scholarly article | Q13442814 |
P819 | ADS bibcode | 1999PNAS...96.8919T |
P356 | DOI | 10.1073/PNAS.96.16.8919 |
P932 | PMC publication ID | 17708 |
P698 | PubMed publication ID | 10430871 |
P5875 | ResearchGate publication ID | 12868625 |
P2093 | author name string | M O'Donnell | |
R Woodgate | |||
X Shen | |||
E G Frank | |||
M F Goodman | |||
M Tang | |||
P2860 | cites work | Deoxycytidyl transferase activity of yeast REV1 protein | Q27931173 |
Efficient bypass of a thymine-thymine dimer by yeast DNA polymerase, Poleta | Q27935465 | ||
The Saccharomyces cerevisiae RAD30 gene, a homologue of Escherichia coli dinB and umuC, is DNA damage inducible and functions in a novel error-free postreplication repair mechanism | Q27938714 | ||
RecA protein-dependent cleavage of UmuD protein and SOS mutagenesis. | Q33559613 | ||
UmuD mutagenesis protein of Escherichia coli: overproduction, purification, and cleavage by RecA. | Q33559649 | ||
RecA-mediated cleavage activates UmuD for mutagenesis: mechanistic relationship between transcriptional derepression and posttranslational activation | Q33559704 | ||
Efficient translesion replication in the absence of Escherichia coli Umu proteins and 3'-5' exonuclease proofreading function | Q33594697 | ||
Ultraviolet mutagenesis and inducible DNA repair in Escherichia coli | Q34072546 | ||
DNA polymerase III of Escherichia coli is required for UV and ethyl methanesulfonate mutagenesis | Q34631905 | ||
Regulation of SOS mutagenesis by proteolysis | Q34734770 | ||
In vivo stability of the Umu mutagenesis proteins: a major role for RecA. | Q35608533 | ||
Isolation and characterization of novel plasmid-encoded umuC mutants | Q35968216 | ||
Involvement of Escherichia coli DNA polymerase II in response to oxidative damage and adaptive mutation | Q35979376 | ||
RecA protein of Escherichia coli has a third essential role in SOS mutator activity | Q36164939 | ||
New recA mutations that dissociate the various RecA protein activities in Escherichia coli provide evidence for an additional role for RecA protein in UV mutagenesis | Q36176522 | ||
Biochemical basis of SOS-induced mutagenesis in Escherichia coli: reconstitution of in vitro lesion bypass dependent on the UmuD'2C mutagenic complex and RecA protein. | Q36275662 | ||
Isolation and Characterization of Thermosensitive Escherichia coli Mutants Defective in Deoxyribonucleic Acid Replication | Q36839028 | ||
Activity of the purified mutagenesis proteins UmuC, UmuD', and RecA in replicative bypass of an abasic DNA lesion by DNA polymerase III | Q37296938 | ||
Analysis of DNA polymerases II and 3 in mutants of Escherichia coli thermosensitive for DNA synthesis | Q37494843 | ||
Mutagenic repair in Escherichia coli: products of the recA gene and of the umuD and umuC genes act at different steps in UV-induced mutagenesis | Q37692184 | ||
The 'A rule' of mutagen specificity: a consequence of DNA polymerase bypass of non-instructional lesions? | Q37713424 | ||
Purification of a soluble UmuD'C complex from Escherichia coli. Cooperative binding of UmuD'C to single-stranded DNA. | Q38358001 | ||
Detection of messenger RNA from the isoleucine-valine operons of Salmonella typhimurium by heterologous DNA-RNA hybridization: Involvement of transfer RNA in transcriptional repression | Q40783410 | ||
Isolation and characterization of mutants of Escherichia coli deficient in induction of mutations by ultraviolet light | Q40850491 | ||
A molecular switch in a replication machine defined by an internal competition for protein rings | Q40952536 | ||
Uvm mutants of Escherichia coli K12 deficient in UV mutagenesis. I. Isolation of uvm mutants and their phenotypical characterization in DNA repair and mutagenesis | Q40958827 | ||
Induction of only one SOS operon, umuDC, is required for SOS mutagenesis in Escherichia coli. | Q42512401 | ||
Gel fidelity assay measuring nucleotide misinsertion, exonucleolytic proofreading, and lesion bypass efficiencies | Q46257980 | ||
Specific RecA amino acid changes affect RecA-UmuD'C interaction | Q47986850 | ||
Deletion of the Saccharomyces cerevisiae gene RAD30 encoding an Escherichia coli DinB homolog confers UV radiation sensitivity and altered mutability. | Q48033074 | ||
Intermolecular cleavage by UmuD-like enzymes: identification of residues required for cleavage and substrate specificity | Q50127776 | ||
Escherichia coli umuDC mutants: DNA sequence alterations and UmuD cleavage | Q54678510 | ||
Mutagenic DNA repair in Escherichia coli. XVI. Mutagenesis by ultraviolet light plus delayed photoreversal in recA strains. | Q54750574 | ||
