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AAA+ ATPases: structural insertions under the magnifying glass

AAA+ ATPases are a diverse protein superfamily which power a vast number of cellular processes, from protein degradation to genome replication and ribosome biogenesis. The latest advances in cryo-EM have resulted in a spectacular increase in the number and quality of AAA+ ATPase structures. This abu...

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Detalles Bibliográficos
Autores principales: Jessop, Matthew, Felix, Jan, Gutsche, Irina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7973254/
https://www.ncbi.nlm.nih.gov/pubmed/33246198
http://dx.doi.org/10.1016/j.sbi.2020.10.027
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author Jessop, Matthew
Felix, Jan
Gutsche, Irina
author_facet Jessop, Matthew
Felix, Jan
Gutsche, Irina
author_sort Jessop, Matthew
collection PubMed
description AAA+ ATPases are a diverse protein superfamily which power a vast number of cellular processes, from protein degradation to genome replication and ribosome biogenesis. The latest advances in cryo-EM have resulted in a spectacular increase in the number and quality of AAA+ ATPase structures. This abundance of new information enables closer examination of different types of structural insertions into the conserved core, revealing discrepancies in the current classification of AAA+ modules into clades. Additionally, combined with biochemical data, it has allowed rapid progress in our understanding of structure-functional relationships and provided arguments both in favour and against the existence of a unifying molecular mechanism for the ATPase activity and action on substrates, stimulating further intensive research.
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spelling pubmed-79732542021-03-23 AAA+ ATPases: structural insertions under the magnifying glass Jessop, Matthew Felix, Jan Gutsche, Irina Curr Opin Struct Biol Article AAA+ ATPases are a diverse protein superfamily which power a vast number of cellular processes, from protein degradation to genome replication and ribosome biogenesis. The latest advances in cryo-EM have resulted in a spectacular increase in the number and quality of AAA+ ATPase structures. This abundance of new information enables closer examination of different types of structural insertions into the conserved core, revealing discrepancies in the current classification of AAA+ modules into clades. Additionally, combined with biochemical data, it has allowed rapid progress in our understanding of structure-functional relationships and provided arguments both in favour and against the existence of a unifying molecular mechanism for the ATPase activity and action on substrates, stimulating further intensive research. Elsevier Science 2021-02 /pmc/articles/PMC7973254/ /pubmed/33246198 http://dx.doi.org/10.1016/j.sbi.2020.10.027 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Jessop, Matthew
Felix, Jan
Gutsche, Irina
AAA+ ATPases: structural insertions under the magnifying glass
title AAA+ ATPases: structural insertions under the magnifying glass
title_full AAA+ ATPases: structural insertions under the magnifying glass
title_fullStr AAA+ ATPases: structural insertions under the magnifying glass
title_full_unstemmed AAA+ ATPases: structural insertions under the magnifying glass
title_short AAA+ ATPases: structural insertions under the magnifying glass
title_sort aaa+ atpases: structural insertions under the magnifying glass
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7973254/
https://www.ncbi.nlm.nih.gov/pubmed/33246198
http://dx.doi.org/10.1016/j.sbi.2020.10.027
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