Cytochrome c oxidase assembly protein COX16 homolog, mitochondrial (COX16)

Homo sapiens — UniProt Q9P0S2

Gene: COX16Homo sapiensSwissProt reviewed

About Cytochrome c oxidase assembly protein COX16 homolog, mitochondrial

Cytochrome c oxidase assembly protein COX16 homolog, mitochondrial (COX16) is a protein from Homo sapiens identified by UniProt accession Q9P0S2, 106 residues long. MolForge cross-references it against 0 known binders and 31 disease associations.

Target properties

Protein nameCytochrome c oxidase assembly protein COX16 homolog, mitochondrial
UniProt accessionQ9P0S2
GeneCOX16
OrganismHomo sapiens
Length106 residues
Molecular weight—
EC numbers—
Target classUNCLASSIFIED
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 (31)

Diseases linked to this target (Open Targets).

  • neurodegenerative disease · score 0.54
  • mitochondrial complex IV deficiency, nuclear type 22 · score 0.48
  • low density lipoprotein cholesterol measurement · score 0.37
  • Isolated cytochrome C oxidase deficiency · score 0.37
  • apolipoprotein B measurement · score 0.32
  • total cholesterol measurement · score 0.26
  • Encephalopathy · score 0.25
  • hypertrophic cardiomyopathy · score 0.25
  • aspartate aminotransferase measurement · score 0.23
  • response to statin · score 0.21

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9P0S2-F1alphafoldPREDICTED75.66—

Amino-acid sequence (106 residues)

MFAPAVMRAF RKNKTLGYGV PMLLLIVGGS FGLREFSQIR YDAVKSKMDP ELEKKLKENK ISLESEYEKI KDSKFDDWKN IRGPRPWEDP DLLQGRNPES LKTKTT

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Quick facts

UniProtQ9P0S2
GeneCOX16
OrganismHomo sapiens
Length106
Binders0
Diseases31
View on UniProt