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Molecule Parameter List for AminoAcids | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 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. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| AminoAcids participated as | Molecule | Sum total of | Enzyme | Substrate of an enzyme | Product of an enzyme | Substrate in Reaction | Product in Reaction |
| No. of occurrences | 8 | 0 | 0 | 6 | 0 | 5 | 0 |
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. | |||
AminoAcids acting as a Molecule in Mammalian_cell_cycle Network
| Name | Accession Name | Pathway Name | Initial Conc. (uM) | Volume (fL) | Buffered | |
| AminoAcids | cycle Accession No. : 85 | Growth Pathway No. : 1069 | 1 | 200 | Yes | |
| AminoAcids | cycle Accession No. : 85 | IE_GRP Pathway No. : 1072 | 1 | 200 | Yes | |
| AminoAcids | cycle Accession No. : 85 | Cdc20_Grp Pathway No. : 1074 | 1 | 200 | Yes | |
| AminoAcids | cycle Accession No. : 85 | CycB_Grp Pathway No. : 1073 | 1 | 200 | Yes | |
| AminoAcids | cycle Accession No. : 85 | CycA_Grp Pathway No. : 1077 | 1 | 200 | Yes | |
| AminoAcids | cycle Accession No. : 85 | CycE_grp Pathway No. : 1078 | 1 | 200 | Yes | |
| AminoAcids | cycle Accession No. : 85 | Genes Pathway No. : 1079 | 1 | 200 | Yes | |
| Amino acid pool, Enters into system indirectly as a scaling factor. Set to 1. | ||||||
| AminoAcids | cycle Accession No. : 85 | CycD_Grp Pathway No. : 1081 | 1 | 200 | Yes | |
AminoAcids 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 | |
| 1 | GM / mu | cycle Accession No. : 85 | Growth Pathway No. : 1069 | 1.00001 | 0.122 | 4 | explicit E-S complex | Substrate AminoAcids Product mass |
| Rate = E.S.kcat/(Km + S) We want to represent dmass/dt = epsilon.mu.GM. Epsilon is 1 for now. mu = 0.061 S here is AA, buffered to 1. We assign Km = 1 for simplicity. Then kcat = 2 * mu = 0.122 | ||||||||
| 2 | CycB / k11 | cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 1 | 3 | 4 | explicit E-S complex | Substrate AminoAcids Product Cdc20notA |
| Represented simply as [CycB]*k11, where k11 is 1.5. As AAs are at 1, we get rate = [AAs].[CycB].kcat / (Km + [AAs]) So if we set Km = [AAs] = 1, then kcat = 3 gives our desired equation. | ||||||||
| 3 | E2FA / k7 | cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 1 | 1.2 | 4 | explicit E-S complex | Substrate AminoAcids Product CycE |
| Represented simply as [E2FA]*k7, where k7 is 0.6 As AAs are at 1, we get rate = [AAs].[E2FA].kcat / (Km + [AAs]) So if we set Km = [AAs] = 1, then kcat = 1.2 gives our desired equation. | ||||||||
| 4 | DRG / k9 | cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 1.00002 | 5 | 4 | explicit E-S complex | Substrate AminoAcids Product CycD |
| Represented simply as [DRG]*k9, where k9 is 2.5. As AAs are at 1, we get rate = [AAs].[DRG].kcat / (Km + [AAs]) So if we set Km = [AAs] = 1, then kcat = 5 gives our desired equation. | ||||||||
| 5 | ERG / k_prime_17 | cycle Accession No. : 85 | CELLDIV Pathway No. : 1070 | 0.999989 | 0.7 | 4 | explicit E-S complex | Substrate AminoAcids Product DRG |
| k17_prime = 0.35. rate = epsilon * k17_prime * [ERG] Assume AA = 1, Km = 1. Then rate = kcat * AA * ERG / (Km + AA) gives kcat = 0.7 | ||||||||
| 6 | ERG_synth / ERG_synth | cycle Accession No. : 85 | Genes Pathway No. : 1079 | 1.00002 | 0.5 | 4 | explicit E-S complex | Substrate AminoAcids Product ERG |
| kcat = 2 * k15 = 0.5 Km = 1 [AA] = 1 | ||||||||
AminoAcids 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 | |
| 1 | k33 | cycle Accession No. : 85 | IE_GRP Pathway No. : 1072 | 0.05 (s^-1) | 0 (s^-1) | - | - | Substrate AminoAcids Product PPX |
| 2 | k11_prime | cycle Accession No. : 85 | Cdc20_Grp Pathway No. : 1074 | 0 (s^-1) | 0 (s^-1) | - | - | Substrate AminoAcids Product Cdc20notA |
| Kind of a silly reaction, with all terms zero, but it is there in the Novak and Tyson equations. | ||||||||
| 3 | k1_prime | cycle Accession No. : 85 | CycB_Grp Pathway No. : 1073 | 0.1 (s^-1) | 0 (s^-1) | - | - | Substrate AminoAcids Product CycB |
| k1_prime = 0.1 | ||||||||
| 4 | k5 | cycle Accession No. : 85 | CycA_Grp Pathway No. : 1077 | 20 (s^-1) | 0 (s^-1) | - | - | Substrate AminoAcids Product Kip1 |
| 5 | k_prime7 | cycle Accession No. : 85 | CycE_grp Pathway No. : 1078 | 0 (s^-1) | 0 (s^-1) | - | - | Substrate AminoAcids Product CycE |
| This is set to zero in the paper, so this reaction isn't really doing anything. | ||||||||
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