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Molecule Parameter List for neurogranin | 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 | Accession and Pathway Details | |
Accession Name | Accession No. | Accession Type | Pathway Link | AMPAR_traff_ model0 | 59 | Network | Shared_Object_AMPAR_traff_model0, CaMKII, CaM, PP1, PP2B, PP1_PSD, PKA, AC, AMPAR, AMPAR_memb | This is model 0 from Hayer and Bhalla, PLoS Comput Biol 2005. It has a bistable model of AMPAR traffick, plus a
non-bistable model of CaMKII. This differs from the reference model (model 1) in that model0 lacks degradation and turno
ver reactions for AMPAR. |
neurogranin acting as a Molecule in AMPAR_traff_model0 Network
Name | Accession Name | Pathway Name | Initial Conc. (uM) | Volume (fL) | Buffered | neurogranin | AMPAR_traff_ model0 Accession No. : 59 | CaM Pathway No. : 236 | 10 | 0.09 | No | Also known as RC3 and p17 and BICKS. Conc in brain >> 2 uM from Martzen and Slemmon J neurosci 64 92-100 1995 but others say less without any #s. Conc in dend spines is much higher than overall, so it could be anywhere from 2 uM to 50. We will estimate 10 uM as a starting point. Gerendasy et al JBC 269:35 22420-22426 1994 have a skeleton model (no numbers) indicating CaM-Ca(n) binding. |
neurogranin acting as a Substrate for an Enzyme in AMPAR_traff_model0 Network
neurogranin acting as a Product of an Enzyme in AMPAR_traff_model0 Network
Enzyme Molecule / Enzyme Activity | Accession Name | Pathway Name | Km (uM) | kcat (s^-1) | Ratio | Enzyme Type | Reagents | CaM_Ca_n-CaNAB / dephosph_ neurogranin
| AMPAR_traff_ model0 Accession No. : 59 | PP2B Pathway No. : 238 | 10.012 | 0.67 | 3.98507 | explicit E-S complex | Substrate neurogranin*
Product neurogranin
| From Seki et al ABB 316(2):673-679 |
neurogranin acting as a Substrate in a reaction in AMPAR_traff_model0 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 | neurogranin-bind -CaM | AMPAR_traff_ model0 Accession No. : 59 | CaM Pathway No. : 236 | 0.3 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 3.3333(uM) | - | Substrate CaM neurogranin
Product neurogranin-CaM
| Surprisingly, no direct info on rates from neurogranin at this time. These rates are based on GAP-43 binding studies. As GAP-43 and neurogranin share near identity in the CaM/PKC binding regions, and also similarity in phosph and dephosph rates, I am borrowing GAP-43 kinetic info. See Alexander et al JBC 262:13 6108-6113 1987 |
neurogranin acting as a Product in a reaction in AMPAR_traff_model0 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 | dephosph-neurogr anin | AMPAR_traff_ model0 Accession No. : 59 | CaM Pathway No. : 236 | 0.005 (s^-1) | 0 (s^-1) | - | - | Substrate neurogranin*
Product neurogranin
| This is put in to keep the basal levels of neurogranin* experimentally reasonable. From various papers, specially Ramakers et al JBC 270:23 1995 13892-13898, it looks like the basal level of phosph is between 20 and 40%. I est around 25 % The kf of 0.005 gives around this level at basal PKC activity levels of 0.1 uM active PKC. |
| Database compilation and code copyright (C) 2022, Upinder S. Bhalla and NCBS/TIFR This Copyright is applied to ensure that the contents of this database remain freely available. Please see FAQ for details. |
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