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FLIP(L): the pseudo‐caspase
Possessing structural homology with their active enzyme counterparts but lacking catalytic activity, pseudoenzymes have been identified for all major enzyme groups. Caspases are a family of cysteine‐dependent aspartate‐directed proteases that play essential roles in regulating cell death and inflamm...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586951/ https://www.ncbi.nlm.nih.gov/pubmed/32096279 http://dx.doi.org/10.1111/febs.15260 |
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author | Smyth, Peter Sessler, Tamas Scott, Christopher J. Longley, Daniel B. |
author_facet | Smyth, Peter Sessler, Tamas Scott, Christopher J. Longley, Daniel B. |
author_sort | Smyth, Peter |
collection | PubMed |
description | Possessing structural homology with their active enzyme counterparts but lacking catalytic activity, pseudoenzymes have been identified for all major enzyme groups. Caspases are a family of cysteine‐dependent aspartate‐directed proteases that play essential roles in regulating cell death and inflammation. Here, we discuss the only human pseudo‐caspase, FLIP(L), a paralog of the apoptosis‐initiating caspases, caspase‐8 and caspase‐10. FLIP(L) has been shown to play a key role in regulating the processing and activity of caspase‐8, thereby modulating apoptotic signaling mediated by death receptors (such as TRAIL‐R1/R2), TNF receptor‐1 (TNFR1), and Toll‐like receptors. In this review, these canonical roles of FLIP(L) are discussed. Additionally, a range of nonclassical pseudoenzyme roles are described, in which FLIP(L) functions independently of caspase‐8. These nonclassical pseudoenzyme functions enable FLIP(L) to play key roles in the regulation of a wide range of biological processes beyond its canonical roles as a modulator of cell death. |
format | Online Article Text |
id | pubmed-7586951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75869512020-10-30 FLIP(L): the pseudo‐caspase Smyth, Peter Sessler, Tamas Scott, Christopher J. Longley, Daniel B. FEBS J Review Articles Possessing structural homology with their active enzyme counterparts but lacking catalytic activity, pseudoenzymes have been identified for all major enzyme groups. Caspases are a family of cysteine‐dependent aspartate‐directed proteases that play essential roles in regulating cell death and inflammation. Here, we discuss the only human pseudo‐caspase, FLIP(L), a paralog of the apoptosis‐initiating caspases, caspase‐8 and caspase‐10. FLIP(L) has been shown to play a key role in regulating the processing and activity of caspase‐8, thereby modulating apoptotic signaling mediated by death receptors (such as TRAIL‐R1/R2), TNF receptor‐1 (TNFR1), and Toll‐like receptors. In this review, these canonical roles of FLIP(L) are discussed. Additionally, a range of nonclassical pseudoenzyme roles are described, in which FLIP(L) functions independently of caspase‐8. These nonclassical pseudoenzyme functions enable FLIP(L) to play key roles in the regulation of a wide range of biological processes beyond its canonical roles as a modulator of cell death. John Wiley and Sons Inc. 2020-03-12 2020-10 /pmc/articles/PMC7586951/ /pubmed/32096279 http://dx.doi.org/10.1111/febs.15260 Text en © 2020 The Authors. The FEBS Journal published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Articles Smyth, Peter Sessler, Tamas Scott, Christopher J. Longley, Daniel B. FLIP(L): the pseudo‐caspase |
title | FLIP(L): the pseudo‐caspase |
title_full | FLIP(L): the pseudo‐caspase |
title_fullStr | FLIP(L): the pseudo‐caspase |
title_full_unstemmed | FLIP(L): the pseudo‐caspase |
title_short | FLIP(L): the pseudo‐caspase |
title_sort | flip(l): the pseudo‐caspase |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7586951/ https://www.ncbi.nlm.nih.gov/pubmed/32096279 http://dx.doi.org/10.1111/febs.15260 |
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