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Sirtuins: Sir2-related NAD-dependent protein deacetylases

Silent information regulator 2 (Sir2) proteins, or sirtuins, are protein deacetylases dependent on nicotine adenine dinucleotide (NAD) and are found in organisms ranging from bacteria to humans. In eukaryotes, sirtuins regulate transcriptional repression, recombination, the cell-division cycle, micr...

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Detalles Bibliográficos
Autores principales: North, Brian J, Verdin, Eric
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC416462/
https://www.ncbi.nlm.nih.gov/pubmed/15128440
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author North, Brian J
Verdin, Eric
author_facet North, Brian J
Verdin, Eric
author_sort North, Brian J
collection PubMed
description Silent information regulator 2 (Sir2) proteins, or sirtuins, are protein deacetylases dependent on nicotine adenine dinucleotide (NAD) and are found in organisms ranging from bacteria to humans. In eukaryotes, sirtuins regulate transcriptional repression, recombination, the cell-division cycle, microtubule organization, and cellular responses to DNA-damaging agents. Sirtuins have also been implicated in regulating the molecular mechanisms of aging. The Sir2 catalytic domain, which is shared among all sirtuins, consists of two distinct domains that bind NAD and the acetyl-lysine substrate, respectively. In addition to the catalytic domain, eukaryotic sirtuins contain variable amino- and carboxy-terminal extensions that regulate their subcellular localizations and catalytic activity.
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spelling pubmed-4164622004-05-22 Sirtuins: Sir2-related NAD-dependent protein deacetylases North, Brian J Verdin, Eric Genome Biol Protein Family Review Silent information regulator 2 (Sir2) proteins, or sirtuins, are protein deacetylases dependent on nicotine adenine dinucleotide (NAD) and are found in organisms ranging from bacteria to humans. In eukaryotes, sirtuins regulate transcriptional repression, recombination, the cell-division cycle, microtubule organization, and cellular responses to DNA-damaging agents. Sirtuins have also been implicated in regulating the molecular mechanisms of aging. The Sir2 catalytic domain, which is shared among all sirtuins, consists of two distinct domains that bind NAD and the acetyl-lysine substrate, respectively. In addition to the catalytic domain, eukaryotic sirtuins contain variable amino- and carboxy-terminal extensions that regulate their subcellular localizations and catalytic activity. BioMed Central 2004 2004-04-28 /pmc/articles/PMC416462/ /pubmed/15128440 Text en Copyright © 2004 BioMed Central Ltd
spellingShingle Protein Family Review
North, Brian J
Verdin, Eric
Sirtuins: Sir2-related NAD-dependent protein deacetylases
title Sirtuins: Sir2-related NAD-dependent protein deacetylases
title_full Sirtuins: Sir2-related NAD-dependent protein deacetylases
title_fullStr Sirtuins: Sir2-related NAD-dependent protein deacetylases
title_full_unstemmed Sirtuins: Sir2-related NAD-dependent protein deacetylases
title_short Sirtuins: Sir2-related NAD-dependent protein deacetylases
title_sort sirtuins: sir2-related nad-dependent protein deacetylases
topic Protein Family Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC416462/
https://www.ncbi.nlm.nih.gov/pubmed/15128440
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