Enhanced phosphoserine insertion during Escherichia coli protein synthesis via partial UAG codon reassignment and release factor 1 deletion. - Wikidata - wikimedia - TriplyDB

Enhanced phosphoserine insertion during Escherichia coli protein synthesis via partial UAG codon reassignment and release factor 1 deletion.

Enhanced phosphoserine insertion during Escherichia coli protein synthesis via partial UAG codon reassignment and release factor 1 deletion.

http://www.wikidata.org/entity/Q36323009

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Non-standard amino acid incorporation into proteins using Escherichia coli cell-free protein synthesis Carbon source-dependent expansion of the genetic code in bacteria Structural Basis of Improved Second-Generation 3-Nitro-tyrosine tRNA Synthetases Expanded cellular amino acid pools containing phosphoserine, phosphothreonine, and phosphotyrosine Revealing the amino acid composition of proteins within an expanded genetic code Efficient genetic encoding of phosphoserine and its nonhydrolyzable analog A flexible codon in genomically recoded Escherichia coli permits programmable protein phosphorylation Robust production of recombinant phosphoproteins using cell-free protein synthesis Genomically recoded organisms expand biological functions Repurposing the translation apparatus for synthetic biology Translation system engineering in Escherichia coli enhances non-canonical amino acid incorporation into proteins.Cell-free protein synthesis from a release factor 1 deficient Escherichia coli activates efficient and multiple site-specific nonstandard amino acid incorporation.Genomes by design.Polyspecific pyrrolysyl-tRNA synthetases from directed evolution Reducing the genetic code induces massive rearrangement of the proteome.Improving cell-free protein synthesis through genome engineering of Escherichia coli lacking release factor 1 Reassignment of a rare sense codon to a non-canonical amino acid in Escherichia coli Genetic code flexibility in microorganisms: novel mechanisms and impact on physiology.Evolution of translation machinery in recoded bacteria enables multi-site incorporation of nonstandard amino acids.Phosphorylation of OPTN by TBK1 enhances its binding to Ub chains and promotes selective autophagy of damaged mitochondria.A facile strategy for selective incorporation of phosphoserine into histones.Transfer RNA misidentification scrambles sense codon recoding.Pyrrolysyl-tRNA synthetase, an aminoacyl-tRNA synthetase for genetic code expansion.Recoding the genetic code with selenocysteine.Expanded genetic code technologies for incorporating modified lysine at multiple sites.Ribonucleosides for an artificially expanded genetic information system.Probing unnatural amino acid integration into enhanced green fluorescent protein by genetic code expansion with a high-throughput screening platform.Expanding the genetic code of Escherichia coli with phosphotyrosine.Chemical pyrophosphorylation of functionally diverse peptides.Nuclear codon reassignments in the genomics era and mechanisms behind their evolution.Highly reproductive Escherichia coli cells with no specific assignment to the UAG codon.Recoded organisms engineered to depend on synthetic amino acids.Near-cognate suppression of amber, opal and quadruplet codons competes with aminoacyl-tRNAPyl for genetic code expansion.Synthesis of Isomeric Phosphoubiquitin Chains Reveals that Phosphorylation Controls Deubiquitinase Activity and Specificity.Designed phosphoprotein recognition in Escherichia coli.Molecular reconstruction of a fungal genetic code alteration.Acetylation Regulates Thioredoxin Reductase Oligomerization and Activity.Increasing the fidelity of noncanonical amino acid incorporation in cell-free protein synthesis.Genetically Incorporating Two Distinct Post-translational Modifications into One Protein Simultaneously.Incorporation of Phosphorylated Tyrosine into Proteins: In Vitro Translation and Study of Phosphorylated IκB-α and Its Interaction with NF-κB.

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Enhanced phosphoserine insertion during Escherichia coli protein synthesis via partial UAG codon reassignment and release factor 1 deletion.

http://www.wikidata.org/entity/Q36323009

description

2012 nî lūn-bûn

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2012年學術文章

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name

Enhanced phosphoserine inserti ...... and release factor 1 deletion.

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Enhanced phosphoserine inserti ...... and release factor 1 deletion.

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Enhanced phosphoserine inserti ...... and release factor 1 deletion.

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Enhanced phosphoserine inserti ...... and release factor 1 deletion.

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Enhanced phosphoserine inserti ...... and release factor 1 deletion.

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Enhanced phosphoserine inserti ...... and release factor 1 deletion.

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J.FEBSLET.2012.08.031

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Enhanced phosphoserine inserti ...... and release factor 1 deletion.

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Alexis J Rovner

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Dieter Söll

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Farren J Isaacs

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Hans R Aerni

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Ilka U Heinemann

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Jesse Rinehart

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Jonathan T Fischer

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Laura Cheng

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Svetlana Rogulina

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William Olds

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P2860

Experimental Determination and System Level Analysis of Essential Genes in Escherichia coli MG1655

Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection

The tRNAscan-SE, snoscan and snoGPS web servers for the detection of tRNAs and snoRNAs

The chemical biology of protein phosphorylation

An SGK1 site in WNK4 regulates Na+ channel and K+ channel activity and has implications for aldosterone signaling and K+ homeostasis

Highly accurate genome sequences of Escherichia coli K-12 strains MG1655 and W3110

Expanding the genetic code of Escherichia coli

Precise manipulation of chromosomes in vivo enables genome-wide codon replacement

Expanding the genetic code of Escherichia coli with phosphoserine

Programming cells by multiplex genome engineering and accelerated evolution

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3716-3722

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Escherichia coli

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