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P-type ATPases: Many more enigmas left to solve

P-type ATPases constitute a large ancient super-family of primary active pumps that have diverse substrate specificities ranging from H(+) to phospholipids. The significance of these enzymes in biology cannot be overstated. They are structurally related, and their catalytic cycles alternate between...

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Autor principal: Palmgren, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10654040/
https://www.ncbi.nlm.nih.gov/pubmed/37838176
http://dx.doi.org/10.1016/j.jbc.2023.105352
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author Palmgren, Michael
author_facet Palmgren, Michael
author_sort Palmgren, Michael
collection PubMed
description P-type ATPases constitute a large ancient super-family of primary active pumps that have diverse substrate specificities ranging from H(+) to phospholipids. The significance of these enzymes in biology cannot be overstated. They are structurally related, and their catalytic cycles alternate between high- and low-affinity conformations that are induced by phosphorylation and dephosphorylation of a conserved aspartate residue. In the year 1988, all P-type sequences available by then were analyzed and five major families, P1 to P5, were identified. Since then, a large body of knowledge has accumulated concerning the structure, function, and physiological roles of members of these families, but only one additional family, P6 ATPases, has been identified. However, much is still left to be learned. For each family a few remaining enigmas are presented, with the intention that they will stimulate interest in continued research in the field. The review is by no way comprehensive and merely presents personal views with a focus on evolution.
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spelling pubmed-106540402023-10-12 P-type ATPases: Many more enigmas left to solve Palmgren, Michael J Biol Chem JBC Reviews P-type ATPases constitute a large ancient super-family of primary active pumps that have diverse substrate specificities ranging from H(+) to phospholipids. The significance of these enzymes in biology cannot be overstated. They are structurally related, and their catalytic cycles alternate between high- and low-affinity conformations that are induced by phosphorylation and dephosphorylation of a conserved aspartate residue. In the year 1988, all P-type sequences available by then were analyzed and five major families, P1 to P5, were identified. Since then, a large body of knowledge has accumulated concerning the structure, function, and physiological roles of members of these families, but only one additional family, P6 ATPases, has been identified. However, much is still left to be learned. For each family a few remaining enigmas are presented, with the intention that they will stimulate interest in continued research in the field. The review is by no way comprehensive and merely presents personal views with a focus on evolution. American Society for Biochemistry and Molecular Biology 2023-10-12 /pmc/articles/PMC10654040/ /pubmed/37838176 http://dx.doi.org/10.1016/j.jbc.2023.105352 Text en © 2023 The Author https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle JBC Reviews
Palmgren, Michael
P-type ATPases: Many more enigmas left to solve
title P-type ATPases: Many more enigmas left to solve
title_full P-type ATPases: Many more enigmas left to solve
title_fullStr P-type ATPases: Many more enigmas left to solve
title_full_unstemmed P-type ATPases: Many more enigmas left to solve
title_short P-type ATPases: Many more enigmas left to solve
title_sort p-type atpases: many more enigmas left to solve
topic JBC Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10654040/
https://www.ncbi.nlm.nih.gov/pubmed/37838176
http://dx.doi.org/10.1016/j.jbc.2023.105352
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