A bioinformatics approach to identifying tail-anchored proteins in the human genome

被引:106
作者
Kalbfleisch, Ted
Cambon, Alex
Wattenberg, Binks W. [1 ]
机构
[1] Univ Louisville, Dept Biochem & Mol Biol, Sch Med, Louisville, KY 40202 USA
[2] Univ Louisville, Sch Med, Ctr Genet & Mol Med, Louisville, KY 40202 USA
[3] Univ Louisville, Sch Publ Hlth & Informat Sci, Dept Bioinformat & Biostat, Louisville, KY 40202 USA
[4] Univ Louisville, Dept Med, Sch Med, Louisville, KY 40202 USA
[5] Univ Louisville, Dept Pharmacol & Toxicol, Sch Med, Louisville, KY 40202 USA
关键词
endoplasmic reticulum; membrane protein; mitochondrial outer membrane; protein targeting; SNARE;
D O I
10.1111/j.1600-0854.2007.00661.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Intracellular proteins with a carboxy-terminal transmembrane domain and the amino-terminus oriented toward the cytosol are known as 'tail-anchored' proteins. Tail-anchored proteins have been of considerable interest because several important classes of proteins, including the vesicle-targeting/fusion proteins known as SNAREs and the apoptosis-related proteins of the Bcl-2 family, among others, utilize this unique membrane-anchoring motif. Here, we use a bioinformatic technique to develop a comprehensive list of potentially tail-anchored proteins in the human genome. Our final list contains 411 entries derived from 325 unique genes. We also analyzed both known and predicted tail-anchored proteins with respect to the amino acid composition of the transmembrane segments. This analysis revealed a distinctive composition of the membrane anchor in SNARE proteins.
引用
收藏
页码:1687 / 1694
页数:8
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