Removal of N-terminal methionine from recombinant proteins by engineered E. coli methionine aminopeptidase.
about
Molecular basis of substrate selection by the N-end rule adaptor protein ClpSCharacterization of a thiamin diphosphate-dependent phenylpyruvate decarboxylase from Saccharomyces cerevisiae.Identification of Staphylococcus aureus proteins recognized by the antibody-mediated immune response to a biofilm infection.A new strategy to produce a defensin: stable production of mutated NP-1 in nitrate reductase-deficient Chlorella ellipsoidea.Overview of the purification of recombinant proteins.Expression and purification of active mouse and human NEIL3 proteins.Microbial factories for recombinant pharmaceuticalsA facile method for expression and purification of the Alzheimer's disease-associated amyloid beta-peptide.Motif-directed redesign of enzyme specificity.Molecular elements of low-oxygen signaling in plants.Co-expression for intracellular processing in microbial protein production.Demethionylation of Pro-1 variants of 4-oxalocrotonate tautomerase in Escherichia coli by co-expression with an engineered methionine aminopeptidase.Development of an improved Pseudoalteromonas haloplanktis TAC125 strain for recombinant protein secretion at low temperature.Targeting the N terminus for site-selective protein modification.Engineering posttranslational proofreading to discriminate nonstandard amino acids.Adenine Enrichment at the Fourth CDS Residue in Bacterial Genes Is Consistent with Error Proofing for +1 Frameshifts.Reduction of product-related species during the fermentation and purification of a recombinant IL-1 receptor antagonist at the laboratory and pilot scale.N-Terminal Methionine Processing.Refining the Ambush Hypothesis: Evidence That GC- and AT-Rich Bacteria Employ Different Frameshift Defence Strategies.Semisynthetic UbH2A reveals different activities of deubiquitinases and inhibitory effects of H2A K119 ubiquitination on H3K36 methylation in mononucleosomes.Strategies for the production of difficult-to-express full-length eukaryotic proteins using microbial cell factories: production of human alpha-galactosidase A.Transfer RNA cleavages by onconase reveal unusual cleavage sites.Reduction of N-terminal methionylation while increasing titer by lowering metabolic and protein production rates in E. coli auto-induced fed-batch fermentation.The proteomics of N-terminal methionine cleavage.High throughput discovery of protein variants using proteomics informed by transcriptomics.
P2860
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P2860
Removal of N-terminal methionine from recombinant proteins by engineered E. coli methionine aminopeptidase.
description
2004 nî lūn-bûn
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2004年の論文
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2004年学术文章
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2004年学术文章
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2004年学术文章
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2004年学术文章
@zh-hans
2004年学术文章
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2004年学术文章
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2004年學術文章
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2004年學術文章
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name
Removal of N-terminal methioni ...... oli methionine aminopeptidase.
@en
Removal of N-terminal methioni ...... oli methionine aminopeptidase.
@nl
type
label
Removal of N-terminal methioni ...... oli methionine aminopeptidase.
@en
Removal of N-terminal methioni ...... oli methionine aminopeptidase.
@nl
prefLabel
Removal of N-terminal methioni ...... oli methionine aminopeptidase.
@en
Removal of N-terminal methioni ...... oli methionine aminopeptidase.
@nl
P2093
P2860
P356
P1433
P1476
Removal of N-terminal methioni ...... oli methionine aminopeptidase.
@en
P2093
Chiu-Feng Wang
Jen-Chong Jeng
Shu-Ting Chang
Sui-Chi Wang
You-Di Liao
P2860
P304
P356
10.1110/PS.04679104
P577
2004-07-01T00:00:00Z