Escherichia coli mutants temperature-sensitive for DNA synthesis | Q69964539 | ||
The mutagenesis proteins UmuD' and UmuC prevent lethal frameshifts while increasing base substitution mutations | Q77231587 | ||
P4510 | describes a project that uses | ImageQuant | Q112270642 |
P433 | issue | 16 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Escherichia coli | Q25419 |
DNA polymerase V complex | Q22326847 | ||
P304 | page(s) | 8919-8924 | |
P577 | publication date | 1999-08-01 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | UmuD'(2)C is an error-prone DNA polymerase, Escherichia coli pol V. | |
P478 | volume | 96 |
Q37482156 | A DinB variant reveals diverse physiological consequences of incomplete TLS extension by a Y-family DNA polymerase. |
Q35219664 | A RecA protein surface required for activation of DNA polymerase V. |
Q47145902 | A Small-Molecule Inducible Synthetic Circuit for Control of the SOS Gene Network without DNA Damage. |
Q34720709 | A constitutively expressed, truncated umuDC operon regulates the recA-dependent DNA damage induction of a gene in Acinetobacter baylyi strain ADP1. |
Q35181456 | A dnaN plasmid shuffle strain for rapid in vivo analysis of mutant Escherichia coli β clamps provides insight into the role of clamp in umuDC-mediated cold sensitivity |
Q32001102 | A model for SOS-lesion-targeted mutations in Escherichia coli |
Q36656088 | A model for targeted substitution mutagenesis during SOS replication of double-stranded DNA containing cis-syn cyclobutane thymine dimers |
Q33770275 | A new class of errant DNA polymerases provides candidates for somatic hypermutation |
Q24609557 | A new model for SOS-induced mutagenesis: how RecA protein activates DNA polymerase V |
Q35111486 | A nucleotide binding rectification Brownian ratchet model for translocation of Y-family DNA polymerases |
Q34383032 | A peptide switch regulates DNA polymerase processivity |
Q43509472 | A single highly mutable catalytic site amino acid is critical for DNA polymerase fidelity |
Q36667427 | A single residue unique to DinB-like proteins limits formation of the polymerase IV multiprotein complex in Escherichia coli |
Q30305550 | A ubiquitous structural core |
Q42274110 | A ΔdinB mutation that sensitizes Escherichia coli to the lethal effects of UV- and X-radiation |
Q34088211 | Adaptive mutation in Escherichia coli |
Q38822086 | Advanced Approaches to Model Xenobiotic Metabolism in Bacterial Genotoxicology In Vitro |
Q34691348 | Aeons of distress: an evolutionary perspective on the bacterial SOS response. |
Q24597093 | All three SOS-inducible DNA polymerases (Pol II, Pol IV and Pol V) are involved in induced mutagenesis |
Q73039820 | Alteration of ultraviolet-induced mutagenesis in yeast through molecular modulation of the REV3 and REV7 gene expression |
Q36300949 | Altering the N-terminal arms of the polymerase manager protein UmuD modulates protein interactions |
Q24683905 | An NMR study on the interaction of Escherichia coli DinI with RecA-ssDNA complexes |
Q35810835 | An ORFan no more: the bacteriophage T4 39.2 gene product, NwgI, modulates GroEL chaperone function |
Q24800880 | An SOS-regulated operon involved in damage-inducible mutagenesis in Caulobacter crescentus |
Q42498856 | An aerobic recA-, umuC-dependent pathway of spontaneous base-pair substitution mutagenesis in Escherichia coli |
Q54516027 | Analysis of translesion replication across an abasic site by DNA polymerase IV of Escherichia coli |
Q43722149 | Anomalous mutagenicity profile of cyclohexanone oxime in bacteria: cell survival in background lawns |
Q24793710 | Answering the Call: Coping with DNA Damage at the Most Inopportune Time |
Q37095712 | Better living with hyper-mutation |
Q36182449 | Bridging the gap: a family of novel DNA polymerases that replicate faulty DNA. |
Q48784313 | Bryn Bridges and mutagenesis: exploring the intellectual space. |
Q34456660 | Cellular determinants of the mutational specificity of 1-nitroso-6-nitropyrene and 1-nitroso-8-nitropyrene in the lacI gene of Escherichia coli |
Q38630779 | Characterization of Escherichia coli UmuC active-site loops identifies variants that confer UV hypersensitivity |
Q54462727 | Characterization of Escherichia coli translesion synthesis polymerases and their accessory factors. |
Q35162442 | Characterization of a new LexA binding motif in the marine magnetotactic bacterium strain MC-1 |
Q58125939 | Chronological Switch from Translesion Synthesis to Homology-Dependent Gap Repair |
Q30437318 | Cleavage of bacteriophage lambda cI repressor involves the RecA C-terminal domain |
