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EC Number
Crystallization
Reference
crystal structure of Sirt3 in complex with fluor-de-Lys peptide and resveratrol and crystal structure of Sirt3 in complex with fluor-de-Lys peptide and piceatannol
crystallization at 4°C by the sitting-drop vapor diffusion method. Crystal structure of human SIRT2 in complex with a macrocyclic peptide inhibitor S2iL5, at 2.5 A resolution
enzyme in a productive complex with NAD+, in a nonproductive NAD+ complex and in the unliganded state, hanging drop vapor diffusion method, using 0.1 M HEPES (pH 7.4), 1.8 M ammonium sulfate, and 1% (w/v) PEG400 at 20°C
enzyme in complex with its acetyl-lysine 16 histone H4 substrate, nicotinamide and the reaction intermediate analog ADP-HPD, vapor diffusion method, using 2.0 M (NH4)2SO4, 100 mM Na citrate, pH 5.6, 200 mM K/Na tartrate or 2.0 M (NH4)2SO4 and 100 mM Na citrate, pH 5.5
hanging drop vapor diffusion using a 1:1 drop ratio. The 2.5 A crystal structure of the SIRT1 catalytic domain bound to NAD+ and 6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide (EX527)
in complex with ADP ribose, microseed matrix seeding, using 17.5% (w/v) PEG 10000, 0.1 M ammonium acetate in 0.1 M bis-Tris buffer pH 6.8 at 20°C; in complex with ADP ribose, microseed matrix seeding, using 25% (w/v) PEG 3350, 0.2 M MgCl2 in 0.1 M bis-Tris buffer pH 5.5
in complex with BHJH-TM1 protein, hanging drop vapor diffusion method, using 25% (w/v) PEG 3350, 0.1 M HEPES buffer, pH 7.5
in complex with [histone H3]-N6-myristoyl-L-lysine9, hanging drop vapor diffusion method, using 16% (w/v) PEG 3350, 0.1 M NaF, 7% (v/v) formamide
isoform SIR2-Af1 in complex with NAD+, hanging drop vapor diffusion method, using 100 mM MES (pH 6.0), and 12% (w/v) PEG-10K
native and selenomethionine-derivatized enzyme in complex with an 11-residue peptide containing residues 12-19 of histone H4 and acetylated at lysine 16, hanging drop vapor diffusion method, using
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