PMID:22001225

From omp dev
Revision as of 19:56, 15 November 2011 by Joncrz (talk | contribs) (Fill PMID: Page!)
Jump to: navigation, search
Citation

Zhang, M, Zhou, Y, Li, T, Wang, H, Cheng, F, Zhou, Y, Bi, L and Zhang, XE (2011) MutL associates with Escherichia coli RecA and inhibits its ATPase activity.Arch Biochem Biophys

Abstract

Different DNA repair systems are known to cooperate to deal with DNA damage. However, the regulatory role of the cross-talk between these pathways is unclear. Here, we have shown that MutL, an essential component of mismatch repair, is a RecA-interacting protein, and that its highly conserved N-terminal domain is sufficient for this interaction. Surface plasmon resonance and capillary electrophoresis analyses revealed that MutL has little effect on RecA-ssDNA filament formation, but dose down-regulate the ATPase activity of RecA. Our findings identify a new role for MutL, and suggest its regulatory role in homologous recombination.

Links

PubMed Online version:10.1016/j.abb.2011.09.013

Keywords


Main Points of the Paper

Please summarize the main points of the paper.

Materials and Methods Used

Please list the materials and methods used in this paper (strains, plasmids, antibodies, etc).

Phenotype Annotations

See Help:AnnotationTable for details on how to edit this table.
<protect>

Phenotype of Taxon Information Genotype Information (if known) Condition Information OMP ID OMP Term Name ECO ID ECO Term Name Notes Status

</protect>

Notes

References

See Help:References for how to manage references in omp dev.