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Results 1 - 10 of 10
EC Number Crystallization (Commentary) Reference
Show all pathways known for 4.2.3.4Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.4- 137643
Show all pathways known for 4.2.3.4Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.4by using the hanging-drop vapour-diffusion method with different screening kits, yields crystals belonging to the tetragonal space group, crystals of DHQS obtained in sitting-drop setups using a hydra automated high-throughput crystal screening machine with different screening kits: (a) 0.1 M sodium malonate pH 4.0, 12% PEG 3350, (b) 0.2 M sodium malonate pH 6.0, 20% PEG 3350, (c) 0.1 M Tris pH 8.5, 2.0 M ammonium sulfate, (d) 0.15 M caesium chloride, 15% PEG 3350, (e) 1.0 M sodium citrate, 0.1 M CHES pH 9.5, (f) 0.2 M ammonium sulfate, 0.1 M bis-Tris pH 5.5, 25% PEG 3350, (g) 0.2 M ammonium sulfate, 0.1 M MES pH 6.5, 30% PEG MME 5000, (h) 0.02 M zinc chloride, 20% PEG 3350. Best crystals are obtained after two weeks from a reservoir containing 0.2 M ammonium sulfate, 0.1 M MES monohydrate pH 6.0 and 31%PEG MME 5000 690254
Show all pathways known for 4.2.3.4Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.4molecular replacement based on the structure of Aspergillus nidulans enzyme, PDB code 1NR5, revealing a homodimeric protein. Each monomer has a NAD+ binding site nestled between the distinct N- and C-terminal domains 729105
Show all pathways known for 4.2.3.4Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.4obtained in a solution containing 20 mM NAD+ 690739
Show all pathways known for 4.2.3.4Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.4oil microbatch method, homodimer 1.8 A resolution 666871
Show all pathways known for 4.2.3.4Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.4sitting-drop vapour-diffusion crystallisation at 4°C utilising microbridges, crystals of unliganded enzyme as well as in complexes with NAD+, the substrate analogue [1R-(1alpha,3beta,4alpha,5beta)]-5-phosphonomethyl-1,3,4-trihydroxycyclohexane-1-carboxylic acid and together with both, NAD+ and [1R-(1alpha,3beta,4alpha,5beta)]-5-phosphonomethyl-1,3,4-trihydroxycyclohexane-1-carboxylic acid 666031
Show all pathways known for 4.2.3.4Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.4sitting-drop vapour-diffusion crystallisation at 4°C utilising microbridges, crystals of unliganded enzyme as well as in complexes with NAD, the substrate analogue [1R-(1alpha,3beta,4alpha,5beta)]-5-phosphonomethyl-1,3,4-trihydroxycyclohexane-1-carboxylic acid and together with both, NAD and [1R-(1alpha,3beta,4alpha,5beta)]-5-phosphonomethyl-1,3,4-trihydroxycyclohexane-1-carboxylic acid 666031
Show all pathways known for 4.2.3.4Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.4sitting-drop vapour-diffusion, crystals of unliganded enzyme, binary complexes with either the substrate analogue, carbaphosphonate or the cofactor NADH, as well as the ternary enzyme-carbaphosphonate-cofactor complex 649156
Show all pathways known for 4.2.3.4Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.4sitting-drop vapour-diffusion, structure at 1.7 A resolution 649245
Show all pathways known for 4.2.3.4Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.4structure in complex with NAD and with NAD plus chlorogenic acid. Chlorogenic acid occupies the substrate position and coordinates with the metal ion in the substrate-binding pocket 763209
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