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. 2015 Jun 27;43(14):7096–7109. doi: 10.1093/nar/gkv647

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© The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Figure 2. — Structure of MRB1590. (A) Overall structure of MRB1590 with the N-domain, central ATPase domain and C-domain labeled and colored blue, yellow and pink, respectively. (B) Ribbon diagram showing the domains in (A) with secondary structural regions labeled. The N-terminal and C-terminal residues are also labeled. C) Size exclusion chromatography analyses of MRB1590. The protein runs as a dimer with a MW of 148 kDa (the monomer MW is 72 kDa). Shown is the elution profile and inset is the generated curve used to determine the MW, where the y axis is the elution volume normalized for column volume and the x axis is the log of the molecular weight (MW). The standards used for the analyses are cytochrome c (12.4 kDa), trypsin (23.3 kDa), albumin (66.4 kDa), alcohol dehydrogenase (150 kDa) and β-amylase (200 kDa).