review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0065-2164(08)00608-4 |
P698 | PubMed publication ID | 19026867 |
P50 | author | Deenah Osman | Q56598976 |
Jennifer Cavet | Q42806437 | ||
P2860 | cites work | The copper chaperone for superoxide dismutase | Q24311669 |
Crystal structure and electron transfer kinetics of CueO, a multicopper oxidase required for copper homeostasis in Escherichia coli | Q24531093 | ||
The zntA gene of Escherichia coli encodes a Zn(II)-translocating P-type ATPase | Q24648949 | ||
Crystal structure of the Atx1 metallochaperone protein at 1.02 A resolution | Q27619033 | ||
Crystal structure of the bacterial membrane protein TolC central to multidrug efflux and protein export | Q27625163 | ||
Copper trafficking: the solution structure of Bacillus subtilis CopZ | Q27636919 | ||
Solution structure of the N-terminal domain of a potential copper-translocating P-type ATPase from Bacillus subtilis in the apo and Cu(I) loaded states | Q27638643 | ||
A new zinc-protein coordination site in intracellular metal trafficking: solution structure of the Apo and Zn(II) forms of ZntA(46-118) | Q27639912 | ||
Crystal structure and dimerization equilibria of PcoC, a methionine-rich copper resistance protein from Escherichia coli | Q27640072 | ||
A redox switch in CopC: An intriguing copper trafficking protein that binds copper(I) and copper(II) at different sites | Q27640760 | ||
Molecular basis of metal-ion selectivity and zeptomolar sensitivity by CueR | Q27641964 | ||
Structural basis for the function of the N-terminal domain of the ATPase CopA from Bacillus subtilis | Q27642229 | ||
Crystal structures of E. coli laccase CueO at different copper concentrations | Q27643511 | ||
Structure and function of the engineered multicopper oxidase CueO from Escherichia coli--deletion of the methionine-rich helical region covering the substrate-binding site | Q27647851 | ||
Cu(I) recognition via cation-π and methionine interactions in CusF | Q27649415 | ||
Crystal structure of a quinoenzyme: copper amine oxidase of Escherichia coli at 2 A resolution | Q27732565 | ||
Solution structure of the fourth metal-binding domain from the Menkes copper-transporting ATPase | Q27748799 | ||
Escherichia coli CopA N-terminal Cys(X)(2)Cys motifs are not required for copper resistance or transport. | Q43703942 | ||
CueO is a multi-copper oxidase that confers copper tolerance in Escherichia coli. | Q43722949 | ||
A copper metallochaperone for photosynthesis and respiration reveals metal-specific targets, interaction with an importer, and alternative sites for copper acquisition | Q43819785 | ||
Copper transfer from the Cu(I) chaperone, CopZ, to the repressor, Zn(II)CopY: metal coordination environments and protein interactions | Q43973869 | ||
Effects of Escherichia coli on iron, copper, and zinc metabolism in chicks | Q70232257 | ||
Characterization of an NADH-linked cupric reductase activity from the Escherichia coli respiratory chain | Q73050248 | ||
Sequential Changes in Fe, Cu, and Zn in Target Organs during Early Coxsackievirus B3 Infection in Mice | Q73327892 | ||
Purification and functional analysis of the copper ATPase CopA of Enterococcus hirae | Q73405469 | ||
Control of copper homeostasis in Escherichia coli by a P-type ATPase, CopA, and a MerR-like transcriptional activator, CopR | Q73414567 | ||
Copper homeostasis in Enterococcus hirae | Q73581016 | ||
The product of the ybdE gene of the Escherichia coli chromosome is involved in detoxification of silver ions | Q73703362 | ||
Characterization of YpmQ, an accessory protein required for the expression of cytochrome c oxidase in Bacillus subtilis | Q73850095 | ||
The independent cue and cus systems confer copper tolerance during aerobic and anaerobic growth in Escherichia coli | Q74001289 | ||
Copper activation of superoxide dismutase 1 (SOD1) in vivo. Role for protein-protein interactions with the copper chaperone for SOD1 | Q74177732 | ||
The Saccharomyces cerevisiae LYS7 gene is involved in oxidative stress protection | Q74267902 | ||
The Pco proteins are involved in periplasmic copper handling in Escherichia coli | Q74416536 | ||
