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Reaction Name | Accession Name / Accession No. | Pathway Name / Pathway No. | Kf | Kb | Kd | tau | Reagents |
1 | CaMKII-bind-CaM | Synaptic_ Network Accession No. 16 | CaMKII
Pathway No. 80 | 49.9998 (uM^-1 s^-1) | 5 (s^-1) | Kd(bf) = 0.1(uM) | - | Substrate: CaM-Ca4 CaMKII
Products: CaMKII-CaM
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| This is tricky. There is some cooperativity here arising from interactions between the subunits of the CAMKII holoenzyme. However, the stoichiometry is 1. Kd = 0.1 uM. Rate is fast (see Hanson et al Neuron 12 943-956 1994) Hanson and Schulman 1992 AnnRev Biochem 61:559-601 give tau for dissoc as 0.2 sec at low Ca, 0.4 at high. Low Ca = 100 nM = physiol. | 2 | CaMKII-bind-CaM | Osc_Ca_ IP3metabolism Accession No. 24 | CaMKII
Pathway No. 121 | 49.9998 (uM^-1 s^-1) | 5 (s^-1) | Kd(bf) = 0.1(uM) | - | Substrate: CaM-Ca4 CaMKII
Products: CaMKII-CaM
|
| This is tricky. There is some cooperativity here arising from interactions between the subunits of the CAMKII holoenzyme. However, the stoichiometry is 1. Kd = 0.1 uM. Rate is fast (see Hanson et al Neuron 12 943-956 1994) Hanson and Schulman 1992 AnnRev Biochem 61:559-601 give tau for dissoc as 0.2 sec at low Ca, 0.4 at high. Low Ca = 100 nM = physiol. | 3 | CaMKII-bind-CaM | Osc_Ca_ IP3metabolism Accession No. 32 | CaMKII
Pathway No. 159 | 49.9998 (uM^-1 s^-1) | 5 (s^-1) | Kd(bf) = 0.1(uM) | - | Substrate: CaM-Ca4 CaMKII
Products: CaMKII-CaM
|
| This is tricky. There is some cooperativity here arising from interactions between the subunits of the CAMKII holoenzyme. However, the stoichiometry is 1. Kd = 0.1 uM. Rate is fast (see Hanson et al Neuron 12 943-956 1994) Hanson and Schulman 1992 AnnRev Biochem 61:559-601 give tau for dissoc as 0.2 sec at low Ca, 0.4 at high. Low Ca = 100 nM = physiol. | 4 | CaMKII-bind-CaM | NonOsc_Ca_ IP3metabolism Accession No. 23 | CaMKII
Pathway No. 106 | 49.9998 (uM^-1 s^-1) | 5 (s^-1) | Kd(bf) = 0.1(uM) | - | Substrate: CaM-Ca4 CaMKII
Products: CaMKII-CaM
|
| This is tricky. There is some cooperativity here arising from interactions between the subunits of the CAMKII holoenzyme. However, the stoichiometry is 1. Kd = 0.1 uM. Rate is fast (see Hanson et al Neuron 12 943-956 1994) Hanson and Schulman 1992 AnnRev Biochem 61:559-601 give tau for dissoc as 0.2 sec at low Ca, 0.4 at high. Low Ca = 100 nM = physiol. | 5 | CaMKII-bind-CaM | NonOsc_Ca_ IP3metabolism Accession No. 31 | CaMKII
Pathway No. 145 | 49.9998 (uM^-1 s^-1) | 5 (s^-1) | Kd(bf) = 0.1(uM) | - | Substrate: CaM-Ca4 CaMKII
Products: CaMKII-CaM
|
| This is tricky. There is some cooperativity here arising from interactions between the subunits of the CAMKII holoenzyme. However, the stoichiometry is 1. Kd = 0.1 uM. Rate is fast (see Hanson et al Neuron 12 943-956 1994) Hanson and Schulman 1992 AnnRev Biochem 61:559-601 give tau for dissoc as 0.2 sec at low Ca, 0.4 at high. Low Ca = 100 nM = physiol. | 6 | CaMKII-bind-CaM | MAPK_network_ 2003 Accession No. 50 | CaMKII
Pathway No. 216 | 49.9998 (uM^-1 s^-1) | 5 (s^-1) | Kd(bf) = 0.1(uM) | - | Substrate: CaM-Ca4 CaMKII
Products: CaMKII-CaM
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| This is tricky. There is some cooperativity here arising from interactions between the subunits of the CAMKII holoenzyme. However, the stoichiometry is 1. Kb/Kf = 6e4 #/cell. Rate is fast (see Hanson et al Neuron 12 943-956 1994) so lets say kb = 10. This gives kf = 1.6667e-4 H&S AnnRev Biochem 92 give tau for dissoc as 0.2 sec at low Ca, 0.4 at high. Low Ca = 100 nM = physiol. | 7 | CaMKII-bind-CaM | fig4_synapse
Accession No. 3 | CaMKII
Pathway No. 26 | 49.9998 (uM^-1 s^-1) | 5 (s^-1) | Kd(bf) = 0.1(uM) | - | Substrate: CaM-Ca4 CaMKII
Products: CaMKII-CaM
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8 | CaMKII-bind-CaM | fig3_CaMKII
Accession No. 2 | CaMKII
Pathway No. 13 | 49.9998 (uM^-1 s^-1) | 5 (s^-1) | Kd(bf) = 0.1(uM) | - | Substrate: CaM-Ca4 CaMKII
Products: CaMKII-CaM
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9 | CaMKII-bind-CaM | CaMKII_noPKA_ model3 Accession No. 62 | CaMKII
Pathway No. 258 | 49.9997 (uM^-1 s^-1) | 5 (s^-1) | Kd(bf) = 0.1(uM) | - | Substrate: CaM-Ca4 CaMKII
