Processing of normal lysosomal and mutant N-acetylgalactosamine 4-sulphatase: BiP (immunoglobulin heavy-chain binding protein) may interact with critical protein contact sites. (Q38323505)

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English	Processing of normal lysosomal and mutant N-acetylgalactosamine 4-sulphatase: BiP (immunoglobulin heavy-chain binding protein) may interact with critical protein contact sites.	scientific article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10377262%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

Processing of normal lysosomal and mutant N-acetylgalactosamine 4-sulphatase: BiP (immunoglobulin heavy-chain binding protein) may interact with critical protein contact sites (English)

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9 December 2019

5

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9 December 2019

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Bradford TM

1

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9 December 2019

Gething MJ

2

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9 December 2019

Davey R

3

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9 December 2019

Hopwood JJ

4

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9 December 2019

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1 July 1999

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9 December 2019

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9

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Biochemical Journal

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9 December 2019

341 ( Pt 1)

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9 December 2019

193-201

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9 December 2019

HSP70 binding sites in the tumor suppressor protein p53.

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6 September 2017

Structure of 20S proteasome from yeast at 2.4 A resolution

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6 September 2017

Structure of a human lysosomal sulfatase

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6 September 2017

Identification, expression, and biochemical characterization of N-acetylgalactosamine-4-sulfatase mutations and relationship with clinical phenotype in MPS-VI patients

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6 September 2017

Review: the immunochemical analysis of enzyme from mucopolysaccharidoses patients.

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6 September 2017

Juvenile form of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). A C-terminal extension causes instability but increases catalytic efficiency of arylsulfatase B.

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6 September 2017

Affinity panning of a library of peptides displayed on bacteriophages reveals the binding specificity of BiP.

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6 September 2017

Two site-directed mutations abrogate enzyme activity but have different effects on the conformation and cellular content of the N-acetylgalactosamine 4-sulphatase protein

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6 September 2017

Participation of the endoplasmic reticulum chaperone calnexin (p88, IP90) in the biogenesis of the cystic fibrosis transmembrane conductance regulator

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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6 September 2017

A shortened beta-hexosaminidase alpha-chain in an Italian patient with infantile Tay-Sachs disease

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6 September 2017

Two mutations produce intron insertion in mRNA and elongated beta-subunit of human beta-hexosaminidase

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6 September 2017

The mucopolysaccharidoses. Diagnosis, molecular genetics and treatment.

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6 September 2017

Analysis of N-acetylgalactosamine-4-sulfatase protein and kinetics in mucopolysaccharidosis type VI patients

1 reference

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6 September 2017

Analysis of the glycosylation and phosphorylation of the alpha-subunit of the lysosomal enzyme, beta-hexosaminidase A, by site-directed mutagenesis

1 reference

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6 September 2017

Defective protein folding as a basis of human disease

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27 September 2017

Immunoglobulin heavy chain-binding protein binds to misfolded mutant insulin receptors with mutations in the extracellular domain

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27 September 2017

ER quality control: the cytoplasmic connection

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27 September 2017

Protein processing: a role in the pathophysiology of genetic disease.

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23 June 2018

Two mutations affecting the transport and maturation of lysosomal alpha-glucosidase in an adult case of glycogen storage disease type II.

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23 June 2018

Mutant (delta F508) cystic fibrosis transmembrane conductance regulator Cl- channel is functional when retained in endoplasmic reticulum of mammalian cells.

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23 June 2018

Human N-acetylgalactosamine-4-sulphate sulphatase. Purification, monoclonal antibody production and native and subunit Mr values

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23 June 2018

Identification of immunoglobulin heavy chain binding protein as glucose-regulated protein 78 on the basis of amino acid sequence, immunological cross-reactivity, and functional activity

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23 June 2018

Juvenile GM2 gangliosidosis caused by substitution of histidine for arginine at position 499 or 504 of the alpha-subunit of beta-hexosaminidase

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23 June 2018

Human N-acetylgalactosamine-4-sulphatase biosynthesis and maturation in normal, Maroteaux-Lamy and multiple-sulphatase-deficient fibroblasts.

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23 June 2018

Hurler syndrome: A patient with abnormally high levels of α-l-iduronidase protein

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23 June 2018

Components and proteolytic processing sites of arylsulfatase B from human placenta

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23 June 2018

Disulfide bond formation during the folding of influenza virus hemagglutinin

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23 June 2018

Cutting complexity down to size.

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31 August 2018

Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation.

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31 August 2018

BiP binding sequences in antibodies.

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31 August 2018

BiP binds type I procollagen pro alpha chains with mutations in the carboxyl-terminal propeptide synthesized by cells from patients with osteogenesis imperfecta

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https://pubmed.ncbi.nlm.nih.gov/10377262

12 December 2020

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Carbohydrate-deficient glycoprotein syndrome (CDGS)--glycosylation, folding and intracellular transport of newly synthesized glycoproteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/10377262

12 December 2020

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Protein C Nagoya, an elongated mutant of protein C, is retained within the endoplasmic reticulum and is associated with GRP78 and GRP94

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Binding sites for Hsp70 molecular chaperones in natural proteins

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https://pubmed.ncbi.nlm.nih.gov/10377262

12 December 2020

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Biosynthesis of human alpha-N-acetylgalactosaminidase: defective phosphorylation and maturation in infantile alpha-NAGA deficiency

1 reference

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12 December 2020

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Identifiers

10.1042/0264-6021:3410193

1 reference

Europe PubMed Central

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2 September 2017

10.1042/BJ3410193

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10377262%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

PMC publication ID

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Europe PubMed Central

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9 December 2019

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Europe PubMed Central

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9 December 2019

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