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Molecule Parameter List for CycA | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 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 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| CycA participated as | Molecule | Sum total of | Enzyme | Substrate of an enzyme | Product of an enzyme | Substrate in Reaction | Product in Reaction |
| No. of occurrences | 1 | 0 | 13 | 1 | 4 | 1 | 1 |
Accession and Pathway Details |
| Accession Name | Accession No. | Accession Type | Pathway Link |
cycle | 85 | Network | Growth, CELLDIV, Rb_grp, IE_GRP, CycB_Grp, Cdc20_Grp, Cdh1_grp, E2F, CycA_Grp, CycE_grp, Early_Response_Genes, Delayed_Response_Genes, CycD_Grp |
| This is a fairly complete mass-action reimplementation of the Novak and Tyson mammalian cell cycle model. It is inexact on two counts. First, it replaces many rather abstracted equations with mass action and Michaelis-Menten forms of enzymes. Second, it does not handle the halving of cellular volume at the division point. Within these limitations, the model does most of what the original paper shows including oscillation of the relevant molecules. | |||
CycA acting as a Molecule in Mammalian_cell_cycle Network
| Name | Accession Name | Pathway Name | Initial Conc. (uM) | Volume (fL) | Buffered | |
| CycA | cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 0 | 200 | No | |
| rate = k4.Gamma_A * [CycA] * [Cdh1]/(J4 + [Cdh1]) J4 = 0.01 k4 = kcat = 40 | ||||||
CycA acting as an Enzyme in Mammalian_cell_cycle Network
| Enzyme Molecule / Enzyme Activity | Accession Name | Pathway Name | Km (uM) | kcat (s^-1) | Ratio | Enzyme Type | Reagents | |
| 1 | CycA / k20_lambdaA | cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 100 | 3000 | 4 | explicit E-S complex | Substrate Rb Product Rb_P |
| Km ~ 0, so rate ~ kcat. Here rate = k20 * lambdaA = 10 * 3 7 Apr 2005: Fix it: rate should have substrate term in it. Set Km = 10 >> substrate. Then, kcat = Km * k20 * lambdaA = 10 * 10 * 3 = 300 | ||||||||
| 2 | CycA / k21_phiE_A | cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 9.99968 | 2500 | 4 | explicit E-S complex | Substrate PP1A Product PP1 |
| phiE is also used for the reaction catalyzed by A. So rates are identical to k21_phiE | ||||||||
| 3 | CycA / Cdh1_CycA | cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 0.01 | 12 | 4 | explicit E-S complex | Substrate Cdh1 Product Cdh1_i |
| J4 = Km = 0.01 k4 = 40. GammaA = 0.3 kcat = k4 * GammaA = 12 | ||||||||
| 4 | CycA / A_phosph_E2F | cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 9.99992 | 10 | 4 | explicit E-S complex | Substrate E2FA Product E2FAP |
| Rate equn has form [CycA].[E2F].k23 k23 = 1 MM equn has form [CycA].[E2F].kcat/(Km + E2F) So, we set kcat = Km * k23 where Km >> E2F 25 Mar. Better: Use explicit enz form. rate = k3.k1/k2 if k3 << k2. Let k3 = 1, k2 = 10, so we get k1 = k23 * 10 = 10. 6 Apr. Problem with explicit form is that the enz-substrate complex may affect the levels of the CycA, B etc. Back to MM. | ||||||||
| 5 | CycA / E2FA.Rb | cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 9.99992 | 10 | 4 | explicit E-S complex | Substrate E2FA.Rb Product E2FAP.Rb |
| Rate equn has form [CycA].[E2F].k23 k23 = 1 MM equn has form [CycA].[E2F].kcat/(Km + E2F) So, we set kcat = Km * k23 where Km >> E2F 25 March 2005 Use explicit form. rate = k23 = 1 = k3*k1/k2 where k3 << k2 So k3 = 1, k2 = 10, k1 = 10. 6 Apr 2005. Back to MM form because enz complex formation is depleting CycA, B etc. | ||||||||
| 6 | CycA / Ak6_etaA | 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 | 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 | 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 | 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 | cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 0.1 | 2 | 4 | explicit E-S complex | Substrate CycE_Kip1 Product Kip1 degraded |
| 11 | CycA / k6_kip1_A | cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 10.0002 | 500 | 4 | explicit E-S complex | Substrate Kip1 Product degraded_kip |
| 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. | ||||||||
| 12 | CycA / k20_lambdaA[1] | cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 100 | 3000 | 4 | explicit E-S complex | Substrate E2FAP.Rb Product E2FAP Rb_P |
| Km ~ 0, so rate ~ kcat. Here rate = k20 * lambdaA = 10 * 3 7 Apr 2005: Fix it: rate should have substrate term in it. Set Km = 10 >> substrate. Then, kcat = Km * k20 * lambdaA = 10 * 10 * 3 = 300 | ||||||||
| 13 | CycA / k20_lambdaA[2] | cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 100 | 3000 | 4 | explicit E-S complex | Substrate E2FA.Rb Product E2FA Rb_P |
| Km ~ 0, so rate ~ kcat. Here rate = k20 * lambdaA = 10 * 3 7 Apr 2005: Fix it: rate should have substrate term in it. Set Km = 10 >> substrate. Then, kcat = Km * k20 * lambdaA = 10 * 10 * 3 = 300 | ||||||||
CycA acting as a Substrate for an Enzyme in Mammalian_cell_cycle Network
| Enzyme Molecule / Enzyme Activity | Accession Name | Pathway Name | Km (uM) | kcat (s^-1) | Ratio | Enzyme Type | Reagents |
| Cdc20 / Cdc20_deg_CycA | 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. | |||||||
CycA acting as a Product of an Enzyme in Mammalian_cell_cycle Network
| Enzyme Molecule / Enzyme Activity | Accession Name | Pathway Name | Km (uM) | kcat (s^-1) | Ratio | Enzyme Type | Reagents | |
| 1 | CycE / Ak6_etaE | 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 | CycA / Ak6_etaA | 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 | ||||||||
| 3 | CycB / Ak6_etaB | 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 | ||||||||
| 4 | E2FA / k29 | cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 1000.02 | 50 | 4 | explicit E-S complex | Substrate Mass_dup Product CycA |
| Represented as eps*k29*[E2FA]*[mass], where k29 is 0.05 Split into two steps, this one deals with the E2FA term. rate = Mass_dup * E2FA * kcat / (Km + Mass_dup) Note that Mass_dup will not change. Let Km >> Mass_dup and kcat = k29 * Km. then rate ~ Mass_dup * E2FA * k29 * Km / Km | ||||||||
CycA acting as a Substrate in a reaction in Mammalian_cell_cycle 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 |
| k25 | cycle Accession No. : 85 | CycA_Grp Pathway No. : 1077 | 999.996 (uM^-1 s^-1) | 10 (s^-1) | Kd(bf) = 0.01(uM) | - | Substrate CycA Kip1 Product CycA_Kip1 |
CycA acting as a Product in a reaction in Mammalian_cell_cycle 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 |
| k_prime6 | cycle Accession No. : 85 | CycA_Grp Pathway No. : 1077 | 10 (s^-1) | 0 (uM^-1 s^-1) | - | - | Substrate CycA_Kip1 Product CycA degraded |
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