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EC Number Crystallization (Commentary)
Show all pathways known for 5.3.3.2Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.2-
Show all pathways known for 5.3.3.2Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.2comparison of orthorhombic, monoclinic and trigonal crystal forms, up to 2.2 A resolution. Crystallization of free enzyme and in complex wih transition-state analogue N,N-dimethyl-2-amino-1-ethyl diphosphate
Show all pathways known for 5.3.3.2Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.2crystal structure of free and metal-bound C67A mutant enzyme
Show all pathways known for 5.3.3.2Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.2crystal structure of the isomerase-bromohydrin complex
Show all pathways known for 5.3.3.2Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.2crystallized at 20°C using the hanging-drop vapor diffusion method with a reservoir solution containing 0.1 M Tris-HCl (pH 8.0), 0.2 M sodium citrate, and 30% (vol/vol) polyethylene glycol 400 (PEG 400)
Show all pathways known for 5.3.3.2Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.2crystallographic investigation of phosphoantigen binding
Show all pathways known for 5.3.3.2Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.2crystals soaked with transition state analogue (N,N-dimethylamino)-1-ethyl diphosphate
Show all pathways known for 5.3.3.2Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.2enzyme shows a flexible N-terminal alpha-helix covering the active pocket and blocking the entrance. Substrate binding induces conformational change in the active site. A water molecule is the direct proton donor for the substrate
Show all pathways known for 5.3.3.2Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.2hanging drop vapor diffusion method, crystal structure of the C67A mutant of isopentenyl diphosphate isomerase complexed with the mechanism-based irreversible inhibitor 3,4-epoxy-3-methyl-1-butyl diphosphate
Show all pathways known for 5.3.3.2Display the word mapDisplay the reaction diagram Show all sequences 5.3.3.2hanging drop vapor diffusion method, crystal structures of complexes with transition state analogue N,N-dimethyl-2-amino-1-ethyl diphosphate and the covalently attached irreversible inhibitors 3,4-epoxy-3-methyl-1-butyl diphosphate at 1.96 A resolution
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