Evidence map›Paper›PMID 37990040›Full record

ArticleScientific reports2023

Prediction of folding patterns for intrinsic disordered protein.

Jiaan Yang, Wen-Xiang Cheng, Gang Wu, Sitong Sheng, Peng Zhang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Expose flexible conformations for intrinsically disordered protein.Current research in structural biology · 2025
    Article
  2. Article
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

5 authors at 3 institutions in 1 country.

Jiaan YangShenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, Guangdong, China. jiaanyang@yahoo.com.
Wen-Xiang ChengShenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, Guangdong, China.
Gang WuSchool of Basic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.
Sitong ShengHYK High-throughput Biotechnology Institute, Shenzhen, 518057, Guangdong, China.
Peng ZhangShenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, Guangdong, China.
Shenzhen Institutes of Advanced Technology · CNChinese Academy of Sciences · CNHuazhong University of Science and Technology · CN

Funding

Key Technologies Research and Development Program 2021YFC1712805National Outstanding Youth Science Fund Project of National Natural Science Foundation of China 82104497National Outstanding Youth Science Fund Project of National Natural Science Foundation of China 82230119National Outstanding Youth Science Fund Project of National Natural Science Foundation of China 92068117Provincial Science and Technology Plan Projects in Guangdong Province 2022A0505020017Science and Technology Innovation Fund of Shenzhen JCYJ20190813114407556Shenzhen International Collaborative Project GJHZ2020073109500902Shenzhen International Collaborative Project GJHZ20210705141405015
6 · The paper itself

Abstract

The conformation flexibility of natural protein causes both complexity and difficulty to understand the relationship between structure and function. The prediction of intrinsically disordered protein primarily is focusing on to disclose the regions with structural flexibility involving relevant biological functions and various diseases. The order of amino acids in protein sequence determines possible conformations, folding flexibility and biological function. Although many methods provided the information of intrinsically disordered protein (IDP), but the results are mainly limited to determine the locations of regions without knowledge of possible folding conformations. Here, the developed protein folding fingerprint adopted the protein folding variation matrix (PFVM) to reveal all possible folding patterns for the intrinsically disordered protein along its sequence. The PFVM integrally exhibited the intrinsically disordered protein with disordering regions, degree of disorder as well as folding pattern. The advantage of PFVM will not only provide rich information for IDP, but also may promote the study of protein folding problem.

Indexed as

Intrinsically Disordered ProteinsAmino AcidsAmino Acid SequenceProtein ConformationProtein FoldingAmino AcidsIntrinsically Disordered Proteins

Identifiers

PMID37990040
PMCPMC10663623
OpenAlexW4388851030

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.