Evidence map›Paper›PMID 39380205›Full record

ArticleGenomics, proteomics & bioinformatics2024

Nphos: Database and Predictor of Protein N-phosphorylation.

Ming-Xiao Zhao, Ruo-Fan Ding, Qiang Chen, Junhua Meng, Fulai Li, Songsen Fu, Biling Huang, Yan Liu, Zhi-Liang Ji, Yufen Zhao

Abstract read
In one paragraph

Article in Genomics, proteomics & bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. 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

10 authors.

Ming-Xiao ZhaoInstitute of Drug Discovery Technology, Ningbo University, Ningbo 315211, China.ORCID 0000-0002-8821-3654
Ruo-Fan DingState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen 361102, China.ORCID 0000-0003-1667-9866
Qiang ChenZhejiang Key Laboratory of Pathophysiology, Department of Biochemistry and Molecular Biology, Health Science Center, Ningbo University, Ningbo 315211, China.ORCID 0000-0003-2624-8904
Junhua MengBGI Genomics, BGI-Shenzhen, Shenzhen 518083, China.ORCID 0009-0001-9021-5114
Fulai LiInstitute of Drug Discovery Technology, Ningbo University, Ningbo 315211, China.ORCID 0000-0002-5710-7795
Songsen FuInstitute of Drug Discovery Technology, Ningbo University, Ningbo 315211, China.ORCID 0000-0002-3524-8108
Biling HuangInstitute of Drug Discovery Technology, Ningbo University, Ningbo 315211, China.ORCID 0000-0002-1060-8787
Yan LiuDepartment of Chemical Biology, Key Laboratory for Chemical Biology of Fujian Province, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, China.ORCID 0000-0001-6112-7898
Zhi-Liang JiState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen 361102, China.ORCID 0000-0003-1190-7655
Yufen ZhaoInstitute of Drug Discovery Technology, Ningbo University, Ningbo 315211, China.ORCID 0000-0002-8513-1354

Funding

Technology and Engineering Center for Space Utilization, Chinese Academy of Sciences
6 · The paper itself

Abstract

Protein N-phosphorylation is widely present in nature and participates in various biological processes. However, current knowledge on N-phosphorylation is extremely limited compared to that on O-phosphorylation. In this study, we collected 11,710 experimentally verified N-phosphosites of 7344 proteins from 39 species and subsequently constructed the database Nphos to share up-to-date information on protein N-phosphorylation. Upon these substantial data, we characterized the sequential and structural features of protein N-phosphorylation. Moreover, after comparing hundreds of learning models, we chose and optimized gradient boosting decision tree (GBDT) models to predict three types of human N-phosphorylation, achieving mean area under the receiver operating characteristic curve (AUC) values of 90.56%, 91.24%, and 92.01% for pHis, pLys, and pArg, respectively. Meanwhile, we discovered 488,825 distinct N-phosphosites in the human proteome. The models were also deployed in Nphos for interactive N-phosphosite prediction. In summary, this work provides new insights and points for both flexible and focused investigations of N-phosphorylation. It will also facilitate a deeper and more systematic understanding of protein N-phosphorylation modification by providing a data and technical foundation. Nphos is freely available at http://www.bio-add.org/Nphos/ and http://ppodd.org.cn/Nphos/.

Indexed as

Databases, ProteinHumansPhosphoproteinsPhosphorylationProteomePhosphoproteinsProteomeBenchmark datasetDatabaseMachine learningN-phosphorylationPost-translational modification

Identifiers

PMID39380205
PMCPMC12016571

What Socratic 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 Socratic graph.