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The cyclophilins
Summary: Cyclophilins (Enzyme Commission (EC) number 5.1.2.8) belong to a group of proteins that have peptidyl-prolyl cis-trans isomerase activity; such proteins are collectively known as immunophilins and also include the FK-506-binding proteins and the parvulins. Cyclophilins are found in all cell...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1175980/ https://www.ncbi.nlm.nih.gov/pubmed/15998457 http://dx.doi.org/10.1186/gb-2005-6-7-226 |
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author | Wang, Ping Heitman, Joseph |
author_facet | Wang, Ping Heitman, Joseph |
author_sort | Wang, Ping |
collection | PubMed |
description | Summary: Cyclophilins (Enzyme Commission (EC) number 5.1.2.8) belong to a group of proteins that have peptidyl-prolyl cis-trans isomerase activity; such proteins are collectively known as immunophilins and also include the FK-506-binding proteins and the parvulins. Cyclophilins are found in all cells of all organisms studied, in both prokaryotes and eukaryotes; humans have a total of 16 cyclophilin proteins, Arabidopsis up to 29 and Saccharomyces 8. The first member of the cyclophilins to be identified in mammals, cyclophilin A, is the major cellular target for, and thus mediates the actions of, the immunosuppressive drug cyclosporin A. Cyclophilin A forms a ternary complex with cyclosporin A and the calcium-calmodulin-activated serine/threonine-specific protein phosphatase calcineurin; formation of this complex prevents calcineurin from regulating cytokine gene transcription. Recent studies have implicated a diverse array of additional cellular functions for cyclophilins, including roles as chaperones and in cell signaling. |
format | Text |
id | pubmed-1175980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-11759802005-07-17 The cyclophilins Wang, Ping Heitman, Joseph Genome Biol Protein Family Review Summary: Cyclophilins (Enzyme Commission (EC) number 5.1.2.8) belong to a group of proteins that have peptidyl-prolyl cis-trans isomerase activity; such proteins are collectively known as immunophilins and also include the FK-506-binding proteins and the parvulins. Cyclophilins are found in all cells of all organisms studied, in both prokaryotes and eukaryotes; humans have a total of 16 cyclophilin proteins, Arabidopsis up to 29 and Saccharomyces 8. The first member of the cyclophilins to be identified in mammals, cyclophilin A, is the major cellular target for, and thus mediates the actions of, the immunosuppressive drug cyclosporin A. Cyclophilin A forms a ternary complex with cyclosporin A and the calcium-calmodulin-activated serine/threonine-specific protein phosphatase calcineurin; formation of this complex prevents calcineurin from regulating cytokine gene transcription. Recent studies have implicated a diverse array of additional cellular functions for cyclophilins, including roles as chaperones and in cell signaling. BioMed Central 2005 2005-06-27 /pmc/articles/PMC1175980/ /pubmed/15998457 http://dx.doi.org/10.1186/gb-2005-6-7-226 Text en Copyright © 2005 BioMed Central Ltd |
spellingShingle | Protein Family Review Wang, Ping Heitman, Joseph The cyclophilins |
title | The cyclophilins |
title_full | The cyclophilins |
title_fullStr | The cyclophilins |
title_full_unstemmed | The cyclophilins |
title_short | The cyclophilins |
title_sort | cyclophilins |
topic | Protein Family Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1175980/ https://www.ncbi.nlm.nih.gov/pubmed/15998457 http://dx.doi.org/10.1186/gb-2005-6-7-226 |
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