Protein disulphide isomerase is required for signal peptide peptidase-mediated protein degradation (Q24322026)

1

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Kwangmin Cho

2

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Sunglim Cho

3

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Ilkwon Kim

4

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Changhoon Oh

5

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Kwangseog Ahn

EDEM1 recognition and delivery of misfolded proteins to the SEL1L-containing ERAD complex

6

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language of work or name

English

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publication date

20 January 2010

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published in

The EMBO Journal

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volume

29

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issue

2

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page(s)

363-75

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cites work

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A membrane protein complex mediates retro-translocation from the ER lumen into the cytosol

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A membrane protein required for dislocation of misfolded proteins from the ER

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A novel ER alpha-mannosidase-like protein accelerates ER-associated degradation

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Alternative conformations of the x region of human protein disulphide-isomerase modulate exposure of the substrate binding b' domain

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Antigen presentation subverted: Structure of the human cytomegalovirus protein US2 bound to the class I molecule HLA-A2

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Roles of protein-disulfide isomerase-mediated disulfide bond formation of yeast Mnl1p in endoplasmic reticulum-associated degradation

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Signal peptide peptidase is required for dislocation from the endoplasmic reticulum

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The human cytomegalovirus US11 gene product dislocates MHC class I heavy chains from the endoplasmic reticulum to the cytosol

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Signal peptide peptidase (SPP) dimer formation as assessed by fluorescence lifetime imaging microscopy (FLIM) in intact cells

27 September 2017

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Derlin-1 promotes the efficient degradation of the cystic fibrosis transmembrane conductance regulator (CFTR) and CFTR folding mutants

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Ubiquitination of MHC class I heavy chains is essential for dislocation by human cytomegalovirus-encoded US2 but not US11.

27 September 2017

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Protein disulfide isomerase-like proteins play opposing roles during retrotranslocation

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27 September 2017

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Subtle sequence variation among MHC class I locus products greatly influences sensitivity to HCMV US2- and US11-mediated degradation

27 September 2017

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Human cytomegalovirus-encoded US2 and US11 target unassembled MHC class I heavy chains for degradation

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Human cytomegalovirus-encoded US2 differentially affects surface expression of MHC class I locus products and targets membrane-bound, but not soluble HLA-G1 for degradation

27 September 2017

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27 September 2017

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Human cytomegalovirus US3 chimeras containing US2 cytosolic residues acquire major histocompatibility class I and II protein degradation properties

27 September 2017

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27 September 2017

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27 September 2017

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Human cytomegalovirus US2 endoplasmic reticulum-lumenal domain dictates association with major histocompatibility complex class I in a locus-specific manner

27 September 2017

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Export of a cysteine-free misfolded secretory protein from the endoplasmic reticulum for degradation requires interaction with protein disulfide isomerase

27 September 2017

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Dislocation of type I membrane proteins from the ER to the cytosol is sensitive to changes in redox potential

27 September 2017

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The HCMV gene products US11 and US2 differ in their ability to attack allelic forms of murine major histocompatibility complex (MHC) class I heavy chains

27 September 2017

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Protein disulfide isomerase. A multifunctional protein resident in the lumen of the endoplasmic reticulum

27 September 2017

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Simian Virus 40 depends on ER protein folding and quality control factors for entry into host cells

27 September 2017

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Real-time fluorescence detection of ERAD substrate retrotranslocation in a mammalian in vitro system.

30 May 2018

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A misassembled transmembrane domain of a polytopic protein associates with signal peptide peptidase

30 May 2018

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EDEM contributes to maintenance of protein folding efficiency and secretory capacity.

30 May 2018

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Ubiquitinylation of the cytosolic domain of a type I membrane protein is not required to initiate its dislocation from the endoplasmic reticulum

21 January 2018

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https://api.crossref.org/works/10.1038%2FEMBOJ.2009.359

The MHC class I homolog of human cytomegalovirus is resistant to down-regulation mediated by the unique short region protein (US)2, US3, US6, and US11 gene products.

21 January 2018

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Molecular characterization of the principal substrate binding site of the ubiquitous folding catalyst protein disulfide isomerase

21 January 2018

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Use of modular substrates demonstrates mechanistic diversity and reveals differences in chaperone requirement of ERAD.

21 January 2018

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US2, a Human Cytomegalovirus-encoded Type I Membrane Protein, Contains a Non-cleavable Amino-terminal Signal Peptide

21 January 2018

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Protein Disulfide Isomerase Acts as a Redox-Dependent Chaperone to Unfold Cholera Toxin

21 January 2018

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PURIFICATION AND PROPERTIES OF A MICROSOMAL ENZYME SYSTEM CATALYZING THE REACTIVATION OF REDUCED RIBONUCLEASE AND LYSOZYME

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19942855

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Lectins sweet-talk proteins into ERAD

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19942855

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EMBOJ.2009.359

1 reference

1879838

1879838

1 reference

1 reference

1 reference