Peripheral myelin protein 22 (PMP22)

Homo sapiens — UniProt Q01453

Gene: PMP22Homo sapiensSwissProt reviewed

About Peripheral myelin protein 22

Peripheral myelin protein 22 (PMP22) is a protein from Homo sapiens identified by UniProt accession Q01453, 160 residues long. MolForge cross-references it against 0 known binders and 684 disease associations.

Target properties

Protein namePeripheral myelin protein 22
UniProt accessionQ01453
GenePMP22
OrganismHomo sapiens
Length160 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 (684)

Diseases linked to this target (Open Targets).

  • Charcot-Marie-Tooth disease type 1A · score 0.82
  • Dejerine-Sottas syndrome · score 0.81
  • Charcot-Marie-Tooth disease type 1E · score 0.78
  • hereditary neuropathy with liability to pressure palsies · score 0.78
  • Charcot-Marie-Tooth disease type 3 · score 0.78
  • chronic inflammatory demyelinating polyneuropathy · score 0.58
  • Charcot-Marie-Tooth disease type 1 · score 0.56
  • Charcot-Marie-Tooth disease · score 0.54
  • Roussy-Lévy syndrome · score 0.54
  • genetic disorder · score 0.49

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q01453-F1alphafoldPREDICTED89.98—

Amino-acid sequence (160 residues)

MLLLLLSIIV LHVAVLVLLF VSTIVSQWIV GNGHATDLWQ NCSTSSSGNV HHCFSSSPNE WLQSVQATMI LSIIFSILSL FLFFCQLFTL TKGGRFYITG IFQILAGLCV MSAAAIYTVR HPEWHLNSDY SYGFAYILAW VAFPLALLSG VIYVILRKRE

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Quick facts

UniProtQ01453
GenePMP22
OrganismHomo sapiens
Length160
Binders0
Diseases684
View on UniProt