» Articles » PMID: 32476995

Computational Prediction of Ubiquitination Proteins Using Evolutionary Profiles and Functional Domain Annotation

Overview
Journal Curr Genomics
Date 2020 Jun 2
PMID 32476995
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Ubiquitination, as a post-translational modification, is a crucial biological process in cell signaling, apoptosis, and localization. Identification of ubiquitination proteins is of fundamental importance for understanding the molecular mechanisms in biological systems and diseases. Although high-throughput experimental studies using mass spectrometry have identified many ubiquitination proteins and ubiquitination sites, the vast majority of ubiquitination proteins remain undiscovered, even in well-studied model organisms.

Objective: To reduce experimental costs, computational methods have been introduced to predict ubiquitination sites, but the accuracy is unsatisfactory. If it can be predicted whether a protein can be ubiquitinated or not, it will help in predicting ubiquitination sites. However, all the computational methods so far can only predict ubiquitination sites.

Methods: In this study, the first computational method for predicting ubiquitination proteins without relying on ubiquitination site prediction has been developed. The method extracts features from sequence conservation information through a grey system model, as well as functional domain annotation and subcellular localization.

Results: Together with the feature analysis and application of the relief feature selection algorithm, the results of 5-fold cross-validation on three datasets achieved a high accuracy of 90.13%, with Matthew's correlation coefficient of 80.34%. The predicted results on an independent test data achieved 87.71% as accuracy and 75.43% of Matthew's correlation coefficient, better than the prediction from the best ubiquitination site prediction tool available.

Conclusion: Our study may guide experimental design and provide useful insights for studying the mechanisms and modulation of ubiquitination pathways. The code is available at: https://github.com/Chunhuixu/UBIPredic_QWRCHX.

Citing Articles

Identification genetic variations in some heat shock protein genes of Tali goat breed and study their structural and functional effects on relevant proteins.

Rezvannejad E, Mousavizadeh S Vet Med Sci. 2023; 9(5):2247-2259.

PMID: 37530404 PMC: 10508551. DOI: 10.1002/vms3.1231.


Thirty years of molecular dynamics simulations on posttranslational modifications of proteins.

Weigle A, Feng J, Shukla D Phys Chem Chem Phys. 2022; 24(43):26371-26397.

PMID: 36285789 PMC: 9704509. DOI: 10.1039/d2cp02883b.


Impact of deleterious missense PRKCI variants on structural and functional dynamics of protein.

Shah H, Khan K, Khan N, Badshah Y, Ashraf N, Shabbir M Sci Rep. 2022; 12(1):3781.

PMID: 35260606 PMC: 8904829. DOI: 10.1038/s41598-022-07526-4.

References
1.
Chou K . Structural bioinformatics and its impact to biomedical science. Curr Med Chem. 2004; 11(16):2105-34. DOI: 10.2174/0929867043364667. View

2.
Chou K . Some remarks on protein attribute prediction and pseudo amino acid composition. J Theor Biol. 2010; 273(1):236-47. PMC: 7125570. DOI: 10.1016/j.jtbi.2010.12.024. View

3.
Hoeller D, Hecker C, Dikic I . Ubiquitin and ubiquitin-like proteins in cancer pathogenesis. Nat Rev Cancer. 2006; 6(10):776-88. DOI: 10.1038/nrc1994. View

4.
Hunter S, Apweiler R, Attwood T, Bairoch A, Bateman A, Binns D . InterPro: the integrative protein signature database. Nucleic Acids Res. 2008; 37(Database issue):D211-5. PMC: 2686546. DOI: 10.1093/nar/gkn785. View

5.
Cai Y, Huang T, Hu L, Shi X, Xie L, Li Y . Prediction of lysine ubiquitination with mRMR feature selection and analysis. Amino Acids. 2011; 42(4):1387-95. DOI: 10.1007/s00726-011-0835-0. View