Steady-state ATPase kinetics for RecG.
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All measurements were carried out at 20°C in the presence 10 µM MDCC-PBP, 10 nM RecG and 500 nM DNA junction (A40:B40) in a buffer described in the materials and methods. (a) kcat and Km for nucleoside triphosphates (b) Ki for non-hydrolyzable or slowly hydrolyzing nucleotides, using 10 µM ATP and varying inhibitor concentration.
创建时间：
2015-12-02
