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Molecule Parameter List for Raf*-GTP-Ras | The statistics table lists the distribution of a molecule acting either as a substrate, product, enzyme or as a molecule within the network.
The text color of a molecule is highlighted by  color. | | Statistics |
Accession and Pathway Details | |
| Accession Name | Accession No. | Accession Type | Pathway Link | Ajay_Bhalla_
2007_ReacDiff2 | 83 | Network | Shared_Object_Ajay_Bhalla_2007_ReacDiff, PKC, MAPK,
Ras, CaM, PKM, chain, kinetics, PKC, MAPK, Ras, CaM, PKM, kinetics[1],
PKC, MAPK, Ras, kinetics[3], CaM, PKM, kinetics[2], PKC, MAPK, Ras,
CaM, PKM, PKC, MAPK, Ras, CaM, PKM, kinetics[4], PKC, MAPK, Ras, CaM,
PKM, kinetics[5], PKC, MAPK, Ras, CaM, PKM, kinetics[6], PKC, MAPK,
Ras, CaM, PKM, kinetics[7], PKC, MAPK, Ras, CaM, PKM, kinetics[8],
PKC, MAPK, Ras, CaM, PKM, kinetics[9], PKC, MAPK, Ras, CaM, PKM, kinetics[10],
PKC, MAPK, Ras, CaM, PKM, kinetics[11], PKC, MAPK, Ras, CaM, PKM, kinetics[12],
PKC, MAPK, Ras, CaM, PKM, kinetics[13], PKC, MAPK, Ras, CaM, PKM, kinetics[14],
PKC, MAPK, Ras, CaM, PKM, kinetics[15], PKC, MAPK, Ras, CaM, PKM, kinetics[16],
PKC, MAPK, Ras, CaM, PKM, kinetics[17], PKC, MAPK, Ras, CaM, PKM, kinetics[18],
PKC, MAPK, Ras, CaM, PKM, kinetics[19], PKC, MAPK, Ras, CaM, PKM, kinetics[20],
PKC, MAPK, Ras, CaM, PKM, kinetics[21], PKC, MAPK, Ras, CaM, PKM, kinetics[22],
PKC, MAPK, Ras, CaM, PKM, kinetics[23], PKC, MAPK, Ras, CaM, PKM, kinetics[24],
PKC, MAPK, Ras, CaM, PKM, kinetics[25], PKC, MAPK, Ras, CaM, PKM, kinetics[26],
PKC, MAPK, Ras, CaM, PKM, kinetics[27], PKC, MAPK, Ras, CaM, PKM, kinetics[28],
PKC, MAPK, Ras, CaM, PKM, kinetics[29], PKC, MAPK, Ras, CaM, PKM, kinetics[30],
PKC, MAPK, Ras, CaM, PKM, kinetics[31], PKC, MAPK, Ras, CaM, PKM, kinetics[32],
PKC, MAPK, Ras, CaM, PKM, kinetics[33], PKC, MAPK, Ras, CaM, PKM, kinetics[34],
PKC, MAPK, Ras, CaM, PKM, kinetics[35], PKC, MAPK, Ras, CaM, PKM, kinetics[36],
PKC, MAPK, Ras, CaM, PKM, kinetics[37], PKC, MAPK, Ras, CaM, PKM, kinetics[38],
PKC, MAPK, Ras, CaM, PKM | This is a 40-compartment reaction-diffusion-transport version of the Ajay_Bhalla_2007_PKM model. The original single-compartment model is repeated 40 times. In addition, a subset (27 out of 42) molecules can diffuse between compartments. Diffusion is implemented as a reaction between corresponding molecules in neighboring compartments. For D = 1e-12 m^2/sec (i.e., 1 micron^2/sec ) the kf and kb of this reaction for these 10 micron compartments are both 0.01/sec In addition, we have a forward (dendrite to soma) transport term of 1 microns/sec. This converts to a rate of 0.1/sec, but applies only to the kf. So the total kf of the diffusion 'reaction' is 0.11 for D = 1 micron^2/sec, and kb is 0.01. If D=0.1 micron^2/sec then kf = 0.101 and kb = 0.001. In addition this model has all molecules buffered in the first and last compartments. This boundary conditions says that the molecules are not drained out of the first compartment, nor do they all pile up in the last one.
The stimulus file pkm_mapk22_transp_endbuf_D1e-13_Fig4CD which was used for the model to replicate Figure 4C and 4D from the paper.