Q41357542 | Comparative analysis of eubacterial DNA polymerase III alpha subunits |
Q27939188 | Comparative analysis of in vivo interactions between Rev1 protein and other Y-family DNA polymerases in animals and yeasts |
Q24515346 | Complementation of defective translesion synthesis and UV light sensitivity in xeroderma pigmentosum variant cells by human and mouse DNA polymerase eta |
Q30494052 | Conformational dynamics of the Escherichia coli DNA polymerase manager proteins UmuD and UmuD'. |
Q36961674 | Controlling mutation: intervening in evolution as a therapeutic strategy |
Q27633840 | Converting a DNA damage checkpoint effector (UmuD2C) into a lesion bypass polymerase (UmuD'2C) |
Q33756174 | Coordinating DNA polymerase traffic during high and low fidelity synthesis |
Q33885426 | Coping with replication 'train wrecks' in Escherichia coli using Pol V, Pol II and RecA proteins |
Q36106867 | Critical amino acids in Escherichia coli UmuC responsible for sugar discrimination and base-substitution fidelity |
Q42157440 | Crucial contribution of the multiple copies of the initiator tRNA genes in the fidelity of tRNA fMet selection on the ribosomal P-site in Escherichia coli |
Q27634747 | Crystal structure of a DinB lesion bypass DNA polymerase catalytic fragment reveals a classic polymerase catalytic domain |
Q27635332 | Crystal structure of a Y-family DNA polymerase in action: a mechanism for error-prone and lesion-bypass replication |
Q26825267 | Culture history and population heterogeneity as determinants of bacterial adaptation: the adaptomics of a single environmental transition |
Q34260300 | DNA damage control by novel DNA polymerases: translesion replication and mutagenesis |
Q33984301 | DNA damage-induced mutation: tolerance via translesion synthesis |
Q44153069 | DNA polymerase III from Escherichia coli cells expressing mutA mistranslator tRNA is error-prone |
Q37726185 | DNA polymerase V activity is autoregulated by a novel intrinsic DNA-dependent ATPase |
Q54446139 | DNA polymerase V allows bypass of toxic guanine oxidation products in vivo. |
Q53879827 | DNA polymerase V-dependent mutator activity in an SOS-induced Escherichia coli strain with a temperature-sensitive DNA polymerase III. |
Q24523653 | DNA polymerase iota and related rad30-like enzymes |
Q37188497 | DNA polymerase switching: effects on spontaneous mutagenesis in Escherichia coli |
Q37261808 | DNA polymerase zeta cooperates with polymerases kappa and iota in translesion DNA synthesis across pyrimidine photodimers in cells from XPV patients. |
Q35978843 | DNA polymerases eta and iota |
Q34311450 | DNA postreplication repair and mutagenesis in Saccharomyces cerevisiae |
Q35978862 | DNA postreplication repair modulated by ubiquitination and sumoylation. |
Q36194928 | DNA repair and genome maintenance in Bacillus subtilis |
Q37455209 | DNA repair in Mycobacterium tuberculosis revisited |
Q36080876 | DNA replication fidelity in Escherichia coli: a multi-DNA polymerase affair. |
Q34176729 | Damage repair DNA polymerases Y. |
Q54541302 | Damage-repair error-prone polymerases of eubacteria: association with mobile genome elements. |
Q40253650 | Defining the position of the switches between replicative and bypass DNA polymerases |
Q28207807 | Deoxycytidyl transferase activity of the human REV1 protein is closely associated with the conserved polymerase domain |
Q35654604 | Directed Evolution of RecA Variants with Enhanced Capacity for Conjugational Recombination |
Q40865910 | Discrimination between translesion synthesis and template switching during bypass replication of thymine dimers in duplex DNA. |
Q44571741 | Disruption of the AtREV3 gene causes hypersensitivity to ultraviolet B light and gamma-rays in Arabidopsis: implication of the presence of a translesion synthesis mechanism in plants |
Q37087848 | Distinct peptide signals in the UmuD and UmuD' subunits of UmuD/D' mediate tethering and substrate processing by the ClpXP protease. |
Q35959590 | Diverse responses to UV light exposure in Acinetobacter include the capacity for DNA damage-induced mutagenesis in the opportunistic pathogens Acinetobacter baumannii and Acinetobacter ursingii |
Q42548215 | Dysfunctional proofreading in the Escherichia coli DNA polymerase III core |
Q44419666 | E. coli BW535, a triple mutant for the DNA repair genes xth, nth, and nfo, chronically induces the SOS response |
Q47609306 | Effect of deletion of SOS-induced polymerases, pol II, IV, and V, on spontaneous mutagenesis in Escherichia coli mutD5. |
