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Result: 1 - 7 of 7 rows are displayed

Reaction List for pathway Gs (Pathway Number 198) in Accession PKA_2003 (Accession Number 47)

Entries are grouped according to Pathway Number and they are alternately color coded using  and  color.
Further ordering can be done to the table header.  indicates that ordering is done according to ascending or descending order.
Keq is calculated only for first order reactions.
Kd is calculated only for second order reactions. [nA+nB <->nC or nA<->nC+nD, where n is number and A,B,C,D are molecules]
  Reaction
Name
Pathway Name / 
Pathway No.
KfKbKdtauReagents
1 L-bind-RGs

Pathway No. 198
0.1
(uM^-1 s^-1)
0.1
(s^-1)
Kd(bf) = 1(uM)-  Substrate:
 R
 L

 Products:
 L.R
  Ligand binding to receptor. From Gether et al JBC 270:28268-28275 (1995) the binding to the purified receptor is at about 1 uM, but the conformational change only happens at 30 uM. We'll take 1 uM for this, since it is already much weaker binding than to the R.Gs complex. The time-course from this paper appears remarkably slow, based on physiological data I estimate more like 10 sec.
2 Activate-GsGs

Pathway No. 198
0.025
(s^-1)
0
(uM^-2 s^-1)
--  Substrate:
 L.R.GDP.Gabc

 Products:
 Gbg
 L.R
 GTP.Ga
  This step combines several stages in GTP.Galpha release. From Berstein et al activation is at .35 - 0.7/min From Fay et al Biochem 30 5066-5075 1991 kf = .01/sec. From Brandt and Ross JBC 261(4):1656-1664 (1986) and Ransan et al Biochem J 283(2):519-524 (1992) rates around 2.5/min to 1.5/min are better.
3 Trimerize-GsGs

Pathway No. 198
6
(uM^-1 s^-1)
0
(s^-1)
--  Substrate:
 GDP.Ga
 Gbg

 Products:
 GDP.Gabc
  Negligible back-reaction.
4 GTPaseGs

Pathway No. 198
0.0667
(s^-1)
0
(s^-1)
--  Substrate:
 GTP.Ga

 Products:
 GDP.Ga
  From Brandt and Ross JBC 261(4):1656-1664, rate is 4/min and is agonist independent. I treat this as irreversible.
5 L-bind-R.GabcGs

Pathway No. 198
5
(uM^-1 s^-1)
0.1
(s^-1)
Kd(bf) = 0.02(uM)-  Substrate:
 L
 R.GDP.Gabc

 Products:
 L.R.GDP.Gabc
  From Seifert et al Mol. Pharmacol 56:348-358 (1999) The EC50 for ISO is about 20 nM.
6 R-bind-GabcGs

Pathway No. 198
0.2
(uM^-1 s^-1)
0.1
(s^-1)
Kd(bf) = 0.5(uM)-  Substrate:
 GDP.Gabc
 R

 Products:
 R.GDP.Gabc
  Receptor binding to Gs. Scale it to the same slow rates described by Fay et al for L.R to L.R.G. From detailed balance, Kd is 50.
7 L.R-bind-GabcGs

Pathway No. 198
10.0002
(uM^-1 s^-1)
0.1
(s^-1)
Kd(bf) = 0.01(uM)-  Substrate:
 GDP.Gabc
 L.R

 Products:
 L.R.GDP.Gabc
  See Fay et al Biochem 30 5066-5075 1991. kf is 0.01/sec but does not account for Gs levels. kb is 0.0001/sec. The fraction of RG is about 50%, so we can estimate Kd at about the same as for Gs basal levels. This rate has to be faster since it has to feed GTP.Ga into the system faster than the GTPase. Waldhoer et al Mol Pharmacol 53:808-818 1988 say affinity for A1adenosine/Gi is 10 nM.

 
Result: 1 - 7 of 7 rows are displayed



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