| Enzyme Molecule / Enzyme Activity | Accession Name | Pathway Name | Km (uM) | kcat (s^-1) | Ratio | Enzyme Type | Reagents |
1 | CycE / Ak6_etaE | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 10.0002 | 500 | 4 | explicit E-S complex | Substrate CycA_Kip1
Product CycA degraded
|
| Rate = V6 * [CycD_Kip1]. 6 Apr 2005. Rates were k1 = 500, k2 = 10, k3 = 1 in explicit E.S reaction form. Changed to MM as Km was too low. New values: Km = 10 kcat = Km * k6 * etaE = 500. |
2 | CycE / k8_CycE | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 0.1 | 2 | 4 | explicit E-S complex | Substrate CycE
Product degraded
|
| Autocatalysis step equation 5. Unfortunately cannot exactly represent the math of Equation 26. Note that we cannot merge this enzyme with k6_etaE because this is in the explicit form to get a little closer to the mathematical form. |
3 | CycE / k6_E_etaE | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 10.0002 | 500 | 4 | explicit E-S complex | Substrate CycE_Kip1
Product CycE degraded
|
| k6 = 100, etaE = 0.5 Assume a large Km of 1000 so that the conc of the enzyme is negligible. Then rate is E.S.Vmax/Km. 6 April 2006 I had changed it over to an explict form earlier. Those values were k1 = 500, k2 = 10, k3 = 1. Cannot use as effective Km is very small so we would end up with lots of E.S complex. Change back to MM: Km = 10, kcat = Km * k6 * etaE = 500. |
4 | CycE / k6_D_etaE | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 10.0002 | 500 | 4 | explicit E-S complex | Substrate CycD_Kip1
Product CycD degraded
|
| Rate = V6 * [CycD_Kip1]. k3.k1/k2 = rate = k6 * etaE = 50. 6 Apr 2005. Old rates in explicit form were k1 = 500, k2 = 10, k3 = 1. Need to go back to MM form because the above explict rates give a very low Km, ie, lots of E.S complex. k6 = 100, etaE = 0.5, Let Km >> substrate, so Km = 10. Then kcat = Km * k6 * etaE = 500. |
5 | CycE / k8_CycE_Kip1 | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 0.1 | 2 | 4 | explicit E-S complex | Substrate CycE_Kip1
Product Kip1 degraded
|
| Autocatalysis step equation 5. Unfortunately cannot exactly represent the math of Equation 26. Note that we cannot merge this enzyme with k6_etaE because this is in the explicit form to get a little closer to the mathematical form. |
6 | CycA / Ak6_etaA | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 10.0002 | 500 | 4 | explicit E-S complex | Substrate CycA_Kip1
Product CycA degraded
|
| See Ak6_etaE |
7 | CycA / k8_CycA | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 0.1 | 2 | 4 | explicit E-S complex | Substrate CycE
Product degraded
|
8 | CycA / k6_E_etaA | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 10.0002 | 500 | 4 | explicit E-S complex | Substrate CycE_Kip1
Product CycE degraded
|
| See notes for k6_E_etaE. Explicit rates had been k1 = 500, k2 = 10, k3 = 1 but this gave a very low Km. So, back to MM: etaA = 0.5 so kcat = 500, Km = 10 as for k6_E_etaE |
9 | CycA / k6_D_etaA | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 10.0002 | 500 | 4 | explicit E-S complex | Substrate CycD_Kip1
Product CycD degraded
|
| k3.k1/k2 = k6.etaA = 100*0.5 = 50 Also k3 << k2. Assume ratio is 10. Let k3 be reasonable, say 1. Then k2 = 10, k1 = 500. 6 April 2005: The above rates are bad because they give a very low Km and too much E.S. complex. So, back to MM: Km >> substrate, so Km = 10. Then kcat = Km * k6 * etaA = 10 * 100 * 0.5 = 500. |
