Structured Summary
Abstract
DNA repair proteins that include the bacterial MutL protein and its eukaryotic homologs. They consist of a conserved N-terminal region with weak ATPase activity, an endonuclease motif, and a C-terminal domain that forms MutL homodimers or heterodimers between MLH1 and the PMS1, MISMATCH REPAIR ENDONUCLEASE PMS2; or MLH3 proteins. These complexes function in DNA repair pathways, primarily DNA MISMATCH REPAIR, where MutL/MLH1 and the MUTS DNA MISMATCH-BINDING PROTEIN are targeted to damaged DNA.
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Synonyms
1 entry terms
- MutL Homologs
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Aspects Covered
29 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
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History Note
2017
MeSH Record
Previous Indexing
- Adenosine Triphosphatases (1992-2016)
- DNA Repair (1982-2016)
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References
- National Library of Medicine. MutL Proteins. Medical Subject Headings (MeSH). 2026. Unique ID D000070956. http://id.nlm.nih.gov/mesh/2026/D000070956
- MutL Proteins. In: Wikidata. https://www.wikidata.org/wiki/Q24723571