Cathepsin W (CTSW)

Homo sapiens — UniProt P56202

Gene: CTSWHomo sapiensSwissProt reviewed

About Cathepsin W

Cathepsin W (CTSW) is a protein from Homo sapiens identified by UniProt accession P56202, 376 residues long. MolForge cross-references it against 0 known binders and 68 disease associations.

Target properties

Protein nameCathepsin W
UniProt accessionP56202
GeneCTSW
OrganismHomo sapiens
Length376 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 (68)

Diseases linked to this target (Open Targets).

  • body height · score 0.16
  • self reported educational attainment · score 0.15
  • Crohn's disease · score 0.15
  • glioblastoma multiforme · score 0.14
  • psoriasis · score 0.14
  • ulcerative colitis · score 0.14
  • sclerosing cholangitis · score 0.14
  • ankylosing spondylitis · score 0.14
  • monocyte count · score 0.13
  • inflammatory bowel disease · score 0.12

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P56202-F1alphafoldPREDICTED83.54—

Amino-acid sequence (376 residues)

MALTAHPSCL LALLVAGLAQ GIRGPLRAQD LGPQPLELKE AFKLFQIQFN RSYLSPEEHA HRLDIFAHNL AQAQRLQEED LGTAEFGVTP FSDLTEEEFG QLYGYRRAAG GVPSMGREIR SEEPEESVPF SCDWRKVASA ISPIKDQKNC NCCWAMAAAG NIETLWRISF WDFVDVSVQE LLDCGRCGDG CHGGFVWDAF ITVLNNSGLA SEKDYPFQGK VRAHRCHPKK YQKVAWIQDF IMLQNNEHRI AQYLATYGPI TVTINMKPLQ LYRKGVIKAT PTTCDPQLVD HSVLLVGFGS VKSEEGIWAE TVSSQSQPQP PHPTPYWILK NSWGAQWGEK GYFRLHRGSN TCGITKFPLT ARVQKPDMKP RVSCPP

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Quick facts

UniProtP56202
GeneCTSW
OrganismHomo sapiens
Length376
Binders0
Diseases68
View on UniProt