Evidence map›Paper›PMID 28340329›Full record

ArticleRNA biology2017

A close-up view of codon selection in eukaryotic initiation.

Christoffer Lind, Mauricio Esguerra, Johan Åqvist

Abstract read
In one paragraph

Article in RNA biology, 2017. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Article
  4. Nucleobase carbonyl groups are poor MgRNA (New York, N.Y.) · 2019
    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

3 authors.

Christoffer Linda Department of Cell and Molecular Biology , Uppsala University , Uppsala , Sweden.
Mauricio Esguerraa Department of Cell and Molecular Biology , Uppsala University , Uppsala , Sweden.ORCID 0000-0002-1775-586X
Johan Åqvista Department of Cell and Molecular Biology , Uppsala University , Uppsala , Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

When given an option to choose among a set of alternatives and only one selection is right, one might stop and reflect over which one is best. However, the ribosome has no time to stop and make such reflections, proteins need to be produced and very fast. Eukaryotic translation initiation is an example of such a conundrum. Here, scanning for the correct codon match must be fast, efficient and accurate. We highlight our recent computational findings, which show how the initiation machinery manages to recognize one specific codon among many possible challengers, by fine-tuning the energetic landscape of base-pairing with the aid of the initiation factors eIF1 and eIF1A. Using a recent 3-dimensional structure of the eukaryotic initiation complex we have performed simulations of codon recognition in atomic detail. These calculations provide an in-depth energetic and structural view of how discrimination against near-cognate codons is achieved by the initiation complex.

Indexed as

Codon, InitiatorComputer SimulationEukaryotic CellsModels, MolecularPeptide Chain Initiation, TranslationalSelection, GeneticThermodynamicsCodon, InitiatorCodon selectionmolecular dynamics simulationribosomestart codontranslation initiation

Identifiers

PMID28340329
PMCPMC5546541

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.