Dynamin-like GTPase OPA1, mitochondrial (OPA1)

Homo sapiens — UniProt O60313

Gene: OPA1Homo sapiensSwissProt reviewed

About Dynamin-like GTPase OPA1, mitochondrial

Dynamin-like GTPase OPA1, mitochondrial (OPA1) is a protein from Homo sapiens identified by UniProt accession O60313, 960 residues long. MolForge cross-references it against 0 known binders and 368 disease associations.

Target properties

Protein nameDynamin-like GTPase OPA1, mitochondrial
UniProt accessionO60313
GeneOPA1
OrganismHomo sapiens
Length960 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—

Approved drugs hitting this target (1)

DrugCentral-linked approved drugs that act on this protein.

Disease associations (368)

Diseases linked to this target (Open Targets).

  • Autosomal dominant optic atrophy, classic type · score 0.83
  • Behr syndrome · score 0.81
  • autosomal dominant optic atrophy, classic form · score 0.80
  • mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type) · score 0.71
  • autosomal dominant optic atrophy plus syndrome · score 0.64
  • neurodegenerative disease · score 0.56
  • genetic disorder · score 0.51
  • optic atrophy · score 0.50
  • mitochondrial disease · score 0.49
  • Retinal dystrophy · score 0.48

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-O60313-F1alphafoldPREDICTED73.98—

Amino-acid sequence (960 residues)

MWRLRRAAVA CEVCQSLVKH SSGIKGSLPL QKLHLVSRSI YHSHHPTLKL QRPQLRTSFQ QFSSLTNLPL RKLKFSPIKY GYQPRRNFWP ARLATRLLKL RYLILGSAVG GGYTAKKTFD QWKDMIPDLS EYKWIVPDIV WEIDEYIDFE KIRKALPSSE DLVKLAPDFD KIVESLSLLK DFFTSGSPEE TAFRATDRGS ESDKHFRKVS DKEKIDQLQE ELLHTQLKYQ RILERLEKEN KELRKLVLQK DDKGIHHRKL KKSLIDMYSE VLDVLSDYDA SYNTQDHLPR VVVVGDQSAG KTSVLEMIAQ ARIFPRGSGE MMTRSPVKVT LSEGPHHVAL FKDSSREFDL TKEEDLAALR HEIELRMRKN VKEGCTVSPE TISLNVKGPG LQRMVLVDLP GVINTVTSGM APDTKETIFS ISKAYMQNPN AIILCIQDGS VDAERSIVTD LVSQMDPHGR RTIFVLTKVD LAEKNVASPS RIQQIIEGKL FPMKALGYFA VVTGKGNSSE SIEAIREYEE EFFQNSKLLK TSMLKAHQVT TRNLSLAVSD CFWKMVRESV EQQADSFKAT RFNLETEWKN NYPRLRELDR NELFEKAKNE ILDEVISLSQ VTPKHWEEIL QQSLWERVST HVIENIYLPA AQTMNSGTFN TTVDIKLKQW TDKQLPNKAV EVAWETLQEE FSRFMTEPKG KEHDDIFDKL KEAVKEESIK RHKWNDFAED SLRVIQHNAL EDRSISDKQQ WDAAIYFMEE ALQARLKDTE NAIENMVGPD WKKRWLYWKN RTQEQCVHNE TKNELEKMLK CNEEHPAYLA SDEITTVRKN LESRGVEVDP SLIKDTWHQV YRRHFLKTAL NHCNLCRRGF YYYQRHFVDS ELECNDVVLF WRIQRMLAIT ANTLRQQLTN TEVRRLEKNV KEVLEDFAED GEKKIKLLTG KRVQLAEDLK KVREIQEKLD AFIEALHQEK

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Quick facts

UniProtO60313
GeneOPA1
OrganismHomo sapiens
Length960
Binders0
Diseases368
View on UniProt