Evidence map›Paper›PMID 27529053›Full record

ArticleScientifica2016

Prediction of G Protein-Coupled Receptors with SVM-Prot Features and Random Forest.

Zhijun Liao, Ying Ju, Quan Zou

Abstract read
In one paragraph

Article in Scientifica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
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  7. A computational model for GPCR-ligand interaction prediction.Journal of integrative bioinformatics · 2020
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  16. Article
  17. IonchanPred 2.0: A Tool to Predict Ion Channels and Their Types.International journal of molecular sciences · 2017
    Article
  18. Review
  19. Article
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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

3 authors.

Zhijun LiaoSchool of Basic Medical Sciences, Fujian Medical University, Fuzhou, Fujian 350108, China; School of Computer Science and Technology, Tianjin University, Tianjin 300350, China.ORCID 0000-0002-7034-8657
Ying JuSchool of Information Science and Technology, Xiamen University, Xiamen, Fujian 361005, China.
Quan ZouSchool of Computer Science and Technology, Tianjin University, Tianjin 300350, China; State Key Laboratory of Medicinal Chemical Biology, Nankai University, Tianjin 300071, China.ORCID 0000-0001-6406-1142

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) are the largest receptor superfamily. In this paper, we try to employ physical-chemical properties, which come from SVM-Prot, to represent GPCR. Random Forest was utilized as classifier for distinguishing them from other protein sequences. MEME suite was used to detect the most significant 10 conserved motifs of human GPCRs. In the testing datasets, the average accuracy was 91.61%, and the average AUC was 0.9282. MEME discovery analysis showed that many motifs aggregated in the seven hydrophobic helices transmembrane regions adapt to the characteristic of GPCRs. All of the above indicate that our machine-learning method can successfully distinguish GPCRs from non-GPCRs.

Identifiers

PMID27529053
PMCPMC4978840

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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.