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. Author manuscript; available in PMC: 2016 Oct 1.
Published in final edited form as: Nat Chem Biol. 2016 Feb 29;12(4):298–303. doi: 10.1038/nchembio.2029

Figure 5. EPR spectra of Ls(AA9)A at 150 K.

Figure 5

* indicates signals from copper site where water was the exogenous ligand, other signals were from species with chloride as exogenous ligand. a, X-band cw EPR spectra in low chloride conditions, Ls(AA9)A-G6 (top) and Ls(AA9)A with no oligosaccharide (bottom). b, X-band cw EPR spectra in high chloride conditions, Ls(AA9)A-G6 (top) and Ls(AA9)A with no oligosaccharide (bottom). c, Contour presentation of the 1H-HYSCORE spectrum of Ls(AA9)A-G6 in the presence of chloride ions (magnetic field 343.6 mT, time between first and second pulse τ = 136 ns, microwave frequency 9.7 GHz). The anti-diagonal cross-peaks are assigned to anisotropic protons, labelled 1H and 2H.