Evidence map›Paper›PMID 28761071›Full record

ArticleScientific reports2017

PhosphoPredict: A bioinformatics tool for prediction of human kinase-specific phosphorylation substrates and sites by integrating heterogeneous feature selection.

Jiangning Song, Huilin Wang, Jiawei Wang, André Leier, Tatiana Marquez-Lago, Bingjiao Yang, Ziding Zhang, Tatsuya Akutsu, Geoffrey I Webb, Roger J Daly

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 93 citations in OpenAlex.

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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

10 authors at 8 institutions in 4 countries.

Jiangning SongBiomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC 3800, Australia.
Huilin WangDepartment of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, Fujian, 361005, China.
Jiawei WangBiomedicine Discovery Institute and Department of Microbiology, Monash University, Melbourne, VIC 3800, Australia.
André LeierInformatics Institute and Department of Genetics, School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
Tatiana Marquez-LagoInformatics Institute and Department of Genetics, School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
Bingjiao YangCollege of Mechanical Engineering, Yanshan University, Qinhuangdao, 066004, China.
Ziding ZhangState Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural University, Beijing, 100193, China.ORCID 0000-0002-9296-571X
Tatsuya AkutsuBioinformatics Center, Institute for Chemical Research, Kyoto University, Kyoto, 611-0011, Japan.ORCID 0000-0001-9763-797X
Geoffrey I WebbMonash Centre for Data Science, Faculty of Information Technology, Monash University, Melbourne, VIC, 3800, Australia. Geoff.Webb@monash.edu.ORCID 0000-0001-9963-5169
Roger J DalyBiomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash University, Melbourne, VIC 3800, Australia. Roger.Daly@monash.edu.
Australian Regenerative Medicine Institute · AUUniversity of Alabama at Birmingham · USChina Agricultural University · CNDiscovery Institute · USKyoto University · JPMonash University · AUXiamen University · CNYanshan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein phosphorylation is a major form of post-translational modification (PTM) that regulates diverse cellular processes. In silico methods for phosphorylation site prediction can provide a useful and complementary strategy for complete phosphoproteome annotation. Here, we present a novel bioinformatics tool, PhosphoPredict, that combines protein sequence and functional features to predict kinase-specific substrates and their associated phosphorylation sites for 12 human kinases and kinase families, including ATM, CDKs, GSK-3, MAPKs, PKA, PKB, PKC, and SRC. To elucidate critical determinants, we identified feature subsets that were most informative and relevant for predicting substrate specificity for each individual kinase family. Extensive benchmarking experiments based on both five-fold cross-validation and independent tests indicated that the performance of PhosphoPredict is competitive with that of several other popular prediction tools, including KinasePhos, PPSP, GPS, and Musite. We found that combining protein functional and sequence features significantly improves phosphorylation site prediction performance across all kinases. Application of PhosphoPredict to the entire human proteome identified 150 to 800 potential phosphorylation substrates for each of the 12 kinases or kinase families. PhosphoPredict significantly extends the bioinformatics portfolio for kinase function analysis and will facilitate high-throughput identification of kinase-specific phosphorylation sites, thereby contributing to both basic and translational research programs.

Indexed as

Protein Processing, Post-TranslationalSoftwareBinding SitesHumansMAP Kinase Signaling SystemPhosphorylationProtein BindingProtein Interaction MappingProtein KinasesProteomeSequence Analysis, ProteinSubstrate SpecificityProtein KinasesProteome

Identifiers

PMID28761071
PMCPMC5537252
OpenAlexW2737403359

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LicenceCC BY
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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.