Evidence map›Paper›PMID 27153555›Full record

ArticleOncotarget2016

iCar-PseCp: identify carbonylation sites in proteins by Monte Carlo sampling and incorporating sequence coupled effects into general PseAAC.

Jianhua Jia, Zi Liu, Xuan Xiao, Bingxiang Liu, Kuo-Chen Chou

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
25.9field-weighted citation impact, top 1% 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

49 citing papers in PubMed, 177 citations in OpenAlex.

  1. Explainable Deep Multilevel Attention Learning for Predicting Protein Carbonylation Sites.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  2. Chemical Carbonylation of Arginine in Peptides and Proteins.Journal of the American Chemical Society · 2025
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  11. Structural Variability in the RLR-MAVS Pathway and Sensitive Detection of Viral RNAs.Medicinal chemistry (Shariqah (United Arab Emirates)) · 2019
    Review
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  13. LAIPT: Lysine Acetylation Site Identification with Polynomial Tree.International journal of molecular sciences · 2018
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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

5 authors at 4 institutions in 3 countries.

Jianhua JiaComputer Department, Jing-De-Zhen Ceramic Institute, Jing-De-Zhen 333403 China.
Zi LiuSchool of Computer Science and Engineering, Nanjing University of Science and Technology, Nanjing, 210094, China.
Xuan XiaoComputer Department, Jing-De-Zhen Ceramic Institute, Jing-De-Zhen 333403 China.
Bingxiang LiuComputer Department, Jing-De-Zhen Ceramic Institute, Jing-De-Zhen 333403 China.
Kuo-Chen ChouGordon Life Science Institute, Boston, MA 02478, USA.
Jingdezhen Ceramic Institute · CNKing Abdulaziz University · SANanjing University of Science and Technology · CNThe Gordon Life Science Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carbonylation is a posttranslational modification (PTM or PTLM), where a carbonyl group is added to lysine (K), proline (P), arginine (R), and threonine (T) residue of a protein molecule. Carbonylation plays an important role in orchestrating various biological processes but it is also associated with many diseases such as diabetes, chronic lung disease, Parkinson's disease, Alzheimer's disease, chronic renal failure, and sepsis. Therefore, from the angles of both basic research and drug development, we are facing a challenging problem: for an uncharacterized protein sequence containing many residues of K, P, R, or T, which ones can be carbonylated, and which ones cannot? To address this problem, we have developed a predictor called iCar-PseCp by incorporating the sequence-coupled information into the general pseudo amino acid composition, and balancing out skewed training dataset by Monte Carlo sampling to expand positive subset. Rigorous target cross-validations on a same set of carbonylation-known proteins indicated that the new predictor remarkably outperformed its existing counterparts. For the convenience of most experimental scientists, a user-friendly web-server for iCar-PseCp has been established at http://www.jci-bioinfo.cn/iCar-PseCp, by which users can easily obtain their desired results without the need to go through the complicated mathematical equations involved. It has not escaped our notice that the formulation and approach presented here can also be used to analyze many other problems in computational proteomics.

Indexed as

AlgorithmsAmino Acid SequenceBacterial ProteinsEscherichia coliHumansMonte Carlo MethodPhotobacteriumProtein CarbonylationProtein Processing, Post-TranslationalSoftwareBacterial ProteinscarbonylationMonte Carlo samplingPseAACrandom forest algorithmsequence-coupling model

Identifiers

PMID27153555
PMCPMC5085176
OpenAlexW2345938495

What OpenQuestion 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 OpenQuestion graph.