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FYCO1 Protein — FYVE and Coiled-Coil Domain Containing 1
FYCO1 Protein — FYVE and Coiled-Coil Domain Containing 1
Introduction
<table class="infobox infobox-protein">
<tr>
<th class="infobox-header" colspan="2">FYCO1 Protein — FYVE and Coiled-Coil Domain Containing 1</th>
</tr>
<tr>
<td class="label">Protein Name</td>
<td>FYCO1 (FYVE and Coiled-Coil Domain Containing 1)</td>
</tr>
<tr>
<td class="label">Gene</td>
<td>FYCO1</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>Q9BQR1</td>
</tr>
<tr>
<td class="label">Molecular Weight</td>
<td>1478 aa (~168 kDa)</td>
</tr>
<tr>
<td class="label">Subcellular Localization</td>
<td>Autophagosomes, late endosomes, lysosomes</td>
</tr>
<tr>
<td class="label">Protein Family</td>
<td>[Autophagy](/entities/autophagy) adaptor family</td>
</tr>
<tr>
<td class="label">Partner</td>
<td>Interaction Domain</td>
</tr>
<tr>
<td class="label">LC3/GABARAP</td>
<td>LIR motif</td>
</tr>
<tr>
<td class="label">RAB7</td>
<td>RUN domain</td>
</tr>
<tr>
<td class="label">RAB11</td>
<td>RUN domain</td>
</tr>
<tr>
<td class="label">PI3P</td>
<td>FYVE domain</td>
</tr>
<tr>
<td class="label">Strategy</td>
<td>Approach</td>
</tr>
<tr>
<td class="label">Autophagy enhancers</td>
<td>Promote autophagy</td>
</tr>
<tr>
<td class="label">Gene therapy</td>
<td>Restore FYCO1</td>
</tr>
<tr>
<td class="label">[mTOR](/entities/mtor) inhibitors</td>
<td>Bypass FYCO1 deficiency</td>
</tr>
<tr>
<td cla
FYCO1 Protein — FYVE and Coiled-Coil Domain Containing 1
Introduction
<table class="infobox infobox-protein">
<tr>
<th class="infobox-header" colspan="2">FYCO1 Protein — FYVE and Coiled-Coil Domain Containing 1</th>
</tr>
<tr>
<td class="label">Protein Name</td>
<td>FYCO1 (FYVE and Coiled-Coil Domain Containing 1)</td>
</tr>
<tr>
<td class="label">Gene</td>
<td>FYCO1</td>
</tr>
<tr>
<td class="label">UniProt ID</td>
<td>Q9BQR1</td>
</tr>
<tr>
<td class="label">Molecular Weight</td>
<td>1478 aa (~168 kDa)</td>
</tr>
<tr>
<td class="label">Subcellular Localization</td>
<td>Autophagosomes, late endosomes, lysosomes</td>
</tr>
<tr>
<td class="label">Protein Family</td>
<td>[Autophagy](/entities/autophagy) adaptor family</td>
</tr>
<tr>
<td class="label">Partner</td>
<td>Interaction Domain</td>
</tr>
<tr>
<td class="label">LC3/GABARAP</td>
<td>LIR motif</td>
</tr>
<tr>
<td class="label">RAB7</td>
<td>RUN domain</td>
</tr>
<tr>
<td class="label">RAB11</td>
<td>RUN domain</td>
</tr>
<tr>
<td class="label">PI3P</td>
<td>FYVE domain</td>
</tr>
<tr>
<td class="label">Strategy</td>
<td>Approach</td>
</tr>
<tr>
<td class="label">Autophagy enhancers</td>
<td>Promote autophagy</td>
</tr>
<tr>
<td class="label">Gene therapy</td>
<td>Restore FYCO1</td>
</tr>
<tr>
<td class="label">[mTOR](/entities/mtor) inhibitors</td>
<td>Bypass FYCO1 deficiency</td>
</tr>
<tr>
<td class="label">Associated Diseases</td>
<td><a href="/wiki/als" style="color:#ef9a9a">Als</a>, <a href="/wiki/cancer" style="color:#ef9a9a">Cancer</a>, <a href="/wiki/cardiovascular" style="color:#ef9a9a">Cardiovascular</a>, <a href="/wiki/ischemia" style="color:#ef9a9a">Ischemia</a>, <a href="/wiki/ms" style="color:#ef9a9a">Ms</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">118 edges</a></td>
</tr>
</table>
Fyco1 Protein — Fyve And Coiled Coil Domain Containing 1 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
This page provides comprehensive information about FYCO1 Protein, including its structure, normal function in the nervous system, and its role in neurodegenerative diseases.
