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Prediction of the burial status of transmembrane residues of helical membrane proteins
BACKGROUND: Helical membrane proteins (HMPs) play a crucial role in diverse cellular processes, yet it still remains extremely difficult to determine their structures by experimental techniques. Given this situation, it is highly desirable to develop sequence-based computational methods for predicti...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2000914/ https://www.ncbi.nlm.nih.gov/pubmed/17708758 http://dx.doi.org/10.1186/1471-2105-8-302 |
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author | Park, Yungki Hayat, Sikander Helms, Volkhard |
author_facet | Park, Yungki Hayat, Sikander Helms, Volkhard |
author_sort | Park, Yungki |
collection | PubMed |
description | BACKGROUND: Helical membrane proteins (HMPs) play a crucial role in diverse cellular processes, yet it still remains extremely difficult to determine their structures by experimental techniques. Given this situation, it is highly desirable to develop sequence-based computational methods for predicting structural characteristics of HMPs. RESULTS: We have developed TMX (TransMembrane eXposure), a novel method for predicting the burial status (i.e. buried in the protein structure vs. exposed to the membrane) of transmembrane (TM) residues of HMPs. TMX derives positional scores of TM residues based on their profiles and conservation indices. Then, a support vector classifier is used for predicting their burial status. Its prediction accuracy is 78.71% on a benchmark data set, representing considerable improvements over 68.67% and 71.06% of previously proposed methods. Importantly, unlike the previous methods, TMX automatically yields confidence scores for the predictions made. In addition, a feature selection incorporated in TMX reveals interesting insights into the structural organization of HMPs. CONCLUSION: A novel computational method, TMX, has been developed for predicting the burial status of TM residues of HMPs. Its prediction accuracy is much higher than that of previously proposed methods. It will be useful in elucidating structural characteristics of HMPs as an inexpensive, auxiliary tool. A web server for TMX is established at http://service.bioinformatik.uni-saarland.de/tmx and freely available to academic users, along with the data set used. |
format | Text |
id | pubmed-2000914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-20009142007-10-05 Prediction of the burial status of transmembrane residues of helical membrane proteins Park, Yungki Hayat, Sikander Helms, Volkhard BMC Bioinformatics Methodology Article BACKGROUND: Helical membrane proteins (HMPs) play a crucial role in diverse cellular processes, yet it still remains extremely difficult to determine their structures by experimental techniques. Given this situation, it is highly desirable to develop sequence-based computational methods for predicting structural characteristics of HMPs. RESULTS: We have developed TMX (TransMembrane eXposure), a novel method for predicting the burial status (i.e. buried in the protein structure vs. exposed to the membrane) of transmembrane (TM) residues of HMPs. TMX derives positional scores of TM residues based on their profiles and conservation indices. Then, a support vector classifier is used for predicting their burial status. Its prediction accuracy is 78.71% on a benchmark data set, representing considerable improvements over 68.67% and 71.06% of previously proposed methods. Importantly, unlike the previous methods, TMX automatically yields confidence scores for the predictions made. In addition, a feature selection incorporated in TMX reveals interesting insights into the structural organization of HMPs. CONCLUSION: A novel computational method, TMX, has been developed for predicting the burial status of TM residues of HMPs. Its prediction accuracy is much higher than that of previously proposed methods. It will be useful in elucidating structural characteristics of HMPs as an inexpensive, auxiliary tool. A web server for TMX is established at http://service.bioinformatik.uni-saarland.de/tmx and freely available to academic users, along with the data set used. BioMed Central 2007-08-20 /pmc/articles/PMC2000914/ /pubmed/17708758 http://dx.doi.org/10.1186/1471-2105-8-302 Text en Copyright © 2007 Park et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Park, Yungki Hayat, Sikander Helms, Volkhard Prediction of the burial status of transmembrane residues of helical membrane proteins |
title | Prediction of the burial status of transmembrane residues of helical membrane proteins |
title_full | Prediction of the burial status of transmembrane residues of helical membrane proteins |
title_fullStr | Prediction of the burial status of transmembrane residues of helical membrane proteins |
title_full_unstemmed | Prediction of the burial status of transmembrane residues of helical membrane proteins |
title_short | Prediction of the burial status of transmembrane residues of helical membrane proteins |
title_sort | prediction of the burial status of transmembrane residues of helical membrane proteins |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2000914/ https://www.ncbi.nlm.nih.gov/pubmed/17708758 http://dx.doi.org/10.1186/1471-2105-8-302 |
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