(Q28264819)

English

UDP-N-acetylglucosamine:lysosomal enzyme precursor N-acetylglucosamine-1-phosphotransferase. Partial purification and characterization of the rat liver Golgi enzyme

scientific article published on October 25, 1982

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30 October 2019

UDP-N-acetylglucosamine:lysosomal enzyme precursor N-acetylglucosamine-1-phosphotransferase. Partial purification and characterization of the rat liver Golgi enzyme (English)

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30 October 2019

Transferases (Other Substituted Phosphate Groups)

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17 September 2023

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10.1016/S0021-9258(18)33717-7

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17 September 2023

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17 September 2023

author name string

A. Waheed

1

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17 September 2023

A. Hasilik

2

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17 September 2023

K. von Figura

3

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1 October 1982

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30 October 2019

25 October 1982

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6288715

17 September 2023

full work available at URL

http://intl.jbc.org/cgi/content/abstract/257/20/12322

online access status

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17 September 2023

https://api.elsevier.com/content/article/PII:S0021925818337177?httpAccept=text/xml

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Journal of Biological Chemistry

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30 October 2019

257

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30 October 2019

12322-12331

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30 October 2019

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30 October 2019

Enzymatic phosphorylation of lysosomal enzymes in the presence of UDP-N-acetylglucosamine. Absence of the activity in I-cell fibroblasts

3

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Phosphorylation of lysosomal enzymes in fibroblasts. Marked deficiency of N-acetylglucosamine-1-phosphotransferase in fibroblasts of patients with mucolipidosis III

5

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Phosphorylated oligosaccharides in lysosomal enzymes: identification of alpha-N-acetylglucosamine(1)phospho(6)mannose diester groups

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

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Enhanced breakdown of arylsulfatase A in multiple sulfatase deficiency

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Synthesis and Processing of Arylsulfatase A in Human Skin Fibroblasts

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Human alpha-N-acetylglucosaminidase. 1. Purification and properties

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A method for rapid isolation of rough and smooth microsomes and Golgi apparatus from rat liver in the same sucrose gradient

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Galactose metabolism in regenerating rat liver

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Studies on uridine-diphosphate-glucose

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DIFFERENTIATION IN VITRO OF EMBRYONIC CARTILAGE AND BONE IN A CHEMICALLY-DEFINED MEDIUM

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The defect in Hurler and Hunter syndromes. II. Deficiency of specific factors involved in mucopolysaccharide degradation

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Structural studies of urinary oligosaccharides from patients with mannosidosis

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Protein measurement with the Folin phenol reagent

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Enzymatic identification of mannose 6-phosphate on the recognition marker for receptor-mediated pinocytosis of beta-glucuronidase by human fibroblasts

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Identification of mannose 6-phosphate in glycoproteins that inhibit the assimilation of β-galactosidase by fibroblasts

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Oligosaccharides in lysosomal enzymes. Distribution of high-mannose and complex oligosaccharides in cathepsin D and beta-hexosaminidase

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Impaired Phosphorylation of Lysosomal Enzymes in Fibroblasts of Patients with Mucolipidosis III

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

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Is there a mechanism for introducing acid hydrolases into liver lysosomes that is independent of mannose 6-phosphate recognition? Evidence from I-cell disease

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Identifiers

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30 October 2019

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