10 | CycA / k8_CycA_Kip1 | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 0.1 | 2 | 4 | explicit E-S complex | Substrate CycE_Kip1
Product Kip1 degraded
|
11 | CycB / Ak6_etaB | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 9.99992 | 1000 | 4 | explicit E-S complex | Substrate CycA_Kip1
Product CycA degraded
|
| See Ak6_etaE |
12 | CycB / k8_CycB | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 0.0999992 | 0.1 | 4 | explicit E-S complex | Substrate CycE
Product degraded
|
13 | CycB / k6_E_etaB | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 9.99992 | 1000 | 4 | explicit E-S complex | Substrate CycE_Kip1
Product CycE degraded
|
| See notes for k6_E_etaE. Here etaB = 1 so kcat = 1000, Km as before is 10 |
14 | CycB / k6_D_etaB | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 9.99992 | 1000 | 4 | explicit E-S complex | Substrate CycD_Kip1
Product CycD degraded
|
| 6 Apr 2005. Earlier used explicit E.S complex form with k1 = 1000, k2 = 10, k3 = 1. This gave low Km and lots of E.S. complex. So shift to MM form: k6 = 100, etaB = 1. Let Km = 10 >> substrate. Then kcat = Km * k6 * etaB = 1000 |
15 | CycB / k8_CycB_Kip1 | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 0.0999992 | 0.1 | 4 | explicit E-S complex | Substrate CycE_Kip1
Product Kip1 degraded
|
| k8 = 0.2, psiB = 0.05, so kcat = 0.1. J8 = 0.1 |
16 | Cdc20 / k2_prime_prime | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 99.9992 | 100 | 4 | explicit E-S complex | Substrate CycB
Product degraded
|
| k2_prime_prime = 1. rate = k2_prime_prime * Cdc20 * CycB Using MM: rate = kcat * Cdc20 * CycB / (CycB + Km) Let Km >> CycB, ie, around 100. Then kcat = k2_prime_prime * Km = 100. |
17 | Cdc20 / Cdc20_deg_CycA | Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 10 | 200 | 4 | explicit E-S complex | Substrate CycA
Product degraded
|
| Rate comes in as k30 = 20 Rate = [Cdc20]*[CycA] * k30. To put in MM form: Rate = [Cdc20]*[CycA] * kcat / (Km + [CycA]) where kcat = k30 * Km and Km >> [CycA]. Put Km = 1000, so kcat = 20000 25 March: use explicit enz form. Use rate = k3*k1/k2 = 20, which works if k2 >> k3. Then let k3 = 1, k2 = 10, k1 becomes 200 7 Apr 2005: Above won't work because of low Km consuming too much of the Cdc20 in the complex form. So use Km = 10, kcat = 200. |
18 | Cdc20 / Cdc20_deg_CycA_ Kip1
| Mammalian_cell_ cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 10 | 200 | 4 | explicit E-S complex | Substrate CycA_Kip1
Product Kip1 degraded
|
| Rate comes in as k30 = 20 Same rate as for CycA alone. Rate = [Cdc20]*[CycA_Kip1] * k30. To put in MM form: Rate = [Cdc20]*[CycA_Kip1] * kcat / (Km + [CycA_Kip1]) where kcat = k30 * Km and Km >> [CycA_Kip1]. Put Km = 1000, so kcat = 20000 Similar to CycA alone, we instead get k2 = 10, k3 = 1, so k1 = 200. 19 Apr 2005: Go back to MM form because of low Km. Let Km = 10, then kcat = Km * k30 = 200. |
19 | Cdh1_i / Cdh1_i_k2_prime | Mammalian_cell_ cycle Accession No. : 85 | Cdh1_grp Pathway No. : 1075 | 100.002 | 5 | 4 | explicit E-S complex | Substrate CycB
Product degraded
|
| k2_prime = 0.05. so actually this reaction is pretty negligible. rate = k2_prime * Cdh1_i * CycB From MM kinetics, rate = kcat * Cdh1_i * CycB / (CycB + Km). Let Km >>CycB, so Km = 10. Then kcat = k2_prime * Km = 0.5 |
20 | Cdh1 / Cdh1_k2 | Mammalian_cell_ cycle Accession No. : 85 | Cdh1_grp Pathway No. : 1075 | 100 | 2000 | 4 | explicit E-S complex | Substrate CycB
Product degraded
|
| k2 = 20 Let Km = 100, so it is >> substrate. Then kcat = Km * k2 = 2000 |