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Predicting helix–helix interactions from residue contacts in membrane proteins

Motivation: Helix–helix interactions play a critical role in the structure assembly, stability and function of membrane proteins. On the molecular level, the interactions are mediated by one or more residue contacts. Although previous studies focused on helix-packing patterns and sequence motifs, fe...

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Autores principales: Lo, Allan, Chiu, Yi-Yuan, Rødland, Einar Andreas, Lyu, Ping-Chiang, Sung, Ting-Yi, Hsu, Wen-Lian
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2666818/
https://www.ncbi.nlm.nih.gov/pubmed/19244388
http://dx.doi.org/10.1093/bioinformatics/btp114
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author Lo, Allan
Chiu, Yi-Yuan
Rødland, Einar Andreas
Lyu, Ping-Chiang
Sung, Ting-Yi
Hsu, Wen-Lian
author_facet Lo, Allan
Chiu, Yi-Yuan
Rødland, Einar Andreas
Lyu, Ping-Chiang
Sung, Ting-Yi
Hsu, Wen-Lian
author_sort Lo, Allan
collection PubMed
description Motivation: Helix–helix interactions play a critical role in the structure assembly, stability and function of membrane proteins. On the molecular level, the interactions are mediated by one or more residue contacts. Although previous studies focused on helix-packing patterns and sequence motifs, few of them developed methods specifically for contact prediction. Results: We present a new hierarchical framework for contact prediction, with an application in membrane proteins. The hierarchical scheme consists of two levels: in the first level, contact residues are predicted from the sequence and their pairing relationships are further predicted in the second level. Statistical analyses on contact propensities are combined with other sequence and structural information for training the support vector machine classifiers. Evaluated on 52 protein chains using leave-one-out cross validation (LOOCV) and an independent test set of 14 protein chains, the two-level approach consistently improves the conventional direct approach in prediction accuracy, with 80% reduction of input for prediction. Furthermore, the predicted contacts are then used to infer interactions between pairs of helices. When at least three predicted contacts are required for an inferred interaction, the accuracy, sensitivity and specificity are 56%, 40% and 89%, respectively. Our results demonstrate that a hierarchical framework can be applied to eliminate false positives (FP) while reducing computational complexity in predicting contacts. Together with the estimated contact propensities, this method can be used to gain insights into helix-packing in membrane proteins. Availability: http://bio-cluster.iis.sinica.edu.tw/TMhit/ Contact: tsung@iis.sinica.edu.tw Supplementary information:Supplementary data are available at Bioinformatics online.
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spelling pubmed-26668182009-04-29 Predicting helix–helix interactions from residue contacts in membrane proteins Lo, Allan Chiu, Yi-Yuan Rødland, Einar Andreas Lyu, Ping-Chiang Sung, Ting-Yi Hsu, Wen-Lian Bioinformatics Original Papers Motivation: Helix–helix interactions play a critical role in the structure assembly, stability and function of membrane proteins. On the molecular level, the interactions are mediated by one or more residue contacts. Although previous studies focused on helix-packing patterns and sequence motifs, few of them developed methods specifically for contact prediction. Results: We present a new hierarchical framework for contact prediction, with an application in membrane proteins. The hierarchical scheme consists of two levels: in the first level, contact residues are predicted from the sequence and their pairing relationships are further predicted in the second level. Statistical analyses on contact propensities are combined with other sequence and structural information for training the support vector machine classifiers. Evaluated on 52 protein chains using leave-one-out cross validation (LOOCV) and an independent test set of 14 protein chains, the two-level approach consistently improves the conventional direct approach in prediction accuracy, with 80% reduction of input for prediction. Furthermore, the predicted contacts are then used to infer interactions between pairs of helices. When at least three predicted contacts are required for an inferred interaction, the accuracy, sensitivity and specificity are 56%, 40% and 89%, respectively. Our results demonstrate that a hierarchical framework can be applied to eliminate false positives (FP) while reducing computational complexity in predicting contacts. Together with the estimated contact propensities, this method can be used to gain insights into helix-packing in membrane proteins. Availability: http://bio-cluster.iis.sinica.edu.tw/TMhit/ Contact: tsung@iis.sinica.edu.tw Supplementary information:Supplementary data are available at Bioinformatics online. Oxford University Press 2009-04-15 2009-02-25 /pmc/articles/PMC2666818/ /pubmed/19244388 http://dx.doi.org/10.1093/bioinformatics/btp114 Text en © 2009 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Papers
Lo, Allan
Chiu, Yi-Yuan
Rødland, Einar Andreas
Lyu, Ping-Chiang
Sung, Ting-Yi
Hsu, Wen-Lian
Predicting helix–helix interactions from residue contacts in membrane proteins
title Predicting helix–helix interactions from residue contacts in membrane proteins
title_full Predicting helix–helix interactions from residue contacts in membrane proteins
title_fullStr Predicting helix–helix interactions from residue contacts in membrane proteins
title_full_unstemmed Predicting helix–helix interactions from residue contacts in membrane proteins
title_short Predicting helix–helix interactions from residue contacts in membrane proteins
title_sort predicting helix–helix interactions from residue contacts in membrane proteins
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2666818/
https://www.ncbi.nlm.nih.gov/pubmed/19244388
http://dx.doi.org/10.1093/bioinformatics/btp114
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