scholarly article | Q13442814 |
P2093 | author name string | J Beckwith | |
F Aslund | |||
E J Stewart | |||
P2860 | cites work | The Minimal Gene Complement of Mycoplasma genitalium | Q22065573 |
Complete sequence analysis of the genome of the bacterium Mycoplasma pneumoniae | Q22066001 | ||
Methods for generating precise deletions and insertions in the genome of wild-type Escherichia coli: application to open reading frame characterization | Q24676777 | ||
Tight regulation, modulation, and high-level expression by vectors containing the arabinose PBAD promoter | Q27860697 | ||
Thioredoxin and glutaredoxin systems | Q28271236 | ||
The reductive enzyme thioredoxin 1 acts as an oxidant when it is exported to the Escherichia coli periplasm | Q33551316 | ||
Formate is the hydrogen donor for the anaerobic ribonucleotide reductase from Escherichia coli | Q33924695 | ||
The Cs sec mutants of Escherichia coli reflect the cold sensitivity of protein export itself | Q33960682 | ||
A signal sequence is not required for protein export in prlA mutants of Escherichia coli | Q34044995 | ||
Evidence for five divergent thioredoxin h sequences in Arabidopsis thaliana. | Q34242244 | ||
Determinants of membrane protein topology | Q34372343 | ||
Ligand interactions of the ArsC arsenate reductase | Q34435846 | ||
Activation of the OxyR transcription factor by reversible disulfide bond formation | Q34459806 | ||
Redox potentials of glutaredoxins and other thiol-disulfide oxidoreductases of the thioredoxin superfamily determined by direct protein-protein redox equilibria | Q34743720 | ||
Two additional glutaredoxins exist in Escherichia coli: glutaredoxin 3 is a hydrogen donor for ribonucleotide reductase in a thioredoxin/glutaredoxin 1 double mutant. | Q35814670 | ||
Thioredoxin or glutaredoxin in Escherichia coli is essential for sulfate reduction but not for deoxyribonucleotide synthesis | Q36159962 | ||
Escherichia coli alkaline phosphatase fails to acquire disulfide bonds when retained in the cytoplasm | Q36241854 | ||
Role of primary structure and disulfide bond formation in beta-lactamase secretion | Q36324284 | ||
An in vivo pathway for disulfide bond isomerization in Escherichia coli | Q36687328 | ||
A collection of strains containing genetically linked alternating antibiotic resistance elements for genetic mapping of Escherichia coli. | Q37055071 | ||
Thioredoxin-catalyzed refolding of disulfide-containing proteins | Q37402702 | ||
Identification and characterization of a new disulfide isomerase-like protein (DsbD) in Escherichia coli | Q37620314 | ||
Evidence for two different classes of redox-active cysteines in ribonucleotide reductase of Escherichia coli | Q38344053 | ||
Characterization of Escherichia coli NrdH. A glutaredoxin-like protein with a thioredoxin-like activity profile | Q38344202 | ||
Effects of signal sequence mutations on the kinetics of alkaline phosphatase export to the periplasm in Escherichia coli | Q39959169 | ||
Identification of a second functional glutaredoxin encoded by the bacteriophage T4 genome | Q42632097 | ||
Cloning, expression, and characterization of a novel Escherichia coli thioredoxin | Q48041278 | ||
Identification of a third thioredoxin gene from Corynebacterium nephridii | Q48063363 | ||
Thioredoxins from Dictyostelium discoideum are a developmentally regulated multigene family | Q48173176 | ||
Identification of a protein required for disulfide bond formation in vivo | Q48201805 | ||
ColE1-type vectors with fully repressible replication | Q48213870 | ||
The role of the thioredoxin and glutaredoxin pathways in reducing protein disulfide bonds in the Escherichia coli cytoplasm. | Q54563918 | ||
Mutations that allow disulfide bond formation in the cytoplasm of Escherichia coli. | Q54646876 | ||
Mutagenesis of structural half-cystine residues in human thioredoxin and effects on the regulation of activity by selenodiglutathione. | Q54651155 | ||
A Pro to His mutation in active site of thioredoxin increases its disulfide-isomerase activity 10-fold. New refolding systems for reduced or randomly oxidized ribonuclease | Q54679075 | ||
The role of thioredoxin in filamentous phage assembly. Construction, isolation, and characterization of mutant thioredoxins. | Q54773035 | ||
