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. 1999 Aug 17;96(17):9551–9556. doi: 10.1073/pnas.96.17.9551

Figure 4.

Figure 4

The peptide QEHA corresponding to amino acid residues 956–982 in ACII attenuates the ability of βγ subunits to inhibit AC activity. (A) IC1a⋅VC2 form of AC was stimulated by G* (80 nM). The ability of βγ subunits (200 nM) to inhibit G*-stimulated activity was monitored in the presence and absence of 200 nM each of the peptides QEHA and SKEE; peptide SKEE corresponds to residues 1,000–1,026 in ACIII, the cognate region of peptide QEHA in ACII. The mean ± SEM (n = 3 experiments) are shown. (B) Same as A except that the VC1aIC1b·IC2 form of AC was used. The mean ± SEM (n = 3 experiments) is presented.