N-glycosylation is crucial for folding, trafficking, and stability of human tripeptidyl-peptidase I. (Q38346370)

2 September 2017

N-glycosylation is crucial for folding, trafficking, and stability of human tripeptidyl-peptidase I. (English)

1 reference

2 September 2017

1 reference

Peter Wujek

1

1 reference

2 September 2017

Elizabeth Kida

2

1 reference

2 September 2017

Marius Walus

3

1 reference

2 September 2017

Krystyna E Wisniewski

4

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2 September 2017

Adam A Golabek

5

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2 September 2017

language of work or name

English

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publication date

31 December 2003

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Journal of Biological Chemistry

2 September 2017

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2 September 2017

279

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2 September 2017

13

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2 September 2017

12827-12839

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Purification and characterisation of a tripeptidyl aminopeptidase I from rat spleen.

2 September 2017

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

The substrate range of tripeptidyl-peptidase I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Characterization of endopeptidase activity of tripeptidyl peptidase-I/CLN2 protein which is deficient in classical late infantile neuronal ceroid lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Mutational analysis of the defective protease in classic late-infantile neuronal ceroid lipofuscinosis, a neurodegenerative lysosomal storage disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Distribution of tripeptidyl peptidase I in human tissues under normal and pathological conditions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

A novel assay for lysosomal pepstatin-insensitive proteinase and its application for the diagnosis of late-infantile neuronal ceroid lipofuscinosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Purification and characterization of bovine brain lysosomal pepstatin-insensitive proteinase, the gene product deficient in the human late-infantile neuronal ceroid lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Rat tripeptidyl peptidase I: molecular cloning, functional expression, tissue localization and enzymatic characterization

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

A lysosomal proteinase, the late infantile neuronal ceroid lipofuscinosis gene (CLN2) product, is essential for degradation of a hydrophobic protein, the subunit c of ATP synthase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Structural organization and sequence of CLN2, the defective gene in classical late infantile neuronal ceroid lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

The human CLN2 protein/tripeptidyl-peptidase I is a serine protease that autoactivates at acidic pH

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Production and characterization of recombinant human CLN2 protein for enzyme-replacement therapy in late infantile neuronal ceroid lipofuscinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Biosynthesis, glycosylation, and enzymatic processing in vivo of human tripeptidyl-peptidase I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Carboxyl proteinase from Pseudomonas defines a novel family of subtilisin-like enzymes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

The biogenesis of lysosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Human alpha-galactosidase A: glycosylation site 3 is essential for enzyme solubility

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Functional analysis of the glycosylation of murine acid sphingomyelinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Late infantile neuronal ceroid lipofuscinosis: quantitative description of the clinical course in patients with CLN2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Site-directed mutagenesis by overlap extension using the polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Protein glucosylation and its role in protein folding

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Glycosidases of the asparagine-linked oligosaccharide processing pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Retro-translocation of proteins from the endoplasmic reticulum into the cytosol

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Protein oligomerization in the endoplasmic reticulum

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Lactacystin and clasto-lactacystin beta-lactone modify multiple proteasome beta-subunits and inhibit intracellular protein degradation and major histocompatibility complex class I antigen presentation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Comparison of cathepsin L synthesized by normal and transformed cells at the gene, message, protein, and oligosaccharide levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Human lysosomal alpha-glucosidase: functional characterization of the glycosylation sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Quality control in the endoplasmic reticulum

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Human acid ceramidase: processing, glycosylation, and lysosomal targeting

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

21 January 2018

Co-translational folding

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

ER quality control: towards an understanding at the molecular level

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Glycoprotein quality control in the endoplasmic reticulum. Mannose trimming by endoplasmic reticulum mannosidase I times the proteasomal degradation of unassembled immunoglobulin subunits

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Role of EDEM in the release of misfolded glycoproteins from the calnexin cycle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

EDEM as an acceptor of terminally misfolded glycoproteins released from calnexin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Enhancement of endoplasmic reticulum (ER) degradation of misfolded Null Hong Kong alpha1-antitrypsin by human ER mannosidase I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Endoplasmic reticulum-associated degradation of mammalian glycoproteins involves sugar chain trimming to Man6-5GlcNAc2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Glucosidase and mannosidase inhibitors mediate increased secretion of mutant alpha1 antitrypsin Z.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Misfolded major histocompatibility complex class I heavy chains are translocated into the cytoplasm and degraded by the proteasome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Identification of proteins that interact with mammalian peptide:N-glycanase and implicate this hydrolase in the proteasome-dependent pathway for protein degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Generation of a lysosomal enzyme targeting signal in the secretory protein pepsinogen.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Lysine-based structure responsible for selective mannose phosphorylation of cathepsin D and cathepsin L defines a common structural motif for lysosomal enzyme targeting.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Role of N-linked oligosaccharide flexibility in mannose phosphorylation of lysosomal enzyme cathepsin L.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Structure and function of the mannose 6-phosphate/insulinlike growth factor II receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Twists and turns of the cation-dependent mannose 6-phosphate receptor. Ligand-bound versus ligand-free receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

Neither type of mannose 6-phosphate receptor is sufficient for targeting of lysosomal enzymes along intracellular routes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M313173200

21 January 2018

Identifiers

DOI

10.1074/JBC.M313173200

1 reference

2 September 2017

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