Kinetic role of a meta-stable native-like two-disulphide species in the folding transition of bovine pancreatic trypsin inhibitor | Q72753383 | ||
Roles of disulfide bonds in bacterial alkaline phosphatase | Q73101164 | ||
The genetics of disulfide bond metabolism | Q77936221 | ||
P433 | issue | 19 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Escherichia coli | Q25419 |
cytoplasm | Q79899 | ||
P304 | page(s) | 5543-5550 | |
P577 | publication date | 1998-10-01 | |
P1433 | published in | The EMBO Journal | Q1278554 |
P1476 | title | Disulfide bond formation in the Escherichia coli cytoplasm: an in vivo role reversal for the thioredoxins | |
P478 | volume | 17 |
Q109649907 | A Bacterial Cell-Based Assay To Study SARS-CoV-2 Protein-Protein Interactions |
Q30964979 | A genetic investigation of the essential role of glutathione: mutations in the proline biosynthesis pathway are the only suppressors of glutathione auxotrophy in yeast |
Q42653676 | A novel monothiol glutaredoxin (Grx4) from Escherichia coli can serve as a substrate for thioredoxin reductase. |
Q33786323 | A novel motif in the NaTrxh N-terminus promotes its secretion, whereas the C-terminus participates in its interaction with S-RNase in vitro |
Q42200622 | A redox trap to augment the intein toolbox. |
Q41703359 | A simple method for expression and purification of Shiga toxin 1 (Stx1) with biological activities by using a single-promoter vector and native signal peptide |
Q54549989 | A unique approach for high level expression and production of a recombinant cobra neurotoxin in Escherichia coli. |
Q51526191 | Aerobic biosynthesis of hydrocinnamic acids in Escherichia coli with a strictly oxygen-sensitive enoate reductase. |
Q46261151 | Aeropyrum pernix membrane topology of protein VKOR promotes protein disulfide bond formation in two subcellular compartments |
Q31144621 | Amino acid residues on the surface of soybean 4-kDa peptide involved in the interaction with its binding protein |
Q27681479 | An Extended Active-site Motif Controls the Reactivity of the Thioredoxin Fold |
Q38106598 | Antimicrobial activity of metals: mechanisms, molecular targets and applications |
Q27930882 | Antioxidant activity of the yeast mitochondrial one-Cys peroxiredoxin is dependent on thioredoxin reductase and glutathione in vivo. |
Q33401000 | Bacterial intein-like domains of predatory bacteria: a new domain type characterized in Bdellovibrio bacteriovorus |
Q40919189 | Bacterial thioredoxin and thioredoxin reductase as mediators for epigallocatechin 3-gallate-induced antimicrobial action |
Q39659628 | Cell migration-promoting and apoptosis-inhibiting activities of Bm-TFF2 require distinct structure basis |
Q47635000 | Cell-free metabolic engineering promotes high-level production of bioactive Gaussia princeps luciferase |
Q35947686 | Characterization and Recombinant Expression of Terebrid Venom Peptide from Terebra guttata. |
Q34104935 | Characterization of Escherichia coli null mutants for glutaredoxin 2. |
Q43566884 | Characterization of a heavy metal ATPase from the apicomplexan Cryptosporidium parvum |
Q39275666 | Cloning of Soluble Human Stem Cell Factor in pET-26b(+) Vector |
Q46911551 | Co-expression of sulphydryl oxidase and protein disulphide isomerase in Escherichia coli allows for production of soluble CRM197. |
Q61807410 | Comparative proteome analysis in an Escherichia coli CyDisCo strain identifies stress responses related to protein production, oxidative stress and accumulation of misfolded protein |
Q37372262 | Comprehensively Characterizing the Thioredoxin Interactome In Vivo Highlights the Central Role Played by This Ubiquitous Oxidoreductase in Redox Control. |
Q38634845 | Conferring specificity in redox pathways by enzymatic thiol/disulfide exchange reactions. |
Q39492391 | Cosecretion of chaperones and low-molecular-size medium additives increases the yield of recombinant disulfide-bridged proteins |
Q27629368 | Crystal structure of the global regulator FlhD from Escherichia coli at 1.8 A resolution |
Q38079490 | Current state and recent advances in biopharmaceutical production in Escherichia coli, yeasts and mammalian cells |
