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Troponin T1, slow skeletal type

mammalian protein found in Homo sapiens
Protein protein Q21116980
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Summary

Troponin T1, slow skeletal type is a protein[1].

Key Facts

  • Troponin T1, slow skeletal type's instance of is recorded as protein[2].
  • Troponin T1, slow skeletal type's UniProt protein ID is recorded as P13805[3].
  • Troponin T1, slow skeletal type's part of is recorded as troponin T[4].
  • Troponin T1, slow skeletal type's part of is recorded as Troponin domain superfamily[5].
  • Troponin T1, slow skeletal type's RefSeq protein ID is recorded as NP_001119604[6].
  • Troponin T1, slow skeletal type's RefSeq protein ID is recorded as NP_001119605[7].
  • Troponin T1, slow skeletal type's RefSeq protein ID is recorded as NP_001278703[8].
  • Troponin T1, slow skeletal type's RefSeq protein ID is recorded as NP_003274[9].
  • Troponin T1, slow skeletal type's RefSeq protein ID is recorded as XP_011525548[10].
  • Troponin T1, slow skeletal type's RefSeq protein ID is recorded as XP_016882675[11].
  • Troponin T1, slow skeletal type's RefSeq protein ID is recorded as XP_016882676[12].
  • Troponin T1, slow skeletal type's molecular function is recorded as troponin T binding[13].
  • Troponin T1, slow skeletal type's molecular function is recorded as tropomyosin binding[14].
  • Troponin T1, slow skeletal type's molecular function is recorded as protein binding[15].
  • Troponin T1, slow skeletal type's molecular function is recorded as calcium ion binding[16].
  • Troponin T1, slow skeletal type's molecular function is recorded as protein binding[17].
  • Troponin T1, slow skeletal type's molecular function is recorded as tropomyosin binding[18].
  • Troponin T1, slow skeletal type's molecular function is recorded as calcium-dependent ATPase activity[19].
  • Troponin T1, slow skeletal type's molecular function is recorded as troponin T binding[20].
  • Troponin T1, slow skeletal type's cell component is recorded as cytosol[21].
  • Troponin T1, slow skeletal type's cell component is recorded as troponin complex[22].
  • Troponin T1, slow skeletal type's cell component is recorded as troponin complex[23].
  • Troponin T1, slow skeletal type's biological process is recorded as regulation of muscle contraction[24].
  • Troponin T1, slow skeletal type's biological process is recorded as skeletal muscle contraction[25].
  • Troponin T1, slow skeletal type's biological process is recorded as slow-twitch skeletal muscle fiber contraction[26].

References

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

Direct Wikidata claims

  1. [2] ↑ . UniProt. Retrieved . wikidata.org.
  2. [3] ↑ . UniProt. 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] ↑ . Q20641742. Retrieved . wikidata.org.
  6. [7] ↑ . Q20641742. Retrieved . wikidata.org.
  7. [8] ↑ . Q20641742. Retrieved . wikidata.org.
  8. [9] ↑ . Q20641742. Retrieved . wikidata.org.
  9. [10] ↑ . Q20641742. Retrieved . wikidata.org.
  10. [11] ↑ . Q20641742. Retrieved . wikidata.org.
  11. [12] ↑ . Q20641742. Retrieved . wikidata.org.
  12. [13] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  13. [14] ↑ . Cellular fate of truncated slow skeletal muscle troponin T produced by Glu180 nonsense mutation in amish nemaline myopathy. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  14. [15] ↑ . A proteome-scale map of the human interactome network. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  15. [16] ↑ . Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  16. [17] ↑ . A proteome-scale map of the human interactome network. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  17. [18] ↑ . Cellular fate of truncated slow skeletal muscle troponin T produced by Glu180 nonsense mutation in amish nemaline myopathy. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] ↑ . Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. 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] ↑ . Cellular fate of truncated slow skeletal muscle troponin T produced by Glu180 nonsense mutation in amish nemaline myopathy. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  22. [23] ↑ . Cellular fate of truncated slow skeletal muscle troponin T produced by Glu180 nonsense mutation in amish nemaline myopathy. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  23. [24] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  24. [25] ↑ . A novel nemaline myopathy in the Amish caused by a mutation in troponin T1. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  25. [26] ↑ . GOA. 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). Troponin T1, slow skeletal type. Retrieved May 3, 2026, from https://4ort.xyz/entity/troponin-t1-slow-skeletal-type
MLA “Troponin T1, slow skeletal type.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/troponin-t1-slow-skeletal-type.
BibTeX @misc{4ortxyz_troponin-t1-slow-skeletal-type_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Troponin T1, slow skeletal type}}, year = {2026}, url = {https://4ort.xyz/entity/troponin-t1-slow-skeletal-type}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Troponin T1, slow skeletal type — https://4ort.xyz/entity/troponin-t1-slow-skeletal-type (retrieved 2026-05-03)

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