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The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching

The metamorphic Mad2 protein acts as a molecular switch in the checkpoint mechanism that monitors proper chromosome attachment to spindle microtubules during cell division. The remarkably slow spontaneous rate of Mad2 switching between its checkpoint inactive and active forms is catalyzed onto a phy...

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Detalles Bibliográficos
Autores principales: Skinner, John J., Wood, Stacey, Shorter, James, Englander, S. Walter, Black, Ben E.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2592820/
https://www.ncbi.nlm.nih.gov/pubmed/19029339
http://dx.doi.org/10.1083/jcb.200808122
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author Skinner, John J.
Wood, Stacey
Shorter, James
Englander, S. Walter
Black, Ben E.
author_facet Skinner, John J.
Wood, Stacey
Shorter, James
Englander, S. Walter
Black, Ben E.
author_sort Skinner, John J.
collection PubMed
description The metamorphic Mad2 protein acts as a molecular switch in the checkpoint mechanism that monitors proper chromosome attachment to spindle microtubules during cell division. The remarkably slow spontaneous rate of Mad2 switching between its checkpoint inactive and active forms is catalyzed onto a physiologically relevant time scale by a self–self interaction between its two forms, culminating in a large pool of active Mad2. Recent structural, biochemical, and cell biological advances suggest that the catalyzed conversion of Mad2 requires a major structural rearrangement that transits through a partially unfolded intermediate.
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spelling pubmed-25928202009-06-01 The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching Skinner, John J. Wood, Stacey Shorter, James Englander, S. Walter Black, Ben E. J Cell Biol Reviews The metamorphic Mad2 protein acts as a molecular switch in the checkpoint mechanism that monitors proper chromosome attachment to spindle microtubules during cell division. The remarkably slow spontaneous rate of Mad2 switching between its checkpoint inactive and active forms is catalyzed onto a physiologically relevant time scale by a self–self interaction between its two forms, culminating in a large pool of active Mad2. Recent structural, biochemical, and cell biological advances suggest that the catalyzed conversion of Mad2 requires a major structural rearrangement that transits through a partially unfolded intermediate. The Rockefeller University Press 2008-12-01 /pmc/articles/PMC2592820/ /pubmed/19029339 http://dx.doi.org/10.1083/jcb.200808122 Text en © 2008 Skinner et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Reviews
Skinner, John J.
Wood, Stacey
Shorter, James
Englander, S. Walter
Black, Ben E.
The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching
title The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching
title_full The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching
title_fullStr The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching
title_full_unstemmed The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching
title_short The Mad2 partial unfolding model: regulating mitosis through Mad2 conformational switching
title_sort mad2 partial unfolding model: regulating mitosis through mad2 conformational switching
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2592820/
https://www.ncbi.nlm.nih.gov/pubmed/19029339
http://dx.doi.org/10.1083/jcb.200808122
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