A Genetic Selection for dinB Mutants Reveals an Interaction between DNA Polymerase IV and the Replicative Polymerase That Is Required for Translesion Synthesis - Wikidata - wikimedia - TriplyDB

A Genetic Selection for dinB Mutants Reveals an Interaction between DNA Polymerase IV and the Replicative Polymerase That Is Required for Translesion Synthesis

A Genetic Selection for dinB Mutants Reveals an Interaction between DNA Polymerase IV and the Replicative Polymerase That Is Required for Translesion Synthesis

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Identification of β Clamp-DNA Interaction Regions That Impair the Ability of E. coli to Tolerate Specific Classes of DNA Damage.DNA Polymerases ImuC and DinB Are Involved in DNA Alkylation Damage Tolerance in Pseudomonas aeruginosa and Pseudomonas putida How MutS finds a needle in a haystack Exchange between Escherichia coli polymerases II and III on a processivity clamp.DNA Polymerase III, but Not Polymerase IV, Must Be Bound to a τ-Containing DnaX Complex to Enable Exchange into Replication Forks.Persistent damaged bases in DNA allow mutagenic break repair in Escherichia coli.MutS regulates access of the error-prone DNA polymerase Pol IV to replication sites: a novel mechanism for maintaining replication fidelity.Sub-Minimum Inhibitory Concentrations of Rhubarb Water Extracts Inhibit Streptococcus suis Biofilm Formation.Collision with duplex DNA renders Escherichia coli DNA polymerase III holoenzyme susceptible to DNA polymerase IV-mediated polymerase switching on the sliding clamp Single-molecule imaging reveals multiple pathways for the recruitment of translesion polymerases after DNA damage.DNA polymerase IV primarily operates outside of DNA replication forks in Escherichia coli.Characterization of a coupled DNA replication and translesion synthesis polymerase supraholoenzyme from archaea.

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A Genetic Selection for dinB Mutants Reveals an Interaction between DNA Polymerase IV and the Replicative Polymerase That Is Required for Translesion Synthesis

http://www.wikidata.org/entity/Q28547796

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A Genetic Selection for dinB M ...... ired for Translesion Synthesis

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A Genetic Selection for dinB M ...... ired for Translesion Synthesis

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A Genetic Selection for dinB M ...... ired for Translesion Synthesis

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A Genetic Selection for dinB M ...... ired for Translesion Synthesis

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A Genetic Selection for dinB M ...... ired for Translesion Synthesis

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A Genetic Selection for dinB M ...... ired for Translesion Synthesis

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A Genetic Selection for dinB M ...... ired for Translesion Synthesis

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A Genetic Selection for dinB M ...... ired for Translesion Synthesis

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A Genetic Selection for dinB M ...... ired for Translesion Synthesis

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JOURNAL.PGEN.1005507

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A Genetic Selection for dinB M ...... ired for Translesion Synthesis

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Anthony J Berdis

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Joseph J Loparo

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Jung-Suk Choi

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Justin M H Heltzel

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Mark D Sutton

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Michelle K Scotland

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P2860

Localization of DNA polymerases eta and iota to the replication machinery is tightly co-ordinated in human cells.

Multiple pathways for SOS-induced mutagenesis in Escherichia coli: an overexpression of dinB/dinP results in strongly enhancing mutagenesis in the absence of any exogenous treatment to damage DNA

Eukaryotic translesion polymerases and their roles and regulation in DNA damage tolerance

Crystal structure of a Y-family DNA polymerase in action: a mechanism for error-prone and lesion-bypass replication

Flexibility revealed by the 1.85 A crystal structure of the beta sliding-clamp subunit of Escherichia coli DNA polymerase III

Structural basis for recruitment of translesion DNA polymerase Pol IV/DinB to the -clamp

Structure of a Sliding Clamp on DNA

Sliding Clamp–DNA Interactions Are Required for Viability and Contribute to DNA Polymerase Management in Escherichia coli

A strategically located serine residue is critical for the mutator activity of DNA polymerase IV from Escherichia coli

Proofreading exonuclease on a tether: the complex between the E. coli DNA polymerase III subunits α, epsilon, θ and β reveals a highly flexible arrangement of the proofreading domain.

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