Cathepsin B (CTSB)

Homo sapiens — UniProt P07858

Gene: CTSBHomo sapiensSwissProt reviewed

About Cathepsin B

Cathepsin B (CTSB) is a protein from Homo sapiens identified by UniProt accession P07858, 339 residues long. MolForge cross-references it against 0 known binders and 835 disease associations.

Target properties

Protein nameCathepsin B
UniProt accessionP07858
GeneCTSB
OrganismHomo sapiens
Length339 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—

Approved drugs hitting this target (4)

DrugCentral-linked approved drugs that act on this protein.

Disease associations (835)

Diseases linked to this target (Open Targets).

  • blood protein measurement · score 0.45
  • keratolytic winter erythema · score 0.37
  • basophil count · score 0.35
  • triglyceride measurement · score 0.34
  • Parkinson disease · score 0.32
  • neurodegenerative disease · score 0.31
  • total cholesterol measurement · score 0.28
  • risk-taking behaviour · score 0.27
  • squalene synthase deficiency · score 0.27
  • basophil percentage of leukocytes · score 0.25

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P07858-F1alphafoldPREDICTED92.14—

Amino-acid sequence (339 residues)

MWQLWASLCC LLVLANARSR PSFHPLSDEL VNYVNKRNTT WQAGHNFYNV DMSYLKRLCG TFLGGPKPPQ RVMFTEDLKL PASFDAREQW PQCPTIKEIR DQGSCGSCWA FGAVEAISDR ICIHTNAHVS VEVSAEDLLT CCGSMCGDGC NGGYPAEAWN FWTRKGLVSG GLYESHVGCR PYSIPPCEHH VNGSRPPCTG EGDTPKCSKI CEPGYSPTYK QDKHYGYNSY SVSNSEKDIM AEIYKNGPVE GAFSVYSDFL LYKSGVYQHV TGEMMGGHAI RILGWGVENG TPYWLVANSW NTDWGDNGFF KILRGQDHCG IESEVVAGIP RTDQYWEKI

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Quick facts

UniProtP07858
GeneCTSB
OrganismHomo sapiens
Length339
Binders0
Diseases835
View on UniProt