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Cytochrome c oxidase assembly factor 3 homolog, mitochondrial (COA3)

Homo sapiens — UniProt Q9Y2R0

Gene: COA3Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Cytochrome c oxidase assembly factor 3 homolog, mitochondrial (COA3) is a protein from Homo sapiens identified by UniProt accession Q9Y2R0, 106 residues long. MolForge cross-references it against 0 known binders and 33 disease associations.

  • UniProt accession: Q9Y2R0; gene symbol COA3.
  • Organism: Homo sapiens.
  • Length: 106 amino acids.
  • Top disease associations (Open Targets): neurodegenerative disease, leigh syndrome due to mitochondrial complex iv deficiency and mitochondrial complex IV deficiency, nuclear type 22.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameCytochrome c oxidase assembly factor 3 homolog, mitochondrial
UniProt accessionQ9Y2R0
GeneCOA3
OrganismHomo sapiens
Length106 residues
Molecular weight—
EC numbers—
Target class—
Subcellular location—
Keywords—

Druggability

Target tractability assessment (Open Targets + pocket analysis). No approved drug

Druggability tierMEDIUM
Druggability score—
Pocket score—
Max clinical phase—

Disease associations (33)

Diseases linked to this target (Open Targets).

  • neurodegenerative disease · score 0.54
  • leigh syndrome due to mitochondrial complex iv deficiency · score 0.42
  • mitochondrial complex IV deficiency, nuclear type 22 · score 0.42
  • mitochondrial complex 4 deficiency, nuclear type 14 · score 0.41
  • Isolated cytochrome C oxidase deficiency · score 0.37
  • BMI-adjusted waist circumference · score 0.04
  • pulse pressure measurement · score 0.03
  • non-small cell lung carcinoma · score 0.03
  • systemic juvenile idiopathic arthritis · score 0.01
  • neuropathy · score 0.01

3D Structure (1)

Experimental (PDB) and predicted (AlphaFold) structures for this protein.

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9Y2R0-F1alphafoldPREDICTED77.38—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9Y2R0.

Amino-acid sequence (106 residues)

MASSGAGDPL DSKRGEAPFA QRIDPTREKL TPEQLHSMRQ AELAQWQKVL PRRRTRNIVT GLGIGALVLA IYGYTFYSIS QERFLDELED EAKAARARAL ARASGS

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

Which diseases are associated with COA3?

The strongest Open Targets associations for COA3 are neurodegenerative disease, leigh syndrome due to mitochondrial complex iv deficiency, mitochondrial complex IV deficiency, nuclear type 22, mitochondrial complex 4 deficiency, nuclear type 14 and Isolated cytochrome C oxidase deficiency.

How long is the COA3 protein?

The Homo sapiens COA3 protein (UniProt Q9Y2R0) is 106 amino acids long.

Browse: Targets: C · all protein targets A–Z · drugs A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

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Quick facts

UniProtQ9Y2R0
GeneCOA3
OrganismHomo sapiens
Length106
Binders0
Diseases33
View on UniProt