review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Michael J Petris | |
Erik Ladomersky | |||
P2860 | cites work | Elemental analysis of Mycobacterium avium-, Mycobacterium tuberculosis-, and Mycobacterium smegmatis-containing phagosomes indicates pathogen-induced microenvironments within the host cell's endosomal system | Q81300400 |
The cop operon is required for copper homeostasis and contributes to virulence in Streptococcus pneumoniae | Q84516987 | ||
The Staphylococcus aureus CsoR regulates both chromosomal and plasmid-encoded copper resistance mechanisms | Q84666106 | ||
Crystal structure and electron transfer kinetics of CueO, a multicopper oxidase required for copper homeostasis in Escherichia coli | Q24531093 | ||
Resistance mechanisms of Mycobacterium tuberculosis against phagosomal copper overload | Q27026445 | ||
A redox switch in CopC: An intriguing copper trafficking protein that binds copper(I) and copper(II) at different sites | Q27640760 | ||
A strategy for the NMR characterization of type II copper(II) proteins: the case of the copper trafficking protein CopC from Pseudomonas Syringae | Q27641422 | ||
Molecular basis of metal-ion selectivity and zeptomolar sensitivity by CueR | Q27641964 | ||
Crystal Structure of the Membrane Fusion Protein CusB from Escherichia coli | Q27657097 | ||
A new structural paradigm in copper resistance in Streptococcus pneumoniae | Q27676018 | ||
Copper-transporting P-type ATPases use a unique ion-release pathway | Q27680830 | ||
A novel copper-responsive regulon in Mycobacterium tuberculosis | Q28486641 | ||
CsoR is a novel Mycobacterium tuberculosis copper-sensing transcriptional regulator | Q28486657 | ||
CtpV: a putative copper exporter required for full virulence of Mycobacterium tuberculosis | Q28487128 | ||
Identification of a copper-binding metallothionein in pathogenic mycobacteria | Q28487141 | ||
CsoR regulates the copper efflux operon copZA in Bacillus subtilis | Q29346694 | ||
Switch or funnel: how RND-type transport systems control periplasmic metal homeostasis. | Q30484886 | ||
Identification of a copper-responsive two-component system on the chromosome of Escherichia coli K-12. | Q30928410 | ||
A role for the ATP7A copper-transporting ATPase in macrophage bactericidal activity | Q33553377 | ||
The multi-copper-ion oxidase CueO of Salmonella enterica serovar Typhimurium is required for systemic virulence | Q33826068 | ||
Mechanism of ATPase-mediated Cu+ export and delivery to periplasmic chaperones: the interaction of Escherichia coli CopA and CusF | Q33946990 | ||
Copper homeostasis in Salmonella is atypical and copper-CueP is a major periplasmic metal complex | Q34055736 | ||
Exploiting innate immune cell activation of a copper-dependent antimicrobial agent during infection | Q34219760 | ||
Old iron, young copper: from Mars to Venus | Q34338955 | ||
Tracking metal ions through a Cu/Ag efflux pump assigns the functional roles of the periplasmic proteins | Q34442184 | ||
Evolution and diversity of periplasmic proteins involved in copper homeostasis in gamma proteobacteria. | Q34465965 | ||
Copper resistance is essential for virulence of Mycobacterium tuberculosis | Q34534178 | ||
Impact of copper limitation on expression and function of multicopper oxidases (ferroxidases) | Q34729814 | ||
Human and swine hosts share vancomycin-resistant Enterococcus faecium CC17 and CC5 and Enterococcus faecalis CC2 clonal clusters harboring Tn1546 on indistinguishable plasmids | Q34741076 | ||
Interactions between CusF and CusB identified by NMR spectroscopy and chemical cross-linking coupled to mass spectrometry | Q34773859 | ||
Identification of Mycobacterium tuberculosis RNAs synthesized in response to phagocytosis by human macrophages by selective capture of transcribed sequences (SCOTS) | Q35656072 | ||
Intracellular copper does not catalyze the formation of oxidative DNA damage in Escherichia coli | Q35759338 | ||
Bacterial infection as assessed by in vivo gene expression | Q35966527 | ||
Copper metabolism during acute inflammation: studies on liver and serum copper concentrations in normal and inflamed rats | Q36097699 | ||
The role of diet and the reticuloendothelial system in the response of rats to Salmonella typhilmurium infection | Q36168069 | ||
