NCBS Home page
Accession List
Pathway List
Search
Authorized Users
Help
News archives

Accession Type:
Network
mRNA synthesis
Shared Object_
mRNA synthesis
 Molecule
 Enzyme
 Reaction
compartment_1compartment_1
compartment_2compartment_2

Enter a Search String

Special character and space not allowed in the query term. Search string should be at least 2 characters long.
Search in: Search for Match By

Molecule List for pathway Shared Object_mRNA synthesis (Pathway Number 1112)

 Name Initial Conc. (uM) Volume (fL) Buffered
1AC10.021000No
   
2AC1_dash_CaM01000No
   
3AC20.0151000No
   
4AC2_star01000No
   
5active_RSK201000No
   
6ATP50001000Yes
   
7Basal_CaMKIV0.00051000No
   
8Basal_MAPK_active0.00011000No
   
9BDNF01000Yes
   
10BDNF_TrkB2_clx01000No
   
11BDNF_TrkB2_star_clx01000No
   
12BDNF_TrkB_clx01000No
   
13BetaGamma01000No
    These exist in a nebulous sense in this model, basically only to balance the conservation equations. The details of their reassociation with G-GDP are not modeled Resting level =0.0094, stim level =.0236 from all42.g ish.
14bRaf0.21000No
   
15braf_dash_GTP_dash_Ras01000No
   
16braf_dash_GTP_dash_Ras1_cplx01000No
   
17braf_dash_GTP_dash_Ras2_cplx01000No
   
18braf_dash_rap1_dash_GTP1_cplx01000No
   
19braf_dash_Rap1_dash_GTP2_cplx01000No
   
20bRaf_Rap1GTP01000No
   
21C3G0.51000No
   
22Ca0.081000Yes
   
23CaM201000No
    There is a LOT of this in the cell: upto 1% of total protein mass. (Alberts et al) Say 25 uM. Meyer et al Science 256 1199-1202 1992 refer to studies saying it is comparable to CaMK levels.
24CaM(Ca)n_dash_CaNAB01000No
   
25CaM.PDE101000No
   
26CaM.PDE1_cplx01000No
   
27CaMCa2_dash_CANAB01000No
   
28CaMCa3_dash_CaNAB01000No
   
29CaMCa4_dash_CaNAB01000No
   
30CaMKIVc11000No
   
31CaMKIVdephos_cplx01000No
   
32CaMKIVphosph_cplx01000No
   
33CaMKIV_CaM_Ca_c01000No
   
34CaMKKdephosph_cplx01000No
   
35CaMKKp01000No
   
36CaMKKphosph_cplx01000No
   
37CaMKK_c0.51000No
    Concentration calculated from PMID: 7883770
38CaMKK_CaM_Ca_c01000No
   
39cAMP01000No
   
40cAMP_dash_PDE0.451000No
   
41cAMP_dash_PDE_star01000No
   
42CaM_dash_Ca01000No
    This is the intermediate where the TR2 end (the high-affinity end) has bound the Ca but the TR1 end has not.
43CaM_dash_Ca201000No
    This is the intermediate where the TR2 end (the high-affinity end) has bound the Ca but the TR1 end has not.
44CaM_dash_Ca301000No
   
45CaM_dash_Ca401000No
   
46CaM_dash_GEF01000No
    See Farnsworth et al Nature 376 524-527 1995
47CaM_dash_GEF_dash_act_dash_ras_cplx01000No
   
48CaNAB11000No
    We assume that the A and B subunits of PP2B are always bound under physiol conditions. Up to 1% of brain protein = 25 uM. I need to work out how it is distributed between cytosolic and particulate fractions. Tallant and Cheung '83 Biochem 22 3630-3635 have conc in many species, average for mammalian brain is around 1 uM.
49CaNAB_dash_Ca201000No
   
