Leptin (LEP)

Homo sapiens — UniProt P41159

Gene: LEPHomo sapiensSwissProt reviewed

About Leptin

Leptin (LEP) is a protein from Homo sapiens identified by UniProt accession P41159, 167 residues long. MolForge cross-references it against 0 known binders and 1,719 disease associations.

Target properties

Protein nameLeptin
UniProt accessionP41159
GeneLEP
OrganismHomo sapiens
Length167 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 (1719)

Diseases linked to this target (Open Targets).

  • obesity due to congenital leptin deficiency · score 0.72
  • BMI-adjusted leptin measurement · score 0.49
  • leptin measurement · score 0.46
  • type 2 diabetes mellitus · score 0.37
  • high density lipoprotein cholesterol measurement · score 0.34
  • body mass index · score 0.27
  • self reported educational attainment · score 0.27
  • interleukin-6 measurement · score 0.24
  • mastiha supplement exposure measurement · score 0.24
  • HbA1c measurement · score 0.21

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P41159-F1alphafoldPREDICTED81.11—

Amino-acid sequence (167 residues)

MHWGTLCGFL WLWPYLFYVQ AVPIQKVQDD TKTLIKTIVT RINDISHTQS VSSKQKVTGL DFIPGLHPIL TLSKMDQTLA VYQQILTSMP SRNVIQISND LENLRDLLHV LAFSKSCHLP WASGLETLDS LGGVLEASGY STEVVALSRL QGSLQDMLWQ LDLSPGC

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Quick facts

UniProtP41159
GeneLEP
OrganismHomo sapiens
Length167
Binders0
Diseases1,719
View on UniProt