Cargando…
Classification of protein motifs based on subcellular localization uncovers evolutionary relationships at both sequence and functional levels
BACKGROUND: Most proteins have evolved in specific cellular compartments that limit their functions and potential interactions. On the other hand, motifs define amino acid arrangements conserved between protein family members and represent powerful tools for assigning function to protein sequences....
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724711/ https://www.ncbi.nlm.nih.gov/pubmed/23865897 http://dx.doi.org/10.1186/1471-2105-14-229 |
_version_ | 1782476713242918912 |
---|---|
author | Parras-Moltó, Marcos Campos-Laborie, Francisco J García-Diéguez, Juan Rodríguez-Griñolo, M Rosario Pérez-Pulido, Antonio J |
author_facet | Parras-Moltó, Marcos Campos-Laborie, Francisco J García-Diéguez, Juan Rodríguez-Griñolo, M Rosario Pérez-Pulido, Antonio J |
author_sort | Parras-Moltó, Marcos |
collection | PubMed |
description | BACKGROUND: Most proteins have evolved in specific cellular compartments that limit their functions and potential interactions. On the other hand, motifs define amino acid arrangements conserved between protein family members and represent powerful tools for assigning function to protein sequences. The ideal motif would identify all members of a protein family but in practice many motifs identify both family members and unrelated proteins, referred to as True Positive (TP) and False Positive (FP) sequences, respectively. RESULTS: To address the relationship between protein motifs, protein function and cellular localization, we systematically assigned subcellular localization data to motif sequences from the comprehensive PROSITE sequence motif database. Using this data we analyzed relationships between localization and function. We find that TPs and FPs have a strong tendency to localize in different compartments. When multiple localizations are considered, TPs are usually distributed between related cellular compartments. We also identified cases where FPs are concentrated in particular subcellular regions, indicating possible functional or evolutionary relationships with TP sequences of the same motif. CONCLUSIONS: Our findings suggest that the systematic examination of subcellular localization has the potential to uncover evolutionary and functional relationships between motif-containing sequences. We believe that this type of analysis complements existing motif annotations and could aid in their interpretation. Our results shed light on the evolution of cellular organelles and potentially establish the basis for new subcellular localization and function prediction algorithms. |
format | Online Article Text |
id | pubmed-3724711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-37247112013-07-30 Classification of protein motifs based on subcellular localization uncovers evolutionary relationships at both sequence and functional levels Parras-Moltó, Marcos Campos-Laborie, Francisco J García-Diéguez, Juan Rodríguez-Griñolo, M Rosario Pérez-Pulido, Antonio J BMC Bioinformatics Research Article BACKGROUND: Most proteins have evolved in specific cellular compartments that limit their functions and potential interactions. On the other hand, motifs define amino acid arrangements conserved between protein family members and represent powerful tools for assigning function to protein sequences. The ideal motif would identify all members of a protein family but in practice many motifs identify both family members and unrelated proteins, referred to as True Positive (TP) and False Positive (FP) sequences, respectively. RESULTS: To address the relationship between protein motifs, protein function and cellular localization, we systematically assigned subcellular localization data to motif sequences from the comprehensive PROSITE sequence motif database. Using this data we analyzed relationships between localization and function. We find that TPs and FPs have a strong tendency to localize in different compartments. When multiple localizations are considered, TPs are usually distributed between related cellular compartments. We also identified cases where FPs are concentrated in particular subcellular regions, indicating possible functional or evolutionary relationships with TP sequences of the same motif. CONCLUSIONS: Our findings suggest that the systematic examination of subcellular localization has the potential to uncover evolutionary and functional relationships between motif-containing sequences. We believe that this type of analysis complements existing motif annotations and could aid in their interpretation. Our results shed light on the evolution of cellular organelles and potentially establish the basis for new subcellular localization and function prediction algorithms. BioMed Central 2013-07-18 /pmc/articles/PMC3724711/ /pubmed/23865897 http://dx.doi.org/10.1186/1471-2105-14-229 Text en Copyright © 2013 Parras-Moltó 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 | Research Article Parras-Moltó, Marcos Campos-Laborie, Francisco J García-Diéguez, Juan Rodríguez-Griñolo, M Rosario Pérez-Pulido, Antonio J Classification of protein motifs based on subcellular localization uncovers evolutionary relationships at both sequence and functional levels |
title | Classification of protein motifs based on subcellular localization uncovers evolutionary relationships at both sequence and functional levels |
title_full | Classification of protein motifs based on subcellular localization uncovers evolutionary relationships at both sequence and functional levels |
title_fullStr | Classification of protein motifs based on subcellular localization uncovers evolutionary relationships at both sequence and functional levels |
title_full_unstemmed | Classification of protein motifs based on subcellular localization uncovers evolutionary relationships at both sequence and functional levels |
title_short | Classification of protein motifs based on subcellular localization uncovers evolutionary relationships at both sequence and functional levels |
title_sort | classification of protein motifs based on subcellular localization uncovers evolutionary relationships at both sequence and functional levels |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724711/ https://www.ncbi.nlm.nih.gov/pubmed/23865897 http://dx.doi.org/10.1186/1471-2105-14-229 |
work_keys_str_mv | AT parrasmoltomarcos classificationofproteinmotifsbasedonsubcellularlocalizationuncoversevolutionaryrelationshipsatbothsequenceandfunctionallevels AT camposlaboriefranciscoj classificationofproteinmotifsbasedonsubcellularlocalizationuncoversevolutionaryrelationshipsatbothsequenceandfunctionallevels AT garciadieguezjuan classificationofproteinmotifsbasedonsubcellularlocalizationuncoversevolutionaryrelationshipsatbothsequenceandfunctionallevels AT rodriguezgrinolomrosario classificationofproteinmotifsbasedonsubcellularlocalizationuncoversevolutionaryrelationshipsatbothsequenceandfunctionallevels AT perezpulidoantonioj classificationofproteinmotifsbasedonsubcellularlocalizationuncoversevolutionaryrelationshipsatbothsequenceandfunctionallevels |