Enter a Search String |
| Special character and space not allowed in the query term. Search string should be at least 2 characters long. |
Molecule Parameter List for CaMKII | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 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 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| CaMKII 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 | 0 | 0 | 2 | 2 | 0 |
Accession and Pathway Details |
| Accession Name | Accession No. | Accession Type | Pathway Link |
2004_PKM_MKP3_ Tuning | 77 | Network | Shared_Object_Ajay_Bhalla_2004_PKM_MKP3_Tuning, PKC, PLA2, PLCbeta, Ras, Gq, MAPK, EGFR, Sos, PLC_g, CaMKII, CaM, PP1, PP2B, PKA, AC, MKP3, PKM |
| This model is based on Ajay SM, Bhalla US. Eur J Neurosci. 2004 Nov;20(10):2671-80. This is the feedforward model with MPK3 from figure 8a. | |||
CaMKII acting as a Molecule in Ajay_Bhalla_2004_PKM_MKP3_Tuning Network
| Name | Accession Name | Pathway Name | Initial Conc. (uM) | Volume (fL) | Buffered | |
| CaMKII | 2004_PKM_MKP3_ Tuning Accession No. : 77 | CaMKII Pathway No. : 339 | 70 | 1.5 | No | |
| Huge conc of CaMKII. In PSD it is 20-40% of protein, so we assume it is around 2.5% of protein in spine as a whole. This level is so high it is unlikely to matter much if we are off a bit. This comes to about 70 uM. | ||||||
CaMKII acting as a Product of an Enzyme in Ajay_Bhalla_2004_PKM_MKP3_Tuning Network
| Enzyme Molecule / Enzyme Activity | Accession Name | Pathway Name | Km (uM) | kcat (s^-1) | Ratio | Enzyme Type | Reagents | |
| 1 | PP1-active / Deph-thr306 | 2004_PKM_MKP3_ Tuning Accession No. : 77 | Ajay_Bhalla_ 2004_PKM_MKP3_ Tuning Pathway No. : 329 | 5.09911 | 0.35 | 4 | explicit E-S complex | Substrate CaMK-thr306 Product CaMKII |
| See Cohen et al | ||||||||
| 2 | PP1-active / Deph_thr286b | 2004_PKM_MKP3_ Tuning Accession No. : 77 | Ajay_Bhalla_ 2004_PKM_MKP3_ Tuning Pathway No. : 329 | 5.09911 | 0.35 | 4 | explicit E-S complex | Substrate CaMKII-thr286 Product CaMKII |
CaMKII acting as a Substrate in a reaction in Ajay_Bhalla_2004_PKM_MKP3_Tuning 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 | CaMKII-bind-CaM | 2004_PKM_MKP3_ Tuning Accession No. : 77 | CaMKII Pathway No. : 339 | 49.9995 (uM^-1 s^-1) | 5 (s^-1) | Kd(bf) = 0.1(uM) | - | Substrate CaM-Ca4 CaMKII Product 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. | ||||||||
| 2 | basal-activity | 2004_PKM_MKP3_ Tuning Accession No. : 77 | CaMKII Pathway No. : 339 | 0.003 (s^-1) | 0 (s^-1) | - | - | Substrate CaMKII Product CaMKII-thr286 |
| This reaction represents one of the big unknowns in CaMK-II biochemistry: what maintains the basal level of phosphorylation on thr 286 ? See Hanson and Schulman Ann Rev Biochem 1992 61:559-601, specially pg 580, for review. I have not been able to find any compelling mechanism in the literature, but fortunately the level of basal activity is well documented. | ||||||||
color.