| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Elizabeth Diago-Navarro | Q82662250 |
| Rolf Boelens | Q28468897 | ||
| P2093 | author name string | Ana J Muñoz-Gómez | |
| Ramón Díaz-Orejas | |||
| Marc Lemonnier | |||
| Monique B Kamphuis | |||
| Juan López-Villarejo | |||
| Ana M Hernandez-Arriaga | |||
| P2860 | cites work | Bacterial toxin-antitoxin systems: more than selfish entities? | Q21145003 |
| Bacterial programmed cell death and multicellular behavior in bacteria | Q21145260 | ||
| New connections in the prokaryotic toxin-antitoxin network: relationship with the eukaryotic nonsense-mediated RNA decay system | Q21194875 | ||
| Prokaryotic DNA segregation by an actin-like filament | Q24536852 | ||
| Kid cleaves specific mRNAs at UUACU sites to rescue the copy number of plasmid R1 | Q24536942 | ||
| Toxin-antitoxin modules may regulate synthesis of macromolecules during nutritional stress | Q24548999 | ||
| Mini-F plasmid genes that couple host cell division to plasmid proliferation | Q24594938 | ||
| An Escherichia coli chromosomal "addiction module" regulated by guanosine [corrected] 3',5'-bispyrophosphate: a model for programmed bacterial cell death | Q24607301 | ||
| Unique type of plasmid maintenance function: postsegregational killing of plasmid-free cells | Q24630262 | ||
| Chromosomal toxin-antitoxin systems may act as antiaddiction modules | Q24646891 | ||
| Molecular mechanisms of HipA-mediated multidrug tolerance and its neutralization by HipB | Q24651429 | ||
| What is the benefit to Escherichia coli of having multiple toxin-antitoxin systems in its genome? | Q24675694 | ||
| Postsegregational killing does not increase plasmid stability but acts to mediate the exclusion of competing plasmids | Q24679732 | ||
| Structural and functional analysis of the kid toxin protein from E. coli plasmid R1 | Q27639783 | ||
| Interactions between the toxin Kid of the bacterial parD system and the antitoxins Kis and MazE. | Q53579152 | ||
| GATEWAY recombinational cloning: application to the cloning of large numbers of open reading frames or ORFeomes. | Q53901952 | ||
| The F plasmid CcdB protein induces efficient ATP-dependent DNA cleavage by gyrase. | Q54223810 | ||
| Isolation and characterization of a conditional replication mutant of the antibiotic resistance factor R1 affected in the gene of the replication protein repA. | Q54354534 | ||
| Messenger RNA interferase RelE controls relBE transcription by conditional cooperativity. | Q54421444 | ||
| Single protein production in living cells facilitated by an mRNA interferase. | Q54487510 | ||
| RelE toxins from bacteria and Archaea cleave mRNAs on translating ribosomes, which are rescued by tmRNA. | Q54524054 | ||
| Rapid induction and reversal of a bacteriostatic condition by controlled expression of toxins and antitoxins. | Q54541820 | ||
| Translational coupling and limited degradation of a polycistronic messenger modulate differential gene expression in the parD stability system of plasmid R1. | Q54603721 | ||
| Kid, a small protein of the parD stability system of plasmid R1, is an inhibitor of DNA replication acting at the initiation of DNA synthesis. | Q54614008 | ||
| Protection of coliphage lambda O initiator protein from proteolysis in the assembly of the replication complex in vivo. | Q54617021 | ||
| Lon-dependent proteolysis of CcdA is the key control for activation of CcdB in plasmid-free segregant bacteria. | Q54639171 | ||
| The kis and kid genes of the parD maintenance system of plasmid R1 form an operon that is autoregulated at the level of transcription by the co-ordinated action of the Kis and Kid proteins. | Q54689585 | ||
| Structural and functional comparison between the stability systems ParD of plasmid R1 and Ccd of plasmid F. | Q54699683 | ||
