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EC Number Crystallization (Commentary)
Display the word mapDisplay the reaction diagram Show all sequences 2.7.7.6-
Display the word mapDisplay the reaction diagram Show all sequences 2.7.7.6a large fragment of subunit PA bound to a fragment of subunit PB1, hanging dropn vapour diffusion method, 20°C, mixing of 0.001 ml of protein solution, containing 10 mg/ml protein in 20 mM Tris-HCl, pH 8.0, and 100 mM sodium chloride, and 0.001 ml of reservoir solution consisting of 100 mM Tris-HCl, pH 7.5, and 2.4 M sodium formate, X-ray diffraction structure determination and analysis at 2.3 A resolution
Display the word mapDisplay the reaction diagram Show all sequences 2.7.7.6ammonium sulfate precipitation
Display the word mapDisplay the reaction diagram Show all sequences 2.7.7.6crystal structure anaysis
Display the word mapDisplay the reaction diagram Show all sequences 2.7.7.6crystal structure determination
Display the word mapDisplay the reaction diagram Show all sequences 2.7.7.6crystal structure determination, structure including the A' subunit jaw and clamp head domains and RpoG and Rpo13 subunits
Display the word mapDisplay the reaction diagram Show all sequences 2.7.7.6crystal structure of the core enzyme at 3.3 A resolution
Display the word mapDisplay the reaction diagram Show all sequences 2.7.7.6crystal structure of the core enzyme at about 3.3 A resolution
Display the word mapDisplay the reaction diagram Show all sequences 2.7.7.6crystallization of RNA polymerase II elongation complex. The purified paused complex forms crystals capable of X-ray diffraction to 3,5 A resolution. The complex remains active in the crystal and, in the presence of nucleoside triphosphates, can efficiently extend the transcript in situ
Display the word mapDisplay the reaction diagram Show all sequences 2.7.7.6crystallization of the enzyme with DNA fragments, crystal growth is optimized using a nanoseeding technique, of the various crystals screened, one diffracts to 4.3 A resolution
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