Structure of the ectodomain of the electron transporter Rv2874 fromMycobacterium tuberculosis Mycobacterium tuberculosis reveals a thioredoxin‐like domain combined with a carbohydrate‐binding module. Issue 1 (1st January 2016)

• Record Type: Journal Article
• Authors: Goldstone, David C.; Metcalf, Peter; Baker, Edward N.
• Is Part Of: Acta crystallographica. Volume 72:Issue 1(2016)
• Page Start: 40
• Page End: 48
• Publication Date: 2016-01-01
• Subjects: membrane-protein ectodomain membrane‐protein ectodomain -- Mycobacterium tuberculosis Mycobacterium tuberculosis -- electron transport electron transport -- carbohydrate binding and modification carbohydrate binding and modification; X-ray crystallography -- Periodicals; Crystallography -- Periodicals; Molecular biology -- Periodicals; Molecular structure -- Periodicals; Biomolecules -- Structure -- Periodicals; Cytology -- Periodicals; Biomolecules -- Structure; Crystallography; Cytology; Molecular biology; Molecular structure; X-ray crystallography; Periodicals; 548
• DOI: 10.1107/S2059798315021488
• Languages: English
• ISSNs: 2059-7983

Abstract

Abstract : The structure of the extramembrane portion of the CcdA‐family member Rv2874 from M. tuberculosis M. tuberculosis reveals a previously unseen juxtaposition of a thioredoxin‐like domain with a carbohydrate‐binding module, suggesting a role in cell‐wall carbohydrate processing. Abstract : The members of the CcdA family are integral membrane proteins that use a disulfide cascade to transport electrons from the thioredoxin–thioredoxin reductase system in the interior of the cell into the extracytoplasmic space. The core transmembrane portion of this family is often elaborated with additional hydrophilic domains that act as adapters to deliver reducing potential to targets outside the cellular membrane. To investigate the function of family members in Mycobacterium tuberculosis Mycobacterium tuberculosis, the structure of the C‐terminal ectodomain from Rv2874, one of three CcdA‐family members present in the genome, was determined. The crystal structure, which was refined at 1.9 Å resolution with R R = 0.195 and R R free free = 0.219, reveals the predicted thioredoxin‐like domain with its conserved Cys‐ X X ‐ X X ‐Cys active‐site motif. Unexpectedly, this domain is combined with a second domain with a carbohydrate‐binding module (CBM) fold, this being the first reported example of a CBM in association with a thioredoxin‐like domain fold. A cavity in the CBM adjacent to the thioredoxin active site suggests a likely carbohydrate‐binding site, representing a broadening of the substrate range for CcdA‐family members and an expansion of the thioredoxin‐domain functionality to carbohydrate modification.