Cytochrome b (MT-CYB)

Homo sapiens — UniProt P00156

Gene: MT-CYBHomo sapiensSwissProt reviewed

About Cytochrome b

Cytochrome b (MT-CYB) is a protein from Homo sapiens identified by UniProt accession P00156, 380 residues long. MolForge cross-references it against 0 known binders and 219 disease associations.

Target properties

Protein nameCytochrome b
UniProt accessionP00156
GeneMT-CYB
OrganismHomo sapiens
Length380 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 (219)

Diseases linked to this target (Open Targets).

  • Leber hereditary optic neuropathy · score 0.72
  • Exercise intolerance · score 0.65
  • mitochondrial disease · score 0.64
  • MELAS · score 0.56
  • MELAS syndrome · score 0.55
  • mitochondrial myopathy with reversible cytochrome C oxidase deficiency · score 0.51
  • mitochondrial encephalomyopathy · score 0.48
  • histiocytoid cardiomyopathy · score 0.45
  • maternally-inherited diabetes and deafness · score 0.45
  • Mitochondrial myopathy · score 0.44

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P00156-F1alphafoldPREDICTED97.74—

Amino-acid sequence (380 residues)

MTPMRKTNPL MKLINHSFID LPTPSNISAW WNFGSLLGAC LILQITTGLF LAMHYSPDAS TAFSSIAHIT RDVNYGWIIR YLHANGASMF FICLFLHIGR GLYYGSFLYS ETWNIGIILL LATMATAFMG YVLPWGQMSF WGATVITNLL SAIPYIGTDL VQWIWGGYSV DSPTLTRFFT FHFILPFIIA ALATLHLLFL HETGSNNPLG ITSHSDKITF HPYYTIKDAL GLLLFLLSLM TLTLFSPDLL GDPDNYTLAN PLNTPPHIKP EWYFLFAYTI LRSVPNKLGG VLALLLSILI LAMIPILHMS KQQSMMFRPL SQSLYWLLAA DLLILTWIGG QPVSYPFTII GQVASVLYFT TILILMPTIS LIENKMLKWA

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Quick facts

UniProtP00156
GeneMT-CYB
OrganismHomo sapiens
Length380
Binders0
Diseases219
View on UniProt