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NOXclass: prediction of protein-protein interaction types
BACKGROUND: Structural models determined by X-ray crystallography play a central role in understanding protein-protein interactions at the molecular level. Interpretation of these models requires the distinction between non-specific crystal packing contacts and biologically relevant interactions. Th...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1386716/ https://www.ncbi.nlm.nih.gov/pubmed/16423290 http://dx.doi.org/10.1186/1471-2105-7-27 |
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author | Zhu, Hongbo Domingues, Francisco S Sommer, lngolf Lengauer, Thomas |
author_facet | Zhu, Hongbo Domingues, Francisco S Sommer, lngolf Lengauer, Thomas |
author_sort | Zhu, Hongbo |
collection | PubMed |
description | BACKGROUND: Structural models determined by X-ray crystallography play a central role in understanding protein-protein interactions at the molecular level. Interpretation of these models requires the distinction between non-specific crystal packing contacts and biologically relevant interactions. This has been investigated previously and classification approaches have been proposed. However, less attention has been devoted to distinguishing different types of biological interactions. These interactions are classified as obligate and non-obligate according to the effect of the complex formation on the stability of the protomers. So far no automatic classification methods for distinguishing obligate, non-obligate and crystal packing interactions have been made available. RESULTS: Six interface properties have been investigated on a dataset of 243 protein interactions. The six properties have been combined using a support vector machine algorithm, resulting in NOXclass, a classifier for distinguishing obligate, non-obligate and crystal packing interactions. We achieve an accuracy of 91.8% for the classification of these three types of interactions using a leave-one-out cross-validation procedure. CONCLUSION: NOXclass allows the interpretation and analysis of protein quaternary structures. In particular, it generates testable hypotheses regarding the nature of protein-protein interactions, when experimental results are not available. We expect this server will benefit the users of protein structural models, as well as protein crystallographers and NMR spectroscopists. A web server based on the method and the datasets used in this study are available at . |
format | Text |
id | pubmed-1386716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-13867162006-04-14 NOXclass: prediction of protein-protein interaction types Zhu, Hongbo Domingues, Francisco S Sommer, lngolf Lengauer, Thomas BMC Bioinformatics Software BACKGROUND: Structural models determined by X-ray crystallography play a central role in understanding protein-protein interactions at the molecular level. Interpretation of these models requires the distinction between non-specific crystal packing contacts and biologically relevant interactions. This has been investigated previously and classification approaches have been proposed. However, less attention has been devoted to distinguishing different types of biological interactions. These interactions are classified as obligate and non-obligate according to the effect of the complex formation on the stability of the protomers. So far no automatic classification methods for distinguishing obligate, non-obligate and crystal packing interactions have been made available. RESULTS: Six interface properties have been investigated on a dataset of 243 protein interactions. The six properties have been combined using a support vector machine algorithm, resulting in NOXclass, a classifier for distinguishing obligate, non-obligate and crystal packing interactions. We achieve an accuracy of 91.8% for the classification of these three types of interactions using a leave-one-out cross-validation procedure. CONCLUSION: NOXclass allows the interpretation and analysis of protein quaternary structures. In particular, it generates testable hypotheses regarding the nature of protein-protein interactions, when experimental results are not available. We expect this server will benefit the users of protein structural models, as well as protein crystallographers and NMR spectroscopists. A web server based on the method and the datasets used in this study are available at . BioMed Central 2006-01-19 /pmc/articles/PMC1386716/ /pubmed/16423290 http://dx.doi.org/10.1186/1471-2105-7-27 Text en Copyright © 2006 Zhu et al; licensee BioMed Central Ltd. |
spellingShingle | Software Zhu, Hongbo Domingues, Francisco S Sommer, lngolf Lengauer, Thomas NOXclass: prediction of protein-protein interaction types |
title | NOXclass: prediction of protein-protein interaction types |
title_full | NOXclass: prediction of protein-protein interaction types |
title_fullStr | NOXclass: prediction of protein-protein interaction types |
title_full_unstemmed | NOXclass: prediction of protein-protein interaction types |
title_short | NOXclass: prediction of protein-protein interaction types |
title_sort | noxclass: prediction of protein-protein interaction types |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1386716/ https://www.ncbi.nlm.nih.gov/pubmed/16423290 http://dx.doi.org/10.1186/1471-2105-7-27 |
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