Evidence map›Paper›PMID 30020831›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2019

Understanding the coupling between DNA damage detection and UvrA's ATPase using bulk and single molecule kinetics.

Jamie T Barnett, Neil M Kad

Open access · hybridAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Microbiology spectrum · 2026
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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.

Jamie T BarnettSchool of Biological Sciences, University of Kent, Canterbury, United Kingdom.
Neil M KadSchool of Biological Sciences, University of Kent, Canterbury, United Kingdom.
University of Kent · GB

Funding

Biotechnology and Biological Sciences Research Council BB/I003460/1Biotechnology and Biological Sciences Research Council BB/M01603X/1Biotechnology and Biological Sciences Research Council BB/M019144/1Biotechnology and Biological Sciences Research Council BB/P00847X/1
6 · The paper itself

Abstract

Nucleotide excision repair (NER) protects cells against diverse types of DNA damage, principally UV irradiation. In Escherichia coli, damage is recognized by 2 key enzymes: UvrA and UvrB. Despite extensive investigation, the role of UvrA's 2 ATPase domains in NER remains elusive. Combining single-molecule fluorescence microscopy and classic biochemical methods, we have investigated the role of nucleotide binding in UvrA's kinetic cycle. Measurement of UvrA's steady-state ATPase activity shows it is stimulated upon binding DNA ( k

Indexed as

DNA DamageDNA RepairAdenosine TriphosphatasesAdenosine TriphosphateDNA, BacterialDNA-Binding ProteinsEscherichia coliEscherichia coli ProteinsKineticsMolecular ImagingSingle-Cell AnalysisAdenosine TriphosphatasesAdenosine TriphosphateDNA, BacterialDNA-Binding ProteinsEscherichia coli ProteinsUvrA protein, E colicooperativityDNA repairDNA tightropesfluorescence imaging

Identifiers

PMID30020831
PMCPMC6355085
OpenAlexW2885017728

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.