Literature DB >> 14675765

Multiple functions of tail-anchor domains of mitochondrial outer membrane proteins.

Shukry J Habib1, Andreja Vasiljev, Walter Neupert, Doron Rapaport.   

Abstract

Tail-anchored proteins form a distinct class of membrane proteins that have a single membrane anchor sequence at their C-terminus, the tail-anchor. Their N-terminal portion is exposed to the cytosol. We have studied the roles of tail-anchor domains of proteins residing in the mitochondrial outer membrane. Four distinct functions of the tail-anchor domain were identified. First, the domain mediates the targeting to mitochondria in a process that probably requires a net positive charge at the C-terminally flanking segment. Second, tail-anchor domains facilitate the insertion into the mitochondrial outer membrane. Third, the tail-anchor is responsible for the assembly of the respective protein into functional multi-subunit complexes; and fourth, tail-anchor domains can stabilize such complexes.

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Year:  2003        PMID: 14675765     DOI: 10.1016/s0014-5793(03)01325-5

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  17 in total

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6.  Ergosterol content specifies targeting of tail-anchored proteins to mitochondrial outer membranes.

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7.  Targeting and function of the mitochondrial fission factor GDAP1 are dependent on its tail-anchor.

Authors:  Konstanze M Wagner; Marcel Rüegg; Axel Niemann; Ueli Suter
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8.  Yeast Miro GTPase, Gem1p, regulates mitochondrial morphology via a novel pathway.

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

Authors:  Joseph T Byers; Rosa M Guzzo; Maysoon Salih; Balwant S Tuana
Journal:  BMC Cell Biol       Date:  2009-06-19       Impact factor: 4.241

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