scholarly article | Q13442814 |
P2093 | author name string | J D Fetherston | |
R D Perry | |||
J W Lillard | |||
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A single amino acid change in AngR, a protein encoded by pJM1-like virulence plasmids, results in hyperproduction of anguibactin | Q33604307 | ||
Regulation of the iron uptake system in Vibrio anguillarum: evidence for a cooperative effect between two transcriptional activators | Q33856152 | ||
Siderochrome production by Yersinia pestis and its relation to virulence | Q34131403 | ||
Trans-complementation-dependent replication of a low molecular weight origin fragment from plasmid R6K | Q34283824 | ||
The gene coding for the 190,000-dalton iron-regulated protein of Yersinia species is present only in the highly pathogenic strains | Q35131521 | ||
Pleiotropic effects of a Yersinia pestis fur mutation | Q35983859 | ||
FptA, the Fe(III)-pyochelin receptor of Pseudomonas aeruginosa: a phenolate siderophore receptor homologous to hydroxamate siderophore receptors | Q36104644 | ||
High-molecular-weight protein 2 of Yersinia enterocolitica is homologous to AngR of Vibrio anguillarum and belongs to a family of proteins involved in nonribosomal peptide synthesis | Q36121385 | ||
Identification and cloning of a fur regulatory gene in Yersinia pestis | Q36125298 | ||
Evolutionary relationship between the TonB-dependent outer membrane transport proteins: nucleotide and amino acid sequences of the Escherichia coli colicin I receptor gene | Q36174455 | ||
Transcriptional regulation by iron of a Vibrio cholerae virulence gene and homology of the gene to the Escherichia coli fur system | Q36191893 | ||
Positive selection procedure for entrapment of insertion sequence elements in gram-negative bacteria | Q36279805 | ||
Genetic analysis of the low calcium response in Yersinia pestis mu d1(Ap lac) insertion mutants | Q36304161 | ||
Mutations to tolerance and resistance to pesticin and colicins in Escherichia coli phi. | Q36317692 | ||
Accumulation of iron by yersiniae | Q36338685 | ||
The pesticin receptor of Yersinia enterocolitica: a novel virulence factor with dual function | Q36729262 | ||
Construction of an eae deletion mutant of enteropathogenic Escherichia coli by using a positive-selection suicide vector | Q36989608 | ||
Expression of iron-regulated proteins in Yersinia species and their relation to virulence | Q37015778 | ||
Resistance to pesticin, storage of iron, and invasion of HeLa cells by Yersiniae | Q37017062 | ||
Comparison of siderophore production and utilization in pathogenic and environmental isolates of Yersinia enterocolitica | Q37069526 | ||
In vivo comparison of avirulent Vwa- and Pgm- or Pstr phenotypes of yersiniae | Q37097219 | ||
Positive transcriptional regulation of an iron-regulated virulence gene in Vibrio cholerae | Q37395794 | ||
Identification and cloning of a hemin storage locus involved in the pigmentation phenotype of Yersinia pestis | Q37608986 | ||
Molecular aspects of regulation of high affinity iron absorption in microorganisms. | Q37953531 | ||
Cloning and nucleotide sequence analysis of the ferripyoverdine receptor gene fpvA of Pseudomonas aeruginosa | Q39929594 | ||
Cloning and sequence analysis of a gene (pchR) encoding an AraC family activator of pyochelin and ferripyochelin receptor synthesis in Pseudomonas aeruginosa | Q39936952 | ||
Novel two-component transmembrane transcription control: regulation of iron dicitrate transport in Escherichia coli K-12. | Q39951971 | ||
Enterobactin-mediated iron transport in Pseudomonas aeruginosa | Q39952078 | ||
Genetics of the iron dicitrate transport system of Escherichia coli | Q39953452 | ||
Chapter 27 Two-Dimensional Polyacrylamide Gel Electrophoretic Fractionation | Q40085913 | ||
The virulence-enhancing effect of iron on nonpigmented mutants of virulent strains of Pasteurella pestis. | Q40294207 | ||
Congo Red-Agar Plating Medium for Detecting Pigmentation in Pasteurella pestis | Q40719844 | ||
Acquisition and storage of inorganic iron and hemin by the yersiniae | Q40733049 | ||
Role for the outer membrane ferric siderophore receptor PupB in signal transduction across the bacterial cell envelope | Q40792238 | ||
The pigmentation locus of Yersinia pestis KIM6+ is flanked by an insertion sequence and includes the structural genes for pesticin sensitivity and HMWP2. | Q41498763 | ||
Purification of yersiniabactin: a siderophore and possible virulence factor of Yersinia enterocolitica | Q41502129 | ||
Virulence of Yersinia enterocolitica is closely associated with siderophore production, expression of an iron-repressible outer membrane polypeptide of 65,000 Da and pesticin sensitivity | Q41503520 | ||
