Evidence map›Paper›PMID 31326273›Full record

ArticleMolecular cell2019

CRISPR-Cas III-A Csm6 CARF Domain Is a Ring Nuclease Triggering Stepwise cA

Ning Jia, Roger Jones, Guangli Yang, Ouathek Ouerfelli, Dinshaw J Patel

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

76 citing papers in PubMed, 129 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Diversity and abundance of ring nucleases in type III CRISPR-Cas loci.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Article
  11. SAM-AMP lyases in type III CRISPR defence.Nucleic acids research · 2025
    Article
  12. Article
  13. Cat1 forms filament networks to degrade NADScience (New York, N.Y.) · 2025
    Article
  14. Characterization of Five CRISPR Systems inInternational journal of molecular sciences · 2025
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

16 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

Ning JiaStructural Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. Electronic address: jian@mskcc.org.
Roger JonesDepartment of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, Piscataway, NJ 08854, USA.
Guangli YangChemical Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Ouathek OuerfelliChemical Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Dinshaw J PatelStructural Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA. Electronic address: pateld@mskcc.org.
Memorial Sloan Kettering Cancer Center · USRutgers, The State University of New Jersey · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
User Training and OutreachP30GM124165 · NIGMS · CORNELL UNIVERSITY · PI MALCOLM S. CAPEL · 2018 to 2026
$34.2M
Development of small molecule cGAS inhibitors for repression of dsDNA-triggered interferon expressionR01AI141507 · NIAID · ROCKEFELLER UNIVERSITY · PI TUSCHL, THOMAS · 2019 to 2022
$2.1M
Pixel Array Detector for X-ray CrystallographyS10RR029205 · NCRR · CORNELL UNIVERSITY · PI EALICK, STEVEN E · 2010 to 2010
$1.8M
'Class I and III Multi-subunit CRISPR-Cas Surveillance Complexes: Recognition, Cleavage, Autoimmunity and Inhibition’R01GM129430 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI PATEL, DINSHAW J · 2019 to 2022
$1.4M
NCI NIH HHS P30 CA008748NCRR NIH HHS S10 RR029205NIAID NIH HHS R01 AI141507NIGMS NIH HHS P30 GM124165NIGMS NIH HHS R01 GM129430
6 · The paper itself

Abstract

Type III-A CRISPR-Cas surveillance complexes containing multi-subunit Csm effector, guide, and target RNAs exhibit multiple activities, including formation of cyclic-oligoadenylates (cA

Indexed as

CRISPR-Cas SystemsAdenine NucleotidesArchaeal ProteinsBinding SitesCRISPR-Associated ProteinsOligoribonucleotidesProtein DomainsRibonucleasesThermococcus2',5'-oligoadenylateAdenine NucleotidesArchaeal ProteinsCRISPR-Associated ProteinsOligoribonucleotidesRibonucleasesA CARF histidine contributes to autoinhibitionCsm6 CARF is a ring nucleaseCsm6 is an adenosine-specific RNaseSequential cleavage bursts regulate RNase activityType III-A CRISPR-Cas Csm

Identifiers

PMID31326273
PMCPMC6731128
OpenAlexW2960176412

What OpenQuestion holds

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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.