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YscN, the putative energizer of the Yersinia Yop secretion machinery.

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TLDR
It is concluded that YscN is a component of the Yop secretion machinery using ATP, and it is hypothesized that it is either the energizer of this machinery or a part of it.
Abstract
Pathogenic yersiniae secrete a set of 11 antihost proteins called Yops. Yop secretion appears as the archetype of the type III secretion pathway. Several components of this machinery are encoded by the virA (lcrA) and virC (lcrC) loci of the 70-kb pYV plasmid. In this paper, we describe yscN, another gene involved in this pathway. It is the first gene of the virB locus. It encodes a 47.8-kDa protein similar to the catalytic subunits of F0F1 and related ATPases, as well as to products of other genes presumed to be involved in a type III secretion pathway. YscN contains the two consensus nucleotide-binding motifs (boxes A and B) described by Walker et al. (J. E. Walker, M. Saraste, M. J. Runswick, and N. J. Gay, EMBO J. 1:945-951, 1982). We engineered a pYV mutant encoding a modified YscN protein lacking box A. This mutant, impaired in Yop secretion, can be complemented in trans by a cloned yscN gene. We conclude that YscN is a component of the Yop secretion machinery using ATP. We hypothesize that it is either the energizer of this machinery or a part of it.

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Citations
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Type III Protein Secretion Systems in Bacterial Pathogens of Animals and Plants

TL;DR: A comparison of the structure, function, regulation, and impact on host cells of the type III secretion systems in the animal pathogens Yersinia spp.
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Yersinia pestis--etiologic agent of plague.

TL;DR: The present understanding of the history, etiology, epidemiology, clinical aspects, and public health issues of plague is updated.
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The type III secretion injectisome.

TL;DR: The principal structural components of the injectisome, from the base located in the bacterial cytosol to the tip of the needle protruding from the cell surface, have been investigated in detail.
References
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Multiple sequence alignment with hierarchical clustering

TL;DR: An algorithm is presented for the multiple alignment of sequences, either proteins or nucleic acids, that is both accurate and easy to use on microcomputers, based on the conventional dynamic-programming method of pairwise alignment.
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