Improving a natural enzyme activity through incorporation of unnatural amino acids.
about
Non-standard amino acid incorporation into proteins using Escherichia coli cell-free protein synthesisRobust production of recombinant phosphoproteins using cell-free protein synthesisManipulation of enzyme properties by noncanonical amino acid incorporation.Controlling enzyme inhibition using an expanded set of genetically encoded amino acids.Enhancing the efficiency and regioselectivity of P450 oxidation catalysts by unnatural amino acid mutagenesis.Cell-free protein synthesis from a release factor 1 deficient Escherichia coli activates efficient and multiple site-specific nonstandard amino acid incorporation.Improving cell-free protein synthesis through genome engineering of Escherichia coli lacking release factor 1Extending enzyme molecular recognition with an expanded amino acid alphabet.From protein engineering to immobilization: promising strategies for the upgrade of industrial enzymesA new synthetic protocol for coumarin amino acid.Detection of dihydrofolate reductase conformational change by FRET using two fluorescent amino acids.Programmable bacterial catalysis - designing cells for biosynthesis of value-added compounds.Protein engineering for metabolic engineering: current and next-generation tools.Overcoming Challenges in Engineering the Genetic CodeBiocatalysis with Unnatural Amino Acids: Enzymology Meets Xenobiology.Pathway Design, Engineering, and Optimization.Designing logical codon reassignment - Expanding the chemistry in biology.Rewriting the Genetic Code.BMP2-modified injectable hydrogel for osteogenic differentiation of human periodontal ligament stem cells.Selective methyl labeling of eukaryotic membrane proteins using cell-free expression.Adaptive evolution of genomically recoded Escherichia coli.Exploring water as building bricks in enzyme engineering.In situ deprotection and incorporation of unnatural amino acids during cell-free protein synthesis.Multiple-site labeling of proteins with unnatural amino acids.Copper-Containing Catalytic Amyloids Promote Phosphoester Hydrolysis and Tandem ReactionsPhase-transfer enantioselective monoalkylation of prochiral nickel(ii) complexes catalyzed by 3,3′-bis[hydroxy(diphenyl)methyl]-1,1′-binaphthyl-2,23′-diol (BIMBOL) as a route to α-amino acids
P2860
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P2860
Improving a natural enzyme activity through incorporation of unnatural amino acids.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
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2010年學術文章
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name
Improving a natural enzyme activity through incorporation of unnatural amino acids.
@en
Improving a natural enzyme activity through incorporation of unnatural amino acids.
@nl
type
label
Improving a natural enzyme activity through incorporation of unnatural amino acids.
@en
Improving a natural enzyme activity through incorporation of unnatural amino acids.
@nl
prefLabel
Improving a natural enzyme activity through incorporation of unnatural amino acids.
@en
Improving a natural enzyme activity through incorporation of unnatural amino acids.
@nl
P2093
P50
P356
P1476
Improving a natural enzyme activity through incorporation of unnatural amino acids
@en
P2093
Anthony J Herlt
Chris Coppin
David L Ollis
Isaac N Ugwumba
Kiyoshi Ozawa
Lewis N Mander
Zhi-Qiang Xu
P304
P356
10.1021/JA106416G
P407
P50
P577
2010-12-16T00:00:00Z