The Tat system proofreads FeS protein substrates and directly initiates the disposal of rejected molecules.
about
A microbial sensor for discovering structural probes of protein misfolding and aggregationStructure of the twin-arginine signal-binding protein DmsD fromEscherichia coliVersatile selection technology for intracellular protein-protein interactions mediated by a unique bacterial hitchhiker transport mechanismVisualizing interactions along the Escherichia coli twin-arginine translocation pathway using protein fragment complementation.Engineering antibody fitness and function using membrane-anchored display of correctly folded proteins.Modified recombinant proteins can be exported via the Sec pathway in Escherichia coli.Interconvertibility of lipid- and translocon-bound forms of the bacterial Tat precursor pre-SufI.The ins and outs of Mycobacterium tuberculosis protein export.Twin-arginine-dependent translocation of folded proteins.Twin-Arginine Protein Translocation.Early contacts between substrate proteins and TatA translocase component in twin-arginine translocation.Co-factor insertion and disulfide bond requirements for twin-arginine translocase-dependent export of the Bacillus subtilis Rieske protein QcrA.TatB functions as an oligomeric binding site for folded Tat precursor proteins.Following the path of a twin-arginine precursor along the TatABC translocase of Escherichia coliMining mammalian genomes for folding competent proteins using Tat-dependent genetic selection in Escherichia coli.Malfolded recombinant Tat substrates are Tat-independently degraded in Escherichia coli.TatD is a central component of a Tat translocon-initiated quality control system for exported FeS proteins in Escherichia coli.Impairment of twin-arginine-dependent export by seemingly small alterations of substrate conformation.Escherichia coli "TatExpress" strains super-secrete human growth hormone into the bacterial periplasm by the Tat pathway.Probing the quality control mechanism of the Escherichia coli twin-arginine translocase with folding variants of a de novo-designed heme protein.
P2860
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P2860
The Tat system proofreads FeS protein substrates and directly initiates the disposal of rejected molecules.
description
2008 nî lūn-bûn
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2008年の論文
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2008年論文
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2008年論文
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2008年論文
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2008年論文
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2008年論文
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2008年论文
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2008年论文
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2008年论文
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name
The Tat system proofreads FeS ...... isposal of rejected molecules.
@en
The Tat system proofreads FeS ...... isposal of rejected molecules.
@nl
type
label
The Tat system proofreads FeS ...... isposal of rejected molecules.
@en
The Tat system proofreads FeS ...... isposal of rejected molecules.
@nl
prefLabel
The Tat system proofreads FeS ...... isposal of rejected molecules.
@en
The Tat system proofreads FeS ...... isposal of rejected molecules.
@nl
P2093
P2860
P356
P1433
P1476
The Tat system proofreads FeS ...... isposal of rejected molecules.
@en
P2093
Alessandra Di Cola
Colin Robinson
Cristina F R O Matos
P2860
P304
P356
10.1038/EMBOJ.2008.132
P407
P577
2008-07-10T00:00:00Z