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. 2017 Aug 17;121(37):8693–8705. doi: 10.1021/acs.jpcb.7b06475

Table 3. Peak Volumesa in 1H–13C and 1H–15N INEPT Spectra of 13C15NCF4Q and 13C15NCF4QΔ34 Assembled with CheA and CheW into Functional Native-Like Arrays on Vesiclesb.

residue/s ω1/1H ω2/13C or 15N CF4Q volume CF4QΔ34 volume mobile region residues CF4Q – CF4QΔ34 = Δ34 volume Δ34 (tail) residues
total Cα (no Gly)     82.8 47.6 48 35.2 34
Arg Nε 7.3 84.9 5.7 2.8 3 2.9 3
Asn Cβ + Tyr Cβ 2.6 39.1 4.1 2.4 1 Asn, 1 Tyr 1.7 2 Asn
Glu Cγ 2.2 36.3 7.1 3.7 5 3.4 3
Gly Cα 4.0 45.4 2.8 2.8 3 0.0 0
Gly N 8.3, 8.2 108.7, 107.4 2.5 2.2 3 0.3 0
His Cβ 3.1 29.7 0.9 0.7 1 0.2 0
His Cε1 7.8 138.4 0.9 0.8 1 0.1 0
Ile Cβ 1.8 38.7 3.2 1.9 2 1.3 1
Ile Cδ1 0.8 13.0 3.3 2.0 2 1.3 1
Leu Cβ 1.6 42.2 4.3 2.5 3 1.7 2
Met Cβ 2.0 17.1 1.5 1.5 1 0.0 0
Phe 7.2 131.8 1.1 0 0 1.1 1
Pro Cδ 3.7 50.7 1.3 0 0 1.3 7
Thr Cβ 4.2 69.8 8.4 5.4 6 3.0 3
Trp Nε 10.0 129.1 1.0 0 0 1.0 1
Tyr Cδ 7.1 133.4 1.1 1.0 1 0.1 0
a

All peak volumes are corrected for differences in nmol of CF in the sample. HC peak volumes are then calibrated based on Tyr Cδ = 2 in the CF4QΔ34 vesicle sample, and then normalized to the number of unresolved correlations contributing to the peak (5 for Phe and 2 for Tyr Cδ) so that the reported volume should correspond to the number of residues. HN peak volumes are calibrated based on Trp Nε = 1 in the CF4Q vesicle sample.

b

Bold columns compare peak volumes to residues of the most probable 50-residue mobile region; italicized columns compare difference volumes to residues of the deleted 34-residue tail.