Pages that link to "Q35930280"
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The following pages link to Altering the conserved nucleotide binding motif in the Salmonella typhimurium MutS mismatch repair protein affects both its ATPase and mismatch binding activities (Q35930280):
Displaying 50 items.
- Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: examination of mutations found in hereditary nonpolyposis colorectal cancer (Q22003969) (← links)
- hMSH4-hMSH5 adenosine nucleotide processing and interactions with homologous recombination machinery (Q24622206) (← links)
- Requirement of mismatch repair genes MSH2 and MSH3 in the RAD1-RAD10 pathway of mitotic recombination in Saccharomyces cerevisiae. (Q27930027) (← links)
- The Saccharomyces cerevisiae Msh2 and Msh6 proteins form a complex that specifically binds to duplex oligonucleotides containing mismatched DNA base pairs (Q27930815) (← links)
- Genetic and biochemical analysis of Msh2p-Msh6p: role of ATP hydrolysis and Msh2p-Msh6p subunit interactions in mismatch base pair recognition. (Q27932001) (← links)
- Saccharomyces cerevisiae Msh2p and Msh6p ATPase activities are both required during mismatch repair (Q27932017) (← links)
- Five SWI/SNF gene products are components of a large multisubunit complex required for transcriptional enhancement (Q27933086) (← links)
- The origin recognition complex in silencing, cell cycle progression, and DNA replication. (Q27936799) (← links)
- Separation-of-function mutations in Saccharomyces cerevisiae MSH2 that confer mismatch repair defects but do not affect nonhomologous-tail removal during recombination (Q27938377) (← links)
- Analysis of the functional domains of the mismatch repair homologue Msh1p and its role in mitochondrial genome maintenance. (Q27938988) (← links)
- Caenorhabditis elegans msh-5 is required for both normal and radiation-induced meiotic crossing over but not for completion of meiosis (Q28140164) (← links)
- Nucleotides and heteroduplex DNA preserve the active conformation of Pseudomonas aeruginosa MutS by preventing protein oligomerization (Q28366275) (← links)
- ATP-dependent interaction of human mismatch repair proteins and dual role of PCNA in mismatch repair (Q28610858) (← links)
- Msh2 blocks an alternative mechanism for non-homologous tail removal during single-strand annealing in Saccharomyces cerevisiae (Q28750609) (← links)
- The swi4+ gene of Schizosaccharomyces pombe encodes a homologue of mismatch repair enzymes (Q31160628) (← links)
- Antibiotics induce redox-related physiological alterations as part of their lethality. (Q33665248) (← links)
- Requirement for Phe36 for DNA binding and mismatch repair by Escherichia coli MutS protein (Q33786744) (← links)
- MutS mediates heteroduplex loop formation by a translocation mechanism (Q33887145) (← links)
- Genotype to phenotype: analyzing the effects of inherited mutations in colorectal cancer families (Q33939068) (← links)
- Isolation and characterization of two Saccharomyces cerevisiae genes encoding homologs of the bacterial HexA and MutS mismatch repair proteins (Q33960283) (← links)
- Enhanced levels of lambda Red-mediated recombinants in mismatch repair mutants (Q34283357) (← links)
- The role of nucleotide binding and hydrolysis in the function of the fission yeast cdc18(+) gene product (Q34606637) (← links)
- Dominant negative mutator mutations in the mutS gene of Escherichia coli (Q34726651) (← links)
- Mutator phenotypes of yeast strains heterozygous for mutations in the MSH2 gene. (Q35063954) (← links)
- Mismatch repair during homologous and homeologous recombination (Q35164333) (← links)
- Human MSH2 (hMSH2) protein controls ATP processing by hMSH2-hMSH6 (Q35562811) (← links)
- The predicted truncation from a cancer-associated variant of the MSH2 initiation codon alters activity of the MSH2-MSH6 mismatch repair complex (Q35563361) (← links)
- A pathogenicity island replicon in Staphylococcus aureus replicates as an unstable plasmid (Q35971709) (← links)
- Azotobacter vinelandii mutS: nucleotide sequence and mutant analysis (Q36124448) (← links)
- Mismatch repair (Q36283640) (← links)
- Contribution of Msh2 and Msh6 subunits to the asymmetric ATPase and DNA mismatch binding activities of Saccharomyces cerevisiae Msh2-Msh6 mismatch repair protein (Q36359452) (← links)
- Single-molecule motions and interactions in live cells reveal target search dynamics in mismatch repair. (Q36394407) (← links)
- Engineered disulfide-forming amino acid substitutions interfere with a conformational change in the mismatch recognition complex Msh2-Msh6 required for mismatch repair (Q36436073) (← links)
- The hMSH2(M688R) Lynch syndrome mutation may function as a dominant negative (Q36447028) (← links)
- Functional domains of the Saccharomyces cerevisiae Mlh1p and Pms1p DNA mismatch repair proteins and their relevance to human hereditary nonpolyposis colorectal cancer-associated mutations (Q36570003) (← links)
- Genetic map of Salmonella typhimurium, edition VIII (Q36669927) (← links)
- A dominant negative mutation in a spliceosomal ATPase affects ATP hydrolysis but not binding to the spliceosome (Q36821799) (← links)
- Hereditary cancer-associated missense mutations in hMSH6 uncouple ATP hydrolysis from DNA mismatch binding (Q36968380) (← links)
- Sequence context effect for hMSH2-hMSH6 mismatch-dependent activation (Q37132714) (← links)
- DNA mismatch repair (MMR)-dependent 5-fluorouracil cytotoxicity and the potential for new therapeutic targets. (Q37602208) (← links)
- DnaK as a thermometer: threonine-199 is site of autophosphorylation and is critical for ATPase activity (Q37611390) (← links)
- An essential virulence protein of Agrobacterium tumefaciens, VirB4, requires an intact mononucleotide binding domain to function in transfer of T-DNA. (Q38301271) (← links)
- ATP-hydrolysis-dependent conformational switch modulates the stability of MutS-mismatch complexes (Q38316177) (← links)
- The Agrobacterium tumefaciens virB4 gene product is an essential virulence protein requiring an intact nucleoside triphosphate-binding domain (Q38321187) (← links)
- hMSH2 and hMSH6 play distinct roles in mismatch binding and contribute differently to the ATPase activity of hMutSalpha (Q38336441) (← links)
- Mismatch recognition-coupled stabilization of Msh2-Msh6 in an ATP-bound state at the initiation of DNA repair (Q39656168) (← links)
- Asymmetric ATP binding and hydrolysis activity of the Thermus aquaticus MutS dimer is key to modulation of its interactions with mismatched DNA. (Q39656345) (← links)
- Mismatch DNA recognition protein from an extremely thermophilic bacterium, Thermus thermophilus HB8 (Q39715504) (← links)
- Identification of the ATP-binding site in the terminase subunit pUL56 of human cytomegalovirus. (Q39733745) (← links)
- Depletion of the cellular amounts of the MutS and MutH methyl-directed mismatch repair proteins in stationary-phase Escherichia coli K-12 cells (Q39841075) (← links)