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Molecule Parameter List for G*GTP | 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 | NonOsc_Ca_ IP3metabolism | 23 | Network | MIPP, CaMKII, CaM, PKC, IP3-3K, CaRegulation, Gq, PLCbeta, 134_dephos, 145_dephos, IP4-system, IHP-system, 1345_dephos | This network models detailed metabolism of Ins(145)P3, integrated with GPCR mediated PLCbeta activation and Ca release by the InsP3 receptor in the neuron. The calcium response is non-oscillatory. Mishra J, Bhalla US. Biophys J. 2002 Sep;83(3):1298-316. |
G*GTP acting as a Molecule in NonOsc_Ca_IP3metabolism Network
Name | Accession Name | Pathway Name | Initial Conc. (uM) | Volume (fL) | Buffered | G*GTP | NonOsc_Ca_ IP3metabolism Accession No. : 23 | Gq Pathway No. : 111 | 0 | 1000 | No | Activated G protein. Berstein et al indicate that about 20-40% of the total Gq alpha should bind GTP at steady stimulus. |
G*GTP acting as a Substrate in a reaction in NonOsc_Ca_IP3metabolism 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 | Inact-G | NonOsc_Ca_ IP3metabolism Accession No. : 23 | Gq Pathway No. : 111 | 0.0133 (s^-1) | 0 (s^-1) | - | - | Substrate G*GTP
Product G*GDP
| | From Berstein et al JBC 267:12 8081-8088 1992, kcat for GTPase activity of Gq is only 0.8/min. | 2 | PLC-bind-Gq | NonOsc_Ca_ IP3metabolism Accession No. : 23 | PLCbeta Pathway No. : 112 | 2.52 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.3968(uM) | - | Substrate G*GTP PLC
Product PLC-Gq
| | this binding does not produce active PLC. This step was needed to implement the described (Smrcka et al) increase in affinity for Ca by PLC once Gq was bound. The tempkin are the same as the binding step for Ca-PLC to Gq. Kd is constrained by detailed balance. | 3 | Act-PLC-by-Gq | NonOsc_Ca_ IP3metabolism Accession No. : 23 | PLCbeta Pathway No. : 112 | 25.2 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.0397(uM) | - | Substrate G*GTP PLC-Ca
Product PLC-Ca-Gq
| | Affinity for Gq is > 20 nM (Smrcka et al Science251 804-807 1991) so [Gq].kf = kb so 40nM * 6e5 = kb/kf = 24e3 so kf = 4.2e-5, kb =1 |
G*GTP acting as a Product in a reaction in NonOsc_Ca_IP3metabolism 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 | Basal-Act-G | NonOsc_Ca_ IP3metabolism Accession No. : 23 | Gq Pathway No. : 111 | 0.0001 (s^-1) | 0 (uM^-1 s^-1) | - | - | Substrate G-GDP
Product BetaGamma G*GTP
| | This is the basal exchange of GTP for GDP. So slow as to be nearly negligible. | 2 | Activate-Gq | NonOsc_Ca_ IP3metabolism Accession No. : 23 | Gq Pathway No. : 111 | 0.01 (s^-1) | 0 (uM^-2 s^-1) | - | - | Substrate Rec-Glu-Gq
Product BetaGamma G*GTP Rec-Glu
| | This reaction is the critical one for activation of Gq. It probably encapsulates multiple steps. In this approximation the receptor-ligand- Gprotein complex splits up into GTP.Galpha, rec.ligand complex, and Gbetagamma. There is a hidden step of exchange of GDP for GTP. The reaction does not take these into account since it is assumed that both GTP and GDP levels are tightly regulated by metabolic control. This is the kcat==k3 stage of the Rec-Glu ezymatic activation of Gq. From Berstein et al actiation is at .35 - 0.7/min From Fay et al Biochem 30 5066-5075 1991 kf = .01/sec From Nakamura et al J physiol Lond 474:1 35-41 1994 see time courses. Also (Berstein) 15-40% of gprot is in GTP-bound form on stim. |
| 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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