Tafazzin (TAFAZZIN)

Homo sapiens — UniProt Q16635

Gene: TAFAZZINHomo sapiensSwissProt reviewed

About Tafazzin

Tafazzin (TAFAZZIN) is a protein from Homo sapiens identified by UniProt accession Q16635, 262 residues long. MolForge cross-references it against 0 known binders and 206 disease associations.

Target properties

Protein nameTafazzin
UniProt accessionQ16635
GeneTAFAZZIN
OrganismHomo sapiens
Length262 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 (206)

Diseases linked to this target (Open Targets).

  • Barth syndrome · score 0.80
  • dilated cardiomyopathy · score 0.50
  • Abnormality of the cardiovascular system · score 0.47
  • cardiomyopathy · score 0.44
  • familial isolated dilated cardiomyopathy · score 0.37
  • left ventricular noncompaction · score 0.33
  • anemia, nonspherocytic hemolytic, due to G6PD deficiency · score 0.27
  • endocardial fibroelastosis · score 0.18
  • gastric carcinoma · score 0.15
  • dilated cardiomyopathy 1A · score 0.12

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q16635-F1alphafoldPREDICTED94.85—

Amino-acid sequence (262 residues)

MPLHVKWPFP AVPPLTWTLA SSVVMGLVGT YSCFWTKYMN HLTVHNREVL YELIEKRGPA TPLITVSNHQ SCMDDPHLWG ILKLRHIWNL KLMRWTPAAA DICFTKELHS HFFSLGKCVP VCRGDGVYQK GMDFILEKLN HGDWVHIFPE GKVNMSSEFL RFKWGIGRLI AECHLNPIIL PLWHVGMNDV LPNSPPYFPR FGQKITVLIG KPFSALPVLE RLRAENKSAV EMRKALTDFI QEEFQHLKTQ AEQLHNHLQP GR

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Quick facts

UniProtQ16635
GeneTAFAZZIN
OrganismHomo sapiens
Length262
Binders0
Diseases206
View on UniProt