Your browser doesn't support javascript.
loading
Inositol Pyrophosphates as Versatile Metabolic Messengers.
Nagpal, Latika; He, Sining; Rao, Feng; Snyder, Solomon H.
Afiliación
  • Nagpal L; The Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA; email: lnagpal1@jhmi.edu.
  • He S; Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Rao F; Current affiliation: Department of Zoology, University of Calcutta, Kolkata, India; email: Lnzoo@caluniv.ac.in.
  • Snyder SH; School of Life Sciences, Southern University of Science and Technology, Shenzhen, Guangdong, China; email: raof@sustech.edu.cn.
Annu Rev Biochem ; 93(1): 317-338, 2024 Aug.
Article en En | MEDLINE | ID: mdl-39094034
ABSTRACT
Discovered in 1993, inositol pyrophosphates are evolutionarily conserved signaling metabolites whose versatile modes of action are being increasingly appreciated. These include their emerging roles as energy regulators, phosphodonors, steric/allosteric regulators, and G protein-coupled receptor messengers. Through studying enzymes that metabolize inositol pyrophosphates, progress has also been made in elucidating the various cellular and physiological functions of these pyrophosphate-containing, energetic molecules. The two main forms of inositol pyrophosphates, 5-IP7 and IP8, synthesized respectively by inositol-hexakisphosphate kinases (IP6Ks) and diphosphoinositol pentakisphosphate kinases (PPIP5Ks), regulate phosphate homeostasis, ATP synthesis, and several other metabolic processes ranging from insulin secretion to cellular energy utilization. Here, we review the current understanding of the catalytic and regulatory mechanisms of IP6Ks and PPIP5Ks, as well as their counteracting phosphatases. We also highlight the genetic and cellular evidence implicating inositol pyrophosphates as essential mediators of mammalian metabolic homeostasis.
Asunto(s)
Palabras clave

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Transducción de Señal / Fosfotransferasas (Aceptor del Grupo Fosfato) / Fosfatos de Inositol Límite: Animals / Humans Idioma: En Revista: Annu Rev Biochem Año: 2024 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Transducción de Señal / Fosfotransferasas (Aceptor del Grupo Fosfato) / Fosfatos de Inositol Límite: Animals / Humans Idioma: En Revista: Annu Rev Biochem Año: 2024 Tipo del documento: Article