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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science
2021
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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. |
format | Online Article Text |
id | pubmed-7973254 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Science |
record_format | MEDLINE/PubMed |
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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