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Items: 1 to 20 of 119

1.

Hydrophobic profiles of the tail anchors in SLMAP dictate subcellular targeting.

Byers JT, Guzzo RM, Salih M, Tuana BS.

BMC Cell Biol. 2009 Jun 19;10:48. doi: 10.1186/1471-2121-10-48.

2.

70-kDa peroxisomal membrane protein related protein (P70R/ABCD4) localizes to endoplasmic reticulum not peroxisomes, and NH2-terminal hydrophobic property determines the subcellular localization of ABC subfamily D proteins.

Kashiwayama Y, Seki M, Yasui A, Murasaki Y, Morita M, Yamashita Y, Sakaguchi M, Tanaka Y, Imanaka T.

Exp Cell Res. 2009 Jan 15;315(2):190-205. doi: 10.1016/j.yexcr.2008.10.031. Epub 2008 Nov 3.

PMID:
19010322
3.

NHE6 protein possesses a signal peptide destined for endoplasmic reticulum membrane and localizes in secretory organelles of the cell.

Miyazaki E, Sakaguchi M, Wakabayashi S, Shigekawa M, Mihara K.

J Biol Chem. 2001 Dec 28;276(52):49221-7. Epub 2001 Oct 18.

4.

Membrane localization of cyclic nucleotide phosphodiesterase 3 (PDE3). Two N-terminal domains are required for the efficient targeting to, and association of, PDE3 with endoplasmic reticulum.

Shakur Y, Takeda K, Kenan Y, Yu ZX, Rena G, Brandt D, Houslay MD, Degerman E, Ferrans VJ, Manganiello VC.

J Biol Chem. 2000 Dec 8;275(49):38749-61.

5.

Novel targeting signals mediate the sorting of different isoforms of the tail-anchored membrane protein cytochrome b5 to either endoplasmic reticulum or mitochondria.

Hwang YT, Pelitire SM, Henderson MP, Andrews DW, Dyer JM, Mullen RT.

Plant Cell. 2004 Nov;16(11):3002-19. Epub 2004 Oct 14.

6.
8.

Bipartite signals mediate subcellular targeting of tail-anchored membrane proteins in Saccharomyces cerevisiae.

Beilharz T, Egan B, Silver PA, Hofmann K, Lithgow T.

J Biol Chem. 2003 Mar 7;278(10):8219-23. Epub 2003 Jan 3.

9.

Characterization of signal that directs C-tail-anchored proteins to mammalian mitochondrial outer membrane.

Horie C, Suzuki H, Sakaguchi M, Mihara K.

Mol Biol Cell. 2002 May;13(5):1615-25.

10.

Molecular determinants of the subcellular localization of the Drosophila Bcl-2 homologues DEBCL and BUFFY.

Doumanis J, Dorstyn L, Kumar S.

Cell Death Differ. 2007 May;14(5):907-15. Epub 2007 Jan 5.

11.

Multiple organelle-targeting signals in the N-terminal portion of peroxisomal membrane protein PMP70.

Iwashita S, Tsuchida M, Tsukuda M, Yamashita Y, Emi Y, Kida Y, Komori M, Kashiwayama Y, Imanaka T, Sakaguchi M.

J Biochem. 2010 Apr;147(4):581-90. doi: 10.1093/jb/mvp205. Epub 2009 Dec 10.

PMID:
20007743
12.

Mammalian vesicle trafficking proteins of the endoplasmic reticulum and Golgi apparatus.

Hay JC, Hirling H, Scheller RH.

J Biol Chem. 1996 Mar 8;271(10):5671-9.

13.

Characterization of the signal that directs Tom20 to the mitochondrial outer membrane.

Kanaji S, Iwahashi J, Kida Y, Sakaguchi M, Mihara K.

J Cell Biol. 2000 Oct 16;151(2):277-88.

14.
15.

Subcellular sorting of small membrane-associated triple gene block proteins: TGBp3-assisted targeting of TGBp2.

Solovyev AG, Stroganova TA, Zamyatnin AA Jr, Fedorkin ON, Schiemann J, Morozov SY.

Virology. 2000 Mar 30;269(1):113-27.

17.
19.

An artificial mitochondrial tail signal/anchor sequence confirms a requirement for moderate hydrophobicity for targeting.

Wattenberg BW, Clark D, Brock S.

Biosci Rep. 2007 Dec;27(6):385-401. Epub 2007 Oct 30.

PMID:
17968654
20.

Triple arginines in the cytoplasmic tail of endomannosidase are not essential for type II membrane topology and Golgi localization.

Stehli J, Torossi T, Ziak M.

Cell Mol Life Sci. 2008 May;65(10):1609-19. doi: 10.1007/s00018-008-8054-x.

PMID:
18425413

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