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Molecule Parameter List for AA | 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 | MAPK_network_ 2003 | 50 | Network | Shared_Object_MAPK_network_2003, PKC, PLA2, PLCbeta, Gq, MAPK, Ras, EGFR, Sos, PLC_g, CaMKII, CaM, PP1, PP2B, PKA, AC | This is a network model of many pathways present at the neuronal synapse. The network has properties of temporal tuning as well as steady-state computational properties. In its default form the network is bistable.Bhalla US Biophys J. 2004 Aug;87(2):745-53 |
AA acting as a Molecule in MAPK_network_2003 Network
AA acting as a Product of an Enzyme in MAPK_network_2003 Network
| Enzyme Molecule / Enzyme Activity | Accession Name | Pathway Name | Km (uM) | kcat (s^-1) | Ratio | Enzyme Type | Reagents | 1 | PLA2-Ca* / kenz | MAPK_network_ 2003 Accession No. : 50 | PLA2 Pathway No. : 208 | 20 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
| | 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 | 2 | PIP2-PLA2* / kenz | MAPK_network_ 2003 Accession No. : 50 | PLA2 Pathway No. : 208 | 20 | 11.04 | 4 | explicit E-S complex | Substrate APC
Product AA
| | 10 X raise oct 22 12 X further raise oct 24 to allow for correct conc of enzyme | 3 | PIP2-Ca-PLA2* / kenz | MAPK_network_ 2003 Accession No. : 50 | PLA2 Pathway No. : 208 | 20 | 36 | 4 | explicit E-S complex | Substrate APC
Product AA
| | 10 x raise oct 22 12 x and rescale for k2 = 4 * k3 convention oct 24 Increase further to get the match to expt, which was spoilt due to large accumulation of PLA2 in the enzyme complexed forms. Lets raise k3, leaving the others at k1 = 1.5e-5 and k2 = 144 since they are large already. | 4 | DAG-Ca-PLA2* / kenz | MAPK_network_ 2003 Accession No. : 50 | PLA2 Pathway No. : 208 | 20 | 60 | 4 | explicit E-S complex | Substrate APC
Product AA
| | 10 X raise oct 22 12 X raise oct 24 + conversion to k2 =4 * k3 | 5 | PLA2*-Ca / kenz | MAPK_network_ 2003 Accession No. : 50 | PLA2 Pathway No. : 208 | 20 | 120 | 4 | explicit E-S complex | Substrate APC
Product AA
| | This form should be 3 to 6 times as fast as the Ca-only form. I have scaled by 4x which seems to give a 5x rise. 10x raise Oct 22 12 x oct 24, changed k2 = 4 * k3 |
AA acting as a Substrate in a reaction in MAPK_network_2003 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 | PKC-act-by-Ca-AA | MAPK_network_ 2003 Accession No. : 50 | PKC Pathway No. : 207 | 0.0012 (uM^-1 s^-1) | 0.1 (s^-1) | Kd(bf) = 83.3333(uM) | - | Substrate AA PKC-Ca
Product PKC-Ca-AA*
| | Schaechter and Benowitz We have to increase Kf for conc scaling Changed kf to 2e-9 on Sept 19, 94. This gives better match. | 2 | PKC-act-by-AA | MAPK_network_ 2003 Accession No. : 50 | PKC Pathway No. : 207 | 0.0001 (uM^-1 s^-1) | 0.1 (s^-1) | Kd(bf) = 833.3333(uM) | - | Substrate AA PKC-cytosolic
Product PKC-AA*
| | Raise kf from 1.667e-10 to 2e-10 to get better match to data. | 3 | PKC-n-DAG-AA | MAPK_network_ 2003 Accession No. : 50 | PKC Pathway No. : 207 | 0.018 (uM^-1 s^-1) | 2 (s^-1) | Kd(bf) = 111.1111(uM) | - | Substrate AA PKC-DAG
Product PKC-DAG-AA
| | Reduced kf to 0.66X to match Shinomura et al data. Initial: kf = 3.3333e-9 New: 2e-9 Newer: 2e-8 kb was 0.2 now 2. | 4 | Degrade-AA | MAPK_network_ 2003 Accession No. : 50 | PLA2 Pathway No. : 208 | 0.4 (s^-1) | 0 (s^-1) | - | - | Substrate AA
Product APC
| | I need to check if the AA degradation pathway really leads back to APC. Anyway, it is a convenient buffered pool to dump it back into. For the purposes of the full model we use a rate of degradation of 0.2/sec Raised decay to 0.4 : see PLA35.g notes for Feb17 |
| 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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