Oligosaccharide modification in the early secretory pathway directs the selection of a misfolded glycoprotein for degradation by the proteasome (Q33852597)

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English	Oligosaccharide modification in the early secretory pathway directs the selection of a misfolded glycoprotein for degradation by the proteasome	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

29 July 2017

Oligosaccharide modification in the early secretory pathway directs the selection of a misfolded glycoprotein for degradation by the proteasome (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

oligosaccharide

1 reference

based on heuristic

inferred from title

author name string

Liu Y

1

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Choudhury P

2

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Cabral CM

3

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Sifers RN

4

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

language of work or name

0 references

publication date

1 February 1999

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Europe PubMed Central

PubMed publication ID

29 July 2017

Journal of Biological Chemistry

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Europe PubMed Central

PubMed publication ID

29 July 2017

274

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

5861-5867

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Protein translocation across the endoplasmic reticulum

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Protein folding in the cell

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Principles that govern the folding of protein chains

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Protein degradation in the endoplasmic reticulum

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Quality control in the secretory pathway

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Proteasomes: multicatalytic proteinase complexes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Degradation of CFTR by the ubiquitin-proteasome pathway

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

ER degradation of a misfolded luminal protein by the cytosolic ubiquitin-proteasome pathway

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Proteasome-dependent endoplasmic reticulum-associated protein degradation: an unconventional route to a familiar fate

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Sec61-mediated transfer of a membrane protein from the endoplasmic reticulum to the proteasome for destruction

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

ER quality control: the cytoplasmic connection

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Ubiquitination is required for the retro-translocation of a short-lived luminal endoplasmic reticulum glycoprotein to the cytosol for degradation by the proteasome

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

The molecular chaperone calnexin binds Glc1Man9GlcNAc2 oligosaccharide as an initial step in recognizing unfolded glycoproteins

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Assembly of ER-associated protein degradation in vitro: dependence on cytosol, calnexin, and ATP.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Defective protein folding as a basis of human disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Intracellular disposal of incompletely folded human alpha1-antitrypsin involves release from calnexin and post-translational trimming of asparagine-linked oligosaccharides

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

The endoplasmic reticulum degradation pathway for mutant secretory proteins alpha1-antitrypsin Z and S is distinct from that for an unassembled membrane protein

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

A lag in intracellular degradation of mutant alpha 1-antitrypsin correlates with the liver disease phenotype in homozygous PiZZ alpha 1-antitrypsin deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Association of folding intermediates of glycoproteins with calnexin during protein maturation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Novel aspects of degradation of T cell receptor subunits from the endoplasmic reticulum (ER) in T cells: importance of oligosaccharide processing, ubiquitination, and proteasome-dependent removal from ER membranes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Degradation of misfolded endoplasmic reticulum glycoproteins in Saccharomyces cerevisiae is determined by a specific oligosaccharide structure

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

How N-linked oligosaccharides affect glycoprotein folding in the endoplasmic reticulum

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

What do dysfunctional serpins tell us about molecular mobility and disease?

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Multiple proteolytic systems, including the proteasome, contribute to CFTR processing

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Inhibition of proteasome activities and subunit-specific amino-terminal threonine modification by lactacystin

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Glycosidases of the asparagine-linked oligosaccharide processing pathway

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Endoplasmic reticulum kifunensine-resistant alpha-mannosidase is enzymatically and immunologically related to the cytosolic alpha-mannosidase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Conformation-independent binding of monoglucosylated ribonuclease B to calnexin

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Glucose trimming and reglucosylation determine glycoprotein association with calnexin in the endoplasmic reticulum

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Role of N-linked oligosaccharide recognition, glucose trimming, and calnexin in glycoprotein folding and quality control

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.9.5861

21 January 2018

Identifiers

10.1074/JBC.274.9.5861

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

ResearchGate publication ID

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