Glutathione-S-Crotonyl-N-Acetylthioethanolamine Alkenetransferase: Properties and Comparison with Other Glutathione-S-Transferases

dc.contributor.author	Speir, Thomas Wilson
dc.date.accessioned	2008-09-02T00:13:19Z
dc.date.accessioned	2022-11-03T02:22:34Z
dc.date.available	2008-09-02T00:13:19Z
dc.date.available	2022-11-03T02:22:34Z
dc.date.copyright	1972
dc.date.issued	1972
dc.identifier.uri	https://ir.wgtn.ac.nz/handle/123456789/29626
dc.description.abstract	A mercapturic acid is an N-acetylated-S-substituted -L-cysteine in which the substitutive group is generally inert to further enzymic reaction (Wood, 1970). Detoxication of foreign compounds to mercapturic acids in mammals has been known for almost 100 years, however the source of cysteine for conjugation has only recently been positively determined.	en_NZ
dc.language	en_NZ
dc.language.iso	en_NZ
dc.publisher	Te Herenga Waka—Victoria University of Wellington	en_NZ
dc.title	Glutathione-S-Crotonyl-N-Acetylthioethanolamine Alkenetransferase: Properties and Comparison with Other Glutathione-S-Transferases	en_NZ
dc.type	Text	en_NZ
vuwschema.type.vuw	Awarded Doctoral Thesis	en_NZ
thesis.degree.discipline	Biochemistry	en_NZ
thesis.degree.grantor	Te Herenga Waka—Victoria University of Wellington	en_NZ
thesis.degree.level	Doctoral	en_NZ
thesis.degree.name	Doctor of Philosophy	en_NZ

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