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The Tat protein export pathway
Abstract
The Tat (t win‐a rginine t ranslocation) system is a bacterial protein export pathway with the remarkable ability to transport folded proteins across the cytoplasmic membrane. Preproteins are directed to the Tat pathway by signal peptides that bear a characteristic sequence motif, which includes consecutive arginine residues. Here, we review recent progress on the characterization of the Tat system and critically discuss the structure and operation of this major new bacterial protein export pathway.
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Cited by
Improved Prediction of Signal Peptides: SignalP 3.0
Dyrløv Bendtsen, J., Nielsen, H., von Heijne, G., & Brunak, S. (2004) · Journal of Molecular Biology · doi:10.1016/j.jmb.2004.05.028 · Cited by 6,350
Microbial arsenic: from geocycles to genes and enzymes
Mukhopadhyay, R., Rosen, B. P., Phung, L. T., & Silver, S. (2002) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2002.tb00617.x · Cited by 726
Genes and enzymes involved in bacterial oxidation and reduction of inorganic arsenic
Silver, S., & Phung, L. T. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.2.599-608.2005 · Cited by 612
A comprehensive review of signal peptides: Structure, roles, and applications
Owji, H., Nezafat, N., Negahdaripour, M., Hajiebrahimi, A., & Ghasemi, Y. (2018) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2018.06.003 · Cited by 523
Recombinant protein secretion in Escherichia coli
Mergulhão, F. J. M., Summers, D. K., & Monteiro, G. A. (2005) · Biotechnology Advances · doi:10.1016/j.biotechadv.2004.11.003 · Cited by 485
Metadata
- Authors
- Berks, B. C., Sargent, F., & Palmer, T.
- Venue
- Molecular Microbiology
- Publisher
- Wiley
- Published
- 2000-01
- Volume
- 35
- Issue
- 2
- Pages
- 260-274
- ISSN
- 0950-382X (ISSN-L)
- 1365-2958
- OpenAlex
- W2108575112
- Cited by
- 574
- References
- 0
- FWCI
- 28.94
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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