Sipa1l3/SPAR3 is targeted to postsynaptic specializations and interacts with the Fezzin ProSAPiP1/Lzts3-Reference-Cited by-同舟云学术

Sipa1l3/SPAR3 is targeted to postsynaptic specializations and interacts with the Fezzin ProSAPiP1/Lzts3

Published:2015-10-08 Issue:1 Volume:136 Page:28-35
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:J. Neurochem.

Author:

Dolnik Anna¹,Kanwal Noreen¹²,Mackert Sarah¹²,Halbedl Sonja¹²,Proepper Christian¹,Bockmann Juergen¹,Schoen Michael¹,Boeckers Tobias M¹,Kühl Susanne J³,Schmeisser Michael J¹⁴

Affiliation:

1. Institute for Anatomy and Cell Biology; Ulm University; Ulm Germany

2. International Graduate School in Molecular Medicine Ulm; IGradU; Ulm University; Ulm Germany

3. Institute for Biochemistry and Molecular Biology; Ulm University; Ulm Germany

4. Department of Neurology; Ulm University; Ulm Germany

Funder

International Graduate School in Molecular Medicine of Ulm University

Helmholtz Gesellschaft

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jnc.13353/fullpdf

Reference27 articles.

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2. C-terminal synaptic targeting elements for postsynaptic density proteins ProSAP1/Shank2 and ProSAP2/Shank3;Boeckers;J. Neurochem.,2005

3. Hippocampal LTP triggers proteasome-mediated SPAR degradation in CA1 neurons;Chen;Synapse,2012

4. Phenotypic and functional analysis of SHANK3 stop mutations identified in individuals with ASD and/or ID;Cochoy;Mol. Autism.,2015

5. In-depth protein profiling of the postsynaptic density from mouse hippocampus using data-independent acquisition proteomics;Distler;Proteomics,2014

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