Laforin, a protein with many faces: glucan phosphatase, adapter protein, et alii. (Q36020483)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22364389%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

title

Laforin, a protein with many faces: glucan phosphatase, adapter protein, et alii (English)

1 reference

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24 January 2020

1 reference

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24 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22364389%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

Matthew S Gentry

1 reference

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24 January 2020

language of work or name

English

0 references

publication date

16 March 2012

1 reference

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24 January 2020

1 reference

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24 January 2020

volume

280

1 reference

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24 January 2020

issue

1 reference

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24 January 2020

page(s)

525-537

1 reference

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Structural and evolutionary aspects of two families of non-catalytic domains present in starch and glycogen binding proteins from microbes, plants and animals

24 January 2020

cites work

1 reference

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Identification and characterization of novel splice variants of the human EPM2A gene mutated in Lafora progressive myoclonus epilepsy

2 October 2017

1 reference

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Laforin, a dual specificity phosphatase involved in Lafora disease, is present mainly as monomeric form with full phosphatase activity

2 October 2017

1 reference

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Neurodegeneration and functional impairments associated with glycogen synthase accumulation in a mouse model of Lafora disease

2 October 2017

1 reference

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Lafora disease E3-ubiquitin ligase malin is related to TRIM32 at both the phylogenetic and functional level

2 October 2017

1 reference

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Laforin, a dual-specificity phosphatase involved in Lafora disease, is phosphorylated at Ser25 by AMP-activated protein kinase.

2 October 2017

1 reference

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Malin and laforin are essential components of a protein complex that protects cells from thermal stress

2 October 2017

1 reference

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PTG depletion removes Lafora bodies and rescues the fatal epilepsy of Lafora disease

2 October 2017

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Phosphate incorporation during glycogen synthesis and Lafora disease

2 October 2017

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Genetic depletion of the malin E3 ubiquitin ligase in mice leads to lafora bodies and the accumulation of insoluble laforin

2 October 2017

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The laforin-malin complex, involved in Lafora disease, promotes the incorporation of K63-linked ubiquitin chains into AMP-activated protein kinase beta subunits.

2 October 2017

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Laforin, the most common protein mutated in Lafora disease, regulates autophagy

2 October 2017

1 reference

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Co-chaperone CHIP stabilizes aggregate-prone malin, a ubiquitin ligase mutated in Lafora disease

2 October 2017

1 reference

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Lafora disease: insights into neurodegeneration from plant metabolism

2 October 2017

1 reference

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Conservation of the glucan phosphatase laforin is linked to rates of molecular evolution and the glucan metabolism of the organism

2 October 2017

1 reference

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Hyperphosphorylation and aggregation of Tau in laforin-deficient mice, an animal model for Lafora disease.

2 October 2017

1 reference

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Increased endoplasmic reticulum stress and decreased proteasomal function in lafora disease models lacking the phosphatase laforin

2 October 2017

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RING domain E3 ubiquitin ligases

2 October 2017

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Deletions and missense mutations of EPM2A exacerbate unfolded protein response and apoptosis of neuronal cells induced by endoplasm reticulum stress

2 October 2017

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Lafora progressive myoclonus epilepsy: a meta-analysis of reported mutations in the first decade following the discovery of the EPM2A and NHLRC1 genes

2 October 2017

1 reference

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AMP-activated protein kinase phosphorylates R5/PTG, the glycogen targeting subunit of the R5/PTG-protein phosphatase 1 holoenzyme, and accelerates its down-regulation by the laforin-malin complex

2 October 2017

1 reference

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Evolution of protein phosphatases in plants and animals

2 October 2017

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Debate: Does genetic information in humans help us treat patients? PRO--genetic information in humans helps us treat patients. CON--genetic information does not help at all.

2 October 2017

1 reference

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The Carbohydrate-Active EnZymes database (CAZy): an expert resource for Glycogenomics

2 October 2017

1 reference

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Laforin negatively regulates cell cycle progression through glycogen synthase kinase 3beta-dependent mechanisms.

2 October 2017

1 reference

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Modulation of functional properties of laforin phosphatase by alternative splicing reveals a novel mechanism for the EPM2A gene in Lafora progressive myoclonus epilepsy

2 October 2017

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Atypical ubiquitin chains: new molecular signals. 'Protein Modifications: Beyond the Usual Suspects' review series

2 October 2017

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

2 October 2017

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Laforin is a glycogen phosphatase, deficiency of which leads to elevated phosphorylation of glycogen in vivo.

2 October 2017

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Regulation of glycogen synthesis by the laforin-malin complex is modulated by the AMP-activated protein kinase pathway

2 October 2017

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

2 October 2017

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Advances in lafora progressive myoclonus epilepsy

2 October 2017

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The phosphatase laforin crosses evolutionary boundaries and links carbohydrate metabolism to neuronal disease.

2 October 2017

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Lafora disease proteins malin and laforin are recruited to aggresomes in response to proteasomal impairment

2 October 2017

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Crystal structure of human dual specificity phosphatase, JNK stimulatory phosphatase-1, at 1.5 A resolution

2 October 2017

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Protein tyrosine phosphatases: from genes, to function, to disease

2 October 2017

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Relationship between glycogen accumulation and the laforin dual specificity phosphatase

2 October 2017

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Starch-binding domains in the post-genome era.

