Evidence map›Paper›PMID 31504772›Full record

ArticleNucleic acids research2019

A protein architecture guided screen for modification dependent restriction endonucleases.

Thomas Lutz, Kiersten Flodman, Alyssa Copelas, Honorata Czapinska, Megumu Mabuchi, Alexey Fomenkov, Xinyi He, Matthias Bochtler, Shuang-Yong Xu

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  3. A methylome-derived mbioRxiv : the preprint server for biology · 2026
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  4. Review
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  6. Article
  7. Article
  8. Article
  9. Article
  10. Pathways of thymidine hypermodification.Nucleic acids research · 2022
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Characterization of BisI Homologs.Frontiers in microbiology · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Frontiers in microbiology · 2020
    Article
  20. Article
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

9 authors at 4 institutions in 3 countries.

Thomas LutzNew England Biolabs, Inc. 240 County Road, Ipswich, MA 01938, USA.
Kiersten FlodmanNew England Biolabs, Inc. 240 County Road, Ipswich, MA 01938, USA.
Alyssa CopelasNew England Biolabs, Inc. 240 County Road, Ipswich, MA 01938, USA.
Honorata CzapinskaInternational Institute of Molecular and Cell Biology, Trojdena 4, 02-109 Warsaw, Poland.
Megumu MabuchiNew England Biolabs, Inc. 240 County Road, Ipswich, MA 01938, USA.
Alexey FomenkovNew England Biolabs, Inc. 240 County Road, Ipswich, MA 01938, USA.
Xinyi HeState Key Laboratory of Microbial Metabolism, School of Life Sciences & Biotechnology, Shanghai Jiao Tong University, 200240 Shanghai, China.
Matthias BochtlerInternational Institute of Molecular and Cell Biology, Trojdena 4, 02-109 Warsaw, Poland.
Shuang-Yong XuNew England Biolabs, Inc. 240 County Road, Ipswich, MA 01938, USA.
New England Biolabs (United States) · USInstitute of Biochemistry and Biophysics, Polish Academy of Sciences · PLInternational Institute of Molecular and Cell Biology · PLShanghai Jiao Tong University · CN

Funding

Studies of DNA MethyltransferasesR44GM105125 · NIGMS · NEW ENGLAND BIOLABS, INC. · PI ROBERTS, RICHARD J · 2012 to 2014
$1.3M
NIGMS NIH HHS R44 GM105125
6 · The paper itself

Abstract

Modification dependent restriction endonucleases (MDREs) often have separate catalytic and modification dependent domains. We systematically looked for previously uncharacterized fusion proteins featuring a PUA or DUF3427 domain and HNH or PD-(D/E)XK catalytic domain. The enzymes were clustered by similarity of their putative modification sensing domains into several groups. The TspA15I (VcaM4I, CmeDI), ScoA3IV (MsiJI, VcaCI) and YenY4I groups, all featuring a PUA superfamily domain, preferentially cleaved DNA containing 5-methylcytosine or 5-hydroxymethylcytosine. ScoA3V, also featuring a PUA superfamily domain, but of a different clade, exhibited 6-methyladenine stimulated nicking activity. With few exceptions, ORFs for PUA-superfamily domain containing endonucleases were not close to DNA methyltransferase ORFs, strongly supporting modification dependent activity of the endonucleases. DUF3427 domain containing fusion proteins had very little or no endonuclease activity, despite the presence of a putative PD-(D/E)XK catalytic domain. However, their expression potently restricted phage T4gt in Escherichia coli cells. In contrast to the ORFs for PUA domain containing endonucleases, the ORFs for DUF3427 fusion proteins were frequently found in defense islands, often also featuring DNA methyltransferases.

Indexed as

Amino Acid SequenceCatalytic DomainDNA CleavageDNA Modification MethylasesDNA Restriction EnzymesEscherichia coliGene Expression Regulation, EnzymologicModels, MolecularProtein Structure, TertiarySequence AlignmentDNA Modification MethylasesDNA Restriction Enzymes

Identifiers

PMID31504772
PMCPMC6765204
OpenAlexW2971864085

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.