Combinatorial protein engineering by incremental truncation - Wikidata - awgldk - TriplyDB

Combinatorial protein engineering by incremental truncation

Combinatorial protein engineering by incremental truncation

http://www.wikidata.org/entity/Q30657935

about

Kinetics of regulated protein-protein interactions revealed with firefly luciferase complementation imaging in cells and living animals Microbial enzymes: tools for biotechnological processes To get what we aim for--progress in diversity generation methods Domain structure and protein interactions of the silent information regulator Sir3 revealed by screening a nested deletion library of protein fragments.Novel folded protein domains generated by combinatorial shuffling of polypeptide segments.Creating multiple-crossover DNA libraries independent of sequence identity.Evolution of highly active enzymes by homology-independent recombination.High-affinity fragment complementation of a fibronectin type III domain and its application to stability enhancement Production of cyclic peptides and proteins in vivo Generating segmental mutations in haloalkane dehalogenase: a novel part in the directed evolution toolbox.DNA family shuffling of hyperthermostable beta-glycosidases.Growth factor engineering by degenerate homoduplex gene family recombination.Rapid generation of incremental truncation libraries for protein engineering using alpha-phosphothioate nucleotides.Using an AraC-based three-hybrid system to detect biocatalysts in vivo.IPRO: an iterative computational protein library redesign and optimization procedure Revealing biases inherent in recombination protocols.High-throughput analysis of the protein sequence-stability landscape using a quantitative yeast surface two-hybrid system and fragment reconstitution Random dissection to select for protein split sites and its application in protein fragment complementation Evolutionary diversification of satellite DNA sequences from Leymus (Poaceae: Triticeae).Comparative molecular cytogenetics of major repetitive sequence families of three Dendrobium species (Orchidaceae) from Bangladesh.Analysis of a c0t-1 library enables the targeted identification of minisatellite and satellite families in Beta vulgaris Sites in the AAV5 capsid tolerant to deletions and tandem duplications.An evolved xylose transporter from Zymomonas mobilis enhances sugar transport in Escherichia coli.Prospecting metagenomic enzyme subfamily genes for DNA family shuffling by a novel PCR-based approach Split-protein systems: beyond binary protein-protein interactions A general approach for receptor and antibody-targeted detection of native proteins utilizing split-luciferase reassembly.Circular permutation in the Ω-loop of TEM-1 β-lactamase results in improved activity and altered substrate specificity Blocking formation of large protein aggregates by small peptides.A 'resource allocator' for transcription based on a highly fragmented T7 RNA polymerase.Combining random gene fission and rational gene fusion to discover near-infrared fluorescent protein fragments that report on protein-protein interactions.Supercoiled Minivector DNA resists shear forces associated with gene therapy delivery.The enzymatic basis for pesticide bioremediation.Primer-Aided Truncation for the Creation of Hybrid Proteins.Directed evolution 2.0: improving and deciphering enzyme properties.Firefly luciferase enzyme fragment complementation for imaging in cells and living animals.Breaking the covalent connection: Chain connectivity and the catalytic reaction of PMM/PGM.A sugar beet (Beta vulgaris L.) reference FISH karyotype for chromosome and chromosome-arm identification, integration of genetic linkage groups and analysis of major repeat family distribution.Using directed evolution to improve the solubility of the C-terminal domain of Escherichia coli aminopeptidase P. Implications for metal binding and protein stability.Evolution of new protein topologies through multistep gene rearrangements α Complementation in the Cre recombinase enzyme

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P2860

Combinatorial protein engineering by incremental truncation

http://www.wikidata.org/entity/Q30657935

description

1999 nî lūn-bûn

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1999 թուականի Մարտին հրատարակուած գիտական յօդուած

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1999 թվականի մարտին հրատարակված գիտական հոդված

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1999年の論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年論文

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1999年论文

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Combinatorial protein engineering by incremental truncation

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Combinatorial protein engineering by incremental truncation

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Combinatorial protein engineering by incremental truncation

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Proceedings of the National Academy of Sciences of the United States of America

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Combinatorial protein engineering by incremental truncation

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P2093

A E Nixon

http://www.w3.org/2001/XMLSchema#string

J H Shim

http://www.w3.org/2001/XMLSchema#string

M Ostermeier

http://www.w3.org/2001/XMLSchema#string

S J Benkovic

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P2860

Towards structure-based drug design: crystal structure of a multisubstrate adduct complex of glycinamide ribonucleotide transformylase at 1.96 A resolution

Unidirectional digestion with exonuclease III creates targeted breakpoints for DNA sequencing

Monitoring protein-protein interactions in intact eukaryotic cells by beta-galactosidase complementation

Characterization by in vitro complementation of a peptide corresponding to an operator-proximal segment of the beta-galactosidase structural gene of Escherichia coli

Directed evolution of enzyme catalysts

DNA shuffling of a family of genes from diverse species accelerates directed evolution

A bacterial two-hybrid system based on a reconstituted signal transduction pathway

Unidirectional digestion with exonuclease III in DNA sequence analysis

A binary plasmid system for shuffling combinatorial antibody libraries.

Crystal structure of glycinamide ribonucleotide transformylase from Escherichia coli at 3.0 A resolution. A target enzyme for chemotherapy.

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