coli: A protein involved in the stabilization of bacterial cell envelope | Q39646127 | ||
Salmonella enterica serovar typhimurium resistance to bile: identification and characterization of the tolQRA cluster | Q39678359 | ||
ZipA is required for recruitment of FtsK, FtsQ, FtsL, and FtsN to the septal ring in Escherichia coli | Q39678952 | ||
Targeting of (D)MinC/MinD and (D)MinC/DicB complexes to septal rings in Escherichia coli suggests a multistep mechanism for MinC-mediated destruction of nascent FtsZ rings. | Q39679140 | ||
Mutational analysis of the TolA C-terminal domain of Escherichia coli and genetic evidence for an interaction between TolA and TolB. | Q39679960 | ||
Pal lipoprotein of Escherichia coli plays a major role in outer membrane integrity | Q39694516 | ||
Effects of multiple deletions of murein hydrolases on viability, septum cleavage, and sensitivity to large toxic molecules in Escherichia coli | Q39741336 | ||
ASAP, a systematic annotation package for community analysis of genomes | Q39790704 | ||
A widely conserved bacterial cell division protein that promotes assembly of the tubulin-like protein FtsZ. | Q39864295 | ||
Induction kinetics and cell surface distribution of Escherichia coli lipoprotein under lac promoter control | Q39961063 | ||
Distribution of newly synthesized lipoprotein over the outer membrane and the peptidoglycan sacculus of an Escherichia coli lac-lpp strain | Q39963079 | ||
fii, a bacterial locus required for filamentous phage infection and its relation to colicin-tolerant tolA and tolB. | Q39964549 | ||
Genetics of resistance to colicins in Escherichia coli K-12: cross-resistance among colicins of group A | Q40035541 | ||
The Escherichia coli amidase AmiC is a periplasmic septal ring component exported via the twin-arginine transport pathway | Q40565200 | ||
Screening for synthetic lethal mutants in Escherichia coli and identification of EnvC (YibP) as a periplasmic septal ring factor with murein hydrolase activity. | Q40567039 | ||
FtsZ ring in bacterial cytokinesis | Q40865464 | ||
Colicin import and pore formation: a system for studying protein transport across membranes? | Q40955264 | ||
Protein Interactions in the Outer Membrane of Escherichia coli | Q41004966 | ||
Bacterial cell division: the cycle of the ring | Q41367414 | ||
Diffusion of green fluorescent protein in three cell environments in Escherichia coli | Q41673126 | ||
Defective O-antigen polymerization in tolA and pal mutants of Escherichia coli in response to extracytoplasmic stress | Q41822623 | ||
The excC gene of Escherichia coli K-12 required for cell envelope integrity encodes the peptidoglycan-associated lipoprotein (PAL). | Q42610591 | ||
Improved methods for producing outer membrane vesicles in Gram-negative bacteria. | Q43662194 | ||
Involvement of N-acetylmuramyl-L-alanine amidases in cell separation and antibiotic-induced autolysis of Escherichia coli | Q43674772 | ||
The Tol/Pal system function requires an interaction between the C-terminal domain of TolA and the N-terminal domain of TolB. | Q43982260 | ||
Proteomic screening and identification of differentially distributed membrane proteins in Escherichia coli | Q44035112 | ||
Peptidoglycan recognition by Pal, an outer membrane lipoprotein | Q46942184 | ||
Organisation and evolution of the tol-pal gene cluster | Q47639043 | ||
TolB protein of Escherichia coli K-12 interacts with the outer membrane peptidoglycan-associated proteins Pal, Lpp and OmpA. | Q47694282 | ||
Tol-Pal proteins are critical cell envelope components of Erwinia chrysanthemi affecting cell morphology and virulence | Q48118243 | ||
Maturation of the Escherichia coli divisome occurs in two steps. | Q50775806 | ||
A membrane metalloprotease participates in the sequential degradation of a Caulobacter polarity determinant. | Q52058791 | ||
The analysis of cell division and cell wall synthesis genes reveals mutationally inactivated ftsQ and mraY in a protoplast-type L-form of Escherichia coli. | Q53625713 | ||
FtsZ-dependent localization of GroEL protein at possible division sites. | Q54500826 | ||
Deletion analyses of the peptidoglycan-associated lipoprotein Pal reveals three independent binding sequences including a TolA box. | Q54512173 | ||
The C-terminal domain of TolA is the coreceptor for filamentous phage infection of E. coli. | Q54561820 | ||
