Steady-state ATPase kinetics for RecG.
收藏NIAID Data Ecosystem2026-03-07 收录
官方服务：
资源简介：
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：
2012-06-06
