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. Author manuscript; available in PMC: 2013 Mar 1.
Published in final edited form as: J Biomol NMR. 2012 Feb 17;52(3):191–195. doi: 10.1007/s10858-012-9606-9

Fig 2.

Fig 2

(A) 600MHz 1H-15N TROSY spectra of wild-type (blue) and M469pAcF/C575A (red) EIC. The NMR spectra were acquired at 37°C. Sample conditions were as follow: 400 μM EIC, 20 mM Tris, pH 7.4, 100 mM NaCl, 4 mM MgCl2, 1 mM EDTA. Under these conditions EIC is present as a 70 kDa dimer (Patel et al., 2006). Resonance assignment for cross-peaks showing large chemical shift differences in the two EIC constructs is reported on the wild-type spectrum. (B) X-ray structure of the wild-type EIC dimer (PDB code 2HWG) (Teplyakov et al., 2006). The monomeric subunits are colored in cyan and orange. Residues whose resonances show large 1HN/15N chemical shift differences (>0.1 ppm) as a consequence of the M469pAcF and C575A mutations are indicated as blue spheres. M469 is shown as yellow sticks.