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Molecule Parameter List for APC | 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 | mkp1_feedback_
effects | 4 | Network |
Shared_Object_mkp1_feedback_effects, Sos, PKC,
MAPK, PLA2, Ras,
PDGFR | | This is a network involving the MAPK-PKC feedback loop with input from the PDGFR in the synapse. The distinctive feature of this model is that it includes MKP-1 induction by MAPK, and the consequent inhibitory regulation of MAPK and the feedback loop. Lots of interesting dynamics arise from this. This link provides supplementary material for the paper Bhalla US et al. Science (2002) 297(5583):1018-23. In the form of several example simulations and demos for the figures in the paper. |
APC acting as a Molecule in mkp1_feedback_effects Network
| Name | Accession Name | Pathway Name | Initial Conc.
(uM) | Volume
(fL) | Buffered | | APC | mkp1_feedback_
effects
Accession No. : 4 | PLA2
Pathway No. : 36 | 30 | 1000 | Yes | | arachodonylphosphatidylcholine is the favoured substrate from Wijkander and Sundler, JBC 202 pp 873-880, 1991. Their assay used 30 uM substrate, which is what the kinetics in this model are based on. For the later model we should locate a more realistic value for APC. For now it is treated as a buffered metabolite. |
APC acting as a Substrate for an Enzyme in mkp1_feedback_effects Network
| | Enzyme Molecule /
Enzyme Activity | Accession Name | Pathway Name | Km (uM) | kcat (s^-1) | Ratio | Enzyme Type | Reagents | | 1 | PLA2-Ca* /
kenz | mkp1_feedback_
effects
Accession No. : 4 | PLA2
Pathway No. : 36 | 20 | 5.4 | 4 | explicit E-S complex | Substrate
APC
Product
AA
| | | Based on Leslie and Channon 1990 BBA 1045:261, in relation to the other PLA2 inputs (not including MAPK). Ca alone is rather a weak input. | | 2 | PIP2-PLA2* /
kenz | mkp1_feedback_
effects
Accession No. : 4 | PLA2
Pathway No. : 36 | 20 | 11.04 | 4 | explicit E-S complex | Substrate
APC
Product
AA
| | | Based on Leslie and Channon 1990 BBA 1045:261. | | 3 | PIP2-Ca-PLA2* /
kenz | mkp1_feedback_
effects
Accession No. : 4 | PLA2
Pathway No. : 36 | 20 | 36 | 4 | explicit E-S complex | Substrate
APC
Product
AA
| | | Based on AA generation by different stimuli according to Leslie and Channon 1990 BBA 1045:261 | | 4 | DAG-Ca-PLA2* /
kenz | mkp1_feedback_
effects
Accession No. : 4 | PLA2
Pathway No. : 36 | 20 | 60 | 4 | explicit E-S complex | Substrate
APC
Product
AA
| | | Based on Leslie and Channon 1990 BBA 1045:261. | | 5 | PLA2*-Ca /
kenz | mkp1_feedback_
effects
Accession No. : 4 | PLA2
Pathway No. : 36 | 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, from Lin et al 1993 Cell 269-278 Nemenoff et al 1993 JBC 268:1960 Several forms contribute to the Ca-stimulated form, so this rate has to be a factor larger than their total contribution. I assign Vmax as the scale factor here because there is lots of APC substrate, so all the PLA2 complex enzymes are limited primarily by Vmax. |
APC acting as a Product in a reaction in mkp1_feedback_effects 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 | | Degrade-AA | mkp1_feedback_
effects
Accession No. : 4 | PLA2
Pathway No. : 36 | 0.4
(s^-1) | 0
(s^-1) | - | - | Substrate
AA
Product
APC
| | Degradation pathway for AA. APC is a convenient buffered pool to dump it back into, though the actual metabolism is probably far more complex. For the purposes of the full model we use a rate of degradation of 0.4/sec to give a dynamic range of AA comparable to what is seen experimentally. Wijkander and Sundler 1991 Eur J Biochem 202:873 Leslie and Channon 1990 BBA 1045:261 |
| Database compilation and code copyright (C) 2022, Upinder S. Bhalla and NCBS/TIFR
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