The Enterococcus hirae copper chaperone CopZ delivers copper(I) to the CopY repressor | Q74589491 | ||
Interaction of the CopZ copper chaperone with the CopA copper ATPase of Enterococcus hirae assessed by surface plasmon resonance | Q74607691 | ||
Cu XAS shows a change in the ligation of CuB upon reduction of cytochrome bo3 from Escherichia coli | Q77293675 | ||
The Haber-Weiss cycle -- 70 years later: an alternative view | Q78021420 | ||
A periplasmic iron-binding protein contributes toward inward copper supply | Q79407657 | ||
Metal ion chaperone function of the soluble Cu(I) receptor Atx1. | Q27934215 | ||
The Menkes/Wilson disease gene homologue in yeast provides copper to a ceruloplasmin-like oxidase required for iron uptake | Q27935957 | ||
Transition Metal Speciation in the Cell: Insights from the Chemistry of Metal Ion Receptors | Q28203407 | ||
Two novel families of bacterial membrane proteins concerned with nodulation, cell division and transport | Q28244411 | ||
Pb(II)-translocating P-type ATPases | Q28289977 | ||
Molecular basis for resistance to silver cations in Salmonella | Q28296192 | ||
Copper chaperone for superoxide dismutase is essential to activate mammalian Cu/Zn superoxide dismutase | Q28343973 | ||
The global responses of Mycobacterium tuberculosis to physiological levels of copper | Q28486613 | ||
CotA of Bacillus subtilis is a copper-dependent laccase | Q28489037 | ||
Characterization of the CopR regulon of Lactococcus lactis IL1403. | Q29346584 | ||
CsoR regulates the copper efflux operon copZA in Bacillus subtilis | Q29346694 | ||
Femtomolar sensitivity of metalloregulatory proteins controlling zinc homeostasis | Q29615199 | ||
Characterization of the binding interface between the copper chaperone Atx1 and the first cytosolic domain of Ccc2 ATPase | Q30658366 | ||
Mechanism of Cu,Zn-superoxide dismutase activation by the human metallochaperone hCCS. | Q30936696 | ||
Purification and physical-chemical properties of methanobactin: a chalkophore from Methylosinus trichosporium OB3b | Q31156801 | ||
The Lys1010-Lys1325 fragment of the Wilson's disease protein binds nucleotides and interacts with the N-terminal domain of this protein in a copper-dependent manner | Q31504267 | ||
Identification of novel staphylococcal virulence genes by in vivo expression technology | Q32071107 | ||
Oxidation of phenolate siderophores by the multicopper oxidase encoded by the Escherichia coli yacK gene | Q33182249 | ||
Isolation of copper biochelates from Methylosinus trichosporium OB3b and soluble methane monooxygenase mutants. | Q33713318 | ||
Periplasmic superoxide dismutase protects Salmonella from products of phagocyte NADPH-oxidase and nitric oxide synthase. | Q33740986 | ||
The copper chelator methanobactin from Methylosinus trichosporium OB3b binds copper(I). | Q33829913 | ||
Metallochaperones, an intracellular shuttle service for metal ions | Q33902264 | ||
Function, structure, and mechanism of intracellular copper trafficking proteins | Q34275487 | ||
Old iron, young copper: from Mars to Venus | Q34338955 | ||
A Salmonella typhimurium genetic locus which confers copper tolerance on copper-sensitive mutants of Escherichia coli | Q34435806 | ||
Evolution of substrate specificities in the P-type ATPase superfamily. | Q34451276 | ||
Potential use of copper surfaces to reduce survival of epidemic meticillin-resistant Staphylococcus aureus in the healthcare environment. | Q34519768 | ||
The delivery of copper for thylakoid import observed by NMR. | Q34694034 | ||
CopA: An Escherichia coli Cu(I)-translocating P-type ATPase. | Q34972315 | ||
The MerR family of transcriptional regulators. | Q35164005 | ||
Escherichia coli mechanisms of copper homeostasis in a changing environment. | Q35164018 | ||
Role of prokaryotic Cu,Zn superoxide dismutase in pathogenesis | Q35594264 | ||
Identification of Mycobacterium tuberculosis RNAs synthesized in response to phagocytosis by human macrophages by selective capture of transcribed sequences (SCOTS) | Q35656072 | ||
P-type ATPase from the cyanobacterium Synechococcus 7942 related to the human Menkes and Wilson disease gene products | Q35803689 | ||
