Synthesis and biological activity of N6-{N[(4-azido-3,5,6-trifluoro)-pyridin-2-yl]-2-aminoethyl}-adenosine 5'-monophosphate, a new AMP photoactivatable derivative. Covalent modification of horse liver alcohol dehydrogenase
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1432-1033.1989.tb14572.x/fullpdf
Reference21 articles.
1. Covalent Binding of an NAD Analogue to Liver Alcohol Dehydrogenase Resulting in an Enzyme-Coenzyme Complex not Requiring Exogenous Coenzyme for Activity
2. Covalent Fixation of NAD⊕to Dehydrogenases and Properties of the Modified Enzymes
3. Activity of NMN+, nicotinamide ribose and analogs in alcohol oxidation promoted by horse-liver alcohol dehydrogenase. Improvement of this activity and structural requirements of the pyridine nucleotide part of the NAD+ coenzyme
4. Covalent modification of the inhibitor binding site(s) of Escherichia coli ADP-glucose synthetase: specific incorporation of the photoaffinity analog 8-azido-adenosine 5'-monophosphate
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Two novel dATP analogs for DNA photoaffinity labeling;Nucleic Acids Research;2000-11-01
2. Wave Chemistry: 2-(4′-Azido 3′,5′,6′-trifluoro 2′-Pyridyl)- Amino Ethylamine as a Key Photoactivatable Building Block with Wide Biological Applications;Synthetic Communications;1996-04
3. Chemical reagents in photoaffinity labeling;Tetrahedron;1995-11
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