| Crystal structure of the MazE/MazF complex: molecular bases of antidote-toxin recognition | Q27641078 | ||
| Crystal structure of the met repressor-operator complex at 2.8 A resolution reveals DNA recognition by beta-strands | Q27642147 | ||
| The Structural Basis for mRNA Recognition and Cleavage by the Ribosome-Dependent Endonuclease RelE | Q27646567 | ||
| The solution structure of ParD, the antidote of the ParDE toxin-antitoxin module, provides the structural basis for DNA and toxin binding | Q27646891 | ||
| Crystal structure of Mycobacterium tuberculosis YefM antitoxin reveals that it is not an intrinsically unstructured protein | Q27652155 | ||
| Inhibitory Mechanism of Escherichia coli RelE-RelB Toxin-Antitoxin Module Involves a Helix Displacement Near an mRNA Interferase Active Site | Q27654200 | ||
| Rejuvenation of CcdB-poisoned gyrase by an intrinsically disordered protein domain | Q27656829 | ||
| A Conserved Mode of Protein Recognition and Binding in a ParD−ParE Toxin−Antitoxin Complex | Q27659672 | ||
| DNA recognition by beta-sheets in the Arc repressor-operator crystal structure | Q27730947 | ||
| Crystal structure of CcdB, a topoisomerase poison from E. coli | Q27766729 | ||
| MOLMOL: a program for display and analysis of macromolecular structures | Q27860873 | ||
| Addiction modules and programmed cell death and antideath in bacterial cultures | Q28146167 | ||
| Toxins-antitoxins: plasmid maintenance, programmed cell death, and cell cycle arrest | Q28206549 | ||
| Antisense RNA-regulated programmed cell death | Q28259967 | ||
| RNA antitoxins | Q28294158 | ||
| Prokaryotic toxin-antitoxin stress response loci | Q29615335 | ||
| Characterization of ChpBK, an mRNA interferase from Escherichia coli | Q30852783 | ||
| Development without germ cells: the role of the germ line in zebrafish sex differentiation. | Q30856433 | ||
| Release of peptide promoted by the GGQ motif of class 1 release factors regulates the GTPase activity of RF3. | Q30868692 | ||
| The YefM antitoxin defines a family of natively unfolded proteins: implications as a novel antibacterial target | Q30886064 | ||
| Structural basis for nucleic acid and toxin recognition of the bacterial antitoxin CcdA. | Q31063061 | ||
| Comprehensive comparative-genomic analysis of type 2 toxin-antitoxin systems and related mobile stress response systems in prokaryotes | Q33459528 | ||
| Cell killing by the F plasmid CcdB protein involves poisoning of DNA-topoisomerase II complexes | Q33969008 | ||
| MazF Cleaves Cellular mRNAs Specifically at ACA to Block Protein Synthesis in Escherichia coli | Q33973437 | ||
| Bacterial toxin-antitoxin gene system as containment control in yeast cells | Q33988395 | ||
| MazG -- a regulator of programmed cell death in Escherichia coli | Q33992667 | ||
| MazF, an mRNA interferase, mediates programmed cell death during multicellular Myxococcus development | Q34009374 | ||
| The art of selective killing: plasmid toxin/antitoxin systems and their technological applications | Q34013680 | ||
| Positive-selection vectors using the F plasmid ccdB killer gene | Q34059638 | ||
| The ratio between CcdA and CcdB modulates the transcriptional repression of the ccd poison-antidote system | Q34083974 | ||
| Identification of components of a new stability system of plasmid R1, ParD, that is close to the origin of replication of this plasmid | Q34174283 | ||
| A linear pentapeptide is a quorum-sensing factor required for mazEF-mediated cell death in Escherichia coli. | Q46930277 | ||
| PIN domains in nonsense-mediated mRNA decay and RNAi | Q47069110 | ||
| Control of segregation of chromosomal DNA by sex factor F in Escherichia coli. Mutants of DNA gyrase subunit A suppress letD (ccdB) product growth inhibition | Q48174226 | ||
