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    CCC2 Cu(2+)-transporting P-type ATPase CCC2 [ Saccharomyces cerevisiae S288C ]

    Gene ID: 851862, updated on 28-Oct-2024

    Summary

    Official Symbol
    CCC2
    Official Full Name
    Cu(2+)-transporting P-type ATPase CCC2
    Primary source
    SGD:S000002678
    Locus tag
    YDR270W
    See related
    AllianceGenome:SGD:S000002678; FungiDB:YDR270W; VEuPathDB:YDR270W
    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 ATPase-coupled monoatomic cation transmembrane transporter activity and copper ion binding activity. Involved in copper ion export and intracellular iron ion homeostasis. Located in trans-Golgi network transport vesicle membrane. Used to study Menkes disease; Wilson disease; occipital horn syndrome; and spinal muscular atrophy. Human ortholog(s) of this gene implicated in Menkes disease; Wilson disease; X-linked distal spinal muscular atrophy 3; cutis laxa; and occipital horn syndrome. Orthologous to several human genes including ATP7A (ATPase copper transporting alpha). [provided by Alliance of Genome Resources, Oct 2024]
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    Genomic context

    See CCC2 in Genome Data Viewer
    Location:
    chromosome: IV
    Exon count:
    1
    Sequence:
    Chromosome: IV; NC_001136.10 (1005675..1008689)

    Chromosome IV - NC_001136.10Genomic Context describing neighboring genes Neighboring gene iron-sulfur cluster assembly protein CIA1 Neighboring gene tryptophan--tRNA ligase MSW1 Neighboring gene hydroxyacylglutathione hydrolase GLO2 Neighboring gene Don1p

    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 hydrolysis activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables ATPase-coupled monoatomic cation transmembrane transporter activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables ATPase-coupled monoatomic cation transmembrane transporter activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables ATPase-coupled monoatomic cation transmembrane transporter activity IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    enables P-type divalent copper transporter activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables P-type monovalent copper transporter activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables copper ion binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables copper ion binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables copper ion binding IEA
    Inferred from Electronic Annotation
    more info
     
    enables metal ion binding IEA
    Inferred from Electronic Annotation
    more info
     
    Process Evidence Code Pubs
    involved_in copper ion export IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in copper ion homeostasis IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in copper ion transport IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in intracellular iron ion homeostasis IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in monoatomic cation transport IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in transmembrane transport IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in Golgi apparatus IEA
    Inferred from Electronic Annotation
    more info
     
    is_active_in membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in membrane IEA
    Inferred from Electronic Annotation
    more info
     
    located_in trans-Golgi network transport vesicle membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 

    General protein information

    Preferred Names
    Cu(2+)-transporting P-type ATPase CCC2
    NP_010556.1
    • Cu(+2)-transporting P-type ATPase; required for export of copper from cytosol into extracytosolic compartment; targeted to vacuole via AP-3 pathway; similar to human proteins involved in Menkes and Wilsons diseases; protein abundance increases in response to DNA replication stress; affects TBSV model (+)RNA virus replication by regulating copper metabolism; human homologs ATP7A and ATP7B both complement yeast null mutant

    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_001136.10 Reference assembly

      Range
      1005675..1008689
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001180578.1NP_010556.1  TPA: Cu(2+)-transporting P-type ATPase CCC2 [Saccharomyces cerevisiae S288C]

      See identical proteins and their annotated locations for NP_010556.1

      Status: REVIEWED

      UniProtKB/Swiss-Prot
      D6VSQ3, P38995
      UniProtKB/TrEMBL
      B3LG21, C7GS90, C8Z5I3, N1P708
      Conserved Domains (2) summary
      cd00371
      Location:667
      HMA; Heavy-metal-associated domain (HMA) is a conserved domain of approximately 30 amino acid residues found in a number of proteins that transport or detoxify heavy metals, for example, the CPx-type heavy metal ATPases and copper chaperones. HMA domain ...
      cd02094
      Location:259938
      P-type_ATPase_Cu-like; P-type heavy metal-transporting ATPase, similar to human copper-transporting ATPases, ATP7A and ATP7B