Bacterial infection as assessed by in vivo gene expression | Q35966527 | ||
Evidence for Cu(I)-thiolate ligation and prediction of a putative copper-binding site in the Escherichia coli NADH dehydrogenase-2. | Q44100726 | ||
Biochemical characterization of CopA, the Escherichia coli Cu(I)-translocating P-type ATPase. | Q44156003 | ||
An atypical linear Cu(I)-S2 center constitutes the high-affinity metal-sensing site in the CueR metalloregulatory protein | Q44602275 | ||
Involvement of reactive oxygen species in bacterial killing within epithelial cells | Q44786511 | ||
Solution structures of a cyanobacterial metallochaperone: insight into an atypical copper-binding motif | Q44838238 | ||
Susceptibility of different bacterial species isolated from food animals to copper sulphate, zinc chloride and antimicrobial substances used for disinfection | Q44890381 | ||
Methanobactin, a copper-acquisition compound from methane-oxidizing bacteria. | Q45054358 | ||
Identification of the transmembrane metal binding site in Cu+-transporting PIB-type ATPases | Q45115007 | ||
AcrA is a highly asymmetric protein capable of spanning the periplasm | Q46186931 | ||
The expression profile of Escherichia coli K-12 in response to minimal, optimal and excess copper concentrations | Q46427809 | ||
Synthesis, analytical characterization and bioactivity of Ag and Cu nanoparticles embedded in poly-vinyl-methyl-ketone films. | Q46609595 | ||
Spectral, kinetic, and thermodynamic properties of Cu(I) and Cu(II) binding by methanobactin from Methylosinus trichosporium OB3b | Q46918114 | ||
Substrate-linked conformational change in the periplasmic component of a Cu(I)/Ag(I) efflux system. | Q46983650 | ||
Chimeras of P-type ATPases and their transcriptional regulators: contributions of a cytosolic amino-terminal domain to metal specificity | Q47269242 | ||
Interaction kinetics of the copper-responsive CopY repressor with the cop promoter of Enterococcus hirae | Q47839920 | ||
Strain specificity in antimicrobial activity of silver and copper nanoparticles | Q47936694 | ||
Bacterial copper- and zinc-cofactored superoxide dismutase contributes to the pathogenesis of systemic salmonellosis | Q48046216 | ||
The functions of Sco proteins from genome-based analysis | Q48081560 | ||
Molecular characterization of an operon, cueAR, encoding a putative P1-type ATPase and a MerR-type regulatory protein involved in copper homeostasis in Pseudomonas putida | Q48284334 | ||
The sctR of Salmonella enterica serova Typhimurium encoding a homologue of MerR protein is involved in the copper-responsive regulation of cuiD. | Q48303329 | ||
GolS controls the response to gold by the hierarchical induction of Salmonella-specific genes that include a CBA efflux-coding operon | Q50067863 | ||
Dissecting the Salmonella response to copper. | Q50068979 | ||
Bacterial sensing of and resistance to gold salts. | Q50074078 | ||
The role of two periplasmic copper- and zinc-cofactored superoxide dismutases in the virulence of Salmonella choleraesuis | Q50110756 | ||
The regulation and role of the periplasmic copper, zinc superoxide dismutase of Escherichia coli | Q50126760 | ||
Susceptibility constants of Escherichia coli and Bacillus subtilis to silver and copper nanoparticles. | Q51093425 | ||
Copper and immunity. | Q52187809 | ||
Two trans-acting metalloregulatory proteins controlling expression of the copper-ATPases of Enterococcus hirae. | Q52511553 | ||
Cobalt-dependent transcriptional switching by a dual-effector MerR-like protein regulates a cobalt-exporting variant CPx-type ATPase. | Q52536197 | ||
Two Menkes-type atpases supply copper for photosynthesis in Synechocystis PCC 6803. | Q52542612 | ||
ZntR is a Zn(II)-responsive MerR-like transcriptional regulator of zntA in Escherichia coli. | Q54104280 | ||
DnaK plays a pivotal role in Tat targeting of CueO and functions beside SlyD as a general Tat signal binding chaperone. | Q54448739 | ||
The multicopper oxidase CutO confers copper tolerance to Rhodobacter capsulatus. | Q54470372 | ||
Transcriptional response of Escherichia coli to external copper. | Q54489547 | ||
Characterisation of CadR from Pseudomonas aeruginosa: a Cd(II)-responsive MerR homologue. | Q54520634 | ||
