The lipid-binding SEC 14 domain

被引：100

作者：

Saito, Kan ^{[1
]}

Tautz, Lutz ^{[1
]}

Mustelin, Tomas ^{[1
]}

机构：

[1] Burnham Inst Med Res, La Jolla, CA 92037 USA

来源：

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2007年 / 1771卷 / 06期

关键词：

SEC14; CRAL_TRIO; CRAL_TRIO_N; PTP-MEG2; PTPN9; TAP; SEC14L; Trio; Dbl; Sec14p;

D O I：

10.1016/j.bbalip.2007.02.010

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Protein-lipid interactions are important for protein targeting, signal transduction, lipid transport, lipid biosynthesis, lipid metabolism, and the maintenance of cellular compartments and membranes. Specific lipid-binding protein domains, such as PH, FYVE, PX, PHD, C2 and SEC14 homology domains, inediate interactions between proteins and specific phospholipids. Here we review the published literature, plus some of our most recent unpublished findings, regarding the biology of the SEC14 domain, also known as CRAL_TRIO domain. (c) 2007 Elsevier B.V. All rights reserved.

引用

页码：719 / 726

页数：8

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