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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...

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Detalles Bibliográficos
Autores principales: Park, Yungki, Hayat, Sikander, Helms, Volkhard
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
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.
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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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