50CaNAB_dash_Ca401000No
   
51CaN_dephos_TORC1_cplx01000No
   
52Ca_input01000No
   
53Cbl0.51000No
   
54Cbl_phospho_cplx01000No
   
55Cbl_star01000No
   
56craf_dash_10.21000No
   
57craf_dash_1_star01000No
   
58craf_dash_1_star_star01000No
    Negative feedback by MAPK* by hyperphosphorylating craf-1* gives rise to this pool. Ueki et al JBC 269(22):15756-15761, 1994
59craf_dash_deph_cplx01000No
   
60craf_star_star_dash_deph_cplx01000No
   
61CRK11000No
   
62CRK_C3G01000No
   
63CRK_C3G_Cbl_star_clx01000No
   
64dephosph_dash_PP1_dash_I_p_cplx01000No
   
65dephosph_inhib1_cplx01000No
   
66dephosph_inhib1_noCaM_cplx01000No
   
67dephosp_S6K_cplx01000No
   
68dephos_S6K_cplx01000No
   
69GAP0.011000No
    GTPase-activating proteins. See Boguski and McCormick. Turn off Ras by helping to hydrolyze bound GTP. This one is probably NF1, ie., Neurofibromin as it is inhibited by AA and lipids, and expressed in neural cells. p120-GAP is also a possible candidate, but is less regulated. Both may exist at similar levels. See Eccleston et al JBC 268(36) pp27012-19 Level=.002 16 May 2003: Increased level to 0.0036, in line with other concentration raises at the synapse.
70GAP_dash_inact_dash_ras_cplx01000No
   
71GAP_star01000No
   
72GDP_dash_Ras0.51000No
    GDP bound form. See Rosen et al Neuron 12 1207-1221 June 1994. the activation loop is based on Boguski and McCormick Nature 366 643-654 93 Assume Ras is present at about the same level as craf-1, 0.2 uM. Hallberg et al JBC 269:6 3913-3916 1994 estimate upto 5-10% of cellular Raf is assoc with Ras. Given that only 5-10% of Ras is GTP-bound, we need similar amounts of Ras as Raf.
73GEF_dash_bg_act_dash_ras_cplx01000No
   
74GEF_dash_Gprot_dash_bg01000No
    Guanine nucleotide exchange factor. This activates raf by exchanging bound GDP with GTP. I have left the GDP/GTP out of this reaction, it would be trivial to put them in. See Boguski & McCormick. Possible candidate molecules: RasGRF, smgGDS, Vav (in dispute). rasGRF: Kcat= 1.2/min Km = 680 nM smgGDS: Kcat: 0.37 /min, Km = 220 nM. vav: Turnover up over baseline by 10X,
75GEF_star01000No
    phosphorylated and thereby activated form of GEF. See, e.g. Orita et al JBC 268:34 25542-25546 1993, Gulbins et al. It is not clear whether there is major specificity for tyr or ser/thr.
76GEF_star_dash_act_dash_ras_cplx01000No
   
77Grb211000No
    There is probably a lot of it in the cell: it is also known as Ash (abundant src homology protein I think). Also Waters et al JBC 271:30 18224 1996 say that only a small fraction of cellular Grb is precipitated out when SoS is precipitated. As most of the Sos seems to be associated with Grb2, it would seem like there is a lot of the latter. Say 1 uM. I haven't been able to find a decent....
78GTP_dash_Ras01000No
    Only a very small fraction (7% unstim, 15% stim) of ras is GTP-bound. Gibbs et al JBC 265(33) 20437
79I11.81000No
    I1 is a 'mixed' inhibitor, but at high enz concs it looks like a non-compet inhibitor (Foulkes et al Eur J Biochem 132 309-313 9183). We treat it as non-compet, so it just turns the enz off without interacting with the binding site. Cohen et al ann rev bioch refer to results where conc is 1.5 to 1.8 uM. In order to get complete inhib of PP1, which is at 1.8 uM, we need >= 1.8 uM.
80I1_star0.0011000No
    Dephosph is mainly by PP2B
81inact_dash_GEF0.11000No
    Assume that SoS is present only at 50 nM. Revised to 100 nM to get equil to experimentally known levels.
82inact_dash_GEF_star01000No
    Phosphorylation-inactivated form of GEF. See Hordijk et al JBC 269:5 3534-3538 1994 and Buregering et al EMBO J 12:11 4211-4220 1993
83inhibited_dash_PKA01000No
   
