Persephin (PSPN)

Homo sapiens — UniProt O60542

Gene: PSPNHomo sapiensSwissProt reviewed

About Persephin

Persephin (PSPN) is a protein from Homo sapiens identified by UniProt accession O60542, 156 residues long. MolForge cross-references it against 0 known binders and 22 disease associations.

Target properties

Protein namePersephin
UniProt accessionO60542
GenePSPN
OrganismHomo sapiens
Length156 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 (22)

Diseases linked to this target (Open Targets).

  • atrial fibrillation · score 0.04
  • oral squamous cell carcinoma · score 0.02
  • neoplasm · score 0.02
  • infection · score 0.01
  • infect · score 0.01
  • Parkinson disease · score 0.01
  • adenocarcinoma · score 0.01
  • bacteriemia · score 0.01
  • McLeod neuroacanthocytosis syndrome · score 0.01
  • inflammatory bowel disease · score 0.01

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-O60542-F1alphafoldPREDICTED77.99—

Amino-acid sequence (156 residues)

MAVGKFLLGS LLLLSLQLGQ GWGPDARGVP VADGEFSSEQ VAKAGGTWLG THRPLARLRR ALSGPCQLWS LTLSVAELGL GYASEEKVIF RYCAGSCPRG ARTQHGLALA RLQGQGRAHG GPCCRPTRYT DVAFLDDRHR WQRLPQLSAA ACGCGG

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Quick facts

UniProtO60542
GenePSPN
OrganismHomo sapiens
Length156
Binders0
Diseases22
View on UniProt