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. 2005 Feb 8;386(Pt 1):103–112. doi: 10.1042/BJ20041222

Figure 3. Kinetic analysis of cABC I on GalAG substrates.

Figure 3

Hanes representations of recombinant cABC I on C4S (●), C6S (○) and DS (▼). Inset, a comparison of enzyme activity on 1 mg/ml C6S substrate in 50 mM Tris buffer, pH 8.0, with 50 mM sodium acetate. Expression of the original clone (▲) results in a protein with negligible activity; expression of the clone manipulated to conform to the desired sequence (△) results in robust enzyme activity.