Q90640712 | Effect of episomally encoded DNA polymerases on chemically induced mutagenesis at the hisG46 target in Ames test |
Q43816434 | Efficiency and accuracy of SOS-induced DNA polymerases replicating benzo[a]pyrene-7,8-diol 9,10-epoxide A and G adducts |
Q64104473 | Enhanced antibiotic resistance development from fluoroquinolone persisters after a single exposure to antibiotic |
Q56902070 | Enzymes of evolutionary change |
Q35582961 | Error-Prone DNA Polymerases: When Making a Mistake is the Only Way to Get Ahead |
Q28646677 | Error-free and error-prone lesion bypass by human DNA polymerase kappa in vitro |
Q78482138 | Error-free recombinational repair predominates over mutagenic translesion replication in E. coli |
Q33700107 | Error-prone DNA polymerase IV is regulated by the heat shock chaperone GroE in Escherichia coli |
Q24604149 | Error-prone bypass of certain DNA lesions by the human DNA polymerase kappa |
Q34049897 | Error‐prone DNA polymerase IV is controlled by the stress‐response sigma factor, RpoS, in Escherichia coli |
Q34311174 | Escherichia coli DNA polymerase III can replicate efficiently past a T-T cis-syn cyclobutane dimer if DNA polymerase V and the 3' to 5' exonuclease proofreading function encoded by dnaQ are inactivated |
Q33994529 | Escherichia coli DNA polymerase IV mutator activity: genetic requirements and mutational specificity |
Q44628475 | Escherichia coli DNA polymerase V subunit exchange: a post-SOS mechanism to curtail error-prone DNA synthesis |
Q35981005 | Escherichia coli DnaE Polymerase Couples Pyrophosphatase Activity to DNA Replication |
Q36164865 | Escherichia coli UmuC active site mutants: effects on translesion DNA synthesis, mutagenesis and cell survival |
Q35192038 | Escherichia coli nucleoside diphosphate kinase mutants depend on translesion DNA synthesis to prevent mutagenesis |
Q39587905 | Escherichia coli responses to a single DNA adduct |
Q33850056 | Eukaryotic DNA polymerases, a growing family |
Q34093113 | Eukaryotic DNA polymerases: proposal for a revised nomenclature. |
Q34244261 | Evolution of the two-step model for UV-mutagenesis |
Q34094904 | Evolutionary changes in mutation rates and spectra and their influence on the adaptation of pathogens |
Q34053164 | Factors that influence the mutagenic patterns of DNA adducts from chemical carcinogens |
Q33995258 | Genetic and biochemical characterization of a novel umuD mutation: insights into a mechanism for UmuD self-cleavage |
Q43984153 | Genetic assays for measuring rates of (CAG).(CTG) repeat instability in Escherichia coli |
Q34011389 | Genetic interactions between the Escherichia coli umuDC gene products and the beta processivity clamp of the replicative DNA polymerase. |
Q42412497 | Genetic interactions of DNA repair pathways in the pathogen Neisseria meningitidis |
Q24563143 | Genome of bacteriophage P1 |
Q22122107 | Genome sequence of the dissimilatory metal ion–reducing bacterium Shewanella oneidensis |
Q34964296 | Highly mutagenic replication by DNA polymerase V (UmuC) provides a mechanistic basis for SOS untargeted mutagenesis |
Q24631768 | Historical overview: searching for replication help in all of the rec places |
Q35026386 | How DNA lesions are turned into mutations within cells? |
Q24534772 | Human DINB1-encoded DNA polymerase kappa is a promiscuous extender of mispaired primer termini |
Q33950961 | Human DNA polymerase iota promiscuous mismatch extension |
Q33826153 | Human DNA polymerase kappa synthesizes DNA with extraordinarily low fidelity |
Q33770256 | Hypermutation in bacteria and other cellular systems |
Q39500181 | Identification of Escherichia coli dnaE (polC) mutants with altered sensitivity to 2',3'-dideoxyadenosine |
Q73270620 | Identification of mucAB-like homologs on two IncT plasmids, R394 and Rts-1 |
Q28486536 | Identification of some DNA damage-inducible genes of Mycobacterium tuberculosis: apparent lack of correlation with LexA binding |
Q92676465 | ImuB and ImuC contribute to UV-induced mutagenesis as part of the SOS regulon in Pseudomonas aeruginosa |
Q54343688 | Increase in UV mutagenesis by heat stress on UV-irradiated E. coli cells. |
Q35585702 | Increase in dNTP pool size during the DNA damage response plays a key role in spontaneous and induced-mutagenesis in Escherichia coli |
Q56900299 | Increase in error threshold for quasispecies by heterogeneous replication accuracy |
Q37282321 | Inducible SOS response system of DNA repair and mutagenesis in Escherichia coli |
Q73945700 | Inducible stable DNA replication (iSDR) and the uvr-dependent tolerance of pyrimidine dimers in UV-irradiated Escherichia coli are two uncoupled processes |
