Cathepsin D

mammalian protein found in Homo sapiens
Protein protein Q21157699
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Cathepsin D

Summary

Cathepsin D is a protein[1].

Key Facts

  • Cathepsin D's instance of is recorded as protein[2].
  • Cathepsin D is a type of protein[3].
  • Cathepsin D is part of Aspartic peptidase domain superfamily[4].
  • Cathepsin D is part of Cathepsin D[5].
  • Cathepsin D is part of Peptidase family A1 domain[6].
  • Cathepsin D is part of Aspartic peptidase, N-terminal domain, protein family[7].
  • Cathepsin D is part of Aspartic peptidase, active site, protein family[8].
  • Cathepsin D comprises Peptidase family A1 domain[9].
  • Cathepsin D comprises Aspartic peptidase, active site[10].
  • Cathepsin D comprises Aspartic peptidase, N-terminal[11].
  • Cathepsin D's molecular function is recorded as peptidase activity[12].
  • Cathepsin D's molecular function is recorded as hydrolase activity[13].
  • Cathepsin D's molecular function is recorded as protein binding[14].
  • Cathepsin D's molecular function is recorded as serine-type endopeptidase activity[15].
  • Cathepsin D's molecular function is recorded as cysteine-type endopeptidase activity[16].
  • Cathepsin D's molecular function is recorded as aspartic-type endopeptidase activity[17].
  • Cathepsin D's molecular function is recorded as peptidase activity[18].
  • Cathepsin D's molecular function is recorded as aspartic-type peptidase activity[19].
  • Cathepsin D's cell component is recorded as lysosomal lumen[20].
  • Cathepsin D's cell component is recorded as extracellular exosome[21].
  • Cathepsin D's cell component is recorded as membrane raft[22].
  • Cathepsin D's cell component is recorded as extracellular matrix[23].
  • Cathepsin D's cell component is recorded as lysosome[24].
  • Cathepsin D's cell component is recorded as melanosome[25].
  • Cathepsin D's cell component is recorded as extracellular space[26].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] . Q905695. Retrieved . wikidata.org.
  2. [3] . Q905695. Retrieved . wikidata.org.
  3. [4] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  4. [5] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  9. [10] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  10. [11] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  11. [12] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  12. [13] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  13. [14] . Aluminum inhibits proteolytic degradation of amyloid beta peptide by cathepsin D: a potential link between aluminum accumulation and neuritic plaque deposition. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  14. [15] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  15. [16] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  16. [17] . Cloning and sequence analysis of cDNA for human cathepsin D. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  17. [18] . Folding, activity and targeting of mutated human cathepsin D that cannot be processed into the double-chain form. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  20. [21] . Large-scale proteomics and phosphoproteomics of urinary exosomes. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  21. [22] . Flotillin-1 facilitates toll-like receptor 3 signaling in human endothelial cells. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  22. [23] . Proteomics characterization of extracellular space components in the human aorta. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  23. [24] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  24. [25] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  25. [26] . Proteomics analysis of cardiac extracellular matrix remodeling in a porcine model of ischemia/reperfusion injury. Retrieved . ebi.ac.uk. Provenance: wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). Cathepsin D. Retrieved May 3, 2026, from https://4ort.xyz/entity/cathepsin-d-q21157699
MLA “Cathepsin D.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cathepsin-d-q21157699.
BibTeX @misc{4ortxyz_cathepsin-d-q21157699_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Cathepsin D}}, year = {2026}, url = {https://4ort.xyz/entity/cathepsin-d-q21157699}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Cathepsin D — https://4ort.xyz/entity/cathepsin-d-q21157699 (retrieved 2026-05-03)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 4w ago · Boghog · 2026-07-24 view diff on Wikidata ↗
    Found in taxon Homo sapiens
    Subclass of protein
    Wikidata description mammalian protein found in Homo sapiens
    Mesh tree code D08.811.277.656.074.500.180, D08.811.277.656.224.187, D08.811.277.656.300.048.180
    + 15 other properties edited (see Wikidata diff for full list)
    "/* wbcreateclaim-create:1| */ [[Property:P591]]: 3.4.23.5, [[:toollabs:quickstatements/#/batch/261491|batch #261491]]"
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