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Glutaryl-CoA oxidase

Two other oxidase activities have been described in rat liver peroxisomes, one acting on glutaryl-CoA, the other on valproyl-CoA. The glutaryl-CoA oxidase activity, however, co-purifies with the inducible pahnitoyl-CoA oxidase. The valproyl-CoA oxidase was claimed to differ from the above described acyl-CoA oxidases, but in our hands this activity was recovered mainly in the cytosol (Casteels, M. Van Veldhoven P. P., unpublished data). [Pg.263]

Bennett, M.J., Pollitt, R.J., Goodman, S.I., Hale, D.E. Vamecq, J. (1991)7. Inherit. Metab. Dis. 14, 165-73. Atypical riboflavin-responsive glutaric aciduria, and deflcient peroxisomal glutaryl-CoA oxidase activity a new peroxisomal disorder. [Pg.270]

Glutaric aciduria type III (glutaryl-CoA oxidase deficiency)... [Pg.207]

Apart from glutaric aciduria II (ETF or ETF dehydrogenase deficiency, see Sect. 14.10) a third disorder with peroxisomal glutaryl-CoA oxidase deficiency leading to glutaric aciduria has been described (glutaric aciduria III, see Chap. 24). [Pg.279]


See other pages where Glutaryl-CoA oxidase is mentioned: [Pg.503]    [Pg.481]    [Pg.506]    [Pg.503]    [Pg.481]    [Pg.506]    [Pg.104]    [Pg.606]   
See also in sourсe #XX -- [ Pg.263 ]

See also in sourсe #XX -- [ Pg.263 ]




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