Cathepsin D (CTSD)

Homo sapiens — UniProt P07339

Gene: CTSDHomo sapiensSwissProt reviewed

About Cathepsin D

Cathepsin D (CTSD) is a protein from Homo sapiens identified by UniProt accession P07339, 412 residues long. MolForge cross-references it against 0 known binders and 673 disease associations.

Target properties

Protein nameCathepsin D
UniProt accessionP07339
GeneCTSD
OrganismHomo sapiens
Length412 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 (3)

DrugCentral-linked approved drugs that act on this protein.

Disease associations (673)

Diseases linked to this target (Open Targets).

  • CLN10 disease · score 0.77
  • neuronal ceroid lipofuscinosis 10 · score 0.73
  • neuronal ceroid lipofuscinosis · score 0.66
  • Congenital neuronal ceroid lipofuscinosis · score 0.55
  • neurodegenerative disease · score 0.50
  • aspartate aminotransferase measurement · score 0.50
  • blood protein measurement · score 0.42
  • cathepsin D measurement · score 0.39
  • lysosomal storage disease · score 0.37
  • genetic disorder · score 0.34

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P07339-F1alphafoldPREDICTED84.99—

Amino-acid sequence (412 residues)

MQPSSLLPLA LCLLAAPASA LVRIPLHKFT SIRRTMSEVG GSVEDLIAKG PVSKYSQAVP AVTEGPIPEV LKNYMDAQYY GEIGIGTPPQ CFTVVFDTGS SNLWVPSIHC KLLDIACWIH HKYNSDKSST YVKNGTSFDI HYGSGSLSGY LSQDTVSVPC QSASSASALG GVKVERQVFG EATKQPGITF IAAKFDGILG MAYPRISVNN VLPVFDNLMQ QKLVDQNIFS FYLSRDPDAQ PGGELMLGGT DSKYYKGSLS YLNVTRKAYW QVHLDQVEVA SGLTLCKEGC EAIVDTGTSL MVGPVDEVRE LQKAIGAVPL IQGEYMIPCE KVSTLPAITL KLGGKGYKLS PEDYTLKVSQ AGKTLCLSGF MGMDIPPPSG PLWILGDVFI GRYYTVFDRD NNRVGFAEAA RL

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Quick facts

UniProtP07339
GeneCTSD
OrganismHomo sapiens
Length412
Binders0
Diseases673
View on UniProt