| Analysis of plasmid genome evolution based on nucleotide-sequence comparison of two related plasmids of Escherichia coli | Q48405680 | ||
| Structure of Arc repressor in solution: evidence for a family of beta-sheet DNA-binding proteins. | Q50464242 | ||
| Recognition of the intrinsically flexible addiction antidote MazE by a dromedary single domain antibody fragment. Structure, thermodynamics of binding, stability, and influence on interactions with DNA. | Q52282024 | ||
| Molecular basis of gyrase poisoning by the addiction toxin CcdB. | Q52287398 | ||
| A mutagenic analysis of the RNase mechanism of the bacterial Kid toxin by mass spectrometry. | Q53376615 | ||
| The Escherichia coli mazEF suicide module mediates thymineless death | Q34181444 | ||
| Toxin-antitoxin loci as stress-response-elements: ChpAK/MazF and ChpBK cleave translated RNAs and are counteracted by tmRNA. | Q34230226 | ||
| Toxin-antitoxin modules as bacterial metabolic stress managers | Q34463800 | ||
| Shutdown decay of mRNA. | Q34542254 | ||
| Role of DNA replication and repair in thymineless death in Escherichia coli | Q34976537 | ||
| Construction of a Vibrio splendidus mutant lacking the metalloprotease gene vsm by use of a novel counterselectable suicide vector | Q35641989 | ||
| Toxin-antitoxin regulation: bimodal interaction of YefM-YoeB with paired DNA palindromes exerts transcriptional autorepression | Q35646662 | ||
| Plasmid R1--replication and its control | Q36274445 | ||
| The extracellular death factor: physiological and genetic factors influencing its production and response in Escherichia coli | Q36594594 | ||
| Structure and function of bacterial kid-kis and related toxin-antitoxin systems | Q36738054 | ||
| ATP-dependent degradation of CcdA by Lon protease. Effects of secondary structure and heterologous subunit interactions | Q36831491 | ||
| Novel Escherichia coli RF1 mutants with decreased translation termination activity and increased sensitivity to the cytotoxic effect of the bacterial toxins Kid and RelE | Q37187273 | ||
| RNase II is important for A-site mRNA cleavage during ribosome pausing | Q37365620 | ||
| Horizontal gene transfer and the earliest stages of the evolution of life | Q37568557 | ||
| The antidote and autoregulatory functions of the F plasmid CcdA protein: a genetic and biochemical survey | Q38304603 | ||
| chpA and chpB, Escherichia coli chromosomal homologs of the pem locus responsible for stable maintenance of plasmid R100 | Q38314758 | ||
| DnaB helicase stimulates primer synthesis activity on short oligonucleotide templates | Q38316011 | ||
| Interference of mRNA function by sequence-specific endoribonuclease PemK. | Q38343561 | ||
| A strand-passage conformation of DNA gyrase is required to allow the bacterial toxin, CcdB, to access its binding site | Q39079987 | ||
| Toxin-antitoxin based transgene expression in mammalian cells | Q39556928 | ||
| Regulatable killing of eukaryotic cells by the prokaryotic proteins Kid and Kis. | Q39696663 | ||
| The stable maintenance system pem of plasmid R100: degradation of PemI protein may allow PemK protein to inhibit cell growth | Q39935070 | ||
| Definition of a minimal plasmid stabilization system from the broad-host-range plasmid RK2. | Q39940253 | ||
| Structure and organization of hip, an operon that affects lethality due to inhibition of peptidoglycan or DNA synthesis | Q39943160 | ||
| Two genes, pemK and pemI, responsible for stable maintenance of resistance plasmid R100. | Q39952666 | ||
| Control of replication of bacterial plasmids: Genetics, molecular biology, and physiology of the plasmid R1 system | Q40112314 | ||
| Programmed cell death in bacterial populations | Q40586191 | ||
| The beta-ribbon DNA recognition motif | Q40627901 | ||
| Bacterial toxin RelE induces apoptosis in human cells | Q40730517 | ||
