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TRIM2 Protein

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wiki page Created: 2026-04-02T07:19:11 By: crosslink-migration Quality: 50% ✓ SciDEX ID: wiki-proteins-trim2-protein
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protein605 wordssynced 2026-04-02

TRIM2 Protein

Introduction

<table class="infobox infobox-protein">
<tr>
<th class="infobox-header" colspan="2">TRIM2 Protein</th>
</tr>
<tr>
<td class="label">Target</td>
<td>Ubiquitination Type</td>
</tr>
<tr>
<td class="label">[Neurofilament Light](/entities/neurofilament-light)</td>
<td>K48-linked</td>
</tr>
<tr>
<td class="label">Synaptic proteins</td>
<td>K63-linked</td>
</tr>
<tr>
<td class="label">[Tau](/proteins/tau)</td>
<td>Mixed</td>
</tr>
<tr>
<td class="label">Strategy</td>
<td>Agent</td>
</tr>
<tr>
<td class="label">Gene therapy</td>
<td>AAV-TRIM2</td>
</tr>
<tr>
<td class="label">Small molecules</td>
<td>Unknown</td>
</tr>
<tr>
<td class="label">Protein replacement</td>
<td>Recombinant TRIM2</td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">9 edges</a></td>
</tr>
</table>

Trim2 Protein is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.

Overview

The TRIM2 protein is a member of the tripartite motif-containing protein family with E3 ubiquitin ligase activity. It plays critical roles in axonal outgrowth, cytoskeletal organization, protein quality control, and neuronal survival. Mutations in TRIM2 cause Charcot-Marie-Tooth disease type 2R and are implicated in neurodegenerative diseases.

Structure

Domain Architecture


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TRIM2PROTEIN
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kg_node_idTRIM2PROTEIN
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wiki_page_idwp-788a26958477
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📊 Evidence Profile
Evidence Balance
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Certainty
45%
Debates
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9
Outgoing
10
0 supporting 0 contradicting 0 neutral
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