[45] Suicide substrates for flavoprotein enzymes
- 1 January 1978
- book chapter
- Published by Elsevier
- Vol. 53, 437-448
- https://doi.org/10.1016/s0076-6879(78)53048-6
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- The structure of the covalent flavin adduct formed between lactate oxidase and the suicide substrate 2-hydroxy-3-butynoateBiochemistry, 1976
- The structure of the covalent adduct formed by the interaction of 3-dimethylamino-1-propyne and the flavine of mitochondrial amine oxidaseBiochemistry, 1976
- Reversible inactivation of vectorial phosphorylation by hydroxybutynoate in Escherichia coli membrane vesiclesBiochemistry, 1975
- Mechanistic studies on the rat kidney flavoenzyme L-α-hydroxy acid oxidaseBiochemistry, 1975
- Active site-directed inactivation of cystathionine γ-synthetase and glutamic pyruvic transaminase by propargylglycineBiochemical and Biophysical Research Communications, 1975
- Irreversible inhibition of aspartate aminotransferase by 2-amino-3-butenoic acidBiochemistry, 1974
- Chemistry and Enzymology of k cat InhibitorsScience, 1974
- Synthesis of α-hydroxy-β-acetylenic acids and their oxidation by and inactivation of flavoprotein oxidasesJournal of the Chemical Society, Chemical Communications, 1974
- Acetylenic enzyme inactivators. Inactivation of .gamma.-cystathionase, in vitro and in vivo by propargylglycineJournal of the American Chemical Society, 1973
- Studies on polypeptides. Part VII, : Synthesis of DL‐, L‐ and D‐2‐amino‐6‐dimethylamino‐4‐hexynoic acidRecueil des Travaux Chimiques des Pays-Bas, 1969