84Int_BDNF_TrKB2_star_clx0.251000Yes
   
85MAPK0.361000No
    conc is from Sanghera et al JBC 265 pp 52 (1990) A second calculation gives 3.1 uM, from same paper. They est MAPK is 1e-4x total protein, and protein is 15% of cell wt, so MAPK is 1.5e-5g/ml = 0.36uM. which is closer to our first estimate. Lets use this. Updated 16 May 2003. Ortiz et al 1995 J Neurosci 15(2):1285-1297 provide estimates of ERK2 levels in hippocampus: 1009 ng/mg. This comes to about 3.6uM, which may still be an underestimate of synaptic levels.
86MAPKK0.181000No
    Conc is from Seger et al JBC 267:20 pp14373 (1992) mwt is 45/46 Kd We assume that phosphorylation on both ser and thr is needed for activiation. See Kyriakis et al Nature 358 417 1992 Init conc of total is 0.18 Ortiz et al 1995 J Neurosci 15(2):1285-1297 suggest that levels are higher in hippocampus than other brain regions, and further elevated in synapses. Estimate 3x higher levels than before, at 0.5 uM. Similar results from Schipper et al 1999 Neuroscience 93(2):585-595 but again lacking in quantitation.
87MAPKKthr_cplx01000No
   
88MAPKKtyr_cplx01000No
   
89MAPKK_dash_deph_cplx01000No
   
90MAPKK_dash_deph_dash_ser_cplx01000No
   
91MAPKK_dash_ser01000No
    Intermediately phophorylated, assumed inactive, form of MAPKK
92MAPKK_star01000No
    MAPKK phosphorylates MAPK on both the tyr and thr residues, first tyr then thr. Refs: Seger et al JBC267:20 pp 14373 1992 The MAPKK itself is phosphorylated on ser as well as thr residues. Let us assume that the ser goes first, and that the sequential phosphorylation is needed. See Kyriakis et al Nature 358 417-421 1992
93MAPK_active_total01000No
   
94MAPK_dash_tyr01000No
    Haystead et al FEBS Lett. 306(1) pp 17-22 show that phosphorylation is strictly sequential, first tyr185 then thr183.
95MAPK_star01000No
   
96MAPK_star_dash_feedback_cplx01000No
   
97MKP1_dash_thr_dash_deph_cplx01000No
   
98MKP1_dash_tyr_dash_deph_cplx01000No
   
99MKP_dash_10.0151000No
    MKP-1 dephosphoryates and inactivates MAPK in vivo: Sun et al Cell 75 487-493 1993. Levels of MKP-1 are regulated, and rise in 1 hour. Kinetics from Charles et al PNAS 90:5292-5296 1993. They refer to Charles et al Oncogene 7 187-190 who show that half-life of MKP1/3CH134 is 40 min. 80% deph of MAPK in 20 min Sep 17 1997: CoInit now 0.4x to 0.0032. See parm searches from jun96 on.
100pCaMKIV_CaM_Ca_c01000No
   
101pCaMKIV_CaM_Ca_c_tot01000No
   
102PDE121000No
   
103PDE1_cplx01000No
   
104PDE_cplx01000No
   
105PDE_p_cplx01000No
   
106PDK111000No
   
107phospho_S6K_cplx01000No
   
108phosph_dash_AC2_cplx01000No
   
109phosph_dash_PDE_cplx01000No
   
110phosph_Sos_cplx01000No
   
111PKA_dash_active01000No
   
112PKA_dash_inhibitor0.251000No
   
113PKA_dash_phosph_dash_GEF_cplx01000No
   
114PKA_dash_phosph_dash_I1_cplx01000No
   
115PKC_dash_active0.011000Yes
   
116PKC_dash_act_dash_GEF_cplx01000No
   
117PKC_dash_act_dash_raf_cplx01000No
   
118PKC_dash_inact_dash_GAP_cplx01000No
   
119PLCg_basal0.00071000No
   
120PLC_g0.11000No
   
121PLC_g_phospho_cplx01000No
   
122PLC_g_phospho_cplx01000No
   
123PLC_g_star01000No
   
124PP1_dash_active_c1.81000No
    Cohen et al Meth Enz 159 390-408 is main source of info conc = 1.8 uM
125PP1_dash_I101000No
   