Q43181792 | Induction and inhibition of ciprofloxacin resistance-conferring mutations in hypermutator bacteria |
Q21146100 | Inhibition of mutation and combating the evolution of antibiotic resistance |
Q26745492 | Insights into the complex levels of regulation imposed on Escherichia coli DNA polymerase V |
Q34311670 | Interaction of the beta sliding clamp with MutS, ligase, and DNA polymerase I. |
Q27935721 | Interaction with PCNA is essential for yeast DNA polymerase eta function |
Q24291530 | Interactions in the error-prone postreplication repair proteins hREV1, hREV3, and hREV7 |
Q34574827 | Interplay between replication and recombination in Escherichia coli: impact of the alternative DNA polymerases |
Q43747964 | Interplay of clamp loader subunits in opening the beta sliding clamp of Escherichia coli DNA polymerase III holoenzyme |
Q33789422 | Intrinsic polymerase activities of UmuD'(2)C and MucA'(2)B are responsible for their different mutagenic properties during bypass of a T-T cis-syn cyclobutane dimer |
Q34317246 | Lack of strand bias in UV-induced mutagenesis in Escherichia coli |
Q47235095 | Lesion Bypass and the Reactivation of Stalled Replication Forks. |
Q34385155 | Lesion bypass DNA polymerases replicate across non-DNA segments |
Q73204355 | Lesion bypass by the Escherichia coli DNA polymerase V requires assembly of a RecA nucleoprotein filament |
Q33832074 | Lesions in DNA: hurdles for polymerases |
Q46014624 | Lessons from 50 years of SOS DNA-damage-induced mutagenesis. |
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Q27936681 | MPH1, a yeast gene encoding a DEAH protein, plays a role in protection of the genome from spontaneous and chemically induced damage. |
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Q33704985 | Mitochondrial DNA toxicity in forebrain neurons causes apoptosis, neurodegeneration, and impaired behavior |
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Q92238970 | Mutagenesis Induced by Sub-Lethal Doses of Ciprofloxacin: Genotypic and Phenotypic Differences Between the Pseudomonas aeruginosa Strain PA14 and Clinical Isolates |
Q42623706 | Mutagenic DNA repair potential in Pseudomonas spp., and characterization of the rulABPc operon from the highly mutable strain Pseudomonas cichorii 302959. |
Q47072057 | Mutagenic and nonmutagenic bypass of DNA lesions by Drosophila DNA polymerases dpoleta and dpoliota |
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Q33942666 | Mutagenic repair of DNA interstrand crosslinks |
Q43722177 | Mutagenicity of nitric oxide-releasing compounds in Escherichia coli: effect of superoxide generation and evidence for two mutagenic mechanisms |
Q36839971 | Mutations for Worse or Better: Low-Fidelity DNA Synthesis by SOS DNA Polymerase V Is a Tightly Regulated Double-Edged Sword |
Q24536098 | Mutations in human DNA polymerase eta motif II alter bypass of DNA lesions |
Q43639973 | Mutator effects of overproducing DNA polymerase eta (Rad30) and its catalytically inactive variant in yeast |
Q34694893 | Nascent DNA processing by RecJ favors lesion repair over translesion synthesis at arrested replication forks in Escherichia coli |
Q35013048 | New structural and mechanistic insight into the A-rule and the instructional and non-instructional behavior of DNA photoproducts and other lesions |
Q47172875 | Noise in the Machine: Alternative Pathway Sampling is the Rule During DNA Replication |
Q34077275 | Nucleotide excision repair or polymerase V-mediated lesion bypass can act to restore UV-arrested replication forks in Escherichia coli |
Q38990962 | Optical and force nanoscopy in microbiology |
Q44312358 | Ordered ATP hydrolysis in the gamma complex clamp loader AAA+ machine. |
Q43762669 | Overexpression of Ogt reduces MNU and ENU induced transition, but not transversion, mutations in E. coli |
Q53990151 | Oxygen free radical damage to DNA. Translesion synthesis by human DNA polymerase eta and resistance to exonuclease action at cyclopurine deoxynucleoside residues. |
Q34311635 | Participation of recombination proteins in rescue of arrested replication forks in UV-irradiated Escherichia coli need not involve recombination |
Q36139867 | Perspective on mutagenesis and repair: the standard model and alternate modes of mutagenesis |
Q28355115 | Physical interactions between DinI and RecA nucleoprotein filament for the regulation of SOS mutagenesis |
Q26822420 | Physiology of the read-write genome |
Q35265889 | Plasmid-encoded MucB protein is a DNA polymerase (pol RI) specialized for lesion bypass in the presence of MucA', RecA, and SSB |
