Inositol pyrophosphates as multifaceted metabolites in the regulation of mammalian signaling networks

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dc.contributor.authorPark, Seung Juko
dc.contributor.authorLee, Seulgiko
dc.contributor.authorPark, Seung-eunko
dc.contributor.authorKim, Seyunko
dc.date.accessioned2018-02-21T06:39:49Z-
dc.date.available2018-02-21T06:39:49Z-
dc.date.created2018-02-19-
dc.date.created2018-02-19-
dc.date.created2018-02-19-
dc.date.issued2018-01-
dc.identifier.citationANIMAL CELLS AND SYSTEMS, v.22, no.1, pp.1 - 6-
dc.identifier.issn1976-8354-
dc.identifier.urihttp://hdl.handle.net/10203/240393-
dc.description.abstractInositol pyrophosphates (PP-IPs) such as 5-diphosphoinositol pentakisphosphate (5-IP7) are inositol metabolites with high-energy phosphoanhydride bonds. The formation of PP-IPs is catalyzed by two groups of enzymes, the IP6 kinases and the PPIP5 kinases, which both phosphorylate inositol hexakisphosphate (IP6). In mammals, PP-IPs are implicated in diverse biological phenomena including cellular growth, vesicular trafficking, apoptosis, and metabolic homeostasis. Mechanistically, all the diverse actions of PP-IPs proceed in one of two ways: the PP-IPs modulate the activity of their target proteins either through allosteric binding or protein pyrophosphorylation. In this review, we highlight recent advances in our understanding of the pleiotropic functions of the mammalian PP-IPs and the metabolic enzymes that produce them. We also discuss some future challenges in the exploration of areas where PP-IPs play important but unknown roles in physiology and disease.-
dc.languageEnglish-
dc.publisherTAYLOR & FRANCIS LTD-
dc.subjectDIPHOSPHOINOSITOL POLYPHOSPHATES-
dc.subjectSACCHAROMYCES-CEREVISIAE-
dc.subjectCONSERVED FAMILY-
dc.subjectHEXAKISPHOSPHATE-
dc.subjectPHOSPHATES-
dc.subjectTURNOVER-
dc.subjectPYROPHOSPHORYLATION-
dc.subjectTETRAKISPHOSPHATE-
dc.subjectPHOSPHORYLATION-
dc.subjectPURIFICATION-
dc.titleInositol pyrophosphates as multifaceted metabolites in the regulation of mammalian signaling networks-
dc.typeArticle-
dc.identifier.wosid000424135500001-
dc.identifier.scopusid2-s2.0-85041597123-
dc.type.rimsART-
dc.citation.volume22-
dc.citation.issue1-
dc.citation.beginningpage1-
dc.citation.endingpage6-
dc.citation.publicationnameANIMAL CELLS AND SYSTEMS-
dc.identifier.doi10.1080/19768354.2017.1408684-
dc.contributor.localauthorKim, Seyun-
dc.description.isOpenAccessY-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorMetabolism-
dc.subject.keywordAuthorinositol pyrophosphate-
dc.subject.keywordAuthorIP6K-
dc.subject.keywordAuthorPPIP5K-
dc.subject.keywordAuthorcell signaling-
dc.subject.keywordAuthorMetabolism-
dc.subject.keywordAuthorinositol pyrophosphate-
dc.subject.keywordAuthorIP6K-
dc.subject.keywordAuthorPPIP5K-
dc.subject.keywordAuthorcell signaling-
dc.subject.keywordPlusDIPHOSPHOINOSITOL POLYPHOSPHATES-
dc.subject.keywordPlusSACCHAROMYCES-CEREVISIAE-
dc.subject.keywordPlusCONSERVED FAMILY-
dc.subject.keywordPlusHEXAKISPHOSPHATE-
dc.subject.keywordPlusPHOSPHATES-
dc.subject.keywordPlusTURNOVER-
dc.subject.keywordPlusPYROPHOSPHORYLATION-
dc.subject.keywordPlusTETRAKISPHOSPHATE-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.subject.keywordPlusPURIFICATION-
dc.subject.keywordPlusDIPHOSPHOINOSITOL POLYPHOSPHATES-
dc.subject.keywordPlusSACCHAROMYCES-CEREVISIAE-
dc.subject.keywordPlusCONSERVED FAMILY-
dc.subject.keywordPlusHEXAKISPHOSPHATE-
dc.subject.keywordPlusPHOSPHATES-
dc.subject.keywordPlusTURNOVER-
dc.subject.keywordPlusPYROPHOSPHORYLATION-
dc.subject.keywordPlusTETRAKISPHOSPHATE-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.subject.keywordPlusPURIFICATION-
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