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Contents 1 Overview 2 Background 3 Structure 4 Function 5 Disease 6 Relevance 7 Structural highlights

Overview

Mycobacterium tuberculosis NrdH is a small glutaredoxin-like protein involved in the electron transport chain that eventually leads to ribonucleotide reduction.

Background

Mycobacterium tuberculosis Wikipediaresides in the lungs of a host and upon becoming active, results in symptoms such as chest pains, weakness, and intense coughing. Left untreated and unmanaged, TB can lead to death (1.5 million in 2013). The disease has a high co-morbidity with HIV/AIDS due to its immunocompromising tendencies. Tuberculosis is one of the most heavily studied diseases today. With over 9 million infections worldwide per year, the necessity for antimicrobial agents to combat emerging multi-drug resistant strands is imperative.

Structure

The structure of M. tuberculosis as determined by x-ray crystallography has 79 residues in a single polypeptide chain. . The active site (shown in green) is dominated by a disulphide bond between Cys-11 and Cys-14, which serves as the site of reduction by Theirodoxin reductase.

Many theirodoxin-like proteins have a similar active site region, denoted as the theirodoxin fold, which occurs directly before the disulfide bond. The residues in this region, denoted by letters CVQC, are the most highly conserved of all areas of the protein across multiple species. Exactly how this structure relates to function is somewhat debated. A Threonine-6 reside directly across the theirodoxin fold from the disulphide bond has been suggested to adopt two different conformations which differentially affect the redox abilities of the Protein. In the A conformation, the alcohol of the threonine side chain points towards the disulfide bond, engaging an ionic interaction between the two that prevents the Therodoxin Reductase from binding. Alternatively, in the B conformation, the alcohol points in the opposite direction, allowing sufficient space for the ligand to bind and reduction to occur. The active site of the protein is stabilized through a network of hydrogen bonds involving the two highly conserved residues, CVQC and WSGFRP. The crystal structure shows that interactions with one water molecule is necessary for the proper coordination between the conserved motifs to occur. These hydrogen bonds orient the important residues in the most optimal position to promote oxidation and reduction.

Function

Disease

Relevance

Similar structures of NrdH have been isolated in other primitive species including E. coli, S. pyogenes, S. typhimurium, D. deserti, S. flexneri 2457T, and S. dysenteriae. In higher order multi-cellular organisms, however the NrdH protein is replaced by more complex glutaredoxins or theirodoxins. This observation leads some to speculate that NrdH is one of the very first ancestors in the ribonucleotide reduction pathway. If this is true, NrdH can be seen as a critical protein that allowed for the development of DNA-based life since deoxyribonucleotides could not have existed without the ribonucleotide reduction pathway. A better understanding of the evolutionary timeline of NrdH and similar proteins could shed greater light onto the RNA Wold Hypothesis, specifically describing the time frame of emergence of DNA based life.

Structural highlights

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