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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...

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Detalles Bibliográficos
Autores principales: Smyth, Peter, Sessler, Tamas, Scott, Christopher J., Longley, Daniel B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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.
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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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