Glycosylation- and phosphorylation-dependent intracellular transport of lysosomal hydrolases (Q37474851)

20 August 2017

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title

Glycosylation- and phosphorylation-dependent intracellular transport of lysosomal hydrolases (English)

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20 August 2017

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Sandra Pohl

1

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20 August 2017

Katrin Marschner

series ordinal

2

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20 August 2017

Stephan Storch

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3

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20 August 2017

Thomas Braulke

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4

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20 August 2017

language of work or name

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1 July 2009

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20 August 2017

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20 August 2017

390

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20 August 2017

521-527

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20 August 2017

7

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Lysosomal disorders: from storage to cellular damage

20 August 2017

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https://api.crossref.org/works/10.1515%2FBC.2009.076

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Sorting of lysosomal proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Molecular analysis of the GlcNac-1-phosphotransferase

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Lysine-based structure in the proregion of procathepsin L is the recognition site for mannose phosphorylation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Strategies for carbohydrate recognition by the mannose 6-phosphate receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Heparan N-sulfatase: in vitro mutagenesis of potential N-glycosylation sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Cloning and sequence analysis of cDNA for human cathepsin D

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Functional characterization of the N-glycosylation sites of human acid sphingomyelinase by site-directed mutagenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Mannose 6-phosphate receptors: new twists in the tale

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Mannose 6-phosphate-independent targeting of lysosomal enzymes in I-cell disease B lymphoblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Localization of the carbohydrate recognition sites of the insulin-like growth factor II/mannose 6-phosphate receptor to domains 3 and 9 of the extracytoplasmic region

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Cellular uptake of saposin (SAP) precursor and lysosomal delivery by the low density lipoprotein receptor-related protein (LRP).

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Overexpression of human alpha-galactosidase A results in its intracellular aggregation, crystallization in lysosomes, and selective secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Assembly of asparagine-linked oligosaccharides

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

The biogenesis of lysosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Molecular cloning and functional expression of two splice forms of human N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Structural requirements for efficient processing and activation of recombinant human UDP-N-acetylglucosamine:lysosomal-enzyme-N-acetylglucosamine-1-phosphotransferase

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

The alpha- and beta-subunits of the human UDP-N-acetylglucosamine:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase [corrected] are encoded by a single cDNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Mucolipidosis II (I-cell disease) and mucolipidosis IIIA (classical pseudo-hurler polydystrophy) are caused by mutations in the GlcNAc-phosphotransferase alpha / beta -subunits precursor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Murine UDP-GlcNAc:lysosomal enzyme N-acetylglucosamine-1-phosphotransferase lacking the gamma-subunit retains substantial activity toward acid hydrolases

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

The lysosomal trafficking of sphingolipid activator proteins (SAPs) is mediated by sortilin

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Recognition of Dictyostelium discoideum lysosomal enzymes is conferred by the amino-terminal carbohydrate binding site of the insulin-like growth factor II/mannose 6-phosphate receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Secretion of phosphomannosyl-deficient arylsulphatase A and cathepsin D from isolated human macrophages

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Transport, enzymatic activity, and stability of mutant sulfamidase (SGSH) identified in patients with mucopolysaccharidosis type III A

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

alpha-Mannosidosis: functional cloning of the lysosomal alpha-mannosidase cDNA and identification of a mutation in two affected siblings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Human alpha-N-acetylgalactosaminidase: site occupancy and structure of N-linked oligosaccharides

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Mucolipidosis II and III alpha/beta: mutation analysis of 40 Japanese patients showed genotype-phenotype correlation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Role of N-oligosaccharide endoplasmic reticulum processing reactions in glycoprotein folding and degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

The two mannose 6-phosphate receptors transport distinct complements of lysosomal proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Molecular basis of variant pseudo-hurler polydystrophy (mucolipidosis IIIC)

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

LIMP-2 is a receptor for lysosomal mannose-6-phosphate-independent targeting of beta-glucocerebrosidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Fibroblasts from patients with I-cell disease and pseudo-Hurler polydystrophy are deficient in uridine 5'-diphosphate-N-acetylglucosamine: glycoprotein N-acetylglucosaminylphosphotransferase activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Glycosylation of a membrane protein is restricted to the growing polypeptide chain but is not necessary for insertion as a transmembrane protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

N-glycan processing in ER quality control

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Molecular and cellular basis of lysosomal transmembrane protein dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

The N370S (Asn370-->Ser) mutation affects the capacity of glucosylceramidase to interact with anionic phospholipid-containing membranes and saposin C

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Localization of the insulin-like growth factor II binding site to amino acids 1508-1566 in repeat 11 of the mannose 6-phosphate/insulin-like growth factor II receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

A novel mutation in UDP-N-acetylglucosamine-1-phosphotransferase gamma subunit (GNPTAG) in two siblings with mucolipidosis type III alters a used glycosylation site

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Mucolipidosis II is caused by mutations in GNPTA encoding the alpha/beta GlcNAc-1-phosphotransferase

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Missense mutation in the N-acetylglucosamine-1-phosphotransferase gene (GNPTA) in a patient with mucolipidosis II induces changes in the size and cellular distribution of GNPTG.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Mutation of the glycosylated asparagine residue 286 in human CLN2 protein results in loss of enzymatic activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Imaging and imagination: understanding the endo-lysosomal system

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

Deficiency of UDP-N-acetylglucosamine: Lysosomal enzyme N-acetylglucosamine-1-phosphotransferase in organs of I-cell patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2009.076

21 January 2018

Identifiers

DOI

10.1515/BC.2009.076

1 reference

20 August 2017

1 reference