Protein complex within Escherichia coli inner membrane. TolA N-terminal domain interacts with TolQ and TolR proteins. | Q54612317 | ||
Peptidoglycan-associated lipoprotein-TolB interaction. A possible key to explaining the formation of contact sites between the inner and outer membranes of Escherichia coli. | Q54612320 | ||
Transmembrane alpha-helix interactions are required for the functional assembly of the Escherichia coli Tol complex. | Q54617237 | ||
Morphological mutants of Escherichia coli. Isolation and ultrastructure of a chain-forming envC mutant. | Q54650691 | ||
A novel peptidoglycan-associated lipoprotein (PAL) found in the outer membrane of Proteus mirabilis and other Gram-negative bacteria | Q71558296 | ||
Evolutionary relationship of uptake systems for biopolymers in Escherichia coli: cross-complementation between the TonB-ExbB-ExbD and the TolA-TolQ-TolR proteins | Q72792046 | ||
Identification of a Sex-factor-affinity Site in E. coli as | Q72911552 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Escherichia coli | Q25419 |
P304 | page(s) | 1008-1025 | |
P577 | publication date | 2007-02-01 | |
P1433 | published in | Molecular Microbiology | Q6895967 |
P1476 | title | The trans-envelope Tol-Pal complex is part of the cell division machinery and required for proper outer-membrane invagination during cell constriction in E. coli | |
P478 | volume | 63 |
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Q76319373 | A conserved RNA seed-pairing domain directs small RNA-mediated stress resistance in enterobacteria |
Q28538240 | A genome-wide screen for bacterial envelope biogenesis mutants identifies a novel factor involved in cell wall precursor metabolism |
Q30156997 | A modular BAM complex in the outer membrane of the alpha-proteobacterium Caulobacter crescentus. |
Q30495590 | A protein critical for cell constriction in the Gram-negative bacterium Caulobacter crescentus localizes at the division site through its peptidoglycan-binding LysM domains |
Q37232478 | ATP-binding site lesions in FtsE impair cell division. |
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Q26786994 | Activities and regulation of peptidoglycan synthases |
Q37799899 | Advances in understanding E. coli cell fission |
Q27657111 | Allosteric β-propeller signalling in TolB and its manipulation by translocating colicins |
Q34484309 | Altered regulation of the OmpF porin by Fis in Escherichia coli during an evolution experiment and between B and K-12 strains |
Q36584033 | An altered FtsA can compensate for the loss of essential cell division protein FtsN in Escherichia coli |
Q41654098 | Antibacterial toxin colicin N and phage protein G3p compete with TolB for a binding site on TolA. |
Q38831310 | Application of Nuclear Magnetic Resonance and Hybrid Methods to Structure Determination of Complex Systems |
Q41779670 | Assembly of the Caulobacter cell division machine |
Q35152795 | BB0323 and novel virulence determinant BB0238: Borrelia burgdorferi proteins that interact with and stabilize each other and are critical for infectivity |
Q38034197 | Bacterial cytokinesis: From Z ring to divisome |
Q37349813 | Biogenesis of bacterial membrane vesicles |
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Q42120871 | Colicin N binds to the periphery of its receptor and translocator, outer membrane protein F. |
Q24671701 | Colicin biology |
Q36345584 | Compensation for the loss of the conserved membrane targeting sequence of FtsA provides new insights into its function. |
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Q37248350 | Computational and experimental approaches to chart the Escherichia coli cell-envelope-associated proteome and interactome |
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Q27683998 | Crystal Structure of Penicillin-Binding Protein 3 (PBP3) from Escherichia coli |
Q27671848 | Crystal Structures of a CTX pIII Domain Unbound and in Complex with a Vibrio cholerae TolA Domain Reveal Novel Interaction Interfaces |
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Q37157051 | Divisome under construction: distinct domains of the small membrane protein FtsB are necessary for interaction with multiple cell division proteins |
Q41929627 | Dual orientation of the outer membrane lipoprotein Pal in Escherichia coli. |
Q51004577 | E. coli Cell Cycle Machinery. |
