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The Tat protein-export system serves to translocate folded proteins, often containing redox cofactors, across the bacterial inner membrane. Substrate proteins are directed to the Tat apparatus by distinctive N-terminal signal peptides containing a consensus SRRxFLK 'twin-arginine' motif. Here we review recent studies of the Tat system with particular emphasis on the assembly of membrane-bound respiratory complexes. We discuss the connection between Tat targeting and topological organisation of the complexes and consider the role of chaperone proteins in cofactor insertion and Tat targeting. The crystal structure of Escherichia coli formate dehydrogenase-N demonstrates that some Tat substrates are integral membrane proteins. Sequence analysis suggests that one-quarter of all traffic on the E. coli Tat pathway is inner-membrane proteins.

Original publication

DOI

10.1007/s00203-002-0434-2

Type

Journal article

Journal

Arch Microbiol

Publication Date

08/2002

Volume

178

Pages

77 - 84

Keywords

Amino Acid Sequence, Bacterial Proteins, Biological Transport, Active, Carrier Proteins, Escherichia coli, Escherichia coli Proteins, Formate Dehydrogenases, Membrane Proteins, Membrane Transport Proteins, Molecular Chaperones, Molecular Sequence Data, Sequence Homology, Amino Acid, Substrate Specificity