Q37904885 | Cyclic ADP-ribose and NAADP: fraternal twin messengers for calcium signaling |
Q34722134 | Cysteine-Based Redox Switches in Enzymes |
Q90709198 | Cystine import is a valuable but risky process whose hazards Escherichia coli minimizes by inducing a cysteine exporter |
Q35063050 | Cytosolic CD38 protein forms intact disulfides and is active in elevating intracellular cyclic ADP-ribose |
Q28472999 | Depletion of Plasmodium berghei plasmoredoxin reveals a non-essential role for life cycle progression of the malaria parasite |
Q44714781 | Disruption of gamma-glutamylcysteine synthetase results in absolute glutathione auxotrophy and apoptosis in Candida albicans |
Q24600389 | Disruption of reducing pathways is not essential for efficient disulfide bond formation in the cytoplasm of E. coli |
Q31046717 | Disulfide bond formation and activation of Escherichia coli β-galactosidase under oxidizing conditions |
Q33723782 | Disulfide bond formation in prokaryotes: history, diversity and design |
Q50947419 | Disulfide bonds and disorder in granulin-3: An unusual handshake between structural stability and plasticity. |
Q45273892 | Effects of selenium on the structure and function of recombinant human S-adenosyl-L-methionine dependent arsenic (+3 oxidation state) methyltransferase in E. coli |
Q24644906 | Efficient folding of proteins with multiple disulfide bonds in the Escherichia coli cytoplasm |
Q30390491 | Efficient production of (2)H, (13)C, (15)N-enriched industrial enzyme Rhizopus chinensis lipase with native disulfide bonds |
Q89553030 | Engineering Biology to Construct Microbial Chassis for the Production of Difficult-to-Express Proteins |
Q34056922 | Enlarging the scope of cell-penetrating prenylated peptides to include farnesylated 'CAAX' box sequences and diverse cell types |
Q36271734 | Evidence for disulfide bonds in SR Protein Kinase 1 (SRPK1) that are required for activity and nuclear localization |
Q44364474 | Evolutionary relationship between defensins in the Poaceae family strengthened by the characterization of new sugarcane defensins. |
Q42502019 | Expression analysis of the nrdHIEF operon from Escherichia coli. Conditions that trigger the transcript level in vivo |
Q39354787 | Expression and characterization of a functional single-chain variable fragment (scFv) protein recognizing MCF7 breast cancer cells in E. coli cytoplasm |
Q44157086 | Expression and purification of the extracellular domain of the human follicle-stimulating hormone receptor using Escherichia coli |
Q54528128 | Expression of proteins using the third domain of the Escherichia coli periplasmic-protein TolA as a fusion partner. |
Q39329667 | Expression of recombinant Ara h 6 in Pichia pastoris but not in Escherichia coli preserves allergic effector function and allows assessment of specific mutations. |
Q36820469 | Expression, purification and identification of CtCVNH, a novel anti-HIV (Human Immunodeficiency Virus) protein from Ceratopteris thalictroides |
Q41704456 | Fluorometric In Situ Monitoring of an Escherichia coli Cell Factory with Cytosolic Expression of Human Glycosyltransferase GalNAcT2: Prospects and Limitations. |
Q34157680 | Formation and transfer of disulphide bonds in living cells |
Q57835066 | Formation of disulphide bonds during secretion of proteins through the periplasmic-independent type I pathway |
Q33952564 | Functional expression of spider neurotoxic peptide huwentoxin-I in E. coli |
Q40714438 | Functional expression, characterization, and purification of the catalytic domain of human 11-beta -hydroxysteroid dehydrogenase type 1. |
Q36638705 | Functional plasticity of a peroxidase allows evolution of diverse disulfide-reducing pathways |
Q27631272 | Functional significance of the beta hairpin in the insecticidal neurotoxin omega-atracotoxin-Hv1a |
Q28486376 | Functional studies of multiple thioredoxins from Mycobacterium tuberculosis |
Q38063935 | Functions and cellular compartmentation of the thioredoxin and glutathione pathways in yeast. |
Q27001688 | Fusion tags for protein solubility, purification and immunogenicity in Escherichia coli: the novel Fh8 system |
