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- Table of Contents
Facts about DNA mismatch repair protein Msh6.
Following mismatch binding, forms a ternary complex with the MutL alpha heterodimer, which is thought to be responsible for directing the downstream MMR occasions, such as strand discrimination, excision, and resynthesis. ATP binding and hydrolysis play a pivotal role in mismatch repair functions.
Human | |
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Gene Name: | MSH6 |
Uniprot: | P52701 |
Entrez: | 2956 |
Belongs to: |
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DNA mismatch repair MutS family |
DNA mismatch repair protein Msh6; G/T mismatch-binding protein; GTBPHNPCC5; GTMBP; hMSH6; HSAP; mutS (E. coli) homolog 6; mutS homolog 6 (E. coli); MutS-alpha 160 kDa subunit; p160; sperm-associated protein
Mass (kDA):
152.786 kDA
Human | |
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Location: | 2p16.3 |
Sequence: | 2; NC_000002.12 (47783082..47806954) |
Nucleus. Chromosome. Associates with H3K36me3 via its PWWP domain.
PMID: 8942985 by Acharya S., et al. hMSH2 forms specific mispair-binding complexes with hMSH3 and hMSH6.
PMID: 9455487 by Shiwaku H.O., et al. Alternative splicing of GTBP in normal human tissues.