Study of the Escherichia coli vsr endonuclease and its interaction with MutL
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Summary
It is concluded that the interaction between Vsr and MutL is not nucleotide dependent, and Vsr stimulation in the presence of MutL was unaffected by the presence or absence of ATP or ADP.
- Type
- dissertation
- Published
- 2008-01-01
- Cited by
- 0
- References
- 95
- Access
- Open access
- OpenAlex
- https://openalex.org/W49530165
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:107424965
Keywords
DNA mismatch repair, Endonuclease, Frameshift mutation, Biology, Escherichia coli
References
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- Methyl-directed DNA mismatch correction.
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- A short course in bacterial genetics
- Deoxyribonucleic acid polymerase III of Escherichia coli. Purification and properties.
- Dominant negative mutator mutations in the mutS gene of Escherichia coli
- Deoxyribonucleic acid polymerase III of Escherichia coli. Characterization of associated exonuclease activities.
- Growth-rate-dependent regulation of the expression and inactivation of thymidylate synthase in Saccharomyces cerevisiae
- Gene conversion in Escherichia coli. Resolution of heteroallelic mismatched nucleotides by co-repair.
- Exonuclease VII of Escherichia coli. Mechanism of action.
- Bacterial genes mutL, mutS, and dcm participate in repair of mismatches at 5-methylcytosine sites
- A gene required for very short patch repair in Escherichia coli is adjacent to the DNA cytosine methylase gene
- Repair of a mismatch is influenced by the base composition of the surrounding nucleotide sequence.
- Base selection, proofreading, and mismatch repair during DNA replication in Escherichia coli.
- Escherichia coli K-12 clones that overproduce dam methylase are hypermutable
- Identification and purification of a single-stranded-DNA-specific exonuclease encoded by the recJ gene of Escherichia coli.
- Separation of DNA binding from the transcription-activating function of a eukaryotic regulatory protein.
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