2 October 2017

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Dimerization of Laforin is required for its optimal phosphatase activity, regulation of GSK3beta phosphorylation, and Wnt signaling

2 October 2017

1 reference

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Epm2a suppresses tumor growth in an immunocompromised host by inhibiting Wnt signaling

2 October 2017

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Phosphorylation of C6- and C3-positions of glucosyl residues in starch is catalysed by distinct dikinases

2 October 2017

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Laforin, a dual specificity phosphatase that dephosphorylates complex carbohydrates

2 October 2017

1 reference

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A chloroplast-localized dual-specificity protein phosphatase in Arabidopsis contains a phylogenetically dispersed and ancient carbohydrate-binding domain, which binds the polysaccharide starch

2 October 2017

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Recent advances in the molecular basis of Lafora's progressive myoclonus epilepsy.

2 October 2017

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Novel glycogen synthase kinase 3 and ubiquitination pathways in progressive myoclonus epilepsy

2 October 2017

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

2 October 2017

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Parkin mediates nonclassical, proteasomal-independent ubiquitination of synphilin-1: implications for Lewy body formation

2 October 2017

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

2 October 2017

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2 October 2017

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Only six kingdoms of life

2 October 2017

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Carbohydrate-binding modules: fine-tuning polysaccharide recognition

2 October 2017

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Protein tyrosine phosphatases in the human genome

2 October 2017

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Laforin, the dual-phosphatase responsible for Lafora disease, interacts with R5 (PTG), a regulatory subunit of protein phosphatase-1 that enhances glycogen accumulation

2 October 2017

1 reference

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Mutations in NHLRC1 cause progressive myoclonus epilepsy

2 October 2017

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The Lafora disease gene product laforin interacts with HIRIP5, a phylogenetically conserved protein containing a NifU-like domain

2 October 2017

1 reference

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Identification of a novel protein interacting with laforin, the EPM2a progressive myoclonus epilepsy gene product

2 October 2017

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2 October 2017

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

2 October 2017

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Structural and evolutionary relationships among protein tyrosine phosphatase domains

2 October 2017

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Regional and developmental expression of Epm2a gene and its evolutionary conservation

2 October 2017

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

2 October 2017

1 reference

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

2 October 2017

1 reference

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

2 October 2017

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T-cell responsiveness to an oncogenic peripheral protein and spontaneous autoimmunity in transgenic mice

2 October 2017

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Glycogen hyperphosphorylation underlies lafora body formation

2 October 2017

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Abnormal metabolism of glycogen phosphate as a cause for Lafora disease

11 July 2018

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Glycogen metabolism in tissues from a mouse model of Lafora disease

11 July 2018

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Myoclonus epilepsy with Lafora bodies. An ultrastruc- tural and cytochemical study

11 July 2018

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Studies in myoclonus epilepsy (Lafora body form). II. Polyglucosans in the systemic deposits of myoclonus epilepsy and in corpora amylacea

11 July 2018

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Studies in myoclonus epilepsy (Lafora body form). I. Isolation and preliminary characterization of Lafora bodies in two cases

11 July 2018

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Lafora bodies and neurological defects in malin-deficient mice correlate with impaired autophagy

11 July 2018

1 reference

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Lafora disease ubiquitin ligase malin promotes proteasomal degradation of neuronatin and regulates glycogen synthesis

23 September 2018

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Preparation of Trojan horse liposomes (THLs) for gene transfer across the blood-brain barrier

23 September 2018

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The malin-laforin complex suppresses the cellular toxicity of misfolded proteins by promoting their degradation through the ubiquitin-proteasome system

23 September 2018

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Mechanism suppressing glycogen synthesis in neurons and its demise in progressive myoclonus epilepsy.

23 September 2018

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Molecular characterization of laforin, a dual-specificity protein phosphatase implicated in Lafora disease.

23 September 2018

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A novel isoform of glucan, water dikinase phosphorylates pre-phosphorylated alpha-glucans and is involved in starch degradation in Arabidopsis

23 September 2018

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Progressive myoclonus epilepsy with polyglucosans (Lafora disease): evidence for a third locus

23 September 2018

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The carbohydrate-binding domain of Lafora disease protein targets Lafora polyglucosan bodies.

23 September 2018

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The evolution of starch-binding domain

23 September 2018

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Beitrag zur Histopathologie der myoklonischen Epilepsie

23 September 2018

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21 January 2018

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Lafora bodies and neurological defects in malin-deficient mice correlate with impaired autophagy

21 January 2018

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Escherichia coli expression, refolding and characterization of human laforin

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12 December 2020

Sequestration of chaperones and proteasome into Lafora bodies and proteasomal dysfunction induced by Lafora disease-associated mutations of malin

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The presence of phosphate in glycogen

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Glycogen contains phosphodiester groups that can be introduced by UDPglucose: glycogen glucose 1-phosphotransferase

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Aminoglycoside antibiotics restore CFTR function by overcoming premature stop mutations

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A new clan of CBM families based on bioinformatics of starch-binding domains from families CBM20 and CBM21

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Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22364389%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22364389%20AND%20SRC:MED&resulttype=core&format=json

24 January 2020

PubMed publication ID

22364389

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22364389%20AND%20SRC:MED&resulttype=core&format=json