Loss of the pigmentation phenotype in Yersinia pestis is due to the spontaneous deletion of 102 kb of chromosomal DNA which is flanked by a repetitive element | Q41505380 | ||
Fur regulation in Yersinia species. | Q41505412 | ||
Analysis of Yersinia pestis chromosomal determinants Pgm+ and Psts associated with virulence. | Q41506457 | ||
Molecular cloning, iron-regulation and mutagenesis of the irp2 gene encoding HMWP2, a protein specific for the highly pathogenic Yersinia | Q41506793 | ||
A highly efficient electroporation system for transformation of Yersinia | Q41511984 | ||
Outer membrane peptides of Yersinia pestis mediating siderophore-independent assimilation of iron | Q41515579 | ||
Nucleotide sequence of the gene for the ferrienterochelin receptor FepA in Escherichia coli. Homology among outer membrane receptors that interact with TonB. | Q41791003 | ||
The ferric-pseudobactin receptor PupA of Pseudomonas putida WCS358: homology to TonB-dependent Escherichia coli receptors and specificity of the protein | Q42613045 | ||
Characterization of a Vibrio cholerae virulence factor homologous to the family of TonB-dependent proteins | Q44399239 | ||
Universal chemical assay for the detection and determination of siderophores. | Q50905929 | ||
The purified SoxABCD quinol oxidase complex of Sulfolobus acidocaldarius contains a novel haem. | Q54026689 | ||
A simple method for the preparation of large quantities of pure plasmid DNA. | Q54100886 | ||
Citrate-dependent iron transport system in Escherichia coli K-12. | Q54534090 | ||
Siderophore-specific induction of iron uptake in Pseudomonas aeruginosa | Q67508797 | ||
Carboxy-terminal phenylalanine is essential for the correct assembly of a bacterial outer membrane protein | Q67914067 | ||
New Tn10 derivatives for transposon mutagenesis and for construction of lacZ operon fusions by transposition | Q72413204 | ||
A small cosmid for efficient cloning of large DNA fragments | Q72886903 | ||
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Yersinia pestis | Q153875 |
P304 | page(s) | 1824-1833 | |
P577 | publication date | 1995-04-01 | |
P1433 | published in | Journal of Bacteriology | Q478419 |
P1476 | title | Analysis of the pesticin receptor from Yersinia pestis: role in iron-deficient growth and possible regulation by its siderophore | |
P478 | volume | 177 |
Q33992155 | A functional 4-hydroxysalicylate/hydroxyquinol degradative pathway gene cluster is linked to the initial dibenzo-p-dioxin pathway genes in Sphingomonas sp. strain RW1. |
Q35959243 | ATP-binding cassette transporters are targets for the development of antibacterial vaccines and therapies |
Q28344997 | Acyl-CoA hydrolysis by the high molecular weight protein 1 subunit of yersiniabactin synthetase: mutational evidence for a cascade of four acyl-enzyme intermediates during hydrolytic editing |
Q32100563 | An ABC transporter system of Yersinia pestis allows utilization of chelated iron by Escherichia coli SAB11. |
Q30156986 | Analysis of HmsH and its role in plague biofilm formation |
Q39492348 | Antimicrobial properties of pyridine-2,6-dithiocarboxylic acid, a metal chelator produced by Pseudomonas spp. |
Q64230622 | Application of filamentous phages in environment: A tectonic shift in the science and practice of ecorestoration |
Q34747000 | Biofilm formation is not required for early-phase transmission of Yersinia pestis |
Q35617313 | Characterization of a large chromosomal "high-pathogenicity island" in biotype 1B Yersinia enterocolitica. |
Q34007128 | Characterization of the Yersinia pestis Yfu ABC inorganic iron transport system |
Q39512306 | Common and specific characteristics of the high-pathogenicity island of Yersinia enterocolitica |
Q37599376 | Developing live vaccines against plague. |
Q40927166 | Environmental modulation of gene expression and pathogenesis in Yersinia |
Q34457319 | Evaluation of Psn, HmuR and a modified LcrV protein delivered to mice by live attenuated Salmonella as a vaccine against bubonic and pneumonic Yersinia pestis challenge |
Q33637474 | Evaluation of YadC protein delivered by live attenuated Salmonella as a vaccine against plague |
Q28492815 | ExsA and LcrF recognize similar consensus binding sites, but differences in their oligomeric state influence interactions with promoter DNA |
Q30788549 | Ferric enterochelin transport in Yersinia enterocolitica: molecular and evolutionary aspects. |
Q35546294 | Genetic organization of the yersiniabactin biosynthetic region and construction of avirulent mutants in Yersinia pestis |
Q34102972 | Genome-wide mutant fitness profiling identifies nutritional requirements for optimal growth of Yersinia pestis in deep tissue |
Q37191735 | Genomic islands of uropathogenic Escherichia coli contribute to virulence |
