Effect of converting individual cysteine residues to serine on IDE kinetics.
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The activity of IDE and its cysteine mutants was determined using a fixed concentration of 10 µM Abz–GGFLRKHGQ-EDDnp as substrate. KA was determined by varying [ATP] at a fixed substrate concentration of 10 µM. Data is expressed as the mean plus or minus the standard deviation. Each value represents measurements made two to four times.
创建时间：
2012-10-15
