scholarly article | Q13442814 |
P2093 | author name string | J. P. Armitage | |
G. A. O'Toole | |||
E. A. Snavely | |||
L. M. Filkins | |||
N. J. Delalez | |||
S. L. Kuchma | |||
P2860 | cites work | The c-di-GMP binding protein YcgR controls flagellar motor direction and speed to affect chemotaxis by a "backstop brake" mechanism | Q24624328 |
Cell cycle-dependent dynamic localization of a bacterial response regulator with a novel di-guanylate cyclase output domain | Q24627219 | ||
Get the message out: cyclic-Di-GMP regulates multiple levels of flagellum-based motility | Q24657841 | ||
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GGDEF and EAL domains inversely regulate cyclic di-GMP levels and transition from sessility to motility | Q27976509 | ||
Flagellar and twitching motility are necessary for Pseudomonas aeruginosa biofilm development | Q27976516 | ||
The bacterial flagellar motor: structure and function of a complex molecular machine | Q28252092 | ||
Genes involved in matrix formation in Pseudomonas aeruginosa PA14 biofilms | Q28492476 | ||
Cleavage, methylation, and localization of the Pseudomonas aeruginosa export proteins XcpT, -U, -V, and -W | Q28492647 | ||
SadB is required for the transition from reversible to irreversible attachment during biofilm formation by Pseudomonas aeruginosa PA14 | Q28492651 | ||
Evidence for two flagellar stators and their role in the motility of Pseudomonas aeruginosa | Q28492878 | ||
BifA, a cyclic-Di-GMP phosphodiesterase, inversely regulates biofilm formation and swarming motility by Pseudomonas aeruginosa PA14. | Q28492929 | ||
The complex flagellar torque generator of Pseudomonas aeruginosa | Q28492947 | ||
The FleQ protein from Pseudomonas aeruginosa functions as both a repressor and an activator to control gene expression from the pel operon promoter in response to c-di-GMP | Q28493013 | ||
Pseudomonas aeruginosa GacA, a factor in multihost virulence, is also essential for biofilm formation | Q28493025 | ||
Identification of FleQ from Pseudomonas aeruginosa as a c-di-GMP-responsive transcription factor | Q28493129 | ||
A broad-host-range Flp-FRT recombination system for site-specific excision of chromosomally-located DNA sequences: application for isolation of unmarked Pseudomonas aeruginosa mutants | Q29547327 | ||
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A bacterial two-hybrid system based on a reconstituted signal transduction pathway | Q29617862 | ||
Regulation of cellulose synthesis in Acetobacter xylinum by cyclic diguanylic acid | Q29620651 | ||
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Stoichiometry and turnover in single, functioning membrane protein complexes. | Q33257539 | ||
Deletion mutant library for investigation of functional outputs of cyclic diguanylate metabolism in Pseudomonas aeruginosa PA14. | Q33601771 | ||
Cyclic-di-GMP-mediated repression of swarming motility by Pseudomonas aeruginosa: the pilY1 gene and its impact on surface-associated behaviors | Q33983265 | ||
The MotA protein of E. coli is a proton-conducting component of the flagellar motor | Q34182677 | ||
Identification and characterization of a cyclic di-GMP-specific phosphodiesterase and its allosteric control by GTP. | Q34430793 | ||
PilZ domain is part of the bacterial c-di-GMP binding protein | Q34462823 | ||
The PilZ domain is a receptor for the second messenger c-di-GMP: the PilZ domain protein YcgR controls motility in enterobacteria | Q34559000 | ||
Cell-cell signaling in Xanthomonas campestris involves an HD-GYP domain protein that functions in cyclic di-GMP turnover. | Q34597994 | ||
The maximum number of torque-generating units in the flagellar motor of Escherichia coli is at least 11 | Q34650102 | ||
Structural and mechanistic determinants of c-di-GMP signalling | Q35003079 | ||