Toward a molecular understanding of metal transport by P(1B)-type ATPases | Q36432934 | ||
Copper trafficking to the mitochondrion and assembly of copper metalloenzymes | Q36456731 | ||
The mechanism of Cu+ transport ATPases: interaction with CU+ chaperones and the role of transient metal-binding sites. | Q36508768 | ||
Copper-boosting compounds: a novel concept for antimycobacterial drug discovery | Q36558441 | ||
The siderophore yersiniabactin binds copper to protect pathogens during infection | Q36692680 | ||
The structure and function of heavy metal transport P1B-ATPases. | Q36706247 | ||
Copper and zinc body levels in inflammation: an overview of the data obtained from animal and human studies | Q36762274 | ||
Copper transport into the secretory pathway is regulated by oxygen in macrophages | Q37166075 | ||
The iron-sulfur clusters of dehydratases are primary intracellular targets of copper toxicity | Q37208556 | ||
Response of gram-positive bacteria to copper stress. | Q37601995 | ||
Cupric yersiniabactin is a virulence-associated superoxide dismutase mimic | Q37602574 | ||
Copper resistance in Pseudomonas syringae mediated by periplasmic and outer membrane proteins | Q37603756 | ||
The copper-responsive RicR regulon contributes to Mycobacterium tuberculosis virulence | Q37621637 | ||
Highly reactive oxygen species: detection, formation, and possible functions. | Q37870856 | ||
Acute phase proteins in acute coronary syndrome: an up-to-date. | Q38020580 | ||
SOD1 aggregation and ALS: role of metallation states and disulfide status | Q38075887 | ||
Human copper-dependent amine oxidases. | Q38177145 | ||
Tyrosinase: the four oxidation states of the active site and their relevance to enzymatic activation, oxidation and inactivation | Q38198344 | ||
Transcriptional activation of an Escherichia coli copper efflux regulon by the chromosomal MerR homologue, cueR. | Q38310027 | ||
Relationships between serum concentrations of C-reactive protein and micronutrients, in patients with tuberculosis. | Q39147140 | ||
Molecular analysis of the copper-transporting efflux system CusCFBA of Escherichia coli | Q39775113 | ||
Copper Hypersensitivity and Uptake in Pseudomonas syringae Containing Cloned Components of the Copper Resistance Operon | Q39857609 | ||
3,3'-Diindolylmethane and genistein decrease the adverse effects of estrogen in LNCaP and PC-3 prostate cancer cells | Q39913846 | ||
Indigenous plasmids in Pseudomonas syringae pv. tomato: conjugative transfer and role in copper resistance | Q39964824 | ||
Plasmid-controlled resistance to copper in Escherichia coli | Q39976079 | ||
Linkage between catecholate siderophores and the multicopper oxidase CueO in Escherichia coli | Q40000513 | ||
Characteristics of fever and acute-phase response induced in rabbits by IL-1 and TNF. | Q40781130 | ||
Mutants in the CtpA copper transporting P-type ATPase reduce virulence of Listeria monocytogenes | Q41130491 | ||
CueR (YbbI) of Escherichia coli is a MerR family regulator controlling expression of the copper exporter CopA. | Q42640041 | ||
Role of copper in reducing hospital environment contamination | Q43311791 | ||
Trace element alterations in infectious diseases | Q43489850 | ||
Acute phase response in horses: changes in plasma cation concentrations after localised tissue injury | Q43495415 | ||
Mutations in the cueA gene encoding a copper homeostasis P-type ATPase reduce the pathogenicity of Pseudomonas aeruginosa in mice | Q43540663 | ||
CueO is a multi-copper oxidase that confers copper tolerance in Escherichia coli. | Q43722949 | ||
Copper deficiency increases the virulence of amyocarditic and myocarditic strains of coxsackievirus B3 in mice | Q44034936 | ||
Respiratory burst and candidacidal activity of peritoneal macrophages are impaired in copper-deficient rats | Q44059090 | ||
Effects of inflammation and antiinflammatory treatment on serum trace elements concentrations | Q44497690 | ||
AcrA is a highly asymmetric protein capable of spanning the periplasm | Q46186931 | ||
Copper stress causes an in vivo requirement for the Escherichia coli disulfide isomerase DsbC. | Q46640858 | ||