Q38314441 | Genes of Escherichia coli O157:H7 that are involved in high-pressure resistance |
Q37364322 | Genetic suppressors and recovery of repressed biochemical memory |
Q43909860 | Glutaredoxins and oxidative stress defense in yeast |
Q91993360 | Heterologous expression and mutagenesis of recombinant Vespa affinis hyaluronidase protein (rVesA2) |
Q40909354 | Heterologous expression and purification of active divercin V41, a class IIa bacteriocin encoded by a synthetic gene in Escherichia coli |
Q28486327 | Heterologous expression, purification, and enzymatic activity of Mycobacterium tuberculosis NAD(+) synthetase |
Q43631394 | High-level bacterial expression of a natively folded, soluble extracellular domain fusion protein of the human luteinizing hormone/chorionic gonadotropin receptor in the cytoplasm of Escherichia coli |
Q47450429 | High-yield expression in Escherichia coli, purification, and characterization of properly folded major peanut allergen Ara h 2. |
Q43061995 | High-yield production, refolding and a molecular modelling of the catalytic module of (1,3)-beta-D-glucan (curdlan) synthase from Agrobacterium sp. |
Q50454673 | Highly efficient folding of multi-disulfide proteins in superoxidizing Escherichia coli cytoplasm. |
Q41902836 | Human Tissue Plasminogen Activator Expression in Escherichia coli using Cytoplasmic and Periplasmic Cumulative Power |
Q42692069 | Identification, characterization and expression of a defensin-like antifungal peptide from the whitefly Bemisia tabaci (Gennadius) (Hemiptera: Aleyrodidae). |
Q58695204 | Identification, expression and characterization of the recombinant Sol g 4.1 protein from the venom of the tropical fire ant |
Q78177288 | Importance of redox potential for the in vivo function of the cytoplasmic disulfide reductant thioredoxin from Escherichia coli |
Q33243139 | In vivo drafting of single-chain antibodies for regulatory duty on the sigma54-promoter Pu of the TOL plasmid |
Q35146828 | Inactivation of the antibacterial and cytotoxic properties of silver ions by biologically relevant compounds |
Q33905769 | Interactions of glutaredoxins, ribonucleotide reductase, and components of the DNA replication system of Escherichia coli. |
Q39471835 | Is oxidized thioredoxin a major trigger for cysteine oxidation? Clues from a redox proteomics approach. |
Q36412331 | Lack of a peroxiredoxin suppresses the lethality of cells devoid of electron donors by channelling electrons to oxidized ribonucleotide reductase |
Q43606301 | Maturation of Pseudomonas aeruginosa elastase. Formation of the disulfide bonds |
Q40731940 | Methionine sulfoxide reduction and assimilation in Escherichia coli: new role for the biotin sulfoxide reductase BisC |
Q35510641 | Microarray analysis of the Escherichia coli response to CdTe-GSH Quantum Dots: understanding the bacterial toxicity of semiconductor nanoparticles |
Q34077498 | Mitochondrial Thioredoxin-Glutathione Reductase from LarvalTaenia crassiceps(Cysticerci) |
Q33799655 | Molecular cloning and comparative sequence analysis of fungal β-Xylosidases |
Q42017043 | Mutations at several loci cause increased expression of ribonucleotide reductase in Escherichia coli |
Q34543949 | Mutations of the membrane-bound disulfide reductase DsbD that block electron transfer steps from cytoplasm to periplasm in Escherichia coli |
Q44097428 | N-Ethylmaleimide inhibits platelet-derived growth factor BB-stimulated Akt phosphorylation via activation of protein phosphatase 2A. |
Q38038614 | Nanomaterials and nanotechnology for skin tissue engineering |
Q34046362 | Native disulfide bond formation in proteins |
Q30729945 | Occurrence of protein disulfide bonds in different domains of life: a comparison of proteins from the Protein Data Bank |
Q33993677 | On the functional interchangeability, oxidant versus reductant, of members of the thioredoxin superfamily |
Q51741818 | Organization and regulation of sex-specific thioredoxin encoding genes in the genus Drosophila. |
Q37592032 | Overcoming the solubility limit with solubility-enhancement tags: successful applications in biomolecular NMR studies |
Q34092832 | Oxidative stress in microorganisms--I. Microbial vs. higher cells--damage and defenses in relation to cell aging and death |
