Myelin P2 protein (PMP2)

Homo sapiens — UniProt P02689

Gene: PMP2Homo sapiensSwissProt reviewed

About Myelin P2 protein

Myelin P2 protein (PMP2) is a protein from Homo sapiens identified by UniProt accession P02689, 132 residues long. MolForge cross-references it against 0 known binders and 55 disease associations.

Target properties

Protein nameMyelin P2 protein
UniProt accessionP02689
GenePMP2
OrganismHomo sapiens
Length132 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 (55)

Diseases linked to this target (Open Targets).

  • Charcot-Marie-Tooth disease type 1G · score 0.73
  • peripheral neuropathy · score 0.33
  • genetic disorder · score 0.32
  • hereditary neuropathy with liability to pressure palsies · score 0.04
  • Charcot-Marie-Tooth disease type 2B2 · score 0.03
  • Barrett's esophagus · score 0.03
  • medulloblastoma · score 0.03
  • atypical teratoid rhabdoid tumor · score 0.02
  • Charcot-Marie-Tooth disease · score 0.02
  • high density lipoprotein cholesterol measurement · score 0.02

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P02689-F1alphafoldPREDICTED96.39—

Amino-acid sequence (132 residues)

MSNKFLGTWK LVSSENFDDY MKALGVGLAT RKLGNLAKPT VIISKKGDII TIRTESTFKN TEISFKLGQE FEETTADNRK TKSIVTLQRG SLNQVQRWDG KETTIKRKLV NGKMVAECKM KGVVCTRIYE KV

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Quick facts

UniProtP02689
GenePMP2
OrganismHomo sapiens
Length132
Binders0
Diseases55
View on UniProt