Q35217472 | Hierarchy of iron uptake systems: Yfu and Yiu are functional in Yersinia pestis |
Q33992694 | High-frequency RecA-dependent and -independent mechanisms of Congo red binding mutations in Yersinia pestis |
Q33207514 | HmsP, a putative phosphodiesterase, and HmsT, a putative diguanylate cyclase, control Hms-dependent biofilm formation in Yersinia pestis |
Q35621220 | Homology with a repeated Yersinia pestis DNA sequence IS100 correlates with pesticin sensitivity in Yersinia pseudotuberculosis |
Q33552328 | Identification and characterization of the hemophore-dependent heme acquisition system of Yersinia pestis |
Q35783832 | Identification of candidates for a subunit vaccine against extraintestinal pathogenic Escherichia coli |
Q31974757 | Iron acquisition in plague: modular logic in enzymatic biogenesis of yersiniabactin by Yersinia pestis. |
Q35510222 | Iron uptake and iron-repressible polypeptides in Yersinia pestis |
Q35959577 | Manganese transporters Yfe and MntH are Fur-regulated and important for the virulence of Yersinia pestis |
Q34001362 | Molecular characterization of the hemin uptake locus (hmu) from Yersinia pestis and analysis of hmu mutants for hemin and hemoprotein utilization. |
Q34077180 | Phenotypic convergence mediated by GGDEF-domain-containing proteins |
Q38813137 | Plague Vaccines: Status and Future |
Q33236998 | Polyamines are essential for the formation of plague biofilm |
Q34576174 | Polyamines are required for the expression of key Hms proteins important for Yersinia pestis biofilm formation |
Q33527554 | Proteomic analysis of iron acquisition, metabolic and regulatory responses of Yersinia pestis to iron starvation |
Q34584584 | Purification, priming, and catalytic acylation of carrier protein domains in the polyketide synthase and nonribosomal peptidyl synthetase modules of the HMWP1 subunit of yersiniabactin synthetase |
Q34747007 | Reduced synthesis of the Ybt siderophore or production of aberrant Ybt-like molecules activates transcription of yersiniabactin genes in Yersinia pestis |
Q34009406 | Regulation of the cytotoxic enterotoxin gene in Aeromonas hydrophila: characterization of an iron uptake regulator |
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Q27679549 | Structural engineering of a phage lysin that targets Gram-negative pathogens |
Q104103245 | Structure elucidation of yersiniabactin, a siderophore from highly virulentYersinia strains |
Q34684486 | Systematic analysis of cyclic di-GMP signalling enzymes and their role in biofilm formation and virulence in Yersinia pestis |
Q36574864 | Temperature regulation of the hemin storage (Hms+) phenotype of Yersinia pestis is posttranscriptional |
Q30756935 | The 102-kilobase pgm locus of Yersinia pestis: sequence analysis and comparison of selected regions among different Yersinia pestis and Yersinia pseudotuberculosis strains |
Q33729765 | The 102-kilobase unstable region of Yersinia pestis comprises a high-pathogenicity island linked to a pigmentation segment which undergoes internal rearrangement |
Q34552737 | The ATP-dependent ClpXP and Lon proteases regulate expression of the Yersinia pestis type III secretion system via regulated proteolysis of YmoA, a small histone-like protein |
Q35618155 | The Bradyrhizobium japonicum fegA gene encodes an iron-regulated outer membrane protein with similarity to hydroxamate-type siderophore receptors |
Q33952323 | The Yersinia high-pathogenicity island: an iron-uptake island |
Q34044097 | The Yersinia pestis siderophore, yersiniabactin, and the ZnuABC system both contribute to zinc acquisition and the development of lethal septicaemic plague in mice. |
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Q41483783 | The high-pathogenicity island of Yersinia pseudotuberculosis can be inserted into any of the three chromosomal asn tRNA genes |
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Q33509883 | TonB-dependent transporters and their occurrence in cyanobacteria |
Q41435969 | Yersinia ironomics: comparison of iron transporters among Yersinia pestis biotypes and its nearest neighbor, Yersinia pseudotuberculosis |
Q33966698 | Yersinia pestis TonB: role in iron, heme, and hemoprotein utilization |
Q34007591 | Yersinia pestis YbtU and YbtT are involved in synthesis of the siderophore yersiniabactin but have different effects on regulation |
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Q38765764 | Zinc transporters YbtX and ZnuABC are required for the virulence of Yersinia pestis in bubonic and pneumonic plague in mice. |
Q34309672 | Znu Is the Predominant Zinc Importer in Yersinia pestis during In Vitro Growth but Is Not Essential for Virulence |
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