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Molecule Parameter List for MAPKK

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
MAPKK participated asMoleculeSum total ofEnzymeSubstrate of an enzymeProduct of an enzymeSubstrate in ReactionProduct in Reaction
No. of occurrences1004100

Accession and Pathway Details
Accession NameAccession No.Accession TypePathway Link
  • Differential syn
    thesis of mRNA
  • 95Network
    kinetics compartment_1 compartment_2 
    The model consists of three major pathways: Calcium-calmodulin dependent protein kinase IV (CaMKIV), Mitogen-activated protein kinase (MAPK) and Protein Phosphatase 1 (PP1). Each of these converged on CREB activation. We also modeled further interactions with Transducer of regulated CREB activity 1 (TORC1) and the protein kinase A (PKA) pathway.

    MAPKK acting as a Molecule in  
    Differential synthesis of mRNA Network
    NameAccession NamePathway NameInitial Conc.
    (uM)
    Volume
    (fL)
    Buffered
    MAPKK
  • Differential syn
    thesis of mRNA

    Accession No. : 95
  • kinetics
    Pathway No. : 1115
    0.181000No
    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.

    MAPKK acting as a Substrate for an Enzyme in  
    Differential synthesis of mRNA Network
     Enzyme Molecule /
    Enzyme Activity
    Accession NamePathway NameKm (uM)kcat (s^-1)RatioEnzyme TypeReagents
    1bRaf_Rap1GTP  /
  • braf_dash_rap1_
    dash_GTP1
  • Differential syn
    thesis of mRNA

    Accession No. : 95
  • kinetics
    Pathway No. : 1115
    0.160.34explicit E-S complexSubstrate
    MAPKK

    Product
    MAPKK_dash_ser
       
    2
  • Raf_dash_GTP_
    dash_Ras
      /
  • Raf_dash_GTP_
    dash_Ras.1
  • Differential syn
    thesis of mRNA

    Accession No. : 95
  • kinetics
    Pathway No. : 1115
    0.15910.34explicit E-S complexSubstrate
    MAPKK

    Product
    MAPKK_dash_ser
        Kinetics are the same as for the craf_1* activity, ie., k1=5.5e-6, k2=0.42, k3 = 0.105 These are basedo n Force et al PNAS USA 91 1270-1274, 1994., but k1 is scaled up 5x (ie., Km is scaled down 5x to the value used here and for craf_1* activity: Km = 0.1591).
    3
  • braf_dash_GTP_
    dash_Ras
      /
  • braf_dash_GTP_
    dash_Ras1
  • Differential syn
    thesis of mRNA

    Accession No. : 95
  • kinetics
    Pathway No. : 1115
    0.160.24explicit E-S complexSubstrate
    MAPKK

    Product
    MAPKK_dash_ser
       
    4
  • Raf_star_dash_
    GTP_dash_Ras
      /
  • Raf_star_dash_
    GTP_dash_Ras.1
  • Differential syn
    thesis of mRNA

    Accession No. : 95
  • kinetics
    Pathway No. : 1115
    0.15910.34explicit E-S complexSubstrate
    MAPKK

    Product
    MAPKK_dash_ser
        Kinetics are the same as for the craf-1* activity, ie., k1=1.1e-6, k2=.42, k3 =0.105 These are based on Force et al PNAS USA 91 1270-1274 1994. These parms cannot reach the observed 4X stim of MAPK. So lets increase the affinity, ie, raise k1 10X to 1.1e-5 Lets take it back down to where it was. Back up to 5X: 5.5e-6

    MAPKK acting as a Product of an Enzyme in  
    Differential synthesis of mRNA Network
    Enzyme Molecule /
    Enzyme Activity
    Accession NamePathway NameKm (uM)kcat (s^-1)RatioEnzyme TypeReagents
    PPhosphatase2A  /
  • MAPKK_dash_
    deph_dash_ser
  • Differential syn
    thesis of mRNA

    Accession No. : 95
  • kinetics
    Pathway No. : 1115
    15.656864explicit E-S complexSubstrate
    MAPKK_dash_ser

    Product
    MAPKK



    Database compilation and code copyright (C) 2022, Upinder S. Bhalla and NCBS/TIFR
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