Evidence map›Paper›PMID 28155714›Full record

ArticleBMC systems biology2016

Pretata: predicting TATA binding proteins with novel features and dimensionality reduction strategy.

Quan Zou, Shixiang Wan, Ying Ju, Jijun Tang, Xiangxiang Zeng

Open access · diamondAbstract read
In one paragraph

Article in BMC systems biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
17.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

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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

79 citing papers in PubMed, 158 citations in OpenAlex.

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  14. A computational model for GPCR-ligand interaction prediction.Journal of integrative bioinformatics · 2020
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19 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Quan ZouSchool of Computer Science and Technology, Tianjin University, Tianjin, China.
Shixiang WanSchool of Computer Science and Technology, Tianjin University, Tianjin, China.
Ying JuSchool of Information Science and Engineering, Xiamen University, Xiamen, China.
Jijun TangSchool of Computer Science and Technology, Tianjin University, Tianjin, China.
Xiangxiang ZengSchool of Information Science and Engineering, Xiamen University, Xiamen, China. xzeng@xmu.edu.cn.
Xiamen University · CNShenzhen Institute of Information Technology · CNUniversity of South Carolina · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIt is necessary and essential to discovery protein function from the novel primary sequences. Wet lab experimental procedures are not only time-consuming, but also costly, so predicting protein structure and function reliably based only on amino acid sequence has significant value. TATA-binding protein (TBP) is a kind of DNA binding protein, which plays a key role in the transcription regulation. Our study proposed an automatic approach for identifying TATA-binding proteins efficiently, accurately, and conveniently. This method would guide for the special protein identification with computational intelligence strategies.

resultsFirstly, we proposed novel fingerprint features for TBP based on pseudo amino acid composition, physicochemical properties, and secondary structure. Secondly, hierarchical features dimensionality reduction strategies were employed to improve the performance furthermore. Currently, Pretata achieves 92.92% TATA-binding protein prediction accuracy, which is better than all other existing methods.

conclusionsThe experiments demonstrate that our method could greatly improve the prediction accuracy and speed, thus allowing large-scale NGS data prediction to be practical. A web server is developed to facilitate the other researchers, which can be accessed at http://server.malab.cn/preTata/ .

Indexed as

Amino Acid SequenceChemical PhenomenaComputational BiologyProtein BindingProtein Structure, SecondarySoftwareSupport Vector MachineTATA-Box Binding ProteinTATA-Box Binding ProteinDimensionality reductionMachine learningProtein sequence featuresSupport vector machineTATA binding protein

Identifiers

PMID28155714
PMCPMC5259984
OpenAlexW2563322674

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.