Restricted role for methionine synthase reductase defined by subcellular localization. (Q37395123)

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1 January 2020

title

Restricted role for methionine synthase reductase defined by subcellular localization (English)

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1 January 2020

1

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1 January 2020

author name string

X Wu

2

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1 January 2020

J Zhang

3

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1 January 2020

R Dumas

4

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1 January 2020

W M Schoel

5

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1 January 2020

M Amrein

6

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1 January 2020

R A Gravel

7

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1 January 2020

publication date

24 January 2008

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Molecular Genetics and Metabolism

1 January 2020

published in

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1 January 2020

volume

94

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1 January 2020

issue

1

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1 January 2020

page(s)

68-77

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Protein interactions in the human methionine synthase-methionine synthase reductase complex and implications for the mechanism of enzyme reactivation

1 January 2020

cites work

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Human methionine synthase reductase is a molecular chaperone for human methionine synthase

6 September 2017

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Energetics of interaction between the G-protein chaperone, MeaB, and B12-dependent methylmalonyl-CoA mutase

6 September 2017

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Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type

6 September 2017

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Human ATP:Cob(I)alamin adenosyltransferase and its interaction with methionine synthase reductase

6 September 2017

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Reduced histone biotinylation in multiple carboxylase deficiency patients: a nuclear role for holocarboxylase synthetase

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Redundancy in the pathway for redox regulation of mammalian methionine synthase: reductive activation by the dual flavoprotein, novel reductase 1.

6 September 2017

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Multiple sequence alignment with the Clustal series of programs

6 September 2017

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Identification of the gene responsible for the cblB complementation group of vitamin B12-dependent methylmalonic aciduria

6 September 2017

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Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements

6 September 2017

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Classification and evolution of P-loop GTPases and related ATPases

6 September 2017

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Human methionine synthase reductase, a soluble P-450 reductase-like dual flavoprotein, is sufficient for NADPH-dependent methionine synthase activation

6 September 2017

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Cloning and characterization of a novel human dual flavin reductase

6 September 2017

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Molecular cloning, expression and physical mapping of the human methionine synthase reductase gene

6 September 2017

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Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism

6 September 2017

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Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria

6 September 2017

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Human methionine synthase. cDNA cloning, gene localization, and expression

6 September 2017

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Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders

6 September 2017

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Cloning, mapping and RNA analysis of the human methionine synthase gene

6 September 2017

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Nitric oxide synthases in mammals

6 September 2017

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Mitochondrial import and processing of mutant human ornithine transcarbamylase precursors in cultured cells

6 September 2017

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Functional methionine synthase deficiency (cblE and cblG): clinical and biochemical heterogeneity

6 September 2017

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Lysosomal cobalamin accumulation in fibroblasts from a patient with an inborn error of cobalamin metabolism (cblF complementation group): visualization by electron microscope radioautography

6 September 2017

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6 September 2017

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14 September 2017

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Crossref

https://api.crossref.org/works/10.1016%2FJ.YMGME.2007.11.019

P450 oxidoreductase deficiency

7 January 2021

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Purification of soluble cytochrome b5 as a component of the reductive activation of porcine methionine synthase

7 January 2021

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10.1016/J.YMGME.2007.11.019

7 January 2021

Identifiers

DOI

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1 January 2020

1 reference

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1 January 2020

PubMed publication ID

18221906

1 reference