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    MEP1 ammonium permease MEP1 [ Saccharomyces cerevisiae S288C ]

    Gene ID: 853019, updated on 9-Dec-2024

    Summary

    Official Symbol
    MEP1
    Official Full Name
    ammonium permease MEP1
    Primary source
    SGD:S000003353
    Locus tag
    YGR121C
    See related
    AllianceGenome:SGD:S000003353; FungiDB:YGR121C; VEuPathDB:YGR121C
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Saccharomyces cerevisiae S288C (strain: S288C)
    Lineage
    Eukaryota; Fungi; Dikarya; Ascomycota; Saccharomycotina; Saccharomycetes; Saccharomycetales; Saccharomycetaceae; Saccharomyces
    Also known as
    AMT1
    Summary
    Enables ammonium channel activity. Involved in ammonium transmembrane transport and nitrogen utilization. Located in plasma membrane. [provided by Alliance of Genome Resources, Dec 2024]
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    Genomic context

    See MEP1 in Genome Data Viewer
    Location:
    chromosome: VII
    Exon count:
    1
    Sequence:
    Chromosome: VII; NC_001139.9 (731449..732927, complement)

    Chromosome VII - NC_001139.9Genomic Context describing neighboring genes Neighboring gene Golgi transport complex subunit COG2 Neighboring gene tRNA-Asn Neighboring gene uncharacterized protein Neighboring gene uncharacterized protein

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Gene Ontology Provided by SGD

    Function Evidence Code Pubs
    enables ammonium channel activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables ammonium channel activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables ammonium channel activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables ammonium channel activity IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    Process Evidence Code Pubs
    involved_in ammonium transmembrane transport IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in ammonium transmembrane transport IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in ammonium transmembrane transport IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in nitrogen utilization IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in endoplasmic reticulum HDA PubMed 
    located_in membrane IEA
    Inferred from Electronic Annotation
    more info
     
    is_active_in plasma membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in plasma membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 

    General protein information

    Preferred Names
    ammonium permease MEP1
    NP_011636.3
    • Ammonium permease; belongs to Mep-Amt-Rh family of well-conserved ammonium (NH4+) transporters that includes the human Rh factors; expression is under the nitrogen catabolite repression regulation; activity regulated by TORC1 effectors, Npr1p and Par32p; human homolog RHCG complements yeast null mutant; mutations in human homolog RHCG implicated in metabolic acidosis; MEP1 has a paralog, MEP3, that arose from the whole genome duplication

    NCBI Reference Sequences (RefSeq)

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    Genome Annotation

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

    Reference assembly

    Genomic

    1. NC_001139.9 Reference assembly

      Range
      731449..732927 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001181250.3NP_011636.3  TPA: ammonium permease MEP1 [Saccharomyces cerevisiae S288C]

      See identical proteins and their annotated locations for NP_011636.3

      Status: REVIEWED

      UniProtKB/Swiss-Prot
      D6VUQ2, P40260
      UniProtKB/TrEMBL
      A6ZUD4, B3LIA8, B5VJ67, C7GSX1, C8Z912, G2WEK3, N1P9W6
      Conserved Domains (1) summary
      TIGR00836
      Location:19424
      amt; ammonium transporter