In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair. - Test2 - elhamkhani - TriplyDB

In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair.

In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair.

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Structural insights into DNA repair by RNase T--an exonuclease processing 3' end of structured DNA in repair pathways The interaction of DNA mismatch repair proteins with human exonuclease I Human exonuclease I is required for 5' and 3' mismatch repair Evidence for involvement of HMGB1 protein in human DNA mismatch repair Mismatch repair proteins collaborate with methyltransferases in the repair of O(6)-methylguanine Molecular mechanisms of the whole DNA repair system: a comparison of bacterial and eukaryotic systems A proteome-wide protein interaction map for Campylobacter jejuni DNA mismatch repair: molecular mechanism, cancer, and ageing PCNA-MutSalpha-mediated binding of MutLalpha to replicative DNA with mismatched bases to induce apoptosis in human cells RecJ exonuclease: substrates, products and interaction with SSB The crystal structure of exonuclease RecJ bound to Mn2+ ion suggests how its characteristic motifs are involved in exonuclease activity Structural basis of Escherichia coli single-stranded DNA-binding protein stimulation of exonuclease I Structure of RecJ Exonuclease Defines Its Specificity for Single-stranded DNA Recognition and processing of double-stranded DNA by ExoX, a distributive 3'-5' exonuclease Saccharomyces cerevisiae Msh2-Msh3 acts in repair of base-base mispairs Inactivation of Exonuclease 1 in mice results in DNA mismatch repair defects, increased cancer susceptibility, and male and female sterility DNA mismatch repair and mutation avoidance pathways Exonuclease 1-dependent and independent mismatch repair DNA mismatch repair in eukaryotes and bacteria Dominant mutations in S. cerevisiae PMS1 identify the Mlh1-Pms1 endonuclease active site and an exonuclease 1-independent mismatch repair pathway Structural and biochemical studies of a moderately thermophilic exonuclease I from Methylocaldum szegediense Partial reconstitution of human DNA mismatch repair in vitro: characterization of the role of human replication protein A Human mismatch repair: reconstitution of a nick-directed bidirectional reaction.Partial reconstitution of DNA large loop repair with purified proteins from Saccharomyces cerevisiae A conserved MutS homolog connector domain interface interacts with MutL homologs.Saccharomyces cerevisiae Msh2-Msh6 DNA binding kinetics reveal a mechanism of targeting sites for DNA mismatch repair.Enhancing multiplex genome editing by natural transformation (MuGENT) via inactivation of ssDNA exonucleases.Evolution in an oncogenic bacterial species with extreme genome plasticity: Helicobacter pylori East Asian genomes.Efficient repair of large DNA loops in Saccharomyces cerevisiae Structure and function of TatD exonuclease in DNA repair.Stabilization of perfect and imperfect tandem repeats by single-strand DNA exonucleases Improving lambda red genome engineering in Escherichia coli via rational removal of endogenous nucleases.Functional interactions and signaling properties of mammalian DNA mismatch repair proteins.Identification of genes subject to positive selection in uropathogenic strains of Escherichia coli: a comparative genomics approach.DNA Mismatch Repair.Probing cellular processes with oligo-mediated recombination and using the knowledge gained to optimize recombineering RecJ-like protein from Pyrococcus furiosus has 3'-5' exonuclease activity on RNA: implications for proofreading of 3'-mismatched RNA primers in DNA replication.The UvrD helicase and its modulation by the mismatch repair protein MutL.A simple and effective method for construction of Escherichia coli strains proficient for genome engineering.Self-assembly of Escherichia coli MutL and its complexes with DNA

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P2860

In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair.

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In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair.

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In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair.

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In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair.

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In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair.

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In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair.

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In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair.

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Proceedings of the National Academy of Sciences of the United States of America

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In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair.

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C Baitinger

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Human strand-specific mismatch repair occurs by a bidirectional mechanism similar to that of the bacterial reaction

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Products of DNA mismatch repair genes mutS and mutL are required for transcription-coupled nucleotide-excision repair of the lactose operon in Escherichia coli

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