Name | Accession Name | Pathway Name | Initial Conc. (uM) | Volume (fL) | Buffered |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 920 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 922 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 933 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 939 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 945 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 951 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 957 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 964 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 970 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 976 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 982 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 988 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 994 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1000 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1005 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1011 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1017 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1023 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1029 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1035 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1041 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1047 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1053 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1059 | 30.0003 | 125.7 | 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. |
APC | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1065 | 30.0003 | 125.7 | 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. |
| Enzyme Molecule / Enzyme Activity | Accession Name | Pathway Name | Km (uM) | kcat (s^-1) | Ratio | Enzyme Type | Reagents |
1 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 920 | 19.9994 | 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 | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 920 | 19.9998 | 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 | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 920 | 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 | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 920 | 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 | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 920 | 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 |
6 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 922 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
7 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 922 | 19.9998 | 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 |
8 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 922 | 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. |
9 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 922 | 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 |
10 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 922 | 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 |
11 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 933 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
12 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 933 | 19.9998 | 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 |
13 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 933 | 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. |
14 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 933 | 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 |
15 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 933 | 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 |
16 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 939 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
17 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 939 | 19.9998 | 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 |
18 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 939 | 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. |
19 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 939 | 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 |
20 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 939 | 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 |
21 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 945 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
22 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 945 | 19.9998 | 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 |
23 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 945 | 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. |
24 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 945 | 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 |
25 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 945 | 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 |
26 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 951 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
27 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 951 | 19.9998 | 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 |
28 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 951 | 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. |
29 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 951 | 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 |
30 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 951 | 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 |
31 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 957 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
32 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 957 | 19.9998 | 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 |
33 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 957 | 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. |
34 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 957 | 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 |
35 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 957 | 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 |
36 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 964 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
37 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 964 | 19.9998 | 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 |
38 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 964 | 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. |
39 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 964 | 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 |
40 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 964 | 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 |
41 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 970 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
42 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 970 | 19.9998 | 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 |
43 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 970 | 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. |
44 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 970 | 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 |
45 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 970 | 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 |
46 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 976 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
47 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 976 | 19.9998 | 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 |
48 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 976 | 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. |
49 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 976 | 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 |
50 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 976 | 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 |
51 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 982 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
52 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 982 | 19.9998 | 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 |
53 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 982 | 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. |
54 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 982 | 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 |
55 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 982 | 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 |
56 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 988 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
57 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 988 | 19.9998 | 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 |
58 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 988 | 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. |
59 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 988 | 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 |
60 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 988 | 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 |
61 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 994 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
62 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 994 | 19.9998 | 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 |
63 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 994 | 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. |
64 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 994 | 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 |
65 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 994 | 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 |
66 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1000 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
67 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1000 | 19.9998 | 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 |
68 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1000 | 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. |
69 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1000 | 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 |
70 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1000 | 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 |
71 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1005 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
72 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1005 | 19.9998 | 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 |
73 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1005 | 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. |
74 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1005 | 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 |
75 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1005 | 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 |
76 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1011 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
77 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1011 | 19.9998 | 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 |
78 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1011 | 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. |
79 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1011 | 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 |
80 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1011 | 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 |
81 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1017 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
82 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1017 | 19.9998 | 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 |
83 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1017 | 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. |
84 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1017 | 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 |
85 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1017 | 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 |
86 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1023 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
87 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1023 | 19.9998 | 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 |
88 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1023 | 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. |
89 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1023 | 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 |
90 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1023 | 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 |
91 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1029 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
92 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1029 | 19.9998 | 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 |
93 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1029 | 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. |
94 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1029 | 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 |
95 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1029 | 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 |
96 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1035 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
97 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1035 | 19.9998 | 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 |
98 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1035 | 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. |
99 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1035 | 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 |
100 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1035 | 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 |
101 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1041 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
102 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1041 | 19.9998 | 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 |
103 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1041 | 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. |
104 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1041 | 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 |
105 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1041 | 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 |
106 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1047 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
107 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1047 | 19.9998 | 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 |
108 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1047 | 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. |
109 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1047 | 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 |
110 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1047 | 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 |
111 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1053 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
112 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1053 | 19.9998 | 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 |
113 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1053 | 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. |
114 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1053 | 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 |
115 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1053 | 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 |
116 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1059 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
117 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1059 | 19.9998 | 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 |
118 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1059 | 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. |
119 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1059 | 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 |
120 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1059 | 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 |
121 | PLA2-Ca* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1065 | 19.9994 | 5.4 | 4 | explicit E-S complex | Substrate APC
Product AA
|
| 10 x raise oct22 12 x oct 24, set k2 = 4 * k3 |
122 | PIP2-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1065 | 19.9998 | 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 |
123 | PIP2-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1065 | 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. |
124 | DAG-Ca-PLA2* / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1065 | 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 |
125 | PLA2*-Ca / kenz | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1065 | 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 |
| Name | Accession Name | Pathway Name | Kf | Kb | Kd | tau | Reagents |
1 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 920 | 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 |
2 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 922 | 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 |
3 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 933 | 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 |
4 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 939 | 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 |
5 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 945 | 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 |
6 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 951 | 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 |
7 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 957 | 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 |
8 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 964 | 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 |
9 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 970 | 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 |
10 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 976 | 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 |
11 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 982 | 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 |
12 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 988 | 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 |
13 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 994 | 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 |
14 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1000 | 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 |
15 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1005 | 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 |
16 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1011 | 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 |
17 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1017 | 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 |
18 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1023 | 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 |
19 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1029 | 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 |
20 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1035 | 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 |
21 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1041 | 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 |
22 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1047 | 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 |
23 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1053 | 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 |
24 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1059 | 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 |
25 | Degrade-AA | Ajay_Bhalla_ 2007_ReacDiff3 Accession No. : 84 | PLA2 Pathway No. : 1065 | 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 |