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Opinion: alternative views of AMP-activated protein kinase.
Brenman, Jay E; Temple, Brenda R S.
Afiliação
  • Brenman JE; Department of Cell and Developmental Biology and Neuroscience Center, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, NC 27599, USA. brenman@med.unc.edu
Cell Biochem Biophys ; 47(3): 321-31, 2007.
Article em En | MEDLINE | ID: mdl-17652778
ABSTRACT
Genes most closely related to adenosine monophosphate (AMP)-activated protein kinase, including SAD kinases and Par-1 regulate cell polarity, although AMP-activated protein kinase (AMPK) modulates cellular energy status. LKB1 (Par-4) is required for normal activation of AMPK in the liver and also regulates cell polarity. AMPK is proposed to inhibit energy consuming activity while initiating energy producing activity during energy limitation. Demonstration that metformin, a common drug for Type 2 diabetes, requires LKB1 for full therapeutic benefit has increased interest in AMPK signaling. Despite the potential importance of AMPK signaling for diabetes, metabolic syndrome and even cancer, the developmental processes regulated by AMPK in genetically mutant animals require further elucidation. Mouse conditional null mutants for AMPK activity will allow genetic elucidation of AMPK function in vivo. This perspective focuses on sequence and structural moieties of AMPK and genetic analysis of AMPK mutations. Interestingly, the predicted protein structure of the carboxy-terminus of AMPKalpha resembles the carboxy-terminal KA-1 domain of MARK3, a Par-1 orthologue.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Monofosfato de Adenosina / Adenilato Quinase / Sistema de Sinalização das MAP Quinases Idioma: En Revista: Cell Biochem Biophys Assunto da revista: BIOFISICA / BIOQUIMICA Ano de publicação: 2007 Tipo de documento: Article País de afiliação: Estados Unidos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Monofosfato de Adenosina / Adenilato Quinase / Sistema de Sinalização das MAP Quinases Idioma: En Revista: Cell Biochem Biophys Assunto da revista: BIOFISICA / BIOQUIMICA Ano de publicação: 2007 Tipo de documento: Article País de afiliação: Estados Unidos