Lafora disease: insights into neurodegeneration from plant metabolism. - Wikidata - wikimedia - TriplyDB

Lafora disease: insights into neurodegeneration from plant metabolism.

Lafora disease: insights into neurodegeneration from plant metabolism.

http://www.wikidata.org/entity/Q37612219

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Starch binding domain-containing protein 1/genethonin 1 is a novel participant in glycogen metabolism Genetics of Lafora progressive myoclonic epilepsy: current perspectives Are there errors in glycogen biosynthesis and is laforin a repair enzyme?Structural basis for the glucan phosphatase activity of Starch Excess4 Structural and functional analysis of PTPMT1, a phosphatase required for cardiolipin synthesis Structure of the Arabidopsis Glucan Phosphatase LIKE SEX FOUR2 Reveals a Unique Mechanism for Starch Dephosphorylation Phosphoglucan-bound structure of starch phosphatase Starch Excess4 reveals the mechanism for C6 specificity Phosphate incorporation during glycogen synthesis and Lafora disease Starch-binding domain-containing protein 1 (Stbd1) and glycogen metabolism: Identification of the Atg8 family interacting motif (AIM) in Stbd1 required for interaction with GABARAPL1 Loss of GABAergic cortical neurons underlies the neuropathology of Lafora disease Structural mechanism of laforin function in glycogen dephosphorylation and lafora disease.Origin and diversification of TRIM ubiquitin ligases.Lafora disease E3-ubiquitin ligase malin is related to TRIM32 at both the phylogenetic and functional level Laforin, a dual specificity phosphatase involved in Lafora disease, is present mainly as monomeric form with full phosphatase activity The laforin-malin complex, involved in Lafora disease, promotes the incorporation of K63-linked ubiquitin chains into AMP-activated protein kinase beta subunits.Genetic depletion of the malin E3 ubiquitin ligase in mice leads to lafora bodies and the accumulation of insoluble laforin Insights into the mechanism of polysaccharide dephosphorylation by a glucan phosphatase Dimerization of Vaccinia virus VH1 is essential for dephosphorylation of STAT1 at tyrosine 701.Dimerization of the glucan phosphatase laforin requires the participation of cysteine 329.Glycogen phosphomonoester distribution in mouse models of the progressive myoclonic epilepsy, Lafora disease.Expression, purification and characterization of soluble red rooster laforin as a fusion protein in Escherichia coli.[When skin biopsy may label an epilepsy].Laforin, a dual-specificity phosphatase involved in Lafora disease, is phosphorylated at Ser25 by AMP-activated protein kinase.Laforin, a protein with many faces: glucan phosphatase, adapter protein, et alii.Muscle glycogen remodeling and glycogen phosphate metabolism following exhaustive exercise of wild type and laforin knockout mice.Modular evolution of phosphorylation-based signalling systems.Deciphering the role of malin in the lafora progressive myoclonus epilepsy Mechanistic Insights into Glucan Phosphatase Activity against Polyglucan Substrates Structural mechanisms of plant glucan phosphatases in starch metabolism Glycogen and its metabolism: some new developments and old themes.A bioassay for Lafora disease and laforin glucan phosphatase activity.Modeling human neurodegenerative diseases in transgenic systems.Protein tyrosine phosphatases in health and disease.Glycogen phosphorylation and Lafora disease.Remarkable evolutionary relatedness among the enzymes and proteins from the α-amylase family.Structural biology of glucan phosphatases from humans to plants The crucial role of protein phosphorylation in cell signaling and its use as targeted therapy (Review).Exploring the structural insights on human laforin mutation K87A in Lafora disease--a molecular dynamics study.Incorporation of phosphate into glycogen by glycogen synthase Laforin and malin knockout mice have normal glucose disposal and insulin sensitivity.

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Lafora disease: insights into neurodegeneration from plant metabolism.

http://www.wikidata.org/entity/Q37612219

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 07 October 2009

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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Lafora disease: insights into neurodegeneration from plant metabolism.

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Lafora disease: insights into neurodegeneration from plant metabolism.

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Lafora disease: insights into neurodegeneration from plant metabolism.

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Lafora disease: insights into neurodegeneration from plant metabolism.

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Lafora disease: insights into neurodegeneration from plant metabolism.

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Lafora disease: insights into neurodegeneration from plant metabolism.

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J.TIBS.2009.08.002

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Trends in Biochemical Sciences

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Lafora disease: insights into neurodegeneration from plant metabolism.

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Carolyn A Worby

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Jack E Dixon

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Matthew S Gentry

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P2860

Ciliate genome sequence reveals unique features of a model eukaryote

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

F ROM B ACTERIAL G LYCOGEN TO S TARCH : Understanding the Biogenesis of the Plant Starch Granule

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

A role for AGL ubiquitination in the glycogen storage disorders of Lafora and Cori's disease

Malin decreases glycogen accumulation by promoting the degradation of protein targeting to glycogen (PTG)

Insights into Lafora disease: malin is an E3 ubiquitin ligase that ubiquitinates and promotes the degradation of laforin.

The starch-related R1 protein is an alpha -glucan, water dikinase.

The Arabidopsis sex1 mutant is defective in the R1 protein, a general regulator of starch degradation in plants, and not in the chloroplast hexose transporter

Identification of a novel enzyme required for starch metabolism in Arabidopsis leaves. The phosphoglucan, water dikinase

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10.1016/J.TIBS.2009.08.002

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12

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2009-10-07T00:00:00Z

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