Skip to main content
. 2015 May 22;71(Pt 6):746–751. doi: 10.1107/S2053230X15007542

Table 1. Crystallization of active and latent cgAUS1.

Crystallization condition (resulting data set) A (1, 2) B (3) C (4) D (5) E (6) F (7)
Protein sample cgAUS1-a1, cgAUS1-a2 cgAUS1-a2 cgAUS1-ln cgAUS1-lr cgAUS1-lr cgAUS1-lr
Protein concentration (mgml1) 36 6 10 14 14 14
Composition of reservoir solution 2325% PEG 4000, 500mM NaCl, 100mM Na formate, 50mM Na citrate pH 6.4 22% PEG 4000, 500mM NaCl, 100mM Na formate, 50mM Na citrate pH 6.4, 100mM 1,4-resorcinol 15% PEG 4000, 100mM MgCl2, 60mM Na citrate pH 7.4 15% PEG 4000, 100mM MgCl2, 60mM Na citrate pH 7.4 12% PEG 4000, 60mM Na citrate pH 6.4, 1mM Na6[TeW6O24] 15% PEG 4000, 60mM Na citrate pH 5.0, 20% glycerol, 1mM Na6[TeW6O24]
Volume of drop (l) 2, 3 2 2 2 2 2
Ratio of drop (protein:reservoir) 1:1; 1:2 1:1 1:1 1:1 1:1 1:1
Cryoprotectant solution 40% PEG 4000, 15% glycerol, 20mM Na citrate pH 6.4 40% PEG 4000, 15% glycerol, 20mM Na citrate pH 6.4, 100mM 1,4-resorcinol 40% PEG 4000, 15% glycerol, 20mM Na citrate pH 7.4 40% PEG 4000, 15% glycerol, 20mM Na citrate pH 7.4 40% PEG 4000, 15% glycerol, 20mM Na citrate pH 6.4 40% PEG 4000, 15% glycerol, 20mM Na citrate pH 5.0, 5mM H2O2

The cryoprotectant solution contained hydrogen peroxide to generate the oxy-form of the dinuclear copper site.