InsP3 Signaling in Apicomplexan Parasites

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GARCIA, Celia R.S., Eduardo ALVES, Pedro H.S. PEREIRA, Paula BARTLETT, Andrew THOMAS, Katsuhiko MIKOSHIBA, Helmut PLATTNER, L. David SIBLEY, 2017. InsP3 Signaling in Apicomplexan Parasites. In: Current Topics in Medicinal Chemistry. 17(19), pp. 2158-2165. ISSN 1568-0266. eISSN 1873-4294

@article{Garcia2017-01-30InsP3-38306, title={InsP3 Signaling in Apicomplexan Parasites}, year={2017}, doi={10.2174/1568026617666170130121042}, number={19}, volume={17}, issn={1568-0266}, journal={Current Topics in Medicinal Chemistry}, pages={2158--2165}, author={Garcia, Celia R.S. and Alves, Eduardo and Pereira, Pedro H.S. and Bartlett, Paula and Thomas, Andrew and Mikoshiba, Katsuhiko and Plattner, Helmut and Sibley, L. David} }

<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/rdf/resource/123456789/38306"> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2017-04-04T12:35:49Z</dcterms:available> <dcterms:title>InsP3 Signaling in Apicomplexan Parasites</dcterms:title> <dc:creator>Plattner, Helmut</dc:creator> <dc:contributor>Sibley, L. David</dc:contributor> <dc:creator>Thomas, Andrew</dc:creator> <dc:contributor>Thomas, Andrew</dc:contributor> <dc:language>eng</dc:language> <dc:creator>Bartlett, Paula</dc:creator> <dc:creator>Garcia, Celia R.S.</dc:creator> <dcterms:issued>2017-01-30</dcterms:issued> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2017-04-04T12:35:49Z</dc:date> <dc:contributor>Plattner, Helmut</dc:contributor> <dc:contributor>Bartlett, Paula</dc:contributor> <dc:contributor>Alves, Eduardo</dc:contributor> <dc:creator>Sibley, L. David</dc:creator> <dc:contributor>Pereira, Pedro H.S.</dc:contributor> <dcterms:abstract xml:lang="eng">Phosphoinositides (PIs) and their derivatives are essential cellular components that form the building blocks for cell membranes and regulate numerous cell functions. Specifically, the ability to generate myo-inositol 1,4,5-trisphosphate (InsP3) via phospholipase C (PLC) dependent hydrolysis of phosphatidylinositol 4,5-bisphosphate (PIP2) to InsP3 and diacylglycerol (DAG) initiates intracellular calcium signaling events representing a fundamental signaling mechanism dependent on PIs. InsP3 produced by PI turnover as a second messenger causes intracellular calcium release, especially from endoplasmic reticulum, by binding to the InsP3 receptor (InsP3R). Various PIs and the enzymes, such as phosphatidylinositol synthase and phosphatidylinositol 4-kinase, necessary for their turnover have been characterized in Apicomplexa, a large phylum of mostly commensal organisms that also includes several clinically relevant parasites. However, InsP3Rs have not been identified in genomes of apicomplexans, despite evidence that these parasites produce InsP3 that mediates intracellular Ca2+ signaling. Evidence to supporting IP3-dependent signaling cascades in apicomplexans suggests that they may harbor a primitive or non-canonical InsP3R. Understanding these pathways may be informative about early branching eukaryotes, where such signaling pathways also diverge from animal systems, thus identifying potential novel and essential targets for therapeutic intervention.</dcterms:abstract> <dc:creator>Pereira, Pedro H.S.</dc:creator> <dc:creator>Mikoshiba, Katsuhiko</dc:creator> <dc:contributor>Garcia, Celia R.S.</dc:contributor> <bibo:uri rdf:resource="https://kops.uni-konstanz.de/handle/123456789/38306"/> <dc:creator>Alves, Eduardo</dc:creator> <dc:contributor>Mikoshiba, Katsuhiko</dc:contributor> </rdf:Description> </rdf:RDF>

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