Evidence map›Paper›PMID 29401372›Full record

ArticleJournal of the American Chemical Society2018

Determinants of Photolyase's DNA Repair Mechanism in Mesophiles and Extremophiles.

Benjamin J G Rousseau, Shoresh Shafei, Agostino Migliore, Robert J Stanley, David N Beratan

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Chemical Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

5 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Theoretical insights into the DNA repair function ofBiophysics and physicobiology · 2020
    Article
  4. Article
  5. 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

5 authors at 2 institutions in 1 country.

Benjamin J G Rousseau
Shoresh Shafei
Agostino Migliore
Robert J StanleyDepartment of Chemistry, Temple University , Philadelphia, Pennsylvania 19122, United States.ORCID 0000-0003-4140-4311
David N BeratanDepartment of Biochemistry, Duke University , Durham, North Carolina 27710, United States.ORCID 0000-0003-4758-8676
Duke University · USTemple University · US

Funding

Shared Services Center NASA 80NSSC17K0033
6 · The paper itself

Abstract

Light-driven DNA repair by extremophilic photolyases is of tremendous importance for understanding the early development of life on Earth. The mechanism for flavin adenine dinucleotide repair of DNA lesions is the subject of debate and has been studied mainly in mesophilic species. In particular, the role of adenine in the repair process is poorly understood. Using molecular docking, molecular dynamics simulations, electronic structure calculations, and electron tunneling pathways analysis, we examined adenine's role in DNA repair in four photolyases that thrive at different temperatures. Our results indicate that the contribution of adenine to the electronic coupling between the flavin and the cyclobutane pyrimidine dimer lesion to be repaired is significant in three (one mesophilic and two extremophilic) of the four enzymes studied. Our analysis suggests that thermophilic and hyperthermophilic photolyases have evolved structurally to preserve the functional position (and thus the catalytic function) of adenine at their high temperatures of operation. Water molecules can compete with adenine in establishing the strongest coupling pathway for the electron transfer repair process, but the adenine contribution remains substantial. The present study also reconciles prior seemingly contradictory conclusions on the role of adenine in mesophile electron transfer repair reactions, showing how adenine-mediated superexchange is conformationally gated.

Indexed as

AdenineDeoxyribodipyrimidine Photo-LyaseDinitrocresolsDNA RepairModels, MolecularPyrimidines4,6-dinitro-o-cresolAdenineDeoxyribodipyrimidine Photo-LyaseDinitrocresolspyrimidinePyrimidines

Identifiers

PMID29401372
PMCPMC7301757
OpenAlexW2785658743

What OpenQuestion holds

Textmetadata
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.