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Molecule Parameter List for inact-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 | Ajay_Bhalla_ 2007_Bistable | 79 | Network | Shared_Object_Ajay_Bhalla_2007_Bistable, PKC, PLA2, MAPK, Ras, CaM | This is a model of ERKII signaling which is bistable due to feedback. The feedback occurs through ERKII phosphorylation of phospholipase A2 (PLA2), leading to increased production of arachidonic acid (AA), which activates protein kinase C (PKC) which activates c-Raf which is upstream of ERKII. The model is a highly simplified variant of more detailed bistable models of MAPK signaling (Bhalla US, Iyengar R. Science. 1999 Jan 15;283(5400):381-7, Ajay SM, Bhalla US. Eur J Neurosci. 2004 Nov;20(10):2671-80) |
inact-GEF acting as a Molecule in Ajay_Bhalla_2007_Bistable Network
Name | Accession Name | Pathway Name | Initial Conc. (uM) | Volume (fL) | Buffered | inact-GEF | Ajay_Bhalla_ 2007_Bistable Accession No. : 79 | Ras Pathway No. : 367 | 0.1 | 125.7 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. |
inact-GEF acting as an Enzyme in Ajay_Bhalla_2007_Bistable Network
Enzyme Molecule / Enzyme Activity | Accession Name | Pathway Name | Km (uM) | kcat (s^-1) | Ratio | Enzyme Type | Reagents | inact-GEF / basal_GEF_ activity
| Ajay_Bhalla_ 2007_Bistable Accession No. : 79 | Ras Pathway No. : 367 | 10.1014 | 0.02 | 4 | explicit E-S complex | Substrate GDP-Ras
Product GTP-Ras
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inact-GEF acting as a Substrate for an Enzyme in Ajay_Bhalla_2007_Bistable Network
Enzyme Molecule / Enzyme Activity | Accession Name | Pathway Name | Km (uM) | kcat (s^-1) | Ratio | Enzyme Type | Reagents | PKC-active / PKC-act-GEF | Ajay_Bhalla_ 2007_Bistable Accession No. : 79 | Shared_Object_ Ajay_Bhalla_ 2007_Bistable Pathway No. : 363 | 3.33331 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| 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 |
inact-GEF acting as a Substrate in a reaction in Ajay_Bhalla_2007_Bistable 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 | CaM-bind-GEF | Ajay_Bhalla_ 2007_Bistable Accession No. : 79 | Ras Pathway No. : 367 | 199.999 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-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 28 Feb 2006: Increased affinity 36-fold to account for Ca input to MAPK cascade, possibly folding in other pathway inputs. 21 April 2006: Altered affinity to same level as pkm_mapk21.g model to prevent spontaneous turnon. Kf = 200, Kb = 1. |
inact-GEF acting as a Product in a reaction in Ajay_Bhalla_2007_Bistable 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 | dephosph-GEF | Ajay_Bhalla_ 2007_Bistable Accession No. : 79 | Ras Pathway No. : 367 | 1 (s^-1) | 0 (s^-1) | - | - | Substrate GEF*
Product inact-GEF
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| 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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