Abstract
MutS, MutL and MutH are the three essential proteins for initiation of methyl-directed DNA mismatch repair to correct mistakes made during DNA replication in Escherichia coli. MutH cleaves a newly synthesized and unmethylated daughter strand 5' to the sequence d(GATC) in a hemi-methylated duplex. Activation of MutH requires the recognition of a DNA mismatch by MutS and MutL. We have crystallized MutH in two space groups and solved the structures at 1.7 and 2.3 A resolution, respectively. The active site of MutH is located at an interface between two subdomains that pivot relative to one another, as revealed by comparison of the crystal structures, and this presumably regulates the nuclease activity. The relative motion of the two subdomains in MutH correlates with the position of a protruding C-terminal helix. This helix appears to act as a molecular lever through which MutS and MutL may communicate the detection of a DNA mismatch and activate MutH. With sequence homology to Sau3AI and structural similarity to PvuII endonuclease, MutH is clearly related to these enzymes by divergent evolution, and this suggests that type II restriction endonucleases evolved from a common ancestor.
MeSH Terms
Amino Acid Sequence
Binding Sites
Crystallography, X-Ray
DNA/chemistry
DNA Repair
DNA Repair Enzymes
DNA-Binding Proteins/chemistry
Deoxyribonucleases, Type II Site-Specific/chemistry
Dimerization
Endodeoxyribonucleases/chemistry
Enzyme Activation
Escherichia coli/enzymology
Escherichia coli Proteins
Models, Molecular
Molecular Sequence Data
Protein Conformation
Protein Structure, Tertiary
Chemicals
DNA-Binding Proteins
Escherichia coli Proteins
DNA
Endodeoxyribonucleases
methyl-directed mismatch repair protein, E coli
Deoxyribonucleases, Type II Site-Specific
DNA Repair Enzymes
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ban C
Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Yang W
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