U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from GEO Profiles

    • Showing Current items.

    MSH3 mismatch repair protein MSH3 [ Saccharomyces cerevisiae S288C ]

    Gene ID: 850454, updated on 9-Dec-2024

    Summary

    Official Symbol
    MSH3
    Official Full Name
    mismatch repair protein MSH3
    Primary source
    SGD:S000000688
    Locus tag
    YCR092C
    See related
    AllianceGenome:SGD:S000000688; FungiDB:YCR092C; VEuPathDB:YCR092C
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Saccharomyces cerevisiae S288C (strain: S288C)
    Lineage
    Eukaryota; Fungi; Dikarya; Ascomycota; Saccharomycotina; Saccharomycetes; Saccharomycetales; Saccharomycetaceae; Saccharomyces
    Summary
    Enables DNA insertion or deletion binding activity and double-strand/single-strand DNA junction binding activity. Contributes to Y-form DNA binding activity and heteroduplex DNA loop binding activity. Involved in DNA metabolic process. Located in cytoplasm and nucleus. Part of MutSbeta complex. Used to study cancer. Human ortholog(s) of this gene implicated in colorectal carcinoma; endometrial cancer; endometrial carcinoma; familial adenomatous polyposis 4; and lung non-small cell carcinoma. Orthologous to human MSH3 (mutS homolog 3). [provided by Alliance of Genome Resources, Dec 2024]
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See MSH3 in Genome Data Viewer
    Location:
    chromosome: III
    Exon count:
    1
    Sequence:
    Chromosome: III; NC_001135.5 (276764..279820, complement)

    Chromosome III - NC_001135.5Genomic Context describing neighboring genes Neighboring gene uncharacterized protein Neighboring gene putative serine/threonine protein kinase KIN82 Neighboring gene CCR4-NOT core subunit CDC39 Neighboring gene aminophospholipid translocase regulatory protein CDC50

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Gene Ontology Provided by SGD

    Function Evidence Code Pubs
    enables ATP binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables ATP-dependent DNA damage sensor activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables DNA binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables DNA insertion or deletion binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    contributes_to Y-form DNA binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables double-strand/single-strand DNA junction binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables double-stranded DNA binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    contributes_to heteroduplex DNA loop binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    contributes_to mismatched DNA binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables mismatched DNA binding IEA
    Inferred from Electronic Annotation
    more info
     
    Process Evidence Code Pubs
    involved_in DNA metabolic process IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in DNA recombination IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in DNA repair IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in meiotic mismatch repair IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in mismatch repair IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in mismatch repair IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in mismatch repair IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in mitotic recombination IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in mitotic recombination IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in removal of nonhomologous ends IGI
    Inferred from Genetic Interaction
    more info
    PubMed 
    involved_in removal of nonhomologous ends IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in replication fork arrest IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    Component Evidence Code Pubs
    part_of MutSbeta complex IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    located_in cytoplasm HDA PubMed 
    located_in nucleus HDA PubMed 
    is_active_in nucleus IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in nucleus IEA
    Inferred from Electronic Annotation
    more info
     

    General protein information

    Preferred Names
    mismatch repair protein MSH3
    NP_010016.2
    • Mismatch repair protein; forms dimers with Msh2p that mediate repair of insertion or deletion mutations and removal of nonhomologous DNA ends, contains a PCNA (Pol30p) binding motif required for genome stability

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    Genome Annotation

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference assembly

    Genomic

    1. NC_001135.5 Reference assembly

      Range
      276764..279820 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001178798.1NP_010016.2  TPA: mismatch repair protein MSH3 [Saccharomyces cerevisiae S288C]

      See identical proteins and their annotated locations for NP_010016.2

      Status: REVIEWED

      UniProtKB/Swiss-Prot
      A6ZTR3, D6VR92, P25336
      UniProtKB/TrEMBL
      N1P7Y1
      Conserved Domains (1) summary
      COG0249
      Location:1271015
      MutS; DNA mismatch repair ATPase MutS [Replication, recombination and repair]