Evidence map›Paper›PMID 29722888›Full record

ArticleBioinformatics (Oxford, England)2018

Applying graph theory to protein structures: an Atlas of coiled coils.

Jack W Heal, Gail J Bartlett, Christopher W Wood, Andrew R Thomson, Derek N Woolfson

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Designability of α-Helical Protein Filaments.Sub-cellular biochemistry · 2026
    Review
  2. Review
  3. Article
  4. CCProtein science : a publication of the Protein Society · 2023
    Article
  5. Article
  6. Coiled coils 9-to-5: rationalChemical science · 2021
    Article
  7. Article
  8. Article
  9. Protein conformational switch discerned via network centrality properties.Computational and structural biotechnology journal · 2021
    Article
  10. 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.

Jack W HealSchool of Chemistry, University of Bristol, Bristol, UK.
Gail J BartlettSchool of Chemistry, University of Bristol, Bristol, UK.
Christopher W WoodSchool of Chemistry, University of Bristol, Bristol, UK.
Andrew R ThomsonSchool of Chemistry, University of Bristol, Bristol, UK.
Derek N WoolfsonSchool of Chemistry, University of Bristol, Bristol, UK.

Funding

Biotechnology and Biological Sciences Research Council BB/J008990/1Biotechnology and Biological Sciences Research Council BB/L01386X/1
6 · The paper itself

Abstract

Motivation: To understand protein structure, folding and function fully and to design proteins de novo reliably, we must learn from natural protein structures that have been characterized experimentally. The number of protein structures available is large and growing exponentially, which makes this task challenging. Indeed, computational resources are becoming increasingly important for classifying and analyzing this resource. Here, we use tools from graph theory to define an Atlas classification scheme for automatically categorizing certain protein substructures. Results: Focusing on the α-helical coiled coils, which are ubiquitous protein-structure and protein-protein interaction motifs, we present a suite of computational resources designed for analyzing these assemblies. iSOCKET enables interactive analysis of side-chain packing within proteins to identify coiled coils automatically and with considerable user control. Applying a graph theory-based Atlas classification scheme to structures identified by iSOCKET gives the Atlas of Coiled Coils, a fully automated, updated overview of extant coiled coils. The utility of this approach is illustrated with the first formal classification of an emerging subclass of coiled coils called α-helical barrels. Furthermore, in the Atlas, the known coiled-coil universe is presented alongside a partial enumeration of the 'dark matter' of coiled-coil structures; i.e. those coiled-coil architectures that are theoretically possible but have not been observed to date, and thus present defined targets for protein design. Availability and implementation: iSOCKET is available as part of the open-source GitHub repository associated with this work (https://github.com/woolfson-group/isocket). This repository also contains all the data generated when classifying the protein graphs. The Atlas of Coiled Coils is available at: http://coiledcoils.chm.bris.ac.uk/atlas/app.

Indexed as

Protein FoldingProtein Conformation, alpha-HelicalProtein Interaction Domains and MotifsProteinsProteins

Identifiers

PMID29722888
PMCPMC6157074

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.