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FEBS Lett. 2006 Apr 17;580(9):2281-4. Epub 2006 Mar 27.

Membrane topology of the human seipin protein.

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  • 1Department of Biochemistry and Biophysics, Stockholm University, SE-10691 Stockholm, Sweden.

Abstract

The Berardinelli-Seip congenital lipodystrophy type 2 (BSCL2) gene encodes an integral membrane protein, called seipin, of unknown function localized to the endoplasmic reticulum of eukaryotic cells. Seipin is associated with the heterogeneous genetic disease BSCL2, and mutations in an N-glycosylation motif links the protein to two other disorders, autosomal-dominant distal hereditary motor neuropathy type V and Silver syndrome. Here, we report a topological study of seipin using an in vitro topology mapping assay. Our results suggest that the predominant form of seipin is 462 residues long and has an N(cyt)-C(cyt) orientation with a long luminal loop between the two transmembrane helices.

PMID:
16574104
DOI:
10.1016/j.febslet.2006.03.040
[PubMed - indexed for MEDLINE]
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