A unique carbohydrate binding domain targets the lafora disease phosphatase to glycogen (Q29347520)

11 April 2017

A unique carbohydrate binding domain targets the lafora disease phosphatase to glycogen (English)

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11 April 2017

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4

Jack E Dixon

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11 April 2017

Jianyong Wang

1

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11 April 2017

Jeanne A Stuckey

series ordinal

2

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11 April 2017

Matthew J Wishart

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3

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11 April 2017

language of work or name

English

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publication date

5 December 2001

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Journal of Biological Chemistry

11 April 2017

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11 April 2017

277

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4

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11 April 2017

2377-2380

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Lafora's disease: towards a clinical, pathologic, and molecular synthesis

11 April 2017

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https://api.crossref.org/works/10.1074%2FJBC.C100686200

Lafora's disease. Comparison of inclusion bodies in skin and in brain.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.C100686200

Axilla skin biopsy: a reliable test for the diagnosis of Lafora's disease

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.C100686200

Diagnosis by axilla skin biopsy in an early case of Lafora's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C100686200

Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.C100686200

A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C100686200

Form and function in protein dephosphorylation

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.C100686200

Laforin, defective in the progressive myoclonus epilepsy of Lafora type, is a dual-specificity phosphatase associated with polyribosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C100686200

Myotubularin, a protein tyrosine phosphatase mutated in myotubular myopathy, dephosphorylates the lipid second messenger, phosphatidylinositol 3-phosphate

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C100686200

The activity of Cdc14p, an oligomeric dual specificity protein phosphatase from Saccharomyces cerevisiae, is required for cell cycle progression

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.C100686200

An assay for phosphoinositide phosphatases utilizing fluorescent substrates

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.C100686200

Sequence homology between putative raw-starch binding domains from different starch-degrading enzymes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C100686200

Protein engineering in the alpha-amylase family: catalytic mechanism, substrate specificity, and stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C100686200

Glucoamylase: structure/function relationships, and protein engineering

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.C100686200

Identification of binding sites on protein targeting to glycogen for enzymes of glycogen metabolism.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.C100686200

Organizing glucose disposal: emerging roles of the glycogen targeting subunits of protein phosphatase-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C100686200

Improved methods for building protein models in electron density maps and the location of errors in these models

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C100686200

The regulation of glycogen synthase by protein phosphatase 1 in 3T3-L1 adipocytes. Evidence for a potential role for DARPP-32 in insulin action.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C100686200

The role of glucose metabolites in the activation and translocation of glycogen synthase by insulin in 3T3-L1 adipocytes

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.C100686200

Glucose induces the translocation of glycogen synthase to the cell cortex in rat hepatocytes

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.C100686200

Glycogen storage diseases. Phenotypic, genetic, and biochemical characteristics, and therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C100686200

Mutational spectrum of the EPM2A gene in progressive myoclonus epilepsy of Lafora: high degree of allelic heterogeneity and prevalence of deletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.C100686200

21 January 2018

Identifiers

DOI

10.1074/JBC.C100686200

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11 April 2017

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