|
Raf*-GTP-Ras acting as a Molecule in Ajay_Bhalla_2007_ReacDiff2 Network
Raf*-GTP-Ras acting as an Enzyme in Ajay_Bhalla_2007_ReacDiff2 Network
| | Enzyme Molecule /
Enzyme Activity | Accession Name | Pathway Name | Km (uM) | kcat (s^-1) | Ratio | Enzyme Type | Reagents | | 1 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 679 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 2 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 679 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 3 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 686 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 4 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 686 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 5 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 692 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 6 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 692 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 7 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 699 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 8 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 699 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 9 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 704 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 10 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 704 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 11 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 710 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 12 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 710 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 13 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 716 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 14 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 716 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 15 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 722 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 16 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 722 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 17 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 728 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 18 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 728 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 19 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 734 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 20 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 734 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 21 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 740 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 22 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 740 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 23 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 746 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 24 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 746 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 25 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 752 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 26 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 752 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 27 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 758 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 28 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 758 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 29 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 764 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 30 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 764 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 31 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 770 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 32 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 770 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 33 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 776 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 34 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 776 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 35 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 782 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 36 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 782 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 37 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 788 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 38 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 788 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 39 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 794 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 40 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 794 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 41 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 800 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 42 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 800 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 43 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 806 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 44 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 806 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 45 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 812 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 46 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 812 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 47 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 818 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 48 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 818 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 49 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 824 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 50 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 824 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 51 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 830 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 52 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 830 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 53 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 836 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 54 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 836 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 55 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 842 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 56 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 842 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 57 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 848 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 58 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 848 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 59 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 854 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 60 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 854 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 61 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 860 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 62 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 860 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 63 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 866 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 64 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 866 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 65 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 872 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 66 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 872 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 67 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 878 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 68 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 878 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 69 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 884 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 70 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 884 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 71 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 890 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 72 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 890 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 73 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 896 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 74 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 896 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 75 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 902 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 76 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 902 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 77 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 908 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 78 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 908 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 | | 79 | Raf*-GTP-Ras /
Raf*-GTP-Ras.1
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 914 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK
Product
MAPKK-ser
| | | Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6 | | 80 | Raf*-GTP-Ras /
Raf*-GTP-Ras.2
| Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | MAPK
Pathway No. : 914 | 0.159096 | 0.3 | 4 | explicit E-S complex | Substrate
MAPKK-ser
Product
MAPKK*
| | | Same kinetics as other c-raf activated forms. See Force et al PNAS 91 1270-1274 1994. k1 = 1.1e-6, k2 = .42, k3 = 1.05 raise k1 to 5.5e-6 |
Raf*-GTP-Ras acting as a Substrate in a reaction in Ajay_Bhalla_2007_ReacDiff2 Network
| Kd is calculated only for second order reactions, like nA+nB <->nC or nA<->nC+nD, where n is number and A,B,C,D are molecules, where as for first order reactions Keq is calculated.
Kd for higher order reaction are not consider. |
Raf*-GTP-Ras acting as a Product in a reaction in Ajay_Bhalla_2007_ReacDiff2 Network
| Kd is calculated only for second order reactions, like nA+nB <->nC or nA<->nC+nD, where n is number and A,B,C,D are molecules, where as for first order reactions Keq is calculated.
Kd for higher order reaction are not consider. |
| | Name | Accession Name | Pathway Name | Kf | Kb | Kd | tau | Reagents | | 1 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 2 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 3 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 4 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics
Pathway No. : 684 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 5 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 6 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[1]
Pathway No. : 690 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 7 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 8 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[2]
Pathway No. : 697 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 9 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 10 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[3]
Pathway No. : 694 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 11 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 12 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[4]
Pathway No. : 708 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 13 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 14 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[5]
Pathway No. : 714 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 15 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 16 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[6]
Pathway No. : 720 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 17 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 18 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[7]
Pathway No. : 726 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 19 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 20 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[8]
Pathway No. : 732 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 21 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 22 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[9]
Pathway No. : 738 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 23 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 24 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[10]
Pathway No. : 744 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 25 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 26 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[11]
Pathway No. : 750 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 27 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 28 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[12]
Pathway No. : 756 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 29 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 30 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[13]
Pathway No. : 762 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 31 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 32 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[14]
Pathway No. : 768 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 33 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 34 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[15]
Pathway No. : 774 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 35 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 36 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[16]
Pathway No. : 780 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 37 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 38 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[17]
Pathway No. : 786 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 39 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 40 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[18]
Pathway No. : 792 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 41 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 42 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[19]
Pathway No. : 798 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 43 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 44 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[20]
Pathway No. : 804 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 45 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 46 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[21]
Pathway No. : 810 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 47 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 48 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[22]
Pathway No. : 816 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 49 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 50 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[23]
Pathway No. : 822 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 51 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 52 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[24]
Pathway No. : 828 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 53 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 54 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[25]
Pathway No. : 834 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 55 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 56 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[26]
Pathway No. : 840 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 57 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 58 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[27]
Pathway No. : 846 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 59 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 60 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[28]
Pathway No. : 852 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 61 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 62 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[29]
Pathway No. : 858 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 63 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 64 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[30]
Pathway No. : 864 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 65 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 66 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[31]
Pathway No. : 870 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 67 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 68 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[32]
Pathway No. : 876 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 69 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 70 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[33]
Pathway No. : 882 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 71 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 72 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[34]
Pathway No. : 888 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 73 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 74 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[35]
Pathway No. : 894 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 75 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 76 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[36]
Pathway No. : 900 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 77 | diff | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | Shared_Object_
Ajay_Bhalla_
2007_ReacDiff
Pathway No. : 677 | 0.101
(s^-1) | 0.001
(s^-1) | Keq = 0.0099(uM) | 9.804sec | Substrate
Raf*-GTP-Ras
Product
Raf*-GTP-Ras
| | 78 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[37]
Pathway No. : 906 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. | | 79 | Ras-act-craf | Ajay_Bhalla_
2007_ReacDiff2
Accession No. : 83 | kinetics[38]
Pathway No. : 912 | 9.9998
(uM^-1 s^-1) | 0.5
(s^-1) | Kd(bf) = 0.05(uM) | - | Substrate
GTP-Ras
craf-1*
Product
Raf*-GTP-Ras
| | | Assume the binding is fast and limited only by the amount of Ras* available. So kf=kb/[craf-1] If kb is 1/sec, then kf = 1/0.2 uM = 1/(0.2 * 6e5) = 8.3e-6 Later: Raise it by 10 X to 4e-5 From Hallberg et al JBC 269:6 3913-3916 1994, 3% of cellular Raf is complexed with Ras. So we raise kb 4x to 4 This step needed to memb-anchor and activate Raf: Leevers et al Nature 369 411-414 May 16, 2003 Changed Ras and Raf to synaptic levels, an increase of about 2x for each. To maintain the percentage of complexed Raf, reduced the kf by 2.4 fold to 10. |
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