Skip to main content
. Author manuscript; available in PMC: 2008 Jun 14.
Published in final edited form as: J Biol Chem. 2007 Jun 1;282(30):21645–21652. doi: 10.1074/jbc.M702368200

Table 2.

Effect of Ca2+ binding in EF hand 2 on activation of RetGC-1 by EF(3,4) mutant

Mutantsa Amaxb nmol cGMP/mg/min K1/2c µM
GCAP-1 EF(3,4) in EGTA 16 ± 3.6 (N=4) 4.4 ± 0.8 (N=4)
GCAP-1 EF(3,4) at 10 µM [Ca]f 22 ± 3.5 (N=3) 1.2 ± 0.3 (N=3)
GCAP-1 E75Q/EF(3,4) in EGTA 18 ± 1.0 (N=3) 6.3 ± 0.3 (N=3)
GCAP-1 E75Q/EF(3,4) at 10 µM [Ca]f 15 ± 1.0 (N=3) 4.2 ± 0.3 (N=3)
a

GCAP-1 EF(3,4) and GCAP-1 E75Q/EF(3,4) represent GCAP-1(D100N/D102G/D144N/D148G) and GCAP-1(E75Q/D100N/D102G/D144N/D148G), respectively.

b

Amax, the maximal level of RetGC-1 activation by GCAP at indicated free Ca2+ in the presence of 5 mM free Mg2+ (mean ± S.D., N is the number of independent measurements)

c

K1/2, the concentration of GCAP required for half-maximal activation of RetGC-1 (mean ± S.D., N is the number of independent measurements)