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Delineation of the TRAK binding regions of the kinesin-1 motor proteins
Understanding specific cargo distribution in differentiated cells is a major challenge. Trafficking kinesin proteins (TRAKs) are kinesin adaptors. They bind the cargo binding domain of kinesin-1 motor proteins forming a link between the motor and their cargoes. To refine the TRAK1/2 binding sites wi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853714/ https://www.ncbi.nlm.nih.gov/pubmed/24161670 http://dx.doi.org/10.1016/j.febslet.2013.09.049 |
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author | Randall, Thomas S. Moores, Carolyn Stephenson, F. Anne |
author_facet | Randall, Thomas S. Moores, Carolyn Stephenson, F. Anne |
author_sort | Randall, Thomas S. |
collection | PubMed |
description | Understanding specific cargo distribution in differentiated cells is a major challenge. Trafficking kinesin proteins (TRAKs) are kinesin adaptors. They bind the cargo binding domain of kinesin-1 motor proteins forming a link between the motor and their cargoes. To refine the TRAK1/2 binding sites within the kinesin-1 cargo domain, rationally designed C-terminal truncations of KIF5A and KIF5C were generated and their co-association with TRAK1/2 determined by quantitative co-immunoprecipitations following co-expression in mammalian cells. Three contributory regions forming the TRAK2 binding site within KIF5A and KIF5C cargo binding domains were delineated. Differences were found between TRAK1/2 with respect to association with KIF5A. |
format | Online Article Text |
id | pubmed-3853714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | John Wiley & Sons Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38537142013-12-09 Delineation of the TRAK binding regions of the kinesin-1 motor proteins Randall, Thomas S. Moores, Carolyn Stephenson, F. Anne FEBS Lett Article Understanding specific cargo distribution in differentiated cells is a major challenge. Trafficking kinesin proteins (TRAKs) are kinesin adaptors. They bind the cargo binding domain of kinesin-1 motor proteins forming a link between the motor and their cargoes. To refine the TRAK1/2 binding sites within the kinesin-1 cargo domain, rationally designed C-terminal truncations of KIF5A and KIF5C were generated and their co-association with TRAK1/2 determined by quantitative co-immunoprecipitations following co-expression in mammalian cells. Three contributory regions forming the TRAK2 binding site within KIF5A and KIF5C cargo binding domains were delineated. Differences were found between TRAK1/2 with respect to association with KIF5A. John Wiley & Sons Ltd 2013-11-29 /pmc/articles/PMC3853714/ /pubmed/24161670 http://dx.doi.org/10.1016/j.febslet.2013.09.049 Text en © 2013 Elsevier B.V. https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Randall, Thomas S. Moores, Carolyn Stephenson, F. Anne Delineation of the TRAK binding regions of the kinesin-1 motor proteins |
title | Delineation of the TRAK binding regions of the kinesin-1 motor proteins |
title_full | Delineation of the TRAK binding regions of the kinesin-1 motor proteins |
title_fullStr | Delineation of the TRAK binding regions of the kinesin-1 motor proteins |
title_full_unstemmed | Delineation of the TRAK binding regions of the kinesin-1 motor proteins |
title_short | Delineation of the TRAK binding regions of the kinesin-1 motor proteins |
title_sort | delineation of the trak binding regions of the kinesin-1 motor proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853714/ https://www.ncbi.nlm.nih.gov/pubmed/24161670 http://dx.doi.org/10.1016/j.febslet.2013.09.049 |
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