Q36581242 | PolA1, a putative DNA polymerase I, is coexpressed with PerR and contributes to peroxide stress defenses of group A Streptococcus |
Q37236724 | Polymerase manager protein UmuD directly regulates Escherichia coli DNA polymerase III α binding to ssDNA. |
Q37424859 | Polymerases leave fingerprints: analysis of the mutational spectrum in Escherichia coli rpoB to assess the role of polymerase IV in spontaneous mutation |
Q36024244 | Portraits of a Y-family DNA polymerase |
Q34024462 | Posttranslational modification of the umuD-encoded subunit of Escherichia coli DNA polymerase V regulates its interactions with the beta processivity clamp |
Q24810491 | Precise temporal modulation in the response of the SOS DNA repair network in individual bacteria |
Q39455619 | Preferential incorporation of G opposite template T by the low-fidelity human DNA polymerase iota |
Q41090654 | Processing closely spaced lesions during Nucleotide Excision Repair triggers mutagenesis in E. coli. |
Q35978849 | Properties and functions of Escherichia coli: Pol IV and Pol V. |
Q35141646 | Prophage induction and differential RecA and UmuDAb transcriptome regulation in the DNA damage responses of Acinetobacter baumannii and Acinetobacter baylyi |
Q40881444 | Protein trafficking on sliding clamps. |
Q36445573 | Proteomic dissection of DNA polymerization |
Q46467417 | Purification and characterization of Escherichia coli DNA polymerase V. |
Q40505709 | Quantitative analysis of translesion DNA synthesis across a benzo[a]pyrene-guanine adduct in mammalian cells: the role of DNA polymerase kappa |
Q34020161 | Quantitative measurement of translesion replication in human cells: evidence for bypass of abasic sites by a replicative DNA polymerase |
Q46457518 | RecA acts in trans to allow replication of damaged DNA by DNA polymerase V. |
Q54490466 | RecA kicks Pol V into gear. |
Q21263032 | RecA proteins from Deinococcus geothermalis and Deinococcus murrayi--cloning, purification and biochemical characterisation |
Q35583008 | RecA-Dependent Recovery of Arrested DNA Replication Forks |
Q38203300 | Recent insight into the kinetic mechanisms and conformational dynamics of Y-Family DNA polymerases |
Q29619755 | Recombinational repair of DNA damage in Escherichia coli and bacteriophage lambda |
Q43686099 | Reduction of ENU-induced transversion mutations by the isoflavone genistein in Escherichia coli |
Q36446093 | Regulation of Escherichia coli SOS mutagenesis by dimeric intrinsically disordered umuD gene products. |
Q27310351 | Regulation of Mutagenic DNA Polymerase V Activation in Space and Time |
Q36761497 | Regulation of bacterial RecA protein function |
Q39501119 | Regulation of the rulAB mutagenic DNA repair operon of Pseudomonas syringae by UV-B (290 to 320 nanometers) radiation and analysis of rulAB-mediated mutability in vitro and in planta |
Q37288891 | Removal of misincorporated ribonucleotides from prokaryotic genomes: an unexpected role for nucleotide excision repair |
Q40430413 | Repair of chromosomal abasic sites in vivo involves at least three different repair pathways |
Q28678572 | Replication of UV-damaged DNA: new insights into links between DNA polymerases, mutagenesis and human disease |
Q43944895 | Replication restart in UV-irradiated Escherichia coli involving pols II, III, V, PriA, RecA and RecFOR proteins |
Q38601246 | Replisome Dynamics during Chromosome Duplication |
Q34552714 | Replisome-mediated translesion synthesis and leading strand template lesion skipping are competing bypass mechanisms |
Q50928301 | Replisome-mediated translesion synthesis by a cellular replicase. |
Q34276876 | Requirement of RAD5 and MMS2 for postreplication repair of UV-damaged DNA in Saccharomyces cerevisiae |
Q38658428 | Response of human DNA polymerase iota to DNA lesions |
Q89417794 | Ribonucleotide discrimination by translesion synthesis DNA polymerases |
Q35130259 | Role of DNA polymerase IV in Escherichia coli SOS mutator activity |
Q33639091 | Role of Escherichia coli DNA polymerase I in chromosomal DNA replication fidelity |
Q90205216 | Role of RNase H enzymes in maintaining genome stability in Escherichia coli expressing a steric-gate mutant of pol VICE391 |
Q36483171 | Role of accessory DNA polymerases in DNA replication in Escherichia coli: analysis of the dnaX36 mutator mutant |
Q33792439 | Role of the dinB gene product in spontaneous mutation in Escherichia coli with an impaired replicative polymerase |
Q24631035 | Roles of DNA polymerases V and II in SOS-induced error-prone and error-free repair in Escherichia coli |
