Lipoyl synthase, mitochondrial (LIAS)

Homo sapiens — UniProt O43766

Gene: LIASHomo sapiensSwissProt reviewed

About Lipoyl synthase, mitochondrial

Lipoyl synthase, mitochondrial (LIAS) is a protein from Homo sapiens identified by UniProt accession O43766, 372 residues long. MolForge cross-references it against 0 known binders and 137 disease associations.

Target properties

Protein nameLipoyl synthase, mitochondrial
UniProt accessionO43766
GeneLIAS
OrganismHomo sapiens
Length372 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 (137)

Diseases linked to this target (Open Targets).

  • lipoic acid synthetase deficiency · score 0.77
  • neurodegenerative disease · score 0.34
  • genetic disorder · score 0.19
  • cholelithiasis · score 0.10
  • low density lipoprotein cholesterol measurement · score 0.09
  • breast cancer · score 0.08
  • esophageal squamous cell carcinoma · score 0.05
  • hemorrhoid · score 0.05
  • cystic fibrosis · score 0.04
  • cancer · score 0.04

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-O43766-F1alphafoldPREDICTED81.16—

Amino-acid sequence (372 residues)

MSLRCGDAAR TLGPRVFGRY FCSPVRPLSS LPDKKKELLQ NGPDLQDFVS GDLADRSTWD EYKGNLKRQK GERLRLPPWL KTEIPMGKNY NKLKNTLRNL NLHTVCEEAR CPNIGECWGG GEYATATATI MLMGDTCTRG CRFCSVKTAR NPPPLDASEP YNTAKAIAEW GLDYVVLTSV DRDDMPDGGA EHIAKTVSYL KERNPKILVE CLTPDFRGDL KAIEKVALSG LDVYAHNVET VPELQSKVRD PRANFDQSLR VLKHAKKVQP DVISKTSIML GLGENDEQVY ATMKALREAD VDCLTLGQYM QPTRRHLKVE EYITPEKFKY WEKVGNELGF HYTASGPLVR SSYKAGEFFL KNLVAKRKTK DL

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Quick facts

UniProtO43766
GeneLIAS
OrganismHomo sapiens
Length372
Binders0
Diseases137
View on UniProt