126PP1_dash_I1_star01000No
   
127PP2A0.151000Yes
    Concentration from DOQCS accession no. 90
128PP2A_dash_dephosph_dash_I1_cplx01000No
   
129PP2A_dash_dephosph_dash_PP1_dash_I_p_cpl01000No
   
130PPhosphatase2A11000No
    Refs: Pato et al Biochem J 293:35-41(93); Takai&Mieskes Biochem J 275:233-239 k1=1.46e-4, k2=1000,k3=250. these use kcat values for calponin. Also, units of kcat may be in min! revert to Vmax base: k3=6, k2=25,k1=3.3e-6 or 6,6,1e-6 CoInit assumed 0.1 uM. See NOTES for MAPK_Ras50.g. CoInit now 0.08 Sep 17 1997: Raise CoInt 1.4x to 0.224, see parm searches from jun 96 on.
131ppRSK01000No
   
132pRSK01000No
   
133pTORC101000No
   
134R201000No
   
135R2C101000No
   
136R2C20.51000No
   
137R2C2_dash_cAMP01000No
   
138R2C2_dash_cAMP201000No
   
139R2C2_dash_cAMP301000No
   
140R2C2_dash_cAMP401000No
   
141R2C_dash_cAMP401000No
   
142R2_dash_cAMP401000No
   
143Raf_dash_GTP_dash_Ras01000No
   
144Raf_dash_GTP_dash_Ras.1_cplx01000No
   
145Raf_dash_GTP_dash_Ras.2_cplx01000No
   
146Raf_star_dash_GTP_dash_Ras01000No
   
147Raf_star_dash_GTP_dash_Ras.1_cplx01000No
   
148Raf_star_dash_GTP_dash_Ras.2_cplx01000No
   
149Rap1GAP0.0121000No
   
150Rap1GDP0.21000No
   
151Rap1GTP01000No
   
152RapGAP1_cplx01000No
   
153RapGAP2_cplx01000No
   
154RSK0.21000No
   
155S6K_phospho_cplx01000No
   
156Shc0.51000No
   
157Shc_phospho_cplx01000No
   
158Shc_star01000No
   
159Shc_star.Sos.Grb201000No
   
160SIK20.51000No
   
161SIK2_phosp_cplx01000No
   
162SIK2_star01000No
   
163Sos0.11000No
   
164Sos.Grb201000No
   
165Sos.Ras_GEF_cplx01000No
   
166Sos_star01000No
   
167Sos_star.Grb201000No
   
168Src0.021000No
   
169Src_phospho_cplx01000No
   
170Src_star01000No
   
171Sum_total_CaMKIV01000No
   
172TORC1c0.11000No
   
173TORC1_phso_enz_cplx01000No
   
174TrKB0.251000No
   

Summed Molecule List

  Target Inputs
1 CaM(Ca)n_dash_CaNAB
  • CaMCa4_dash_
    CaNAB

  • CaMCa3_dash_
    CaNAB

  • CaMCa2_dash_
    CANAB

  • 2 MAPK_active_totalMAPK_star
  • Basal_MAPK_
    active

  • Basal_MAPK_
    active

  • 3 pCaMKIV_CaM_Ca_c_tot
  • pCaMKIV_CaM_Ca_
    c

    Basal_CaMKIV
  • 4 Sum_total_CaMKIV
  • pCaMKIV_CaM_Ca_
    c_tot

  • pCaMKIV_CaM_Ca_
    c_tot



  • Pathway Details  Molecule List   Enzyme List   Reaction List  


    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.