Q41734679 | Roles of E. coli DNA polymerases IV and V in lesion-targeted and untargeted SOS mutagenesis |
Q34810207 | Roles of YqjH and YqjW, homologs of the Escherichia coli UmuC/DinB or Y superfamily of DNA polymerases, in stationary-phase mutagenesis and UV-induced mutagenesis of Bacillus subtilis |
Q34124367 | Roles of the Escherichia coli RecA protein and the global SOS response in effecting DNA polymerase selection in vivo |
Q54458103 | RuvABC is required to resolve holliday junctions that accumulate following replication on damaged templates in Escherichia coli. |
Q35822001 | SOS mutator activity: unequal mutagenesis on leading and lagging strands. |
Q59064993 | SOS polymerases |
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Q90727217 | SetRICE391, a negative transcriptional regulator of the integrating conjugative element 391 mutagenic response |
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Q54522641 | Silencing of the gene coding for the epsilon subunit of DNA polymerase III slows down the growth rate of Escherichia coli populations. |
Q36317166 | Simple and efficient purification of Escherichia coli DNA polymerase V: cofactor requirements for optimal activity and processivity in vitro |
Q38294175 | Single-stranded DNA-binding protein recruits DNA polymerase V to primer termini on RecA-coated DNA. |
Q33885007 | Sloppier copier DNA polymerases involved in genome repair |
Q43022010 | Sloppy bypass of an abasic lesion catalyzed by a Y-family DNA polymerase |
Q50134974 | Sources of spontaneous mutagenesis in bacteria. |
Q27933149 | Specificity of DNA lesion bypass by the yeast DNA polymerase eta. |
Q36961669 | Stationary phase mutagenesis in B. subtilis: a paradigm to study genetic diversity programs in cells under stress |
Q37274991 | Steric gate variants of UmuC confer UV hypersensitivity on Escherichia coli. |
Q36646366 | Strand-biased cytosine deamination at the replication fork causes cytosine to thymine mutations in Escherichia coli. |
Q35986593 | Stress responses and genetic variation in bacteria. |
Q37355812 | Stress-induced beta-lactam antibiotic resistance mutation and sequences of stationary-phase mutations in the Escherichia coli chromosome. |
Q27642458 | Structural basis for recruitment of translesion DNA polymerase Pol IV/DinB to the -clamp |
Q27634744 | Structure of the catalytic core of S. cerevisiae DNA polymerase eta: implications for translesion DNA synthesis |
Q34490504 | Subunit-specific degradation of the UmuD/D' heterodimer by the ClpXP protease: the role of trans recognition in UmuD' stability |
Q36337954 | Suffering in silence: the tolerance of DNA damage |
Q35562059 | Suppression of the E. coli SOS response by dNTP pool changes |
Q24561825 | Survival of Shewanella oneidensis MR-1 after UV radiation exposure |
Q37579017 | Telomere-mediated effects on melanogenesis and skin aging |
Q35037449 | The "A" rule revisited: polymerases as determinants of mutational specificity |
Q33957289 | The "tale" of UmuD and its role in SOS mutagenesis |
Q36331197 | The Acinetobacter regulatory UmuDAb protein cleaves in response to DNA damage with chimeric LexA/UmuD characteristics |
Q36538298 | The Escherichia coli SOS mutagenesis proteins UmuD and UmuD' interact physically with the replicative DNA polymerase |
Q34102902 | The Escherichia coli lacZ reversion mutagenicity assay |
Q42414957 | The Roles of UmuD in Regulating Mutagenesis |
Q33903483 | The SOS response regulates adaptive mutation |
Q93185974 | The SOS system: A complex and tightly regulated response to DNA damage |
Q27935826 | The Saccharomyces cerevisiae RAD6 group is composed of an error-prone and two error-free postreplication repair pathways |
Q27678899 | The UmuC subunit of the E. coli DNA polymerase V shows a unique interaction with the β-clamp processivity factor |
Q37317368 | The active form of DNA polymerase V is UmuD'(2)C-RecA-ATP. |
Q24531220 | The aflatoxin B(1) formamidopyrimidine adduct plays a major role in causing the types of mutations observed in human hepatocellular carcinoma |
Q36018582 | The aminoglycoside antibiotic kanamycin damages DNA bases in Escherichia coli: caffeine potentiates the DNA-damaging effects of kanamycin while suppressing cell killing by ciprofloxacin in Escherichia coli and Bacillus anthracis |
Q42287231 | The antirepressor needed for induction of linear plasmid-prophage N15 belongs to the SOS regulon. |
Q33937507 | The bacteriophage 434 repressor dimer preferentially undergoes autoproteolysis by an intramolecular mechanism |