Measurement of cytoplasmic copper, silver, and gold with a lux biosensor shows copper and silver, but not gold, efflux by the CopA ATPase of Escherichia coli. | Q54522639 | ||
The Escherichia coli copper-responsive copA promoter is activated by gold. | Q54534686 | ||
Bacillus subtilis cytochrome oxidase mutants: biochemical analysis and genetic evidence for two aa3-type oxidases. | Q54693977 | ||
Role of a Streptococcus gordonii copper-transport operon, copYAZ, in biofilm detachment. | Q54696923 | ||
Changes in the total content of iron, copper, and zinc in serum, heart, liver, spleen, and skeletal muscle tissues of rats infected withTrypanosoma cruzi | Q58844301 | ||
CopZ fromBacillus subtilisinteracts in vivo with a copper exporting CPx-type ATPase CopA | Q60393072 | ||
Feed additive studies with newly weaned pigs: efficacy of supplemental copper, antibiotics and organic acids | Q70089756 | ||
Copper chaperone cycling and degradation in the regulation of the cop operon of Enterococcus hirae. | Q36255839 | ||
Understanding how cells allocate metals using metal sensors and metallochaperones | Q36289346 | ||
Virulent Salmonella typhimurium has two periplasmic Cu, Zn-superoxide dismutases | Q36398159 | ||
Multiple metal binding domains enhance the Zn(II) selectivity of the divalent metal ion transporter AztA | Q36580046 | ||
Structural basis for metal binding specificity: the N-terminal cadmium binding domain of the P1-type ATPase CadA. | Q36583819 | ||
The biogenesis of c-type cytochromes in Escherichia coli requires a membrane-bound protein, DipZ, with a protein disulphide isomerase-like domain | Q36688584 | ||
Atx1-like chaperones and their cognate P-type ATPases: copper-binding and transfer. | Q36709019 | ||
Copper resistance determinants in bacteria | Q36783743 | ||
Function and regulation of human copper-transporting ATPases | Q36872228 | ||
Basic and applied features of multicopper oxidases, CueO, bilirubin oxidase, and laccase | Q36896571 | ||
The temporal expression profile of Mycobacterium tuberculosis infection in mice. | Q37358252 | ||
Cuprous oxidase activity of CueO from Escherichia coli | Q37596274 | ||
Mechanisms for activating Cu- and Zn-containing superoxide dismutase in the absence of the CCS Cu chaperone | Q37646146 | ||
Functional analysis of chimeric proteins of the Wilson Cu(I)-ATPase (ATP7B) and ZntA, a Pb(II)/Zn(II)/Cd(II)-ATPase from Escherichia coli | Q38297342 | ||
Transcriptional activation of an Escherichia coli copper efflux regulon by the chromosomal MerR homologue, cueR. | Q38310027 | ||
DNA distortion mechanism for transcriptional activation by ZntR, a Zn(II)-responsive MerR homologue in Escherichia coli | Q38317199 | ||
Recent developments in trace element metabolism and function: trace elements, disease resistance and immune responsiveness in ruminants | Q38668911 | ||
Cloning and functional analysis of the pbr lead resistance determinant of Ralstonia metallidurans CH34. | Q39505004 | ||
Molecular analysis of the copper-transporting efflux system CusCFBA of Escherichia coli | Q39775113 | ||
Silver-resistant mutants of Escherichia coli display active efflux of Ag+ and are deficient in porins | Q39847399 | ||
ATP-dependent cadmium transport by the cadA cadmium resistance determinant in everted membrane vesicles of Bacillus subtilis | Q39932848 | ||
Linkage between catecholate siderophores and the multicopper oxidase CueO in Escherichia coli | Q40000513 | ||
Copper toxicity: Evidence for the conversion of cupric to cuprous copper in vivo under anaerobic conditions | Q40006968 | ||
Differential accumulation of Salmonella[Cu, Zn] superoxide dismutases SodCI and SodCII in intracellular bacteria: correlation with their relative contribution to pathogenicity | Q40699610 | ||
Construction and characterization of a mercury-independent MerR activator (MerRAC): transcriptional activation in the absence of Hg(II) is accompanied by DNA distortion. | Q40871898 | ||
Mutants in the CtpA copper transporting P-type ATPase reduce virulence of Listeria monocytogenes | Q41130491 | ||
Oxygen-induced maturation of SOD1: a key role for disulfide formation by the copper chaperone CCS. | Q41987289 | ||
