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Molecule Parameter List for inact_dash_GEF | 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 | Differential syn thesis of mRNA | 95 | Network | kinetics, compartment_1, compartment_2 | The model consists of three major pathways: Calcium-calmodulin dependent protein kinase IV (CaMKIV), Mitogen-activated protein kinase (MAPK) and Protein Phosphatase 1 (PP1). Each of these converged on CREB activation. We also modeled further interactions with Transducer of regulated CREB activity 1 (TORC1) and the protein kinase A (PKA) pathway. |
inact_dash_GEF acting as a Molecule in Differential synthesis of mRNA Network
Name | Accession Name | Pathway Name | Initial Conc. (uM) | Volume (fL) | Buffered | inact_dash_GEF | Differential syn thesis of mRNA Accession No. : 95 | kinetics Pathway No. : 1115 | 0.1 | 1000 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. |
inact_dash_GEF acting as a Substrate for an Enzyme in Differential synthesis of mRNA Network
| Enzyme Molecule / Enzyme Activity | Accession Name | Pathway Name | Km (uM) | kcat (s^-1) | Ratio | Enzyme Type | Reagents | 1 | PKC_dash_active / PKC_dash_act_ dash_GEF
| Differential syn thesis of mRNA Accession No. : 95 | kinetics Pathway No. : 1115 | 3.3333 | 4 | 4 | explicit E-S complex | Substrate inact_dash_GEF
Product GEF_star
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 2 | PKA_dash_active / PKA_dash_ phosph_dash_GEF
| Differential syn thesis of mRNA Accession No. : 95 | kinetics Pathway No. : 1115 | 7.5 | 9 | 4 | explicit E-S complex | Substrate inact_dash_GEF
Product inact_dash_GEF_ star
| | This pathway inhibits Ras when cAMP is elevated. See: Hordijk et al JBC 269:5 3534-3538 1994 Burgering et al EMBO J 12:11 4211-4220 1993 The rates are the same as used in PKA-phosph-I1 |
inact_dash_GEF acting as a Substrate in a reaction in Differential synthesis of mRNA 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 | bg_dash_act_ dash_GEF | Differential syn thesis of mRNA Accession No. : 95 | kinetics Pathway No. : 1115 | 6 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.1667(uM) | - | Substrate BetaGamma inact_dash_GEF
Product GEF_dash_Gprot_ dash_bg
| | SoS/GEF is present at 50 nM ie 3e4/cell. BetaGamma maxes out at 9e4. Assume we have 1/3 of the GEF active when the BetaGamma is 1.5e4. so 1e4 * kb = 2e4 * 1.5e4 * kf, so kf/kb = 3e-5. The rate of this equil should be reasonably fast, say 1/sec | 2 | CaM_dash_bind_ dash_GEF | Differential syn thesis of mRNA Accession No. : 95 | kinetics Pathway No. : 1115 | 60 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.0167(uM) | - | Substrate CaM_dash_Ca4 inact_dash_GEF
Product CaM_dash_GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 |
inact_dash_GEF acting as a Product in a reaction in Differential synthesis of mRNA 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. |
| Database compilation and code copyright (C) 2022, Upinder S. Bhalla and NCBS/TIFR This Copyright is applied to ensure that the contents of this database remain freely available. Please see FAQ for details. |
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