Products: CaMKII-CaM
|
| This is tricky. There is some cooperativity here arising from interactions between the subunits of the CAMKII holoenzyme. However, the stoichiometry is 1. Kb/Kf = 6e4 #/cell. Rate is fast (see Hanson et al Neuron 12 943-956 1994) so lets say kb = 10. This gives kf = 1.6667e-4 H&S AnnRev Biochem 92 give tau for dissoc as 0.2 sec at low Ca, 0.4 at high. Low Ca = 100 nM = physiol. | 10 | CaMKII-bind-CaM- PSD | CaMKII_noPKA_ model3 Accession No. 62 | Shared_Object_ CaMKII_noPKA_ model3 Pathway No. 257 | 49.9998 (uM^-1 s^-1) | 0 (s^-1) | - | - | Substrate: CaMKII-PSD CaM-Ca4-PSD
Products: CaMKII-CaM-PSD
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11 | CaMKII-thr286-bi nd-CaM-PSD | CaMKII_noPKA_ model3 Accession No. 62 | Shared_Object_ CaMKII_noPKA_ model3 Pathway No. 257 | 1000.02 (uM^-1 s^-1) | 0.1 (s^-1) | Kd(bf) = 0.0001(uM) | - | Substrate: CaMKII-thr286-PS D CaM-Ca4-PSD
Products: CaMKII-thr286-Ca M-PSD
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| Same values as for the main compartment Can the main compartment pool of Ca/CaM be used? | 12 | CaMKII-diss-CaM | CaMKII_noPKA_ model3 Accession No. 62 | Shared_Object_ CaMKII_noPKA_ model3 Pathway No. 257 | 5 (s^-1) | 0 (uM^-1 s^-1) | - | - | Substrate: CaMKII-CaM-PSD
Products: CaM-Ca4-PSD CaMKII-PSD
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13 | Stoch_Basal_ CaMKII_PSD | CaMKII_noPKA_ model3 Accession No. 62 | Shared_Object_ CaMKII_noPKA_ model3 Pathway No. 257 | 1 (s^-1) | 1 (s^-1) | Keq = 1(uM) | 0.5sec | Substrate: basal_CaMKII_ PSD_control
Products: basal_CaMKII_ PSD
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14 | CaMKII-bind-CaM | CaMKII_model3
Accession No. 63 | CaMKII
Pathway No. 264 | 49.9997 (uM^-1 s^-1) | 5 (s^-1) | Kd(bf) = 0.1(uM) | - | Substrate: CaM-Ca4 CaMKII
Products: CaMKII-CaM
|
| This is tricky. There is some cooperativity here arising from interactions between the subunits of the CAMKII holoenzyme. However, the stoichiometry is 1. Kb/Kf = 6e4 #/cell. Rate is fast (see Hanson et al Neuron 12 943-956 1994) so lets say kb = 10. This gives kf = 1.6667e-4 H&S AnnRev Biochem 92 give tau for dissoc as 0.2 sec at low Ca, 0.4 at high. Low Ca = 100 nM = physiol. | 15 | CaMKII-bind-CaM- PSD | CaMKII_model3
Accession No. 63 | Shared_Object_ CaMKII_model3 Pathway No. 263 | 49.9998 (uM^-1 s^-1) | 0 (s^-1) | - | - | Substrate: CaMKII-PSD CaM-Ca4-PSD
Products: CaMKII-CaM-PSD
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16 | CaMKII-thr286-bi nd-CaM-PSD | CaMKII_model3
Accession No. 63 | Shared_Object_ CaMKII_model3 Pathway No. 263 | 1000.02 (uM^-1 s^-1) | 0.1 (s^-1) | Kd(bf) = 0.0001(uM) | - | Substrate: CaMKII-thr286-PS D CaM-Ca4-PSD
Products: CaMKII-thr286-Ca M-PSD
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| Same values as for the main compartment Can the main compartment pool of Ca/CaM be used? | 17 | CaMKII-diss-CaM | CaMKII_model3
Accession No. 63 | Shared_Object_ CaMKII_model3 Pathway No. 263 | 5 (s^-1) | 0 (uM^-1 s^-1) | - | - | Substrate: CaMKII-CaM-PSD
Products: CaM-Ca4-PSD CaMKII-PSD
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18 | Stoch_Basal_ CaMKII_PSD | CaMKII_model3
Accession No. 63 | Shared_Object_ CaMKII_model3 Pathway No. 263 | 1 (s^-1) | 1 (s^-1) | Keq = 1(uM) | 0.5sec | Substrate: basal_CaMKII_ PSD_control
Products: basal_CaMKII_ PSD
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19 | CaMKII-bind-CaM | CaMKII_2003
Accession No. 49 | CaMKII
Pathway No. 202 | 49.9998 (uM^-1 s^-1) | 5 (s^-1) | Kd(bf) = 0.1(uM) | - | Substrate: CaM-Ca4 CaMKII
Products: CaMKII-CaM
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| This is tricky. There is some cooperativity here arising from interactions between the subunits of the CAMKII holoenzyme. However, the stoichiometry is 1. Kb/Kf = 6e4 #/cell. Rate is fast (see Hanson et al Neuron 12 943-956 1994) so lets say kb = 10. This gives kf = 1.6667e-4 H&S AnnRev Biochem 92 give tau for dissoc as 0.2 sec at low Ca, 0.4 at high. Low Ca = 100 nM = physiol. | 20 | dephosp_CaMKIII | CaMKIII
Accession No. 90 | Shared_Object_ CaMKIII Pathway No. 1093 | 0.07 (s^-1) | 0 (s^-1) | - | - | Substrate: CaMKIII*
Products: CaMKIII
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