High-level expression and characterization of the recombinant enzyme, and tissue distribution of human succinic semialdehyde dehydrogenase (Q24337367)

identical protein binding

GOA release 2020-03-11

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GOA release 2020-03-11

author name string

Jeong Han Kang

1

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Yong Bok Park

2

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Tae-Lin Huh

3

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Won-Ha Lee

4

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Myung-Sook Choi

5

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Oh-Shin Kwon

Protein Expression and Purification

6

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language of work or name

English

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publication date

November 2005

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published in

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volume

44

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issue

1

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page(s)

16-22

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cites work

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Succinic semialdehyde dehydrogenase deficiency: an inborn error of gamma-aminobutyric acid metabolism

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Succinic semialdehyde dehydrogenase from mammalian brain: subunit analysis using polyclonal antiserum

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Brain succinic semialdehyde dehydrogenase: identification of reactive lysyl residues labeled with pyridoxal-5'-phosphate

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Oxidation of 4-hydroxy-2-nonenal by succinic semialdehyde dehydrogenase (ALDH5A)

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4-Hydroxybutyric acid and the clinical phenotype of succinic semialdehyde dehydrogenase deficiency, an inborn error of GABA metabolism

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Molecular cloning of the mature NAD(+)-dependent succinic semialdehyde dehydrogenase from rat and human. cDNA isolation, evolutionary homology, and tissue expression

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Two exon-skipping mutations as the molecular basis of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria)

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Plant succinic semialdehyde dehydrogenase. Cloning, purification, localization in mitochondria, and regulation by adenine nucleotides.

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The kinetics of pig brain aldehyde dehydrogenase.

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The binding of NADH to succinic semialdehyde dehydrogenase

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Succinic semialdehyde dehydrogenases of Escherichia coli: their role in the degradation of p-hydroxyphenylacetate and gamma-aminobutyrate

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Brain succinic semialdehyde dehydrogenase. Reactions of sulfhydryl residues connected with catalytic activity

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The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients.

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