Zobrazeno 1 - 10
of 327
pro vyhledávání: '"Mandelate racemase"'
Autor:
Joshua A Hayden, Meghan C Hamilton, Lia Grandinetti, Nicole M. Easton, Oliver P Kuehm, Stephen L. Bearne, Colin D. Douglas, Martin St. Maurice
Publikováno v:
Biochemistry. 60:2508-2518
o-Carbonyl arylboronic acids such as 2-formylphenylboronic acid (2-FPBA) are employed in biocompatible conjugation reactions with the resulting iminoboronate adduct stabilized by an intramolecular N-B interaction. However, few studies have utilized t
Publikováno v:
Protein Engineering, Design and Selection. 32:261-270
Dihydroxy-acid dehydratase (DHAD) catalyzes the dehydration of R-2,3-dihydroxyisovalerate (DHIV) to 2-ketoisovalerate (KIV) using an Fe-S cluster as a cofactor, which is sensitive to oxidation and expensive to synthesize. In contrast, sugar acid dehy
Autor:
Christopher M. Fetter, Mitesh Nagar, Colin D. Douglas, Stephen L. Bearne, Zachary A. Morrison
Publikováno v:
Archives of Biochemistry and Biophysics. 666:116-126
Mandelate racemase (MR) catalyzes the interconversion of the enantiomers of mandelate using a two-base mechanism with Lys 166 acting as the Bronsted base to abstract the α-proton from (S)-mandelate. The resulting intermediate is subsequently re-prot
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Akademický článek
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Publikováno v:
Organic Process Research & Development. 22:1761-1771
Conventional enantioselective preparative chromatographic separation using columns packed with chiral stationary phase is characterized by a 50% yield constraint. Racemization of the undesired enan...
Autor:
Xiang Li, Lin-Feng Wang, Jian-He Xu, Yuan-Yuan Jia, Kan Yunchao, Lun-Guang Yao, Tang Cunduo, Hong-Ling Shi
Publikováno v:
Enzyme and microbial technology. 136
L-Phenylglycine (L-PHG) is a member of unnatural amino acids, and becoming more and more important as intermediate for pharmaceuticals, food additives and agrochemicals. However, the existing synthetic methods for L-PHG mainly rely on toxic cyanide c
Publikováno v:
Protein Engineering, Design and Selection. 31:135-145
Mandelate racemase (MR) serves as a paradigm for our understanding of enzyme-catalyzed deprotonation of a carbon acid substrate. To facilitate structure-function studies on MR using non-natural amino acid substitutions, we engineered the Cys92Ser/Cys
Publikováno v:
Biochemical and Biophysical Research Communications. 491:217-222
3,6-Anydro- l -galatonate cycloisomerase (ACI) catalyzes the cycloisomerization of a 3,6-anhydro- l -galactonic acid known as a novel metabolite in agarolytic bacteria. Here, we present 3-D structures of ACI from Vibrio sp. strain EJY3 ( Vej ACI) in
Autor:
Stephen L. Bearne
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1865:619-630
Background Enzymes of the enolase superfamily (ENS) are mechanistically diverse, yet share a common partial reaction (abstraction of the α-proton from a carboxylate substrate). While the catalytic machinery responsible for the deprotonation reaction