The rotary motor of bacterial flagella | Q35034069 | ||
Identification of flgZ as a flagellar gene encoding a PilZ domain protein that regulates swimming motility and biofilm formation in Pseudomonas | Q35087901 | ||
Flagellar movement driven by proton translocation | Q35146235 | ||
Cyclic di-guanosine-monophosphate comes of age: a novel secondary messenger involved in modulating cell surface structures in bacteria? | Q35737977 | ||
Inverse regulation of biofilm formation and swarming motility by Pseudomonas aeruginosa PA14 | Q35759797 | ||
Distinct roles of highly conserved charged residues at the MotA-FliG interface in bacterial flagellar motor rotation | Q36559339 | ||
Second messenger regulation of biofilm formation: breakthroughs in understanding c-di-GMP effector systems | Q37074141 | ||
Load-dependent assembly of the bacterial flagellar motor | Q37105691 | ||
Molecular motors of the bacterial flagella | Q37291882 | ||
Electrostatic interactions between rotor and stator in the bacterial flagellar motor | Q37421534 | ||
Tuning the flagellar motor | Q37702667 | ||
Positive control of swarming, rhamnolipid synthesis, and lipase production by the posttranscriptional RsmA/RsmZ system in Pseudomonas aeruginosa PAO1. | Q37734986 | ||
Protein dynamics and mechanisms controlling the rotational behaviour of the bacterial flagellar motor | Q37940123 | ||
You've come a long way: c-di-GMP signaling | Q37973939 | ||
Two genetic loci produce distinct carbohydrate-rich structural components of the Pseudomonas aeruginosa biofilm matrix | Q40993746 | ||
Saccharomyces cerevisiae-based molecular tool kit for manipulation of genes from gram-negative bacteria | Q41485900 | ||
Minor pilins of the type IV pilus system participate in the negative regulation of swarming motility | Q42106502 | ||
Coordinated cyclic-di-GMP repression of Salmonella motility through YcgR and cellulose | Q42721538 | ||
Cyclic diguanylate (c-di-GMP) regulates Vibrio cholerae biofilm formation. | Q42851824 | ||
A post-translational, c-di-GMP-dependent mechanism regulating flagellar motility | Q43073468 | ||
Second messenger-mediated adjustment of bacterial swimming velocity | Q44130151 | ||
Plate-based assay for swarming motility in Pseudomonas aeruginosa | Q47597702 | ||
Charged residues in the cytoplasmic loop of MotA are required for stator assembly into the bacterial flagellar motor. | Q50044992 | ||
Restoration of torque in defective flagellar motors. | Q52249128 | ||
Allelic exchange in Pseudomonas aeruginosa using novel ColE1-type vectors and a family of cassettes containing a portable oriT and the counter-selectable Bacillus subtilis sacB marker | Q68129217 | ||
Two novel flagellar components and H-NS are involved in the motor function of Escherichia coli | Q73076418 | ||
Charged residues of the rotor protein FliG essential for torque generation in the flagellar motor of Escherichia coli | Q73221940 | ||
Residues of the cytoplasmic domain of MotA essential for torque generation in the bacterial flagellar motor | Q73820872 | ||
Roles for flagellar stators in biofilm formation by Pseudomonas aeruginosa | Q80392603 | ||
Two different stator systems drive a single polar flagellum in Shewanella oneidensis MR-1 | Q83242265 | ||
Plate-based assay for swimming motility in Pseudomonas aeruginosa | Q87855852 | ||
P4510 | describes a project that uses | ImageJ | Q1659584 |
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Pseudomonas aeruginosa | Q31856 |
P304 | page(s) | 420–430 | |
P577 | publication date | 2015-02-01 | |
P1433 | published in | Journal of Bacteriology | Q478419 |
P1476 | title | Cyclic di-GMP-mediated repression of swarming motility by Pseudomonas aeruginosa PA14 requires the MotAB stator | |
P478 | volume | 197 |
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