Evidence map›Paper›PMID 26788119›Full record

ArticleComputational and mathematical methods in medicine2015

Prediction of Protein Structural Classes for Low-Similarity Sequences Based on Consensus Sequence and Segmented PSSM.

Yunyun Liang, Sanyang Liu, Shengli Zhang

Abstract read
In one paragraph

Article in Computational and mathematical methods in medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Yunyun LiangSchool of Mathematics and Statistics, Xidian University, Xi'an 710071, China.
Sanyang LiuSchool of Mathematics and Statistics, Xidian University, Xi'an 710071, China.
Shengli ZhangSchool of Mathematics and Statistics, Xidian University, Xi'an 710071, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prediction of protein structural classes for low-similarity sequences is useful for understanding fold patterns, regulation, functions, and interactions of proteins. It is well known that feature extraction is significant to prediction of protein structural class and it mainly uses protein primary sequence, predicted secondary structure sequence, and position-specific scoring matrix (PSSM). Currently, prediction solely based on the PSSM has played a key role in improving the prediction accuracy. In this paper, we propose a novel method called CSP-SegPseP-SegACP by fusing consensus sequence (CS), segmented PsePSSM, and segmented autocovariance transformation (ACT) based on PSSM. Three widely used low-similarity datasets (1189, 25PDB, and 640) are adopted in this paper. Then a 700-dimensional (700D) feature vector is constructed and the dimension is decreased to 224D by using principal component analysis (PCA). To verify the performance of our method, rigorous jackknife cross-validation tests are performed on 1189, 25PDB, and 640 datasets. Comparison of our results with the existing PSSM-based methods demonstrates that our method achieves the favorable and competitive performance. This will offer an important complementary to other PSSM-based methods for prediction of protein structural classes for low-similarity sequences.

Indexed as

Consensus SequencePosition-Specific Scoring MatricesComputational BiologyDatabases, ProteinPrincipal Component AnalysisProteinsProtein Structure, SecondarySupport Vector MachineProteins

Identifiers

PMID26788119
PMCPMC4693000

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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.