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Hybrid and Rogue Kinases Encoded in the Genomes of Model Eukaryotes

The highly modular nature of protein kinases generates diverse functional roles mediated by evolutionary events such as domain recombination, insertion and deletion of domains. Usually domain architecture of a kinase is related to the subfamily to which the kinase catalytic domain belongs. However o...

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Autores principales: Rakshambikai, Ramaswamy, Gnanavel, Mutharasu, Srinivasan, Narayanaswamy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177888/
https://www.ncbi.nlm.nih.gov/pubmed/25255313
http://dx.doi.org/10.1371/journal.pone.0107956
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author Rakshambikai, Ramaswamy
Gnanavel, Mutharasu
Srinivasan, Narayanaswamy
author_facet Rakshambikai, Ramaswamy
Gnanavel, Mutharasu
Srinivasan, Narayanaswamy
author_sort Rakshambikai, Ramaswamy
collection PubMed
description The highly modular nature of protein kinases generates diverse functional roles mediated by evolutionary events such as domain recombination, insertion and deletion of domains. Usually domain architecture of a kinase is related to the subfamily to which the kinase catalytic domain belongs. However outlier kinases with unusual domain architectures serve in the expansion of the functional space of the protein kinase family. For example, Src kinases are made-up of SH2 and SH3 domains in addition to the kinase catalytic domain. A kinase which lacks these two domains but retains sequence characteristics within the kinase catalytic domain is an outlier that is likely to have modes of regulation different from classical src kinases. This study defines two types of outlier kinases: hybrids and rogues depending on the nature of domain recombination. Hybrid kinases are those where the catalytic kinase domain belongs to a kinase subfamily but the domain architecture is typical of another kinase subfamily. Rogue kinases are those with kinase catalytic domain characteristic of a kinase subfamily but the domain architecture is typical of neither that subfamily nor any other kinase subfamily. This report provides a consolidated set of such hybrid and rogue kinases gleaned from six eukaryotic genomes–S.cerevisiae, D. melanogaster, C.elegans, M.musculus, T.rubripes and H.sapiens–and discusses their functions. The presence of such kinases necessitates a revisiting of the classification scheme of the protein kinase family using full length sequences apart from classical classification using solely the sequences of kinase catalytic domains. The study of these kinases provides a good insight in engineering signalling pathways for a desired output. Lastly, identification of hybrids and rogues in pathogenic protozoa such as P.falciparum sheds light on possible strategies in host-pathogen interactions.
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spelling pubmed-41778882014-10-02 Hybrid and Rogue Kinases Encoded in the Genomes of Model Eukaryotes Rakshambikai, Ramaswamy Gnanavel, Mutharasu Srinivasan, Narayanaswamy PLoS One Research Article The highly modular nature of protein kinases generates diverse functional roles mediated by evolutionary events such as domain recombination, insertion and deletion of domains. Usually domain architecture of a kinase is related to the subfamily to which the kinase catalytic domain belongs. However outlier kinases with unusual domain architectures serve in the expansion of the functional space of the protein kinase family. For example, Src kinases are made-up of SH2 and SH3 domains in addition to the kinase catalytic domain. A kinase which lacks these two domains but retains sequence characteristics within the kinase catalytic domain is an outlier that is likely to have modes of regulation different from classical src kinases. This study defines two types of outlier kinases: hybrids and rogues depending on the nature of domain recombination. Hybrid kinases are those where the catalytic kinase domain belongs to a kinase subfamily but the domain architecture is typical of another kinase subfamily. Rogue kinases are those with kinase catalytic domain characteristic of a kinase subfamily but the domain architecture is typical of neither that subfamily nor any other kinase subfamily. This report provides a consolidated set of such hybrid and rogue kinases gleaned from six eukaryotic genomes–S.cerevisiae, D. melanogaster, C.elegans, M.musculus, T.rubripes and H.sapiens–and discusses their functions. The presence of such kinases necessitates a revisiting of the classification scheme of the protein kinase family using full length sequences apart from classical classification using solely the sequences of kinase catalytic domains. The study of these kinases provides a good insight in engineering signalling pathways for a desired output. Lastly, identification of hybrids and rogues in pathogenic protozoa such as P.falciparum sheds light on possible strategies in host-pathogen interactions. Public Library of Science 2014-09-25 /pmc/articles/PMC4177888/ /pubmed/25255313 http://dx.doi.org/10.1371/journal.pone.0107956 Text en © 2014 Rakshambikai et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Rakshambikai, Ramaswamy
Gnanavel, Mutharasu
Srinivasan, Narayanaswamy
Hybrid and Rogue Kinases Encoded in the Genomes of Model Eukaryotes
title Hybrid and Rogue Kinases Encoded in the Genomes of Model Eukaryotes
title_full Hybrid and Rogue Kinases Encoded in the Genomes of Model Eukaryotes
title_fullStr Hybrid and Rogue Kinases Encoded in the Genomes of Model Eukaryotes
title_full_unstemmed Hybrid and Rogue Kinases Encoded in the Genomes of Model Eukaryotes
title_short Hybrid and Rogue Kinases Encoded in the Genomes of Model Eukaryotes
title_sort hybrid and rogue kinases encoded in the genomes of model eukaryotes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4177888/
https://www.ncbi.nlm.nih.gov/pubmed/25255313
http://dx.doi.org/10.1371/journal.pone.0107956
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