Evidence map›Paper›PMID 22369665›Full record

ArticleBMC genomics2011

Cutoff Scanning Matrix (CSM): structural classification and function prediction by protein inter-residue distance patterns.

Douglas E V Pires, Raquel C de Melo-Minardi, Marcos A dos Santos, Carlos H da Silveira, Marcelo M Santoro, Wagner Meira

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Article in BMC genomics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

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35citing papers in PubMed
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3 · Its place in the literature

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35 citing papers in PubMed.

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  11. Using Graph-Based Signatures to Guide Rational Antibody Engineering.Methods in molecular biology (Clifton, N.J.) · 2023
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  20. Network-based protein structural classification.Royal Society open science · 2020
    Article
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Douglas E V PiresDepartment of Biochemistry and Immunology, Universidade Federal de Minas Gerais, Belo Horizonte, 31270-901, Brazil. dpires@dcc.ufmg.br
Raquel C de Melo-Minardi
Marcos A dos Santos
Carlos H da Silveira
Marcelo M Santoro
Wagner Meira

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe unforgiving pace of growth of available biological data has increased the demand for efficient and scalable paradigms, models and methodologies for automatic annotation. In this paper, we present a novel structure-based protein function prediction and structural classification method: Cutoff Scanning Matrix (CSM). CSM generates feature vectors that represent distance patterns between protein residues. These feature vectors are then used as evidence for classification. Singular value decomposition is used as a preprocessing step to reduce dimensionality and noise. The aspect of protein function considered in the present work is enzyme activity. A series of experiments was performed on datasets based on Enzyme Commission (EC) numbers and mechanistically different enzyme superfamilies as well as other datasets derived from SCOP release 1.75.

resultsCSM was able to achieve a precision of up to 99% after SVD preprocessing for a database derived from manually curated protein superfamilies and up to 95% for a dataset of the 950 most-populated EC numbers. Moreover, we conducted experiments to verify our ability to assign SCOP class, superfamily, family and fold to protein domains. An experiment using the whole set of domains found in last SCOP version yielded high levels of precision and recall (up to 95%). Finally, we compared our structural classification results with those in the literature to place this work into context. Our method was capable of significantly improving the recall of a previous study while preserving a compatible precision level.

conclusionsWe showed that the patterns derived from CSMs could effectively be used to predict protein function and thus help with automatic function annotation. We also demonstrated that our method is effective in structural classification tasks. These facts reinforce the idea that the pattern of inter-residue distances is an important component of family structural signatures. Furthermore, singular value decomposition provided a consistent increase in precision and recall, which makes it an important preprocessing step when dealing with noisy data.

Indexed as

SoftwareDatabases, ProteinEnzymesProtein FoldingProtein Structure, TertiaryEnzymes

Identifiers

PMID22369665
PMCPMC3287581

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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.