Titlebook: Cholesterol Transporters of the START Domain Protein Family in Health and Disease; START Proteins - Str Barbara J. Clark,Douglas‘M. Stocco

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Cholesterol Transporters of the START Domain Protein Family in Health and Disease978-1-4939-1112-7

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,Abkürzungen, Bezeichnungen und Symbole,n START family members, e.g., STARD1, STARD11, and STARD2 are well characterized for their roles in cholesterol, ceramide, and phosphatidylcholine transfer, respectively, while much remains to be learned about the remaining family members. The purpose of this book is to present a compendium of the h

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https://doi.org/10.1007/978-3-642-81608-6RD11) binding have conserved residues that play a structural role in the formation of a cavity that fits the shape of their specific ligands. We also expose a correlation between structural fluctuations reported to occur in secondary and tertiary structure elements of START domains and we suggest co

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,Hydrostatische Anlagen — Stand der Technik,of its action remains unclear. Lipoid CAH is caused by StAR mutations and is thus the StAR knockout experiment of nature. Recent work has shown that P450scc mutations cause a disease that is a phenocopy of lipoid CAH. The discovery of StAR led to the discovery of the broader family of structurally r

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https://doi.org/10.1007/978-3-642-81608-6fflux process mediated by adenosine triphosphate (ATP)-binding cassette transporters (ABCA1/G1) and apolipoprotein acceptors, and inhibits nuclear factor-κB signalling, resulting in repression of an array of inflammatory genes. Thus, StAR/STARD1 may represent a novel target for treatment of atherosc

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Struktursynthese hydrostatischer Anlagen,loosely with specific subcellular membranes. (4) STARD4 can bind cholesterol and efficiently transfer it between membranes. (5) STARD4 can mediate transfer of cholesterol to the ER resident enzyme acyl-coenzyme A cholesterol acyltransferase (ACAT) for esterification. (6) STARD5 does not have these A

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