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ATPázy transportujúce meď

  1. Subject h.ATPázy transportujúce meď
    Subject h.Copper-Transporting ATPases
    Entry termsmeď transportujúce ATPázy
    meď transportujúca ATPáza 1
    meď transportujúca ATPáza 2
    ATP7A proteín
    ATP7B Cu-viažuca ATPáza typu P
    ATP7B Cu-viažuca ATPáza, P-typ
    meď transportujúca ATPáza alfa
    ATPáza, Cu++ transportujúca, beta polypeptid (Wilsonova choroba)
    meď prenášajúca pumpa 1
    meď transportujúce adenozíntrifosfatázy
    proteín asociovaný s Menkesovou chorobou
    proteín spojený s Menkesovou chorobou
    Cu(+)-transportujúce ATP-ázy
    Cu-transportujúce ATP-ázy
    PINA enzým
    ATP-áza pineálna špecifická nočná
    proteín Wilsonovej choroby
    English X referencesATP7B Cu-Binding P Type ATPase
    ATPase, Cu++ Transporting, beta Polypeptide (Wilson Disease)
    Copper-Transporting ATPase
    Copper-Transporting ATPase 1
    Copper-Transporting ATPase 2
    Copper-Transporting Adenosine Triphosphatases
    Cu(+)-Transporting ATPases
    Cu-Transporting ATPases
    Menkes Disease-Associated Protein
    Pineal Night-Specific ATPase
    Wilson Disease Cu-Binding P Type ATPase
    Scope note in EnglishP-type ATPases which transport copper ions across membranes in prokaryotic and eukaryotic cells. They possess a conserved CYSTEINE-HISTIDINE-SERINE (CPx) amino acid motif within their transmembrane helices that functions in cation translocation and catalytic activation, and an N-terminal copper-binding CxxC motif that regulates enzyme activity. They play essential roles in intracellular copper homeostasis through regulating the uptake, efflux and storage of copper ions, and in cuproprotein biosynthesis.
    See also reference (FX) in Slovak degenerácia hepatolentikulárna
    Menkesov syndróm
    See also reference (FX) in English Hepatolenticular Degeneration
    Menkes Kinky Hair Syndrome
    Links (2) - MeSH descriptor
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Number of the records: 1  

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