Evidence map›Paper›PMID 23879571›Full record

ArticleBMC bioinformatics2013

A strategy to select suitable physicochemical attributes of amino acids for protein fold recognition.

Alok Sharma, Kuldip K Paliwal, Abdollah Dehzangi, James Lyons, Seiya Imoto, Satoru Miyano

Abstract read
In one paragraph

Article in BMC bioinformatics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

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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

13 citing papers in PubMed.

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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

6 authors.

Alok SharmaLaboratory of DNA Information Analysis, University of Tokyo, Minato-ku, Tokyo, Japan. aloks@ims.u-tokyo.ac.jp
Kuldip K Paliwal
Abdollah Dehzangi
James Lyons
Seiya Imoto
Satoru Miyano

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAssigning a protein into one of its folds is a transitional step for discovering three dimensional protein structure, which is a challenging task in bimolecular (biological) science. The present research focuses on: 1) the development of classifiers, and 2) the development of feature extraction techniques based on syntactic and/or physicochemical properties.

resultsApart from the above two main categories of research, we have shown that the selection of physicochemical attributes of the amino acids is an important step in protein fold recognition and has not been explored adequately. We have presented a multi-dimensional successive feature selection (MD-SFS) approach to systematically select attributes. The proposed method is applied on protein sequence data and an improvement of around 24% in fold recognition has been noted when selecting attributes appropriately.

conclusionThe MD-SFS has been applied successfully in selecting physicochemical attributes of the amino acids. The selected attributes show improved protein fold recognition performance.

Indexed as

Chemical PhenomenaComputational BiologyProtein FoldingProtein Interaction MappingAlgorithmsAmino AcidsAmino Acid SequenceDrug DesignProteinsAmino AcidsProteins

Identifiers

PMID23879571
PMCPMC3724710

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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.