Killin (KLLN)

Homo sapiens — UniProt B2CW77

Gene: KLLNHomo sapiensSwissProt reviewed

About Killin

Killin (KLLN) is a protein from Homo sapiens identified by UniProt accession B2CW77, 178 residues long. MolForge cross-references it against 0 known binders and 118 disease associations.

Target properties

Protein nameKillin
UniProt accessionB2CW77
GeneKLLN
OrganismHomo sapiens
Length178 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 (118)

Diseases linked to this target (Open Targets).

  • Cowden disease · score 0.41
  • neurodegenerative disease · score 0.37
  • type 2 diabetes mellitus · score 0.32
  • BMI-adjusted waist-hip ratio · score 0.28
  • waist-hip ratio · score 0.26
  • monocyte count · score 0.25
  • systolic blood pressure · score 0.24
  • mean platelet volume · score 0.22
  • monocyte percentage of leukocytes · score 0.22
  • mean corpuscular volume · score 0.21

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-B2CW77-F1alphafoldPREDICTED50.89—

Amino-acid sequence (178 residues)

MDRPGPGSAR PGRTVHVWGY RVEWKVRNGR KLQPSEWAGR GDLGGFKRRW KDTRATVGTT FRRRSRVSLV GELSKFPLPS DSSGGKSSSS FARGALAWCR QRNPNPSCAA AETGARTSLP KERCRGWRLG NWLHKHPHPN TCPRLPACWL PPILTERGER VPKLVPLLAC YPKSKPKD

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Quick facts

UniProtB2CW77
GeneKLLN
OrganismHomo sapiens
Length178
Binders0
Diseases118
View on UniProt