Evidence map›Paper›PMID 38158653›Full record

ArticleBiophysical journal2024

Efficient enumeration and visualization of helix-coil ensembles.

Roy G Hughes, Shiwen Zhao, Terrence G Oas, Scott C Schmidler

Abstract read
In one paragraph

Article in Biophysical journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Roy G HughesDepartment of Biochemistry, Duke University, Durham, North Carolina.
Shiwen ZhaoProgram in Computational Biology and Bioinformatics, Duke University, Durham, North Carolina.
Terrence G OasDepartment of Biochemistry, Duke University, Durham, North Carolina.
Scott C SchmidlerProgram in Computational Biology and Bioinformatics, Duke University, Durham, North Carolina; Department of Statistical Science, Duke University, Durham, North Carolina. Electronic address: scott.schmidler@duke.edu.

Funding

A New Approach to Phylogenetic Analysis Using Structural InformationR01GM090201 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI RODRIGUEZ, ABEL · 2009 to 2013
$1.4M
NIGMS NIH HHS R01 GM090201
6 · The paper itself

Abstract

Helix-coil models are routinely used to interpret circular dichroism data of helical peptides or predict the helicity of naturally-occurring and designed polypeptides. However, a helix-coil model contains significantly more information than mean helicity alone, as it defines the entire ensemble-the equilibrium population of every possible helix-coil configuration-for a given sequence. Many desirable quantities of this ensemble are either not obtained as ensemble averages or are not available using standard helicity-averaging calculations. Enumeration of the entire ensemble can allow calculation of a wider set of ensemble properties, but the exponential size of the configuration space typically renders this intractable. We present an algorithm that efficiently approximates the helix-coil ensemble to arbitrary accuracy by sequentially generating a list of the M highest populated configurations in descending order of population. Truncating this list of (configuration, population) pairs at a desired accuracy provides an approximating sub-ensemble. We demonstrate several uses of this approach for providing insight into helix-coil ensembles and folding mechanisms, including landscape visualization.

Indexed as

PeptidesCircular DichroismPeptides

Identifiers

PMID38158653
PMCPMC10870177

What OpenQuestion holds

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Registered trials

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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.