Q42378984 | Phage-assisted continuous evolution of proteases with altered substrate specificity |
Q42574521 | Pre-expression of a sulfhydryl oxidase significantly increases the yields of eukaryotic disulfide bond containing proteins expressed in the cytoplasm of E.coli |
Q83889863 | Primer-independent initiation of RNA synthesis by SeMV recombinant RNA-dependent RNA polymerase |
Q33530332 | Production of a soluble disulfide bond-linked TCR in the cytoplasm of Escherichia coli trxB gor mutants. |
Q44523646 | Production of bioactive chicken follistatin315 in Escherichia coli |
Q54420959 | Production of biologically active forms of recombinant hepcidin, the iron-regulatory hormone. |
Q44038146 | Production of functional single-chain Fv antibodies in the cytoplasm of Escherichia coli |
Q36734714 | Production of the catalytic core of human peptidylglycine α-hydroxylating monooxygenase (hPHMcc) in Escherichia coli |
Q47151186 | Prokaryotic soluble expression and purification of bioactive human fibroblast growth factor 21 using maltose-binding protein. |
Q42224883 | Properties of a novel intracellular poly(3-hydroxybutyrate) depolymerase with high specific activity (PhaZd) in Wautersia eutropha H16. |
Q36247264 | Protection against Th17 cells differentiation by an interleukin-23 receptor cytokine-binding homology region |
Q43279398 | Protein denitrosylation: enzymatic mechanisms and cellular functions. |
Q36575813 | Protein disulfides and protein disulfide oxidoreductases in hyperthermophiles |
Q36569895 | Protein folding and conformational stress in microbial cells producing recombinant proteins: a host comparative overview |
Q43917524 | Protein levels of Escherichia coli thioredoxins and glutaredoxins and their relation to null mutants, growth phase, and function |
Q36574940 | Proteome analyses of heme-dependent respiration in Lactococcus lactis: involvement of the proteolytic system |
Q28473892 | Quorum sensing primes the oxidative stress response in the insect endosymbiont, Sodalis glossinidius |
Q33883304 | Reactivity of glutaredoxins 1, 2, and 3 from Escherichia coli shows that glutaredoxin 2 is the primary hydrogen donor to ArsC-catalyzed arsenate reduction. |
Q44387477 | Real-time kinetics of the interaction between the two subunits, Escherichia coli thioredoxin and gene 5 protein of phage T7 DNA polymerase |
Q57281801 | Recombinant AfusinC, an anionic fungal CSαβ defensin from Aspergillus fumigatus, exhibits antimicrobial activity against gram-positive bacteria |
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Q35940945 | Recombinant protein folding and misfolding in Escherichia coli |
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Q43920319 | Redox state of cytoplasmic thioredoxin |
Q35699713 | Regulation of redox homeostasis in the yeast Saccharomyces cerevisiae |
Q47665859 | Relationship between the occurrence of cysteine in proteins and the complexity of organisms |
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Q52647762 | Repurposing Auranofin, Ebselen, and PX-12 as Antimicrobial Agents Targeting the Thioredoxin System. |
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Q35918506 | Role and location of the unusual redox-active cysteines in the hydrophobic domain of the transmembrane electron transporter DsbD. |
Q43648141 | Role of individual disulfide bonds in the structural maturation of a low molecular weight glutenin subunit |
Q34052736 | Roles of the glutathione- and thioredoxin-dependent reduction systems in the Escherichia coli and saccharomyces cerevisiae responses to oxidative stress. |
Q36478560 | SHuffle, a novel Escherichia coli protein expression strain capable of correctly folding disulfide bonded proteins in its cytoplasm |
Q33557755 | Salmonella enterica serovar typhimurium trxA mutants are protective against virulent challenge and induce less inflammation than the live-attenuated vaccine strain SL3261. |
Q40739794 | Scanning mutagenesis of a Janus-faced atracotoxin reveals a bipartite surface patch that is essential for neurotoxic function |
Q33913069 | Selenoproteins: molecular pathways and physiological roles. |
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