» Articles » PMID: 26422468

Identify Beta-Hairpin Motifs with Quadratic Discriminant Algorithm Based on the Chemical Shifts

Overview
Journal PLoS One
Date 2015 Oct 1
PMID 26422468
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Successful prediction of the beta-hairpin motif will be helpful for understanding the of the fold recognition. Some algorithms have been proposed for the prediction of beta-hairpin motifs. However, the parameters used by these methods were primarily based on the amino acid sequences. Here, we proposed a novel model for predicting beta-hairpin structure based on the chemical shift. Firstly, we analyzed the statistical distribution of chemical shifts of six nuclei in not beta-hairpin and beta-hairpin motifs. Secondly, we used these chemical shifts as features combined with three algorithms to predict beta-hairpin structure. Finally, we achieved the best prediction, namely sensitivity of 92%, the specificity of 94% with 0.85 of Mathew's correlation coefficient using quadratic discriminant analysis algorithm, which is clearly superior to the same method for the prediction of beta-hairpin structure from 20 amino acid compositions in the three-fold cross-validation. Our finding showed that the chemical shift is an effective parameter for beta-hairpin prediction, suggesting the quadratic discriminant analysis is a powerful algorithm for the prediction of beta-hairpin.

Citing Articles

MultiToxPred 1.0: a novel comprehensive tool for predicting 27 classes of protein toxins using an ensemble machine learning approach.

Beltran J, Herrera-Belen L, Parraguez-Contreras F, Farias J, Machuca-Sepulveda J, Short S BMC Bioinformatics. 2024; 25(1):148.

PMID: 38609877 PMC: 11010298. DOI: 10.1186/s12859-024-05748-z.


Linear discriminant analysis reveals hidden patterns in NMR chemical shifts of intrinsically disordered proteins.

Romero J, Putko P, Urbanczyk M, Kazimierczuk K, Zawadzka-Kazimierczuk A PLoS Comput Biol. 2022; 18(10):e1010258.

PMID: 36201530 PMC: 9578625. DOI: 10.1371/journal.pcbi.1010258.


Current Approaches in Supersecondary Structures Investigation.

Rudnev V, Kulikova L, Nikolsky K, Malsagova K, Kopylov A, Kaysheva A Int J Mol Sci. 2021; 22(21).

PMID: 34769310 PMC: 8584461. DOI: 10.3390/ijms222111879.


Improving Protein Gamma-Turn Prediction Using Inception Capsule Networks.

Fang C, Shang Y, Xu D Sci Rep. 2018; 8(1):15741.

PMID: 30356073 PMC: 6200818. DOI: 10.1038/s41598-018-34114-2.


iNuc-ext-PseTNC: an efficient ensemble model for identification of nucleosome positioning by extending the concept of Chou's PseAAC to pseudo-tri-nucleotide composition.

Tahir M, Hayat M, Khan S Mol Genet Genomics. 2018; 294(1):199-210.

PMID: 30291426 DOI: 10.1007/s00438-018-1498-2.


References
1.
Cavalli A, Salvatella X, Dobson C, Vendruscolo M . Protein structure determination from NMR chemical shifts. Proc Natl Acad Sci U S A. 2007; 104(23):9615-20. PMC: 1887584. DOI: 10.1073/pnas.0610313104. View

2.
Xiao X, Wang P, Lin W, Jia J, Chou K . iAMP-2L: a two-level multi-label classifier for identifying antimicrobial peptides and their functional types. Anal Biochem. 2013; 436(2):168-77. DOI: 10.1016/j.ab.2013.01.019. View

3.
Kou G, Feng Y . Identify five kinds of simple super-secondary structures with quadratic discriminant algorithm based on the chemical shifts. J Theor Biol. 2015; 380:392-8. DOI: 10.1016/j.jtbi.2015.06.006. View

4.
Wishart D, Case D . Use of chemical shifts in macromolecular structure determination. Methods Enzymol. 2001; 338:3-34. DOI: 10.1016/s0076-6879(02)38214-4. View

5.
Case D . The use of chemical shifts and their anisotropies in biomolecular structure determination. Curr Opin Struct Biol. 1998; 8(5):624-30. DOI: 10.1016/s0959-440x(98)80155-3. View