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http://purl.uniprot.org/citations/30389354http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/30389354http://www.w3.org/2000/01/rdf-schema#comment"Extensive research conducted in the last three decades has identified the roles for the main bioactive sphingolipids, namely ceramide, sphingosine, and sphingosine 1-phosphate (S1P) as key regulators of cellular homeostasis, growth and death. One of the major groups of enzymes in the ceramide pathway, ceramidases, converts ceramide into sphingosine and fatty acids, with sphingosine being further metabolized to S1P. Thus, these enzymes play important roles in the network controlling the functions associated with these bioactive sphingolipids. Among the family of ceramidases, neutral ceramidase (nCDase), which is named according to its optimal pH for catalytic activity, has received increased attention in the last decade. The goal of this review is to provide a brief background on bioactive sphingolipids and the ceramidases. We then describe more recent advances on nCDase, specifically the resolution of its crystal structure and understanding its roles in cell biology and physiology."xsd:string
http://purl.uniprot.org/citations/30389354http://purl.org/dc/terms/identifier"doi:10.1016/j.jbior.2018.10.005"xsd:string
http://purl.uniprot.org/citations/30389354http://purl.uniprot.org/core/author"Hannun Y.A."xsd:string
http://purl.uniprot.org/citations/30389354http://purl.uniprot.org/core/author"Coant N."xsd:string
http://purl.uniprot.org/citations/30389354http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/30389354http://purl.uniprot.org/core/name"Adv Biol Regul"xsd:string
http://purl.uniprot.org/citations/30389354http://purl.uniprot.org/core/pages"141-146"xsd:string
http://purl.uniprot.org/citations/30389354http://purl.uniprot.org/core/title"Neutral ceramidase: Advances in mechanisms, cell regulation, and roles in cancer."xsd:string
http://purl.uniprot.org/citations/30389354http://purl.uniprot.org/core/volume"71"xsd:string
http://purl.uniprot.org/citations/30389354http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/30389354
http://purl.uniprot.org/citations/30389354http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/30389354
http://purl.uniprot.org/uniprot/#_A0A0C4DFQ8-mappedCitation-30389354http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30389354
http://purl.uniprot.org/uniprot/#_Q9NR71-mappedCitation-30389354http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/30389354
http://purl.uniprot.org/uniprot/A0A0C4DFQ8http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/30389354
http://purl.uniprot.org/uniprot/Q9NR71http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/30389354