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. Author manuscript; available in PMC: 2014 Jul 1.
Published in final edited form as: Nat Commun. 2014;5:3009. doi: 10.1038/ncomms4009

Figure 3. Co-substrate-binding sites.

Figure 3

a, Wall-eyed stereo view from the periplasmic side of the internal cavity in Mol-A with the N- and C-halves in green and blue, respectively. b, Identical view of Mol-B with N- and C-halves in cyan and blue, respectively. c, Steady-state levels of [3H]melibiose accumulation by intact cells at 10 min presented as histograms. DW2, cells without MelB. Error bar, s.e.m.; n = 2 for all mutants with a single-site mutation, and n = 10 for the WT and DW2. d, Trp→D2G FRET with RSO vesicles. The emission signals were collected at wavelength of 490 nm after excited at wavelength of 290 nm. Λ, adding 10 μM D2G; pink arrows Inline graphic adding 120 mM melibiose; gray arrows Inline graphic adding water; black arrows ↓, adding 20 mM or 50 mM Na+ or Li+. Black double-headed arrows ↔, Na+ or Li+ stimulation; pink double-headed arrows Inline graphic, melibiose displacement of D2G.