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. 2014 Jan 29;70(Pt 2):384–391. doi: 10.1107/S1399004713028393

Figure 1.

Figure 1

(a) GtgE43–214 was subjected to limited proteolysis by subtilisin protease (Sigma–Aldrich) as described. Edman sequencing indicated that the two main cleavage products were N-terminally truncated to residue 79. C-­terminal residue limits were estimated based on the molecular weight of the cleavage products as observed by SDS–PAGE. The crystallized construct is shown in red. Molecular-mass markers (left lane) are labelled in kDa. (b) Native and selenomethionine-derivative crystals of GtgE79–214 grown in 0.2 M Li2SO4, 1.75 M ammonium sulfate, 0.1 M Tris pH 7.0 at 4°C. (c) 2F o − F c model-phased electron-density map contoured at 2σ shown in blue with the final refined model shown.