Essential trace elements selenium, zinc, copper, and iron concentrations and their related acute-phase proteins in patients with vivax malaria | Q48014379 | ||
The Bradyrhizobium japonicum fixGHIS genes are required for the formation of the high-affinity cbb3-type cytochrome oxidase | Q48064505 | ||
Menkes' disease: case report | Q48209920 | ||
Neuronal and vascular disorders of the brain and spinal cord in Menkes kinky hair disease | Q48249207 | ||
The sctR of Salmonella enterica serova Typhimurium encoding a homologue of MerR protein is involved in the copper-responsive regulation of cuiD. | Q48303329 | ||
Biodistribution of 64Cu in inflamed rats following administration of two anti-inflammatory copper complexes | Q48449768 | ||
Difficulties in the neonatal diagnosis of Menkes' kinky hair syndrome--trichopoliodystrophy | Q48628210 | ||
The copper supply pathway to a Salmonella Cu,Zn-superoxide dismutase (SodCII) involves P(1B)-type ATPase copper efflux and periplasmic CueP. | Q50020969 | ||
GolS controls the response to gold by the hierarchical induction of Salmonella-specific genes that include a CBA efflux-coding operon | Q50067863 | ||
Bacterial sensing of and resistance to gold salts. | Q50074078 | ||
Clinical and biochemical consequences of copper-histidine therapy in Menkes disease. | Q52222718 | ||
Corynebacterium glutamicum CsoR acts as a transcriptional repressor of two copper/zinc-inducible P(1B)-type ATPase operons. | Q52631035 | ||
Interaction of nutrition and infection: effect of copper deficiency on resistance to Trypanosoma lewisi. | Q54264859 | ||
Copper resistance in E. coli: the multicopper oxidase PcoA catalyzes oxidation of copper(I) in Cu(I)Cu(II)-PcoC. | Q54421399 | ||
Correlation of hypercupremia with other acute phase reactants in malignant lymphoma. | Q54472488 | ||
Trace elements and some extracellular antioxidant proteins levels in serum of patients with systemic lupus erythematosus. | Q54785143 | ||
Copper status and function of neutrophils are reversibly depressed in marginally and severely copper-deficient rats | Q68490471 | ||
Redistribution of minerals and trace elements in chronic inflammation--a study on isolated blood cells from patients with ankylosing spondylitis | Q69229759 | ||
Serum copper concentration as an index of experimental lung injury | Q69274073 | ||
Copper deficiency suppresses the immune response of mice | Q70810089 | ||
The effect of copper deficiency on the resistance of mice to infection with Pasteurella haemolytica | Q71709747 | ||
Effects of metal chelating agents on the oxidation of lipids induced by copper and iron | Q72648811 | ||
Some effects of copper deficiency on leucocyte function in sheep and cattle | Q72919151 | ||
Effects of selenium and copper deficiency on neutrophil function in cattle | Q72936432 | ||
The independent cue and cus systems confer copper tolerance during aerobic and anaerobic growth in Escherichia coli | Q74001289 | ||
The Haber-Weiss cycle -- 70 years later: an alternative view | Q78021420 | ||
P433 | issue | 6 | |
P304 | page(s) | 957-964 | |
P577 | publication date | 2015-06-01 | |
P1433 | published in | Metallomics | Q3307262 |
P1476 | title | Copper tolerance and virulence in bacteria | |
P478 | volume | 7 |
Q56988952 | An important role for periplasmic storage in Pseudomonas aeruginosa copper homeostasis revealed by a combined experimental and computational modeling study |
Q28073414 | Bacterial Proteasomes: Mechanistic and Functional Insights |
Q38679535 | Biotechnological and Biochemical Utilization of Lignin |
Q36103181 | Candida albicans adapts to host copper during infection by swapping metal cofactors for superoxide dismutase |
Q55338658 | Chemical Warfare at the Microorganismal Level: A Closer Look at the Superoxide Dismutase Enzymes of Pathogens. |
Q98467209 | Chromium-catechin complex, synthesis and toxicity check using bacterial models |
Q90153840 | Comparative differential cuproproteomes of Rhodobacter capsulatus reveal novel copper homeostasis related proteins |
Q92879087 | CopA Protects Streptococcus suis against Copper Toxicity |
Q52647045 | Copper Influences the Antibacterial Outcomes of a β-Lactamase-Activated Prochelator against Drug-Resistant Bacteria. |