Q33993202 | The bacteriophage P1 HumD protein is a functional homolog of the prokaryotic UmuD'-like proteins and facilitates SOS mutagenesis in Escherichia coli |
Q30641251 | The beta clamp targets DNA polymerase IV to DNA and strongly increases its processivity |
Q35132450 | The biochemical basis and in vivo regulation of SOS-induced mutagenesis promoted by Escherichia coli DNA polymerase V (UmuD'2C). |
Q34263814 | The contribution of endogenous sources of DNA damage to the multiple mutations in cancer |
Q34536932 | The dimeric SOS mutagenesis protein UmuD is active as a monomer |
Q34244975 | The discovery of error-prone DNA polymerase V and its unique regulation by RecA and ATP |
Q35165373 | The diverse spectrum of sliding clamp interacting proteins |
Q33892878 | The early detection of frameshift mutations induced by a food-borne carcinogen in rats: a new tool for molecular epidemiology. |
Q28834627 | The efficiency of the translesion synthesis across abasic sites by mitochondrial DNA polymerase is low in mitochondria of 3T3 cells |
Q28298627 | The eureka enzyme: the discovery of DNA polymerase |
Q34186298 | The expanding polymerase universe |
Q24683573 | The human DINB1 gene encodes the DNA polymerase Poltheta |
Q29614220 | The importance of repairing stalled replication forks |
Q36099918 | The many faces of DNA polymerases: strategies for mutagenesis and for mutational avoidance |
Q27692575 | The mechanisms of UV mutagenesis |
Q31422789 | The mutagenesis protein UmuC is a DNA polymerase activated by UmuD', RecA, and SSB and is specialized for translesion replication |
Q40634197 | The pKO2 linear plasmid prophage of Klebsiella oxytoca. |
Q35013042 | The property of DNA polymerase zeta: REV7 is a putative protein involved in translesion DNA synthesis and cell cycle control |
Q93350332 | The recombination mediator proteins RecFOR maintain RecA* levels for maximal DNA polymerase V Mut activity |
Q34614165 | The roles of Klenow processing and flap processing activities of DNA polymerase I in chromosome instability in Escherichia coli K12 strains |
Q54440494 | The two inducible responses, SOS and heat-shock, in Escherichia coli act synergistically during Weigle reactivation of the bacteriophage phiX174. |
Q44192202 | The two-step model for translesion synthesis: then and now. |
Q41820110 | Transcriptional modulator NusA interacts with translesion DNA polymerases in Escherichia coli. |
Q34205013 | Transcriptional responses to DNA damage |
Q34509062 | Translesion DNA Synthesis |
Q34356338 | Translesion DNA polymerases |
Q39171293 | Translesion DNA polymerases in eukaryotes: what makes them tick? |
Q34389241 | Translesion DNA synthesis and mutagenesis in prokaryotes. |
Q37952001 | Translesion DNA synthesis in the context of cancer research |
Q37775587 | Translesion DNA synthesis polymerases in DNA interstrand crosslink repair |
Q39079498 | Translesion Synthesis: Insights into the Selection and Switching of DNA Polymerases. |
Q33953024 | Translesion synthesis by the UmuC family of DNA polymerases |
Q39095697 | Translesion synthesis by yeast DNA polymerase zeta from templates containing lesions of ultraviolet radiation and acetylaminofluorene |
Q34036796 | Two distinct modes of RecA action are required for DNA polymerase V-catalyzed translesion synthesis |
Q54472760 | Two processivity clamp interactions differentially alter the dual activities of UmuC. |
Q33400985 | Two-polymerase mechanisms dictate error-free and error-prone translesion DNA synthesis in mammals |
Q33279151 | UV-induced mutagenesis in Escherichia coli SOS response: a quantitative model |
Q41887546 | UmuD and RecA directly modulate the mutagenic potential of the Y family DNA polymerase DinB. |
Q35969100 | UmuDAb: An Error-Prone Polymerase Accessory Homolog Whose N-Terminal Domain Is Required for Repression of DNA Damage Inducible Gene Expression in Acinetobacter baylyi |
Q36023692 | What a difference a decade makes: insights into translesion DNA synthesis |
Q34464872 | Why do cells have multiple error-prone DNA polymerases? |
Q36778894 | Y-family DNA polymerases and their role in tolerance of cellular DNA damage. |
Q24604217 | poliota, a remarkably error-prone human DNA polymerase |
Q35013038 | poliota-dependent lesion bypass in vitro |
Q33995520 | umuDC-dnaQ Interaction and its implications for cell cycle regulation and SOS mutagenesis in Escherichia coli. |
Q33995559 | umuDC-mediated cold sensitivity is a manifestation of functions of the UmuD(2)C complex involved in a DNA damage checkpoint control |
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