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Co-staining of cells expressing the XPG-V5 fusion protein with GFP in the pLenti CMV GFP backbone is shown in Figure S2A.

The frequency of hydrogen bond formation between the carbonyl groups of NQTrp and the amide backbone is shown in Figure 6.

The molecule backbone is shown in Figure S5.

The TAR phosphate backbone is shown in orange with bases in blue.

The protein backbone is shown in cartoon representation with the region of interest (residues 105 121) shown as sticks.

The predicted structures of the engineered pre-amiRNAs incorporated into the pSM155 backbone are shown in Fig. 1.

The chemical shift differences along the peptide backbone are shown in Figure 6 for Aβ42 in the presence and absence of curcumin or resveratrol.

The ribo-phosphate backbone is shown as a thin tube, in salmon and pale yellow color for the RNA and DNA strands, respectively, and the bases are depicted as rungs of a ladder.

An initial "manual" structure calculation with CYANA[ 28] used only the manually identified 48 unambiguous restraints (Table S1) in addition to hydrogen bonds defining the β-sheets and 56 dihedral angle restraints from TALOS+.[ 29] The resulting backbone structure is shown in Figure  3 a; for details see the Supporting Information.

The backbone of MdfA is shown in cartoon representation.

The chromophore backbone for TagRFP is shown in orange.