about
Bioorthogonal chemistry: fishing for selectivity in a sea of functionalityEvolution of proteins with genetically encoded "chemical warheads"Click chemistry in complex mixtures: bioorthogonal bioconjugationBioorthogonal chemistry: strategies and recent developmentsBoron Mimetics: 1,2-Dihydro-1,2-azaborines Bind inside a Nonpolar Cavity of T4 LysozymeSite-directed spin labeling of a genetically encoded unnatural amino acidImportance of single molecular determinants in the fidelity of expanded genetic codesAn Evolved Aminoacyl-tRNA Synthetase with Atypical Polysubstrate Specificity,From Chemical Mutagenesis to Post-Expression Mutagenesis: A 50 Year OdysseyBeyond the canonical 20 amino acids: expanding the genetic lexiconGenetic incorporation of unnatural amino acids into proteins in Mycobacterium tuberculosisBioconjugatable azo-based dark-quencher dyes: synthesis and application to protease-activatable far-red fluorescent probes.4R- and 4S-iodophenyl hydroxyproline, 4R-pentynoyl hydroxyproline, and S-propargyl-4-thiolphenylalanine: conformationally biased and tunable amino acids for bioorthogonal reactions.Fast and Tight Boronate Formation for Click Bioorthogonal Conjugation.One plasmid selection system for the rapid evolution of aminoacyl-tRNA synthetasesSynthesis and carbohydrate binding studies of fluorescent alpha-amidoboronic acids and the corresponding bisboronic acids.Bioorthogonal chemistry: recent progress and future directions.Storable N-phenylcarbamate palladacycles for rapid functionalization of an alkyne-encoded proteinSite-specific coupling and sterically controlled formation of multimeric antibody fab fragments with unnatural amino acidsProtein conjugation with genetically encoded unnatural amino acids.Evolution, ecology and the engineered organism: lessons for synthetic biology.Synthesis of non-linear protein dimers through a genetically encoded Thiol-ene reaction.An efficient protocol for incorporation of an unnatural amino acid in perdeuterated recombinant proteins using glucose-based media.A new class of fluorescent boronic acids that have extraordinarily high affinities for diols in aqueous solution at physiological pHGenetic incorporation of twelve meta-substituted phenylalanine derivatives using a single pyrrolysyl-tRNA synthetase mutantSynthesis at the interface of chemistry and biology.Aminoboronic acids and esters: from synthetic challenges to the discovery of unique classes of enzyme inhibitors.Biochemical analysis with the expanded genetic lexicon.Transition metal-mediated bioorthogonal protein chemistry in living cells.Selective chemical protein modification.Designing logical codon reassignment - Expanding the chemistry in biology.Evolution of amber suppressor tRNAs for efficient bacterial production of proteins containing nonnatural amino acids.Photocleavage of the polypeptide backbone by 2-nitrophenylalanine.Copper(II)-mediated O-arylation of protected serines and threonines.Investigation of Trimethyllysine Binding by the HP1 Chromodomain via Unnatural Amino Acid Mutagenesis.A serendipitous phosphonocarboxylate complex of boron: when vessel becomes reagent.Genetically encoding phosphotyrosine and its nonhydrolyzable analog in bacteria.Unnatural amino acid mutagenesis of fluorescent proteins.Ascorbate as a pro-oxidant: mild N-terminal modification with vinylboronic acids.Genetic Incorporation of a Reactive Isothiocyanate Group into Proteins.
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
A genetically encoded boronate-containing amino acid.
@en
type
label
A genetically encoded boronate-containing amino acid.
@en
prefLabel
A genetically encoded boronate-containing amino acid.
@en
P2093
P2860
P356
P1476
A genetically encoded boronate-containing amino acid.
@en
P2093
Eric Brustad
Jae Wook Lee
Mark L Bushey
Peter G Schultz
Wenshe Liu
P2860
P304
P356
10.1002/ANIE.200803240
P407
P577
2008-01-01T00:00:00Z