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. Author manuscript; available in PMC: 2008 Sep 9.
Published in final edited form as: Biochemistry. 2007 May 27;46(25):7514–7524. doi: 10.1021/bi700082v

Table 3.

Assigned quadrupolar splittings from WALP19 peptides in DMPC at 40°C, based on results for selectively labeled tryptophans. The last column lists the averaged θ angles between the C-D bond and the membrane normal (assuming isotropic order parameters of 0.75 (Trp-2&3) and 0.55 (Trp-17&18), along with the error associated with an estimated experimental error of 2 kHz in Δνq.

Labeled Trp Bond C-2 Bond C-5

Δνq (kHz) θ (°) Δνq (kHz) θ (°)
Trp-2 76 40.2 ± 0.4; 73.2 ± 0.7 155 23.3 ± 0.5
Trp-3 53 44.6 ± 0.4; 66.5 ± 0.5 155 23.3 ± 0.5
Trp-17 62 38.5 ± 0.5; 76.4 ± 1.1 a a
Trp-18 11 51.8 ± 0.5, 57.8 ± 0.6 63 38.3 ± 0.5; 77.0 ± 1.2
a

No weaker C-5 peak could be identified for Trp-17.