Q40392431 | Copper Is a Host Effector Mobilized to Urine during Urinary Tract Infection To Impair Bacterial Colonization. |
Q33736716 | Copper Resistance in Aspergillus nidulans Relies on the PI-Type ATPase CrpA, Regulated by the Transcription Factor AceA. |
Q89965275 | Copper and Melanin Play a Role in Myxococcus xanthus Predation on Sinorhizobium meliloti |
Q27010264 | Copper at the Fungal Pathogen-Host Axis |
Q57801718 | Copper signalling: causes and consequences |
Q47781903 | Cytoplasmic Copper Detoxification in Salmonella Can Contribute to SodC Metalation but Is Dispensable during Systemic Infection |
Q91807691 | Development of Antibacterial Ti-Cux Alloys for Dental Applications: Effects of Ageing for Alloys with Up to 10 wt% Cu |
Q58780928 | Environmental Concentrations of Copper, Alone or in Mixture With Arsenic, Can Impact River Sediment Microbial Community Structure and Functions |
Q92733416 | Essential Gene Clusters Involved in Copper Tolerance Identified in Acinetobacter baumannii Clinical and Environmental Isolates |
Q55686770 | Experimental Warming Differentially Influences the Vulnerability of Phototrophic and Heterotrophic Periphytic Communities to Copper Toxicity. |
Q90633003 | Genetically encoded RNA-based sensors for intracellular imaging of silver ions |
Q116816598 | Genome analysis of Pollutimonas subterranea gen. nov., sp. nov. and Pollutimonas nitritireducens sp. nov., isolated from nitrate- and radionuclide-contaminated groundwater, and transfer of several Pusillimonas species into three new genera… |
Q97524200 | Genome wide transcriptomic analysis of the soil ammonia oxidizing archaeon Nitrososphaera viennensis upon exposure to copper limitation |
Q52334530 | Genome-wide analysis of the regulation of Cu metabolism in Cryptococcus neoformans. |
Q36064900 | Host-Imposed Copper Poisoning Impacts Fungal Micronutrient Acquisition during Systemic Candida albicans Infections |
Q49235486 | Identification of membrane-associated proteins with pathogenic potential expressed by Corynebacterium pseudotuberculosis grown in animal serum. |
Q60949768 | Insight Into the Diversity and Possible Role of Plasmids in the Adaptation of Psychrotolerant and Metalotolerant spp. to Extreme Antarctic Environments |
Q90455757 | Integrative Conjugative Element ICEHs1 Encodes for Antimicrobial Resistance and Metal Tolerance in Histophilus somni |
Q94599792 | Metallothioneins regulate ATP7A trafficking and control cell viability during copper deficiency and excess |
Q92060246 | New insights into copper homeostasis in filamentous fungi |
Q92828195 | Pathotyping the Zoonotic Pathogen Streptococcus suis: Novel Genetic Markers To Differentiate Invasive Disease-Associated Isolates from Non-Disease-Associated Isolates from England and Wales |
Q60938644 | Proteogenomic Analysis of BBCC367, a Relevant Marine Bacterium Isolated From the South Pacific Ocean |
Q92377301 | Random peptide mixtures entrapped within a copper-cuprite matrix: new antimicrobial agent against methicillin-resistant Staphylococcus aureus |
Q36204464 | Rapid bacteria identification from environmental mining samples using MALDI-TOF MS analysis |
Q90681006 | Relationships Between Copper-Related Proteomes and Lifestyles in β Proteobacteria |
Q50282683 | Relevance of tcrYAZB operon acquisition for Enterococcus survival at high copper concentrations under anaerobic conditions. |
Q64106903 | The Combined Effect of Cold and Copper Stresses on the Proliferation and Transcriptional Response of |
Q27704298 | The CopC Family: Structural and Bioinformatic Insights into a Diverse Group of Periplasmic Copper Binding Proteins |
Q38704529 | The Yin and Yang of copper during infection |
Q40813624 | Towards understanding the biological function of the unusual chaperonin Cpn60.1 (GroEL1) of Mycobacterium tuberculosis |
Q40628234 | Understanding the 7-Cys module amplification of C. neoformans metallothioneins: how high capacity Cu-binding polypeptides are built to neutralize host nutritional immunity. |
Q91956794 | Whole-genome analysis of extraintestinal Escherichia coli sequence type 73 from a single hospital over a 2 year period identified different circulating clonal groups |
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