Evidence map›Paper›PMID 29975698›Full record

ArticlePloS one2018

SAFlex: A structural alphabet extension to integrate protein structural flexibility and missing data information.

Ikram Allam, Delphine Flatters, Géraldine Caumes, Leslie Regad, Vincent Delos, Gregory Nuel, Anne-Claude Camproux

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 94% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 2 institutions in 1 country.

Ikram AllamMolécules thérapeutiques in silico (MTi), INSERM UMR-S973, University Paris Diderot, Paris 7, France.
Delphine FlattersMolécules thérapeutiques in silico (MTi), INSERM UMR-S973, University Paris Diderot, Paris 7, France.
Géraldine CaumesMolécules thérapeutiques in silico (MTi), INSERM UMR-S973, University Paris Diderot, Paris 7, France.
Leslie RegadMolécules thérapeutiques in silico (MTi), INSERM UMR-S973, University Paris Diderot, Paris 7, France.
Vincent DelosProbability Statistique and Biology (PSB), LPMA laboratory, CNRS INSMI UMR 7599, University Pierre et Marie Curie, Paris 6, France.
Gregory NuelProbability Statistique and Biology (PSB), LPMA laboratory, CNRS INSMI UMR 7599, University Pierre et Marie Curie, Paris 6, France.
Anne-Claude CamprouxMolécules thérapeutiques in silico (MTi), INSERM UMR-S973, University Paris Diderot, Paris 7, France.ORCID 0000-0001-8821-9952
Inserm · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this paper, we describe SAFlex (Structural Alphabet Flexibility), an extension of an existing structural alphabet (HMM-SA), to better explore increasing protein three dimensional structure information by encoding conformations of proteins in case of missing residues or uncertainties. An SA aims to reduce three dimensional conformations of proteins as well as their analysis and comparison complexity by simplifying any conformation in a series of structural letters. Our methodology presents several novelties. Firstly, it can account for the encoding uncertainty by providing a wide range of encoding options: the maximum a posteriori, the marginal posterior distribution, and the effective number of letters at each given position. Secondly, our new algorithm deals with the missing data in the protein structure files (concerning more than 75% of the proteins from the Protein Data Bank) in a rigorous probabilistic framework. Thirdly, SAFlex is able to encode and to build a consensus encoding from different replicates of a single protein such as several homomer chains. This allows localizing structural differences between different chains and detecting structural variability, which is essential for protein flexibility identification. These improvements are illustrated on different proteins, such as the crystal structure of an eukaryotic small heat shock protein. They are promising to explore increasing protein redundancy data and obtain useful quantification of their flexibility.

Indexed as

Amino Acid SequenceModels, MolecularProtein ConformationAlgorithmsDatabases, ProteinMarkov ChainsMolecular ConformationProteinsProteins

Identifiers

PMID29975698
PMCPMC6033379
OpenAlexW2867951924

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.