A possible regulatory role for the metal-binding domain of CadA, the Listeria monocytogenes Cd2+-ATPase | Q42053104 | ||
Allosteric underwinding of DNA is a critical step in positive control of transcription by Hg-MerR | Q42617709 | ||
Molecular genetics and transport analysis of the copper-resistance determinant (pco) from Escherichia coli plasmid pRJ1004. | Q42627691 | ||
CueR (YbbI) of Escherichia coli is a MerR family regulator controlling expression of the copper exporter CopA. | Q42640041 | ||
Characterization of a copper-transport operon, copYAZ, from Streptococcus mutans | Q42644478 | ||
The Listeria monocytogenes gene ctpA encodes a putative P-type ATPase involved in copper transport | Q42650481 | ||
ActP controls copper homeostasis in Rhizobium leguminosarum bv. viciae and Sinorhizobium meliloti preventing low pH-induced copper toxicity | Q42673846 | ||
Molecular genetics of a chromosomal locus involved in copper tolerance in Escherichia coli K-12. | Q42679774 | ||
Copper resistance in Enterococcus faecium, mediated by the tcrB gene, is selected by supplementation of pig feed with copper sulfate | Q43153923 | ||
Mutations in the cueA gene encoding a copper homeostasis P-type ATPase reduce the pathogenicity of Pseudomonas aeruginosa in mice | Q43540663 | ||
The regulation of catalytic activity of the menkes copper-translocating P-type ATPase. Role of high affinity copper-binding sites | Q43617499 | ||
The cysteine-rich amino-terminal domain of ZntA, a Pb(II)/Zn(II)/Cd(II)-translocating ATPase from Escherichia coli, is not essential for its function | Q43644754 | ||
Copper stabilizes a heterodimer of the yCCS metallochaperone and its target superoxide dismutase | Q43687960 | ||
P921 | main subject | copper | Q753 |
bacteria | Q10876 | ||
P304 | page(s) | 217-247 | |
P577 | publication date | 2008-01-01 | |
P1433 | published in | Advances in Applied Microbiology | Q15753069 |
P1476 | title | Copper homeostasis in bacteria | |
P478 | volume | 65 |
Q56988952 | An important role for periplasmic storage in Pseudomonas aeruginosa copper homeostasis revealed by a combined experimental and computational modeling study |
Q38910492 | Bacterial Cu(+)-ATPases: models for molecular structure-function studies. |
Q35220353 | Beyond iron: non-classical biological functions of bacterial siderophores |
Q49090745 | Caulobacter crescentus intrinsic dimorphism provides a prompt bimodal response to copper stress |
Q28277615 | Cellular copper distribution: a mechanistic systems biology approach |
Q52580803 | Chalkophores. |
Q36156223 | Characterization of the PIB-Type ATPases present in Thermus thermophilus |
Q57701081 | Chemical and structural status of copper associated with oxygenic and anoxygenic phototrophs and heterotrophs: possible evolutionary consequences |
Q35783508 | Chemistry and biology of the copper chelator methanobactin. |
Q57200781 | ClostridiumSpecies as Metallic Copper-Forming Bacteria in Soil under Reducing Conditions |
Q34787334 | Control of copper resistance and inorganic sulfur metabolism by paralogous regulators in Staphylococcus aureus |
Q41642913 | CopM is a novel copper-binding protein involved in copper resistance in Synechocystis sp. PCC 6803. |
Q41988674 | Copper efflux is induced during anaerobic amino acid limitation in Escherichia coli to protect iron-sulfur cluster enzymes and biogenesis |
Q34055736 | Copper homeostasis in Salmonella is atypical and copper-CueP is a major periplasmic metal complex |
Q42777244 | Copper homeostasis networks in the bacterium Pseudomonas aeruginosa. |
Q35773696 | Copper in microbial pathogenesis: meddling with the metal |
Q36075898 | Copper(II)-Bis(Thiosemicarbazonato) Complexes as Antibacterial Agents: Insights into Their Mode of Action and Potential as Therapeutics. |
Q45734884 | Coproporphyrin III excretion identifies the anaerobic coproporphyrinogen III oxidase HemN as a copper target in the Cu⁺-ATPase mutant copA⁻ of Rubrivivax gelatinosus |
Q33926855 | CorE from Myxococcus xanthus is a copper-dependent RNA polymerase sigma factor. |
Q33911352 | CtpA, a copper-translocating P-type ATPase involved in the biogenesis of multiple copper-requiring enzymes |
