Evidence map›Paper›PMID 30311130›Full record

ArticleMolecular biology reports2018

iPhosY-PseAAC: identify phosphotyrosine sites by incorporating sequence statistical moments into PseAAC.

Yaser Daanial Khan, Nouman Rasool, Waqar Hussain, Sher Afzal Khan, Kuo-Chen Chou

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.3field-weighted citation impact, top 3% 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

15 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. CNNLSTMac4CPred: A Hybrid Model for N4-Acetylcytidine Prediction.Interdisciplinary sciences, computational life sciences · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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 4 institutions in 3 countries.

Yaser Daanial KhanDepartment of Computer Science, School of Systems and Technology, University of Management and Technology, C-II Johar Town, Lahore, Pakistan. yaser.khan@umt.edu.pk.
Nouman RasoolDepartment of Life Sciences, School of Science, University of Management and Technology, Lahore, Pakistan.
Waqar HussainDepartment of Computer Science, School of Systems and Technology, University of Management and Technology, C-II Johar Town, Lahore, Pakistan.
Sher Afzal KhanFaculty of Computing and Information Technology in Rabigh, King Abdul Aziz University, Jeddah, 21577, Kingdom of Saudi Arabia.
Kuo-Chen ChouGordon Life Science Institute, Boston, MA, 02478, USA.
University of Management and Technology · PKAbdul Wali Khan University Mardan · PKThe Gordon Life Science Institute · USUniversity of Karachi · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein phosphorylation is one of the most fundamental types of post-translational modifications and it plays a vital role in various cellular processes of eukaryotes. Among three types of phosphorylation i.e. serine, threonine and tyrosine phosphorylation, tyrosine phosphorylation is one of the most frequent and it is important for mediation of signal transduction in eukaryotic cells. Site-directed mutagenesis and mass spectrometry help in the experimental determination of cellular signalling networks, however, these techniques are costly, time taking and labour associated. Thus, efficient and accurate prediction of these sites through computational approaches can be beneficial to reduce cost and time. Here, we present a more accurate and efficient sequence-based computational method for prediction of phosphotyrosine (PhosY) sites by incorporation of statistical moments into PseAAC. The study is carried out based on Chou's 5-step rule, and various position-composition relative features are used to train a neural network for the prediction purpose. Validation of results through Jackknife testing is performed to validate the results of the proposed prediction method. Overall accuracy validated through Jackknife testing was calculated 93.9%. These results suggest that the proposed prediction model can play a fundamental role in the prediction of PhosY sites in an accurate and efficient way.

Indexed as

AlgorithmsAmino AcidsBiometryComputational BiologyDatabases, ProteinForecastingPhosphorylationPhosphotyrosineProtein Processing, Post-TranslationalSequence Analysis, DNAAmino AcidsPhosphotyrosineNeural networkPhosphotyrosinePredictionPseAACStatistical moments

Identifiers

PMID30311130
OpenAlexW2896188973

What OpenQuestion holds

Textmetadata
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.