Cytochrome c oxidase assembly factor SCO2 (SCO2)

Homo sapiens — UniProt O43819

Gene: SCO2Homo sapiensSwissProt reviewed

About Cytochrome c oxidase assembly factor SCO2

Cytochrome c oxidase assembly factor SCO2 (SCO2) is a protein from Homo sapiens identified by UniProt accession O43819, 266 residues long. MolForge cross-references it against 0 known binders and 114 disease associations.

Target properties

Protein nameCytochrome c oxidase assembly factor SCO2
UniProt accessionO43819
GeneSCO2
OrganismHomo sapiens
Length266 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 (114)

Diseases linked to this target (Open Targets).

  • cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 · score 0.80
  • myopia 6 · score 0.79
  • fatal infantile encephalocardiomyopathy · score 0.75
  • Rare isolated myopia · score 0.69
  • mitochondrial DNA depletion syndrome 1 · score 0.56
  • neurodegenerative disease · score 0.50
  • mitochondrial neurogastrointestinal encephalomyopathy · score 0.48
  • genetic disorder · score 0.47
  • Leigh syndrome · score 0.37
  • Charcot-Marie-Tooth disease type 4 · score 0.37

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-O43819-F1alphafoldPREDICTED83.72—

Amino-acid sequence (266 residues)

MLLLTRSPTA WHRLSQLKPR VLPGTLGGQA LHLRSWLLSR QGPAETGGQG QPQGPGLRTR LLITGLFGAG LGGAWLALRA EKERLQQQKR TEALRQAAVG QGDFHLLDHR GRARCKADFR GQWVLMYFGF THCPDICPDE LEKLVQVVRQ LEAEPGLPPV QPVFITVDPE RDDVEAMARY VQDFHPRLLG LTGSTKQVAQ ASHSYRVYYN AGPKDEDQDY IVDHSIAIYL LNPDGLFTDY YGRSRSAEQI SDSVRRHMAA FRSVLS

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Quick facts

UniProtO43819
GeneSCO2
OrganismHomo sapiens
Length266
Binders0
Diseases114
View on UniProt