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Ferritin Mitochondrial (FTMT)

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<table class="infobox infobox-protein">
<tr><th class="infobox-header" colspan="2">Ferritin Mitochondrial (FTMT)</th></tr>
<tr><td class="label">Gene</td><td>[FTMT](/genes/ftmt)</td></tr>
<tr><td class="label">UniProt</td><td><a href="https://www.uniprot.org/uniprot/P04183" target="_blank">P04183</a></td></tr>
<tr><td class="label">PDB</td><td><a href="https://www.rcsb.org/structure/5ML2" target="_blank">5ML2</a></td></tr>
<tr><td class="label">Molecular Weight</td><td>~25 kDa (subunit), 200 kDa (24-mer)</td></tr>
<tr><td class="label">Subcellular Localization</td><td>Mitochondria (mitochondrial matrix)</td></tr>
<tr><td class="label">Protein Family</td><td>Ferritin family</td></tr>
<tr><td class="label">Aliases</td><td>MtF, Mitochondrial Ferritin</td></tr>
</table>

Ferritin Mitochondrial (FTMT)

Introduction

Mitochondrial Ferritin (FTMT) is a specialized iron-storage protein encoded by the [FTMT](/genes/ftmt) gene. Unlike cytosolic ferritin, FTMT is targeted to mitochondria and plays crucial roles in iron homeostasis, oxidative stress protection, and cellular survival. FTMT has attracted significant attention in neurodegenerative disease research due to the well-established role of iron dysregulation and oxidative stress in [Alzheimer's disease](/diseases/alzheimers-disease) and [Parkinson's disease](/diseases/parkinsons-disease) [1].

Structure

FTMT has a unique structure adapted for mitochondrial function:

Monomer Structure

  • ~25 kDa per subunit
  • Contains the classic ferritin fold
  • Iron-binding sites in the ferroxidase center

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Related Entities
FTMTPROTEIN
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slugproteins-ftmt-protein
kg_node_idFTMTPROTEIN
entity_typeprotein
origin_typev1_polymorphic_backfill
source_tablewiki_pages
wiki_page_idwp-718ac85583a5
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📊 Evidence Profile Foundational
Evidence Balance
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Certainty
100%
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Outgoing
32
0 supporting 0 contradicting 0 neutral
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