Structure
FYCO1 is a large autophagy adaptor protein containing multiple domains:
- FYVE domain (residues 1-50) - binds PI3P on autophagosomes
- Coiled-coil regions (multiple) - mediate protein interactions
- LIR (LC3-interacting region) (residues 400-420) - binds LC3/GABARAP
- RUN domain (residues 900-1100) - interacts with RAB GTPases
- C-terminal regions - contain multiple protein-binding sites
Binding Partners
Normal Function
FYCO1 is a selective autophagy receptor that coordinates:
Autophagosome Transport
- Recruits autophagosomes to microtubules
- Facilitates transport from periphery to perinuclear region
- Promotes autophagosome-lysosome fusion
Autophagy Flux
- Enhances autophagosome-lysosome fusion
- Coordinates endosomal maturation
- Supports selective autophagy
Cellular Homeostasis
- Clears damaged organelles
- Removes protein aggregates
- Maintains neuronal health
Role in Disease
Hereditary Spastic Paraplegia (SPG59)
FYCO1 mutations cause HSP through:
- Impaired autophagic flux
- Accumulation of damaged organelles
- Axonal transport defects
- Degeneration of corticospinal tract
Neurodegeneration
FYCO1 deficiency leads to:
- Impaired protein aggregate clearance
- Mitochondrial dysfunction
- Enhanced oxidative stress
- Lysosomal storage abnormalities
Therapeutic Targeting
Key Publications
See Also
- [FYCO1 Gene](/proteins/fyco1-protein)
- [Hereditary Spastic Paraplegia](/diseases/hereditary-spastic-paraplegia)
- [Autophagy-Lysosomal Pathway](/mechanisms/autophagy-lysosomal-pathway)
- [RAB Proteins](/entities/rab-proteins)
- [LC3/GABARAP](/entities/lc3-gabarap)
- [Protein Quality Control](/mechanisms/protein-quality-control-network)
External Links
- [UniProt: FYCO1](https://www.uniprot.org/uniprot/Q9BQR1)
- [NCBI Protein: FYCO1](https://www.ncbi.nlm.nih.gov/protein/Q9BQR1)
Disease Associations
Hereditary Spastic Paraplegia (SPG59)
- [FYCO1 mutations* cause AR-SPG59](/genes/ar)
- [First described in 2014 (Moiretti)](/genes/scrib)
- [Characterized by:](/genes/ar)
- [Early-onset spastic paraplegia](/genes/ar)
- [Thin corpus callosum](/brain-regions/corpus-callosum)
- [Cerebellar ataxia](/diseases/cerebellar-ataxia)
- [Peripheral neuropathy](/cell-types/dorsal-root-ganglion-neuropathy)
Alzheimer's Disease
- [FYCO1 in autophagosome-lysosome pathway](/genes/fyco1)
- [Impaired autophagy in AD brains](/mechanisms/autophagy)
- [Role in [tau](/proteins/tau) clearance](/proteins)
- May contribute to protein aggregate accumulation
Parkinson's Disease
- [FYCO1 ex](/genes/fyco1)pression in dopaminergic [neurons](/entities/neurons)
- Role in [alpha-synuclein](/proteins/alpha-synuclein) clearance
- Lysosomal dysfunction in PD
- Autophagy impairment
Neurodegeneration
- Autophagy-lysosomal pathway dysfunction
- Protein aggregate accumulation
- Mitochondrial quality control
- Synaptic dysfunction
Therapeutic Approaches
Autophagy Enhancement
- Rapamycin - [mTOR](/mechanisms/mtor-signaling-pathway) inhibition
- Metformin - AMPK activation
- Trehalose - autophagy inducer
- Lithium - autophagy enhancement
Gene Therapy
- AAV-FYCO1 delivery
- CRISPR-based approaches
- siRNA targeting
- Viral vector development
Small Molecules
- [TFEB](/proteins/tfeb) activators
- Autophagy modulators
- Lysosomal function enhancers
Research Directions
- Understanding FYCO1 mutation spectrum
- Developing gene therapy approaches
- Biomarker potential
- Role in specific neuronal populations
Background
The study of Fyco1 Protein — Fyve And Coiled Coil Domain Containing 1 has evolved significantly over the past decades. Research in this area has revealed important insights into the underlying mechanisms of neurodegeneration and continues to drive therapeutic development.
Historical context and key discoveries in this field have shaped our current understanding and will continue to guide future research directions.
References
▸Metadataorigin_type: v1_polymorphic_backfill
| slug | proteins-fyco1-protein |
| kg_node_id | FYCO1PROTEIN |
| entity_type | protein |
| origin_type | v1_polymorphic_backfill |
| source_table | wiki_pages |
| wiki_page_id | wp-65811f75d88e |
| __merged_from | {'merged_at': '2026-05-13', 'unprefixed_id': 'proteins-fyco1-protein'} |
| _schema_version | 1 |
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