Mapping Lysosomal Storage Disorders with Neurological Features by Cellular Pathways: Towards Precision Medicine. [PDF]
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Therapeutic potential of the sphingosine kinase 2 inhibitor opaganib. [PDF]
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Spider venom phospholipase D toxin structure: Interfacial binding site, mechanism, activation, and head group preference. [PDF]
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Interorgan crosstalk in metabolic dysfunction-associated steatotic liver disease. [PDF]
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The Biological Significance of Calmodulin Binding to Lipids. [PDF]
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Activator proteins and topology of lysosomal sphingolipid catabolism
Lipids and Lipid Metabolism, 1992The lysosomal degradation of several sphingolipids by acid hydrolases is dependent on small non-enzymic cofactors, called sphingolipid activator proteins some of which have been identified as sphingolipid binding proteins. This review summarizes the information available on the structure, function, biosynthesis, gene organization and pathobiochemistry ...
Konrad Sandhoff, W Fürst
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Stimulation of lysosomal sphingomyelin degradation by sphingolipid activator proteins
Chemistry and Physics of Lipids, 1999Lysosomal breakdown of glycosphingolipids with short hydrophilic carbohydrate headgroups is achieved by the simultaneous action of specific hydrolases and sphingolipid activator proteins (SAPs). Activator proteins are considered to facilitate the enzyme/substrate interaction between water-soluble enzymes and membrane-bound substrates.
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