ArticleBMC genomics2009
Functional diversity of human protein kinase splice variants marks significant expansion of human kinome.
Article in BMC genomics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- Bayesian reconstruction and differential testing of excised introns.Bioinformatics (Oxford, England) · 2025Article
- Review
- Inhibitors of Serine/Threonine Protein Phosphatases: Biochemical and Structural Studies Provide Insight for Further Development.Current medicinal chemistry · 2019Review
- Bayesian nonparametric discovery of isoforms and individual specific quantification.Nature communications · 2018Article
- Identification of functional metabolic biomarkers from lung cancer patient serum using PEP technology.Biomarker research · 2016Article
- Human tRNA synthetase catalytic nulls with diverse functions.Science (New York, N.Y.) · 2014Article
- Exploring the function of protein kinases in schistosomes: perspectives from the laboratory and from comparative genomics.Frontiers in genetics · 2014Article
- Alternative splicing in oncogenic kinases: from physiological functions to cancer.Journal of nucleic acids · 2012Article
- Reversible and irreversible protein glutathionylation: biological and clinical aspects.Expert opinion on drug metabolism & toxicology · 2011Review
- Classification of protein kinases on the basis of both kinase and non-kinase regions.PloS one · 2010Article
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3 authors.
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Abstract
backgroundProtein kinases are involved in diverse spectrum of cellular processes. Availability of draft version of the human genomic data in the year 2001 enabled recognition of repertoire of protein kinases. However, over the years the human genomic data is being refined and the current release of human genomic data has helped us to recognize a larger repertoire of over 900 human protein kinases represented mainly by splice variants.
resultsMany of these identified protein kinases are alternatively spliced products. Interestingly, some of the human kinase splice variants appear to be significantly diverged in terms of their functional properties as represented by incorporation or absence of one or more domains. Many sets of protein kinase splice variants have substantially different domain organization and in a few sets of splice variants kinase domains belong to different subfamilies of kinases suggesting potential participation in different signal transduction pathways.
conclusionsAddition or deletion of a domain between splice variants of multi-domain kinases appears to be a means of generating differences in the functional features of otherwise similar kinases. It is intriguing that marked sequence diversity within the catalytic regions of some of the splice variant kinases result in kinases belonging to different subfamilies. These human kinase splice variants with different functions might contribute to diversity of eukaryotic cellular signaling.
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