Q40148823 | Electrostatic interactions between the CTX phage minor coat protein and the bacterial host receptor TolA drive the pathogenic conversion of Vibrio cholerae |
Q38062003 | Energetics of colicin import revealed by genetic cross-complementation between the Tol and Ton systems |
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Q36208004 | From Homodimer to Heterodimer and Back: Elucidating the TonB Energy Transduction Cycle. |
Q37957146 | From individual cell motility to collective behaviors: insights from a prokaryote, Myxococcus xanthus. |
Q33694168 | From the regulation of peptidoglycan synthesis to bacterial growth and morphology. |
Q34536796 | FtsEX acts on FtsA to regulate divisome assembly and activity |
Q42688895 | FtsN--trigger for septation |
Q92341279 | Functional Regulators of Bacterial Flagella |
Q33871108 | Gene Transfer Agent Promotes Evolvability within the Fittest Subpopulation of a Bacterial Pathogen |
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Q92159079 | High-throughput time-resolved morphology screening in bacteria reveals phenotypic responses to antibiotics |
Q34927322 | High-throughput, quantitative analyses of genetic interactions in E. coli |
Q37418450 | How do bacteria localize proteins to the cell pole? |
Q34740554 | Identification of Escherichia coli ZapC (YcbW) as a component of the division apparatus that binds and bundles FtsZ polymers |
Q61800053 | Identification of Genes Involved in Biogenesis of Outer Membrane Vesicles (OMVs) in Serovar Typhi |
Q46463260 | Identification of New Virulence Factors and Vaccine Candidates for Yersinia pestis |
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Q41491505 | Increased Outer Membrane Vesicle Formation in a Helicobacter pylori tolB Mutant |
Q57910516 | Induced conformational changes activate the peptidoglycan synthase PBP1B |
Q36422274 | Interactions of the energy transducer TonB with noncognate energy-harvesting complexes |
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Q42154160 | Interplay between Penicillin-binding proteins and SEDS proteins promotes bacterial cell wall synthesis |
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Q38055247 | Lipoproteins in bacteria: structures and biosynthetic pathways |
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Q34719857 | Mapping the interactions between Escherichia coli TolQ transmembrane segments |
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Q38856034 | Membrane remodelling in bacteria |
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Q33876882 | Multiple interaction domains in FtsL, a protein component of the widely conserved bacterial FtsLBQ cell division complex. |
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Q37438985 | New fluorescence microscopy methods for microbiology: sharper, faster, and quantitative |
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Q33387670 | Proinflammatory effect in whole blood by free soluble bacterial components released from planktonic and biofilm cells |
Q36788005 | Proteolysis of BB0323 results in two polypeptides that impact physiologic and infectious phenotypes in Borrelia burgdorferi |
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Q34453150 | Roles for both FtsA and the FtsBLQ subcomplex in FtsN-stimulated cell constriction in Escherichia coli. |
Q53686632 | Salmonella Tol-Pal reduces outer-membrane glycerophopholipid levels for envelope homeostasis and survival during bacteremia. |
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Q27656662 | The crystal structure of the TolB box of colicin A in complex with TolB reveals important differences in the recruitment of the common TolB translocation portal used by group A colicins |
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Q39158631 | The divisome at 25: the road ahead. |
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Q53521792 | The essential cell division protein FtsN interacts with the murein (peptidoglycan) synthase PBP1B in Escherichia coli. |
Q90245651 | The lipoprotein Pal stabilises the bacterial outer membrane during constriction by a mobilisation-and-capture mechanism |
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Q39137955 | The multicellular nature of filamentous heterocyst-forming cyanobacteria. |
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Q38065215 | The physiology of bacterial cell division |
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