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Characterization and Prediction of Protein Phosphorylation Hotspots in Arabidopsis thaliana
The regulation of protein function by modulating the surface charge status via sequence-locally enriched phosphorylation sites (P-sites) in so called phosphorylation “hotspots” has gained increased attention in recent years. We set out to identify P-hotspots in the model plant Arabidopsis thaliana....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Research Foundation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3433687/ https://www.ncbi.nlm.nih.gov/pubmed/22973286 http://dx.doi.org/10.3389/fpls.2012.00207 |
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author | Christian, Jan-Ole Braginets, Rostyslav Schulze, Waltraud X. Walther, Dirk |
author_facet | Christian, Jan-Ole Braginets, Rostyslav Schulze, Waltraud X. Walther, Dirk |
author_sort | Christian, Jan-Ole |
collection | PubMed |
description | The regulation of protein function by modulating the surface charge status via sequence-locally enriched phosphorylation sites (P-sites) in so called phosphorylation “hotspots” has gained increased attention in recent years. We set out to identify P-hotspots in the model plant Arabidopsis thaliana. We analyzed the spacing of experimentally detected P-sites within peptide-covered regions along Arabidopsis protein sequences as available from the PhosPhAt database. Confirming earlier reports (Schweiger and Linial, 2010), we found that, indeed, P-sites tend to cluster and that distributions between serine and threonine P-sites to their respected closest next P-site differ significantly from those for tyrosine P-sites. The ability to predict P-hotspots by applying available computational P-site prediction programs that focus on identifying single P-sites was observed to be severely compromised by the inevitable interference of nearby P-sites. We devised a new approach, named HotSPotter, for the prediction of phosphorylation hotspots. HotSPotter is based primarily on local amino acid compositional preferences rather than sequence position-specific motifs and uses support vector machines as the underlying classification engine. HotSPotter correctly identified experimentally determined phosphorylation hotspots in A. thaliana with high accuracy. Applied to the Arabidopsis proteome, HotSPotter-predicted 13,677 candidate P-hotspots in 9,599 proteins corresponding to 7,847 unique genes. Hotspot containing proteins are involved predominantly in signaling processes confirming the surmised modulating role of hotspots in signaling and interaction events. Our study provides new bioinformatics means to identify phosphorylation hotspots and lays the basis for further investigating novel candidate P-hotspots. All phosphorylation hotspot annotations and predictions have been made available as part of the PhosPhAt database at http://phosphat.mpimp-golm.mpg.de. |
format | Online Article Text |
id | pubmed-3433687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
spelling | pubmed-34336872012-09-12 Characterization and Prediction of Protein Phosphorylation Hotspots in Arabidopsis thaliana Christian, Jan-Ole Braginets, Rostyslav Schulze, Waltraud X. Walther, Dirk Front Plant Sci Plant Science The regulation of protein function by modulating the surface charge status via sequence-locally enriched phosphorylation sites (P-sites) in so called phosphorylation “hotspots” has gained increased attention in recent years. We set out to identify P-hotspots in the model plant Arabidopsis thaliana. We analyzed the spacing of experimentally detected P-sites within peptide-covered regions along Arabidopsis protein sequences as available from the PhosPhAt database. Confirming earlier reports (Schweiger and Linial, 2010), we found that, indeed, P-sites tend to cluster and that distributions between serine and threonine P-sites to their respected closest next P-site differ significantly from those for tyrosine P-sites. The ability to predict P-hotspots by applying available computational P-site prediction programs that focus on identifying single P-sites was observed to be severely compromised by the inevitable interference of nearby P-sites. We devised a new approach, named HotSPotter, for the prediction of phosphorylation hotspots. HotSPotter is based primarily on local amino acid compositional preferences rather than sequence position-specific motifs and uses support vector machines as the underlying classification engine. HotSPotter correctly identified experimentally determined phosphorylation hotspots in A. thaliana with high accuracy. Applied to the Arabidopsis proteome, HotSPotter-predicted 13,677 candidate P-hotspots in 9,599 proteins corresponding to 7,847 unique genes. Hotspot containing proteins are involved predominantly in signaling processes confirming the surmised modulating role of hotspots in signaling and interaction events. Our study provides new bioinformatics means to identify phosphorylation hotspots and lays the basis for further investigating novel candidate P-hotspots. All phosphorylation hotspot annotations and predictions have been made available as part of the PhosPhAt database at http://phosphat.mpimp-golm.mpg.de. Frontiers Research Foundation 2012-09-05 /pmc/articles/PMC3433687/ /pubmed/22973286 http://dx.doi.org/10.3389/fpls.2012.00207 Text en Copyright © 2012 Christian, Braginets, Schulze and Walther. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Plant Science Christian, Jan-Ole Braginets, Rostyslav Schulze, Waltraud X. Walther, Dirk Characterization and Prediction of Protein Phosphorylation Hotspots in Arabidopsis thaliana |
title | Characterization and Prediction of Protein Phosphorylation Hotspots in Arabidopsis thaliana |
title_full | Characterization and Prediction of Protein Phosphorylation Hotspots in Arabidopsis thaliana |
title_fullStr | Characterization and Prediction of Protein Phosphorylation Hotspots in Arabidopsis thaliana |
title_full_unstemmed | Characterization and Prediction of Protein Phosphorylation Hotspots in Arabidopsis thaliana |
title_short | Characterization and Prediction of Protein Phosphorylation Hotspots in Arabidopsis thaliana |
title_sort | characterization and prediction of protein phosphorylation hotspots in arabidopsis thaliana |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3433687/ https://www.ncbi.nlm.nih.gov/pubmed/22973286 http://dx.doi.org/10.3389/fpls.2012.00207 |
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