Literature DB >> 23369641

Sampling the membrane: function of rhomboid-family proteins.

Marius K Lemberg1.   

Abstract

Rhomboids constitute a conserved protein superfamily that specifically binds membrane proteins and directs them into various different cellular pathways ranging from regulated secretion to endoplasmic reticulum (ER)-associated degradation (ERAD). Rhomboid proteases are known to release protein domains from membranes by a cut in their membrane anchor, whereas an emerging new class of rhomboid-family proteins lacks key catalytic residues and is not proteolytically active. Recent work has shown that these rhomboid pseudoproteases, including iRhoms and derlins, bind membrane proteins to regulate their fate, but the underlying molecular mechanism is not known. This review summarizes recent advances in the molecular understanding of rhomboid-family proteins and discusses common principles in how they recognize and bind proteins in the plane of the membrane.
Copyright © 2013 Elsevier Ltd. All rights reserved.

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Year:  2013        PMID: 23369641     DOI: 10.1016/j.tcb.2013.01.002

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  19 in total

1.  Mapping the energy landscape for second-stage folding of a single membrane protein.

Authors:  Duyoung Min; Robert E Jefferson; James U Bowie; Tae-Young Yoon
Journal:  Nat Chem Biol       Date:  2015-10-19       Impact factor: 15.040

Review 2.  Proteolytic ectodomain shedding of membrane proteins in mammals-hardware, concepts, and recent developments.

Authors:  Stefan F Lichtenthaler; Marius K Lemberg; Regina Fluhrer
Journal:  EMBO J       Date:  2018-07-05       Impact factor: 11.598

3.  Signal peptide peptidase functions in ERAD to cleave the unfolded protein response regulator XBP1u.

Authors:  Chia-yi Chen; Nicole S Malchus; Beate Hehn; Walter Stelzer; Dönem Avci; Dieter Langosch; Marius K Lemberg
Journal:  EMBO J       Date:  2014-09-19       Impact factor: 11.598

4.  How does the exosite of rhomboid protease affect substrate processing and inhibition?

Authors:  Michael Shokhen; Amnon Albeck
Journal:  Protein Sci       Date:  2017-10-24       Impact factor: 6.725

5.  Intramembrane protease PARL defines a negative regulator of PINK1- and PARK2/Parkin-dependent mitophagy.

Authors:  Cathrin Meissner; Holger Lorenz; Beate Hehn; Marius K Lemberg
Journal:  Autophagy       Date:  2015       Impact factor: 16.016

Review 6.  Ubiquitin-dependent protein degradation at the yeast endoplasmic reticulum and nuclear envelope.

Authors:  Dimitrios Zattas; Mark Hochstrasser
Journal:  Crit Rev Biochem Mol Biol       Date:  2014-09-18       Impact factor: 8.250

7.  A Golgi rhomboid protease Rbd2 recruits Cdc48 to cleave yeast SREBP.

Authors:  Jiwon Hwang; Diedre Ribbens; Sumana Raychaudhuri; Leah Cairns; He Gu; Adam Frost; Siniša Urban; Peter J Espenshade
Journal:  EMBO J       Date:  2016-09-21       Impact factor: 11.598

8.  Subunit architecture of the Golgi Dsc E3 ligase required for sterol regulatory element-binding protein (SREBP) cleavage in fission yeast.

Authors:  S Julie-Ann Lloyd; Sumana Raychaudhuri; Peter J Espenshade
Journal:  J Biol Chem       Date:  2013-06-12       Impact factor: 5.157

9.  Quality control of integral membrane proteins by assembly-dependent membrane integration.

Authors:  Matthias J Feige; Linda M Hendershot
Journal:  Mol Cell       Date:  2013-08-08       Impact factor: 17.970

10.  Substrate recruitment of γ-secretase and mechanism of clinical presenilin mutations revealed by photoaffinity mapping.

Authors:  Akio Fukumori; Harald Steiner
Journal:  EMBO J       Date:  2016-05-23       Impact factor: 11.598

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