Evidence map›Paper›PMID 33198762›Full record

ReviewCell communication and signaling : CCS2020

The tail of cryptochromes: an intrinsically disordered cog within the mammalian circadian clock.

Gian Carlo G Parico, Carrie L Partch

Open access · goldAbstract readReview
In one paragraph

Review in Cell communication and signaling : CCS, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.2field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
  3. AProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Antarctic MicroalgaMarine drugs · 2026
    Article
  5. Targeting Cryptochromes in Chronic Diseases.Cell biology international · 2025
    Review
  6. Review
  7. Review
  8. Article
  9. c-Jun N-terminal kinase signaling in aging.Frontiers in aging neuroscience · 2024
    Review
  10. Review
  11. Article
  12. Article
  13. Dimerization of European Robin Cryptochrome 4a.The journal of physical chemistry. B · 2023
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Gian Carlo G ParicoDepartment of Chemistry and Biochemistry, UC Santa Cruz, Santa Cruz, USA.
Carrie L PartchDepartment of Chemistry and Biochemistry, UC Santa Cruz, Santa Cruz, USA. cpartch@ucsc.edu.ORCID 0000-0002-4677-2861
University of California, Santa Cruz · US

Funding

Exploring the structural basis for 24-hour timekeeping in mammalsR01GM107069 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI PARTCH, CARRIE L · 2013 to 2020
$3.2M
An Octet Bio-layer Interferometer for Macromolecular Interaction Studies at UCSCS10OD027012 · OD · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI RUBIN, SETH MICHAEL · 2019 to 2019
$370k
Howard Hughes Medical InstituteNIGMS NIH HHS R01 GM107069NIH HHS S10 OD027012
6 · The paper itself

Abstract

Cryptochrome (CRY) proteins play an essential role in regulating mammalian circadian rhythms. CRY is composed of a structured N-terminal domain known as the photolyase homology region (PHR), which is tethered to an intrinsically disordered C-terminal tail. The PHR domain is a critical hub for binding other circadian clock components such as CLOCK, BMAL1, PERIOD, or the ubiquitin ligases FBXL3 and FBXL21. While the isolated PHR domain is necessary and sufficient to generate circadian rhythms, removing or modifying the cryptochrome tails modulates the amplitude and/or periodicity of circadian rhythms, suggesting that they play important regulatory roles in the molecular circadian clock. In this commentary, we will discuss how recent studies of these intrinsically disordered tails are helping to establish a general and evolutionarily conserved model for CRY function, where the function of PHR domains is modulated by reversible interactions with their intrinsically disordered tails. Video abstract.

Indexed as

Circadian ClocksAmino Acid SequenceAnimalsCircadian RhythmCLOCK ProteinsCryptochromesHumansIntrinsically Disordered ProteinsMammalsCLOCK ProteinsCryptochromesIntrinsically Disordered ProteinsAutoinhibitionCircadian rhythmsCryptochromeC-terminal tailIntrinsically disordered proteinIntrinsically disordered region

Identifiers

PMID33198762
PMCPMC7667820
OpenAlexW3099227530

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.