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Molecule Parameter List for PLA2-cytosolic | 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 | |
PLA2-cytosolic acting as a Molecule in MAPK-bistability-fig1c Network
Name | Accession Name | Pathway Name | Initial Conc. (uM) | Volume (fL) | Buffered | PLA2-cytosolic | MAPK-bistability -fig1c Accession No. : 35 | PLA2 Pathway No. : 183 | 0.4 | 1000 | No | cPLA2 IV form has mol wt of 85 Kd. Glaser et al 1993 TIPS 14:92-98. Calculated cytosolic concentration is ~300 nM from Wijkander and Sundler 1991 Eur J Biochem 202:873 Leslie and Channon 1990 BBA 1045:261 use about 400 nM. Decent match. Use 400 nM. |
PLA2-cytosolic acting as a Substrate for an Enzyme in MAPK-bistability-fig1c Network
Enzyme Molecule / Enzyme Activity | Accession Name | Pathway Name | Km (uM) | kcat (s^-1) | Ratio | Enzyme Type | Reagents | MAPK* / MAPK* | MAPK-bistability -fig1c Accession No. : 35 | Shared_Object_ MAPK-bistability -fig1c Pathway No. : 179 | 25.641 | 20 | 4 | explicit E-S complex | Substrate PLA2-cytosolic
Product PLA2*
| Km = 25uM @ 50 uM ATP and 1mg/ml MBP (huge XS of substrate) Vmax = 4124 pmol/min/ml at a conc of 125 pmol/ml of enz. Numbers are from Sanghera et al JBC 265 pp 52 , 1990. From Nemenoff et al 1993 JBC 268(3):1960-1964 - using Sanghera's 1e-4 ratio of MAPK to protein, we get k3 = 7/sec from 1000 pmol/min/mg total protein in fig 5 I take the Vmax to be higher for PLA2 given the fold activation of PLA2 by MAPK. This is actually a balance term between MAPK and the dephosphorylation step. |
PLA2-cytosolic acting as a Substrate in a reaction in MAPK-bistability-fig1c 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 | PLA2-Ca-act | MAPK-bistability -fig1c Accession No. : 35 | PLA2 Pathway No. : 183 | 1 (uM^-1 s^-1) | 0.1 (s^-1) | Kd(bf) = 0.1(uM) | - | Substrate Ca PLA2-cytosolic
Product PLA2-Ca*
| | Direct activation of PLA2 by Ca. From Leslie and Channon BBA 1045 (1990) 261-270 fig6 pp267. | 2 | PIP2-PLA2-act | MAPK-bistability -fig1c Accession No. : 35 | PLA2 Pathway No. : 183 | 0.0012 (uM^-1 s^-1) | 0.5 (s^-1) | Kd(bf) = 416.6667(uM) | - | Substrate PLA2-cytosolic temp-PIP2
Product PIP2-PLA2*
| | Activation of PLA2 by PIP2. From Leslie and Channon 1990 BBA 1045:261 the stimulation of PLA2 activity by high PIP2 is 7x. In this model we don't really expect any PIP2 stimulus. |
PLA2-cytosolic acting as a Product in a reaction in MAPK-bistability-fig1c 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 | dephosphorylate- PLA2* | MAPK-bistability -fig1c Accession No. : 35 | PLA2 Pathway No. : 183 | 0.17 (s^-1) | 0 (s^-1) | - | - | Substrate PLA2*
Product PLA2-cytosolic
| Dephosphorylation reaction to balance MAPK phosphorylation of PLA2. This is probably mediated by PP2A. Rates determined to keep the balance of phosphorylated and non-phosphorylated PLA2 reasonable. The constraining factor is the fold activation of PLA2 by MAPK. |
| 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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