Author pages are created from data sourced from our academic publisher partnerships and public sources.
Biotransformations in Organic Chemistry. A Textbook
- J. B. Jones
- 1 August 2001
Chemical modification of enzymes for enhanced functionality.
The explosion in commercial and synthetic applications of enzymes has stimulated much of the interest in enhancing enzyme functionality and stability. Covalent chemical modification, the original… Expand
Structure-based design guides the improved efficacy of deacylation transition state analogue inhibitors of TEM-1 beta-Lactamase(,).
Transition state analogue boronic acid inhibitors mimicking the structures and interactions of good penicillin substrates for the TEM-1 beta-lactamase of Escherchia coli were designed using graphic… Expand
Differences in binding modes of enantiomers of 1-acetamido boronic acid based protease inhibitors: crystal structures of gamma-chymotrypsin and subtilisin Carlsberg complexes.
- V. Stoll, B. Eger, R. Hynes, V. Martichonok, J. B. Jones, E. Pai
- Chemistry, Medicine
- 13 January 1998
In order to probe the structural basis of stereoselectivity in the serine protease family, a series of enantiomeric boronic acids RCH2CH(NHCOCH3)B(OH)2 has been synthesized and kinetically… Expand
Enzymes in organic synthesis. 47. Active-site model for interpreting and predicting the specificity of pig liver esterase
Nicotinamide coenzyme regeneration. Flavin mononucleotide (riboflavin phosphate) as an efficient, economical, and enzyme-compatible recycling agent
The high cost of nicotinamide coenzymes currently acts as a deterrent to the widespread adoption of alcohol dehydrogenases as chiral catalysts for effecting stereospecific and selective… Expand
Alteration of the specificity of subtilisin BPN' by site-directed mutagenesis in its S1 and S1' binding sites
Glycomethanethiosulfonates: powerful reagents for protein glycosylation
Abstract Twelve novel glycomethanethiosulfonate (glyco-MTS) protein glycosylation reagents have been prepared. Their use in a controlled site-selective glycosylation strategy that combines… Expand
Carcinogenicity of lactones. IV. Alkylation of analogues of DNA guanine groups such as imidazole, N-methylimidazole, and guanosine by α, β-unsaturated acids
Studies on the reactions of carcinogenic γ-lactones and related compounds with analogues of guanine DNA residues indicate that the lactones themselves will not effect permanent alkylation of the gu...
Alkylations of the Side-chain Nucleophiles of Cysteine, Methionine, Histidine, and Lysine Derivatives with Allyl Bromide, 1-Bromo-2-butyne, and 2-Bromoacetophenone
Comparative studies on the reactions of cysteine, methionine, histidine, and lysine derivatives with allyl bromide, 1-bromo-2-butyne, and 2-bromoacetophenone have been carried out in connection wit...