Peroxisomal biogenesis factor 19 (PEX19)

Homo sapiens — UniProt P40855

Gene: PEX19Homo sapiensSwissProt reviewed

About Peroxisomal biogenesis factor 19

Peroxisomal biogenesis factor 19 (PEX19) is a protein from Homo sapiens identified by UniProt accession P40855, 299 residues long. MolForge cross-references it against 0 known binders and 60 disease associations.

Target properties

Protein namePeroxisomal biogenesis factor 19
UniProt accessionP40855
GenePEX19
OrganismHomo sapiens
Length299 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 (60)

Diseases linked to this target (Open Targets).

  • peroxisome biogenesis disorder 12A (Zellweger) · score 0.76
  • Zellweger syndrome · score 0.75
  • neurodegenerative disease · score 0.50
  • peroxisome biogenesis disorder · score 0.46
  • genetic disorder · score 0.41
  • peroxisome biogenesis disorder, complementation group 7 · score 0.37
  • lysosomal storage disease · score 0.37
  • Zellweger spectrum disorders · score 0.33
  • peroxisome biogenesis disorder 1A (Zellweger) · score 0.17
  • cutaneous melanoma · score 0.13

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P40855-F1alphafoldPREDICTED70.60—

Amino-acid sequence (299 residues)

MAAAEEGCSV GAEADRELEE LLESALDDFD KAKPSPAPPS TTTAPDASGP QKRSPGDTAK DALFASQEKF FQELFDSELA SQATAEFEKA MKELAEEEPH LVEQFQKLSE AAGRVGSDMT SQQEFTSCLK ETLSGLAKNA TDLQNSSMSE EELTKAMEGL GMDEGDGEGN ILPIMQSIMQ NLLSKDVLYP SLKEITEKYP EWLQSHRESL PPEQFEKYQE QHSVMCKICE QFEAETPTDS ETTQKARFEM VLDLMQQLQD LGHPPKELAG EMPPGLNFDL DALNLSGPPG ASGEQCLIM

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Quick facts

UniProtP40855
GenePEX19
OrganismHomo sapiens
Length299
Binders0
Diseases60
View on UniProt