Q44638569 | Cu binding by the Escherichia coli metal-efflux accessory protein RcnB. |
Q45351024 | Cupriavidus pinatubonensis AEO106 deals with copper-induced oxidative stress before engaging in biodegradation of the herbicide 4-chloro-2-methylphenoxyacetic acid |
Q37451149 | Differential roles for the Co(2+) /Ni(2+) transporting ATPases, CtpD and CtpJ, in Mycobacterium tuberculosis virulence. |
Q37604815 | Direct ROS scavenging activity of CueP from Salmonella enterica serovar Typhimurium. |
Q55027458 | Dissection of the sensor domain of the copper-responsive histidine kinase CorS from Myxococcus xanthus. |
Q54375441 | Distinct functional roles of homologous Cu+ efflux ATPases in Pseudomonas aeruginosa. |
Q35948071 | Dynamic Clustering of the Bacterial Sensory Kinase BaeS |
Q34465965 | Evolution and diversity of periplasmic proteins involved in copper homeostasis in gamma proteobacteria. |
Q41916820 | Expression and physiological role of three Myxococcus xanthus copper-dependent P1B-type ATPases during bacterial growth and development |
Q35287196 | Global transcriptional profiles of the copper responses in the cyanobacterium Synechocystis sp. PCC 6803 |
Q38333599 | Luminescence resonance energy transfer in the cytoplasm of live Escherichia coli cells |
Q33946990 | Mechanism of ATPase-mediated Cu+ export and delivery to periplasmic chaperones: the interaction of Escherichia coli CopA and CusF |
Q37279465 | Mechanisms of copper homeostasis in bacteria |
Q39123632 | Membrane Anchoring and Ion-Entry Dynamics in P-type ATPase Copper Transport. |
Q35922313 | Metal transport across biomembranes: emerging models for a distinct chemistry. |
Q27008192 | Metals in cyanobacteria: analysis of the copper, nickel, cobalt and arsenic homeostasis mechanisms |
Q38037538 | Nutrient acquisition and metabolism by Campylobacter jejuni |
Q41730425 | Oxygen-dependent copper toxicity: targets in the chlorophyll biosynthesis pathway identified in the copper efflux ATPase CopA deficient mutant |
Q38189393 | Pathogenic adaptations to host-derived antibacterial copper |
Q52633724 | Periplasmic response upon disruption of transmembrane Cu transport in Pseudomonas aeruginosa. |
Q46424461 | Peroxide reduction by a metal-dependent catalase in Nostoc punctiforme (cyanobacteria). |
Q35870713 | Regulation of Cu(I)/Ag(I) efflux genes in Escherichia coli by the sensor kinase CusS. |
Q36016362 | Role in metal homeostasis of CtpD, a Co²⁺ transporting P(1B4)-ATPase of Mycobacterium smegmatis. |
Q35192451 | Staphylococcus lugdunensis IsdG liberates iron from host heme |
Q92488437 | Structural basis and mechanism for metallochaperone-assisted assembly of the CuA center in cytochrome oxidase |
Q28261249 | Structural biology of copper trafficking |
Q47362089 | Study of the Expression of Bacterial Multidrug Efflux Pumps in Anaerobic Conditions |
Q53161687 | The CopRS two-component system is responsible for resistance to copper in the cyanobacterium Synechocystis sp. PCC 6803. |
Q36508768 | The mechanism of Cu+ transport ATPases: interaction with CU+ chaperones and the role of transient metal-binding sites. |
Q34970478 | The transport mechanism of bacterial Cu+-ATPases: distinct efflux rates adapted to different function |
Q28742385 | The two-component signal transduction system CopRS of Corynebacterium glutamicum is required for adaptation to copper-excess stress |
Q36432934 | Toward a molecular understanding of metal transport by P(1B)-type ATPases |
Q57928829 | Toxicity and Bioremediation of Heavy Metals Contaminated Ecosystem from Tannery Wastewater: A Review |
Q35076247 | Transcriptomic and genomic evidence for Streptococcus agalactiae adaptation to the bovine environment. |
Q38005941 | Two-component signal transduction in Corynebacterium glutamicum and other corynebacteria: on the way towards stimuli and targets |
Q36496575 | Uncovering the Transmembrane Metal Binding Site of the Novel Bacterial Major Facilitator Superfamily-Type Copper Importer CcoA. |
Q90495155 | Zinc excess increases cellular demand for iron and decreases tolerance to copper in Escherichia coli |
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