Disorderness in <i>Escherichia coli</i> proteome: perception of folding fidelity and protein–protein interactions

2013-05-01T00:00:00Z (GMT) by Bratati Kahali Tapash Chandra Ghosh
<div><p>Traditionally biased usage of synonymous codons renders selective advantage to proteins expressed at high levels with a few exceptions like in <i>Escherichia coli</i>. Proteome-wide characteristics indicative of trends in highly expressed proteins of <i>E. coli</i> is analyzed in this communication. Implications for the nature of interactions performed by these two groups of highly expressed proteins are discussed here. The group of highly expressed proteins having optimized codon usage through employment of most abundant tRNAs is already shielded from misfolding by their improved error-prone translational machinery. Our data also provide evidence for mechanism by which a significant proportion of highly expressed proteins with high intrinsic disorder evade degradation and successfully carry out their function.</p> </div>