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Molecule Parameter List for inact-GEF | 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 | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 | 81 | Network | Shared_Object_Ajay_bhalla_2007_ReacDiff1_1e-12, PKC, MAPK, Ras, CaM, PKM, chain, kinetics, PKC, MAPK, Ras, CaM, PKM, kinetics[1], PKC, MAPK, Ras, CaM, PKM, kinetics[2], PKC, MAPK, Ras, CaM, PKM, kinetics[3], PKC, MAPK, MAPK, Ras, CaM, PKM, kinetics[4], PKC, MAPK, Ras, CaM, PKM, kinetics[5], PKC, MAPK, Ras, kinetics[6], CaM, PKM, PKC, MAPK, Ras, CaM, PKM, kinetics[7], PKC, Ras, CaM, PKM, kinetics[8], PKC, MAPK, Ras, CaM, PKM, kinetics[9], PKC, MAPK, Ras, CaM, PKM, kinetics[10], PKC, MAPK, Ras, CaM, PKM, kinetics[11], PKC, MAPK, Ras, CaM, PKM, kinetics[12], PKC, MAPK, Ras, CaM, PKM, kinetics[13], PKC, MAPK, Ras, CaM, PKM, kinetics[14], PKC, MAPK, Ras, CaM, PKM, kinetics[15], PKC, MAPK, Ras, CaM, PKM, kinetics[16], PKC, MAPK, Ras, CaM, PKM, kinetics[17], PKC, MAPK, Ras, CaM, PKM, kinetics[18], PKC, MAPK, Ras, CaM, PKM, kinetics[19], PKC, MAPK, Ras, CaM, PKM, kinetics[20], PKC, MAPK, Ras, CaM, PKM, kinetics[21], PKC, MAPK, Ras, CaM, PKM, kinetics[22], PKC, MAPK, Ras, CaM, PKM, kinetics[23], PKC, MAPK, Ras, CaM, PKM | This is a 25-compartment reaction-diffusion version of the Ajay_Bhalla_2007_PKM model. The original single-compartment model is repeated 25 times. In addition, a subset (27 out of 42) molecules can diffuse between compartments. Diffusion is implemented as a reaction between corresponding molecules in neighboring compartments. For D = 1e-12 m^2/sec (i.e., 1 micron^2/sec ) the kf and kb of this reaction for these 10 micron compartments are both 0.01/sec. For D = 1e-13 m^2/sec (i.e., 0.1 micron^2/sec ) the kf and kb are 0.001/sec.
The stimulus file pkm_mapk22_diff_1e-12_Fig4A which was used for the model to replicate Figure 4A from the paper.
This stimulus file pkm_mapk22_diff_1e-12_Fig4G which was used for the model to replicate Figure 4G from the paper |
inact-GEF acting as a Molecule in Ajay_bhalla_2007_ReacDiff1_1e-12 Network
Name | Accession Name | Pathway Name | Initial Conc. (uM) | Volume (fL) | Buffered | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 378 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 385 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 391 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 397 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 404 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 410 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 416 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 422 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 427 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 433 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 439 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 445 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 451 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 457 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 463 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 469 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 475 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 481 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 487 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 493 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 499 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 505 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 511 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 517 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. | inact-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 523 | 0.1 | 1.5 | No | Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels. |
inact-GEF acting as an Enzyme in Ajay_bhalla_2007_ReacDiff1_1e-12 Network
inact-GEF acting as a Substrate for an Enzyme in Ajay_bhalla_2007_ReacDiff1_1e-12 Network
| Enzyme Molecule / Enzyme Activity | Accession Name | Pathway Name | Km (uM) | kcat (s^-1) | Ratio | Enzyme Type | Reagents | 1 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 2 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics Pathway No. : 382 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 3 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[1] Pathway No. : 388 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 4 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[2] Pathway No. : 394 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 5 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[3] Pathway No. : 400 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 6 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[4] Pathway No. : 407 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 7 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[5] Pathway No. : 413 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 8 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[6] Pathway No. : 417 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 9 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[7] Pathway No. : 425 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 10 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[8] Pathway No. : 430 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 11 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[9] Pathway No. : 436 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 12 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[10] Pathway No. : 442 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 13 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[11] Pathway No. : 448 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 14 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[12] Pathway No. : 454 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 15 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[13] Pathway No. : 460 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 16 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[14] Pathway No. : 466 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 17 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[15] Pathway No. : 472 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 18 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[16] Pathway No. : 478 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 19 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[17] Pathway No. : 484 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 20 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[18] Pathway No. : 490 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 21 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[19] Pathway No. : 496 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 22 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[20] Pathway No. : 502 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 23 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[21] Pathway No. : 508 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 24 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[22] Pathway No. : 514 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X | 25 | PKC-active / PKC-act-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | kinetics[23] Pathway No. : 520 | 3.33333 | 4 | 4 | explicit E-S complex | Substrate inact-GEF
Product GEF*
| | Rate consts from PKC-act-raf. This reaction activates GEF. It can lead to at least 2X stim of ras, and a 2X stim of MAPK over and above that obtained via direct phosph of c-raf. Note that it is a push-pull reaction, and there is also a contribution through the phosphorylation and inactivation of GAPs. The original PKC-act-raf rate consts are too fast. We lower K1 by 10 X |
inact-GEF acting as a Substrate in a reaction in Ajay_bhalla_2007_ReacDiff1_1e-12 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 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 2 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 378 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 3 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 4 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 385 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 5 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 6 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 391 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 7 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 8 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 397 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 9 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 10 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 404 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 11 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 12 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 410 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 13 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 14 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 416 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 15 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 16 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 422 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 17 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 18 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 427 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 19 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 20 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 433 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 21 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 22 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 439 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 23 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 24 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 445 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 25 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 26 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 451 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 27 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 28 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 457 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 29 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 30 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 463 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 31 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 32 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 469 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 33 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 34 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 475 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 35 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 36 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 481 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 37 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 38 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 487 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 39 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 40 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 493 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 41 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 42 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 499 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 43 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 44 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 505 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 45 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 46 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 511 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 47 | diff | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Shared_Object_ Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Pathway No. : 375 | 0.01 (s^-1) | 0.01 (s^-1) | Keq = 1(uM) | 50sec | Substrate inact-GEF
Product inact-GEF
| 48 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 517 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 | 49 | CaM-bind-GEF | Ajay_bhalla_ 2007_ReacDiff1_ 1e-12 Accession No. : 81 | Ras Pathway No. : 523 | 199.995 (uM^-1 s^-1) | 1 (s^-1) | Kd(bf) = 0.005(uM) | - | Substrate CaM-Ca4 inact-GEF
Product CaM-GEF
| | We have no numbers for this. It is probably between the two extremes represented by the CaMKII phosph states, and I have used guesses based on this. kf=1e-4 kb=1 The reaction is based on Farnsworth et al Nature 376 524-527 1995 |
inact-GEF acting as a Product in a reaction in Ajay_bhalla_2007_ReacDiff1_1e-12 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. |
| 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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