Competitive processivity-clamp usage by DNA polymerases during DNA replication and repair.
about
Structure of a Sliding Clamp on DNASliding Clamp–DNA Interactions Are Required for Viability and Contribute to DNA Polymerase Management in Escherichia coliM. tuberculosis Sliding β-Clamp Does Not Interact Directly with the NAD+ -Dependent DNA LigaseThe UmuC subunit of the E. coli DNA polymerase V shows a unique interaction with the β-clamp processivity factorThe 9-1-1 checkpoint clamp physically interacts with polzeta and is partially required for spontaneous polzeta-dependent mutagenesis in Saccharomyces cerevisiae.A Genetic Selection for dinB Mutants Reveals an Interaction between DNA Polymerase IV and the Replicative Polymerase That Is Required for Translesion SynthesisParallel multiplicative target screening against divergent bacterial replicases: identification of specific inhibitors with broad spectrum potentialRole of Escherichia coli DNA polymerase I in chromosomal DNA replication fidelity.Roles of the Escherichia coli RecA protein and the global SOS response in effecting DNA polymerase selection in vivoInteraction of the sliding clamp beta-subunit and Hda, a DnaA-related protein.The interplay of primer-template DNA phosphorylation status and single-stranded DNA binding proteins in directing clamp loaders to the appropriate polarity of DNA.T4 replication: what does "processivity" really mean?The dynamic processivity of the T4 DNA polymerase during replicationTranslesion DNA Synthesis.Interplay between replication and recombination in Escherichia coli: impact of the alternative DNA polymerases.Two forms of ribosomal protein L2 of Escherichia coli that inhibit DnaA in DNA replication.Exchange of DNA polymerases at the replication fork of bacteriophage T7.Transposase interaction with the β sliding clamp: effects on insertion sequence proliferation and transposition rateSelective disruption of the DNA polymerase III α-β complex by the umuD gene products.Escherichia coli DNA polymerase IV (Pol IV), but not Pol II, dynamically switches with a stalled Pol III* replicaseIdentification of β Clamp-DNA Interaction Regions That Impair the Ability of E. coli to Tolerate Specific Classes of DNA Damage.Replisome architecture and dynamics in Escherichia coli.Dynamics of loading the Escherichia coli DNA polymerase processivity clamp.Escherichia coli DNA polymerase III is responsible for the high level of spontaneous mutations in mutT strainsA direct proofreader-clamp interaction stabilizes the Pol III replicase in the polymerization mode.Controlling mutation: intervening in evolution as a therapeutic strategy.Contributions of the individual hydrophobic clefts of the Escherichia coli beta sliding clamp to clamp loading, DNA replication and clamp recyclingLoading clamps for DNA replication and repairThe clamp loader assembles the beta clamp onto either a 3' or 5' primer terminus: the underlying basis favoring 3' loading.Cycling of the E. coli lagging strand polymerase is triggered exclusively by the availability of a new primer at the replication forkRegulation of interactions with sliding clamps during DNA replication and repair.Chromosomal replication dynamics and interaction with the β sliding clamp determine orientation of bacterial transposable elements.Maturation of bacteriophage T4 lagging strand fragments depends on interaction of T4 RNase H with T4 32 protein rather than the T4 gene 45 clamp.Increased dNTP binding affinity reveals a nonprocessive role for Escherichia coli beta clamp with DNA polymerase IV.Replisome Dynamics during Chromosome Duplication.Characterization of Escherichia coli UmuC active-site loops identifies variants that confer UV hypersensitivity.Recent Advances in Helicobacter pylori Replication: Possible Implications in Adaptation to a Pathogenic Lifestyle and Perspectives for Drug Design.The rate of polymerase release upon filling the gap between Okazaki fragments is inadequate to support cycling during lagging strand synthesisThe Escherichia coli dnaN159 mutant displays altered DNA polymerase usage and chronic SOS induction.Defining the position of the switches between replicative and bypass DNA polymerases.
P2860
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P2860
Competitive processivity-clamp usage by DNA polymerases during DNA replication and repair.
description
2003 nî lūn-bûn
@nan
2003 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Competitive processivity-clamp ...... ng DNA replication and repair.
@ast
Competitive processivity-clamp ...... ng DNA replication and repair.
@en
Competitive processivity-clamp ...... ng DNA replication and repair.
@nl
type
label
Competitive processivity-clamp ...... ng DNA replication and repair.
@ast
Competitive processivity-clamp ...... ng DNA replication and repair.
@en
Competitive processivity-clamp ...... ng DNA replication and repair.
@nl
prefLabel
Competitive processivity-clamp ...... ng DNA replication and repair.
@ast
Competitive processivity-clamp ...... ng DNA replication and repair.
@en
Competitive processivity-clamp ...... ng DNA replication and repair.
@nl
P2860
P356
P1433
P1476
Competitive processivity-clamp usage by DNA polymerases during DNA replication and repair
@en
P2093
Myron F Goodman
Roxana E Georgescu
P2860
P304
P356
10.1093/EMBOJ/CDG603
P407
P577
2003-12-01T00:00:00Z