complement factor properdin

mammalian protein found in Homo sapiens
Protein protein Q22677535
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complement factor properdin

Summary

complement factor properdin is a protein[1].

Key Facts

  • complement factor properdin's instance of is recorded as protein[2].
  • complement factor properdin's subclass of is recorded as protein[3].
  • complement factor properdin's UniProt protein ID is recorded as P27918[4].
  • complement factor properdin's part of is recorded as Thrombospondin type-1 (TSP1) repeat superfamily[5].
  • complement factor properdin's part of is recorded as Thrombospondin type-1 (TSP1) repeat, protein family[6].
  • complement factor properdin's MeSH descriptor ID is recorded as D011414[7].
  • complement factor properdin's has part is recorded as Thrombospondin type-1 (TSP1) repeat[8].
  • complement factor properdin's RefSeq protein ID is recorded as NP_001138724[9].
  • complement factor properdin's RefSeq protein ID is recorded as NP_002612[10].
  • complement factor properdin's RefSeq protein ID is recorded as XP_016885064[11].
  • complement factor properdin's PDB structure ID is recorded as 1W0R[12].
  • complement factor properdin's PDB structure ID is recorded as 1W0S[13].
  • complement factor properdin's MeSH tree code is recorded as D12.776.124.486.274.965[14].
  • complement factor properdin's MeSH tree code is recorded as D12.776.124.790.223.624[15].
  • complement factor properdin's MeSH tree code is recorded as D12.776.377.715.182.624[16].
  • complement factor properdin's molecular function is recorded as protein binding[17].
  • complement factor properdin's molecular function is recorded as serine-type endopeptidase activity[18].
  • complement factor properdin's cell component is recorded as extracellular matrix[19].
  • complement factor properdin's cell component is recorded as endoplasmic reticulum lumen[20].
  • complement factor properdin's cell component is recorded as extracellular region[21].
  • complement factor properdin's cell component is recorded as extracellular space[22].
  • complement factor properdin's cell component is recorded as specific granule lumen[23].
  • complement factor properdin's cell component is recorded as tertiary granule lumen[24].
  • complement factor properdin's cell component is recorded as collagen-containing extracellular matrix[25].
  • complement factor properdin's biological process is recorded as immune response[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] . Q905695. Retrieved . wikidata.org.
  4. [5] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  8. [9] . Q20641742. Retrieved . wikidata.org.
  9. [10] . Q20641742. Retrieved . wikidata.org.
  10. [11] . Q20641742. Retrieved . wikidata.org.
  11. [12] . Q905695. Retrieved . wikidata.org.
  12. [13] . Q905695. Retrieved . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . Complement factor P is a ligand for the natural killer cell-activating receptor NKp46.. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  17. [18] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] . Proteomics characterization of extracellular space components in the human aorta. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  20. [21] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  21. [22] . Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  22. [23] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  23. [24] . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  24. [25] . Proteomics characterization of extracellular space components in the human aorta. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  25. [26] . Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency. Retrieved . ebi.ac.uk. Provenance: wikidata.org.

Class ancestry

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

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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). complement factor properdin. Retrieved May 3, 2026, from https://4ort.xyz/entity/complement-factor-properdin-q22677535
MLA “complement factor properdin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/complement-factor-properdin-q22677535.
BibTeX @misc{4ortxyz_complement-factor-properdin-q22677535_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{complement factor properdin}}, year = {2026}, url = {https://4ort.xyz/entity/complement-factor-properdin-q22677535}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): complement factor properdin — https://4ort.xyz/entity/complement-factor-properdin-q22677535 (retrieved 2026-05-03)

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