| Broad-host-range plasmid replication: an open question. | Q41172958 | ||
| Cooperative tandem binding of met repressor of Escherichia coli | Q41298156 | ||
| Comparison of ccd of F, parDE of RP4, and parD of R1 using a novel conditional replication control system of plasmid R1. | Q41654669 | ||
| Conditionally lethal genes associated with bacterial plasmids | Q41655129 | ||
| Interactions of Kid-Kis toxin-antitoxin complexes with the parD operator-promoter region of plasmid R1 are piloted by the Kis antitoxin and tuned by the stoichiometry of Kid-Kis oligomers. | Q41811686 | ||
| RNase/anti-RNase activities of the bacterial parD toxin-antitoxin system | Q42054469 | ||
| Driving forces of gyrase recognition by the addiction toxin CcdB. | Q42136192 | ||
| Model for RNA binding and the catalytic site of the RNase Kid of the bacterial parD toxin-antitoxin system. | Q42167261 | ||
| Analysis of an Escherichia coli mutant strain resistant to the cell-killing function encoded by the gef gene family | Q42611510 | ||
| The chromosomal relBE2 toxin-antitoxin locus of Streptococcus pneumoniae: characterization and use of a bioluminescence resonance energy transfer assay to detect toxin-antitoxin interaction | Q42678581 | ||
| A toxin-antitoxin module as a target for antimicrobial development | Q43267764 | ||
| The regulation of the Escherichia coli mazEF promoter involves an unusual alternating palindrome | Q43509583 | ||
| Non-cytotoxic variants of the Kid protein that retain their auto-regulatory activity | Q44558880 | ||
| Separate-component-stabilization system for protein and DNA production without the use of antibiotics | Q45884103 | ||
| P433 | issue | 15 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | biotechnology | Q7108 |
| P304 | page(s) | 3097-3117 | |
| P577 | publication date | 2010-06-21 | |
| P1433 | published in | FEBS Journal | Q1388041 |
| P1476 | title | parD toxin-antitoxin system of plasmid R1--basic contributions, biotechnological applications and relationships with closely-related toxin-antitoxin systems | |
| P478 | volume | 277 |
| Q21133955 | A common origin for the bacterial toxin-antitoxin systems parD and ccd, suggested by analyses of toxin/target and toxin/antitoxin interactions |
| Q27666599 | A processed noncoding RNA regulates an altruistic bacterial antiviral system |
| Q27028105 | Antibiotic-free selection in biotherapeutics: now and forever |
| Q41494477 | Coupling between the basic replicon and the Kis-Kid maintenance system of plasmid R1: modulation by Kis antitoxin levels and involvement in control of plasmid replication |
| Q35604307 | Expression of the Streptococcus pneumoniae yoeB chromosomal toxin gene causes cell death in the model plant Arabidopsis thaliana |
| Q37895333 | Identification of bacterial plasmids based on mobility and plasmid population biology. |
| Q26751512 | Keeping the Wolves at Bay: Antitoxins of Prokaryotic Type II Toxin-Antitoxin Systems |
| Q88702084 | Next-generation biocontainment systems for engineered organisms |
| Q34495366 | Recent advancements in toxin and antitoxin systems involved in bacterial programmed cell death |
| Q37576199 | Regulating toxin-antitoxin expression: controlled detonation of intracellular molecular timebombs |
| Q89878402 | Safety Aspects of Genetically Modified Lactic Acid Bacteria |
| Q46296325 | Structural analyses of the MazEF4 toxin-antitoxin pair in Mycobacterium tuberculosis provide evidence for a unique extracellular death factor. |
| Q28079157 | Structure, Evolution, and Functions of Bacterial Type III Toxin-Antitoxin Systems |
| Q38064401 | Toxin-antitoxin genes of the Gram-positive pathogen Streptococcus pneumoniae: so few and yet so many. |
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