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Tof1p YNL273W

fungal protein found in Saccharomyces cerevisiae S288c
Protein protein Q27549478
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Tof1p YNL273W

Summary

Tof1p YNL273W is a protein[1].

Key Facts

  • Tof1p YNL273W's instance of is recorded as protein[2].
  • Tof1p YNL273W's subclass of is recorded as protein[3].
  • Tof1p YNL273W's UniProt protein ID is recorded as P53840[4].
  • Tof1p YNL273W's part of is recorded as Timeless protein family[5].
  • Tof1p YNL273W's has part is recorded as Timeless protein[6].
  • Tof1p YNL273W's RefSeq protein ID is recorded as NP_014126[7].
  • Tof1p YNL273W's molecular function is recorded as protein binding[8].
  • Tof1p YNL273W's molecular function is recorded as molecular function[9].
  • Tof1p YNL273W's molecular function is recorded as DNA binding[10].
  • Tof1p YNL273W's cell component is recorded as replication fork protection complex[11].
  • Tof1p YNL273W's cell component is recorded as nucleus[12].
  • Tof1p YNL273W's cell component is recorded as nuclear replication fork[13].
  • Tof1p YNL273W's cell component is recorded as cytosol[14].
  • Tof1p YNL273W's cell component is recorded as nuclear chromosome[15].
  • Tof1p YNL273W's cell component is recorded as nuclear chromosome[16].
  • Tof1p YNL273W's cell component is recorded as nucleus[17].
  • Tof1p YNL273W's cell component is recorded as replication fork protection complex[18].
  • Tof1p YNL273W's biological process is recorded as negative regulation of DNA replication[19].
  • Tof1p YNL273W's biological process is recorded as DNA replication[20].
  • Tof1p YNL273W's biological process is recorded as DNA repair[21].
  • Tof1p YNL273W's biological process is recorded as replication fork arrest[22].
  • Tof1p YNL273W's biological process is recorded as meiosis[23].
  • Tof1p YNL273W's biological process is recorded as maintenance of DNA repeat elements[24].
  • Tof1p YNL273W's biological process is recorded as cell cycle[25].
  • Tof1p YNL273W's biological process is recorded as DNA replication checkpoint signaling[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] ↑ . Q20641742. Retrieved . wikidata.org.
  3. [4] ↑ . Q905695. Retrieved . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . InterPro Release 71.0. ebi.ac.uk. Provenance: wikidata.org.
  6. [7] ↑ . Q20641742. Retrieved . wikidata.org.
  7. [8] ↑ . High-quality binary protein interaction map of the yeast interactome network. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  8. [9] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  9. [10] ↑ . Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  10. [11] ↑ . GINS maintains association of Cdc45 with MCM in replisome progression complexes at eukaryotic DNA replication forks. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  11. [12] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  12. [13] ↑ . Molecular anatomy and regulation of a stable replisome at a paused eukaryotic DNA replication fork.. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  13. [14] ↑ . The nuclear localization of SWI/SNF proteins is subjected to oxygen regulation. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  14. [15] ↑ . S-phase checkpoint proteins Tof1 and Mrc1 form a stable replication-pausing complex. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  15. [16] ↑ . S-phase checkpoint proteins Tof1 and Mrc1 form a stable replication-pausing complex. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  16. [17] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  17. [18] ↑ . GINS maintains association of Cdc45 with MCM in replisome progression complexes at eukaryotic DNA replication forks. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  18. [19] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  19. [20] ↑ . Mrc1 and Tof1 promote replication fork progression and recovery independently of Rad53.. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  20. [21] ↑ . Genetic analysis of Saccharomyces cerevisiae H2A serine 129 mutant suggests a functional relationship between H2A and the sister-chromatid cohesion partners Csm3-Tof1 for the repair of topoisomerase I-induced DNA damage. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  21. [22] ↑ . The Tof1p-Csm3p protein complex counteracts the Rrm3p helicase to control replication termination of Saccharomyces cerevisiae. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  22. [23] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  23. [24] ↑ . Mrc1, Tof1 and Csm3 inhibit CAG.CTG repeat instability by at least two mechanisms.. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  24. [25] ↑ . GOA. Retrieved . ebi.ac.uk. Provenance: wikidata.org.
  25. [26] ↑ . S-phase checkpoint proteins Tof1 and Mrc1 form a stable replication-pausing complex. 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). Tof1p YNL273W. Retrieved May 3, 2026, from https://4ort.xyz/entity/tof1p-ynl273w
MLA “Tof1p YNL273W.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/tof1p-ynl273w.
BibTeX @misc{4ortxyz_tof1p-ynl273w_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Tof1p YNL273W}}, year = {2026}, url = {https://4ort.xyz/entity/tof1p-ynl273w}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Tof1p YNL273W — https://4ort.xyz/entity/tof1p-ynl273w (retrieved 2026-05-03)

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