Succinate-semialdehyde dehydrogenase: Difference between revisions
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== Structural highlights == | == Structural highlights == | ||
The active site of SSD contains the <scene name='59/590825/Cv/4'>substrate succinate semialdehyde</scene> and the <scene name='59/590825/Cv/7'>cofactor NADP</scene><ref>PMID:23500184</ref>. <scene name='59/590825/Cv/9'>Whole binding site</scene>. | The active site of SSD contains the <scene name='59/590825/Cv/4'>substrate succinate semialdehyde</scene> and the <scene name='59/590825/Cv/7'>cofactor NADP</scene><ref>PMID:23500184</ref>. <scene name='59/590825/Cv/9'>Whole binding site</scene>. | ||
</StructureSection> | </StructureSection> | ||
Revision as of 01:42, 21 September 2018
FunctionSuccinate-semialdehyde dehydrogenase (SSD) catalyzes the conversion of succinate semialdehyde, NAD+ and water to succinate, NADH and H+. SSD participates in glutamate and butyrate metabolism[1]. DiseaseSSD deficiency is a disorder of GABA metabolism with symptoms of seizures, delayed development and hypotonia[2]. Structural highlightsThe active site of SSD contains the and the [3]. .
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3D structures of succinate-semialdehyde dehydrogenase3D structures of succinate-semialdehyde dehydrogenase
Updated on 21-September-2018
ReferencesReferences
- ↑ JAKOBY WB, SCOTT EM. Aldehyde oxidation. III. Succinic semialdehyde dehydrogenase. J Biol Chem. 1959 Apr;234(4):937-40. PMID:13654295
- ↑ Gordon N. Succinic semialdehyde dehydrogenase deficiency (SSADH) (4-hydroxybutyric aciduria, gamma-hydroxybutyric aciduria). Eur J Paediatr Neurol. 2004;8(5):261-5. PMID:15341910 doi:http://dx.doi.org/10.1016/j.ejpn.2004.06.004
- ↑ Yuan Z, Yin B, Wei D, Yuan YR. Structural basis for cofactor and substrate selection by cyanobacterium succinic semialdehyde dehydrogenase. J Struct Biol. 2013 May;182(2):125-35. doi: 10.1016/j.jsb.2013.03.001. Epub 2013 , Mar 13. PMID:23500184 doi:10.1016/j.jsb.2013.03.001