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Multifaceted Roles of ALG-2 in Ca(2+)-Regulated Membrane Trafficking
ALG-2 (gene name: PDCD6) is a penta-EF-hand Ca(2+)-binding protein and interacts with a variety of proteins in a Ca(2+)-dependent fashion. ALG-2 recognizes different types of identified motifs in Pro-rich regions by using different hydrophobic pockets, but other unknown modes of binding are also use...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037681/ https://www.ncbi.nlm.nih.gov/pubmed/27571067 http://dx.doi.org/10.3390/ijms17091401 |
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author | Maki, Masatoshi Takahara, Terunao Shibata, Hideki |
author_facet | Maki, Masatoshi Takahara, Terunao Shibata, Hideki |
author_sort | Maki, Masatoshi |
collection | PubMed |
description | ALG-2 (gene name: PDCD6) is a penta-EF-hand Ca(2+)-binding protein and interacts with a variety of proteins in a Ca(2+)-dependent fashion. ALG-2 recognizes different types of identified motifs in Pro-rich regions by using different hydrophobic pockets, but other unknown modes of binding are also used for non-Pro-rich proteins. Most ALG-2-interacting proteins associate directly or indirectly with the plasma membrane or organelle membranes involving the endosomal sorting complex required for transport (ESCRT) system, coat protein complex II (COPII)-dependent ER-to-Golgi vesicular transport, and signal transduction from membrane receptors to downstream players. Binding of ALG-2 to targets may induce conformational change of the proteins. The ALG-2 dimer may also function as a Ca(2+)-dependent adaptor to bridge different partners and connect the subnetwork of interacting proteins. |
format | Online Article Text |
id | pubmed-5037681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-50376812016-09-29 Multifaceted Roles of ALG-2 in Ca(2+)-Regulated Membrane Trafficking Maki, Masatoshi Takahara, Terunao Shibata, Hideki Int J Mol Sci Review ALG-2 (gene name: PDCD6) is a penta-EF-hand Ca(2+)-binding protein and interacts with a variety of proteins in a Ca(2+)-dependent fashion. ALG-2 recognizes different types of identified motifs in Pro-rich regions by using different hydrophobic pockets, but other unknown modes of binding are also used for non-Pro-rich proteins. Most ALG-2-interacting proteins associate directly or indirectly with the plasma membrane or organelle membranes involving the endosomal sorting complex required for transport (ESCRT) system, coat protein complex II (COPII)-dependent ER-to-Golgi vesicular transport, and signal transduction from membrane receptors to downstream players. Binding of ALG-2 to targets may induce conformational change of the proteins. The ALG-2 dimer may also function as a Ca(2+)-dependent adaptor to bridge different partners and connect the subnetwork of interacting proteins. MDPI 2016-08-26 /pmc/articles/PMC5037681/ /pubmed/27571067 http://dx.doi.org/10.3390/ijms17091401 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Maki, Masatoshi Takahara, Terunao Shibata, Hideki Multifaceted Roles of ALG-2 in Ca(2+)-Regulated Membrane Trafficking |
title | Multifaceted Roles of ALG-2 in Ca(2+)-Regulated Membrane Trafficking |
title_full | Multifaceted Roles of ALG-2 in Ca(2+)-Regulated Membrane Trafficking |
title_fullStr | Multifaceted Roles of ALG-2 in Ca(2+)-Regulated Membrane Trafficking |
title_full_unstemmed | Multifaceted Roles of ALG-2 in Ca(2+)-Regulated Membrane Trafficking |
title_short | Multifaceted Roles of ALG-2 in Ca(2+)-Regulated Membrane Trafficking |
title_sort | multifaceted roles of alg-2 in ca(2+)-regulated membrane trafficking |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037681/ https://www.ncbi.nlm.nih.gov/pubmed/27571067 http://dx.doi.org/10.3390/ijms17091401 |
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