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

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 Parameter List for nuc_MAPK*

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
nuc_MAPK* participated asMoleculeSum total ofEnzymeSubstrate of an enzymeProduct of an enzymeSubstrate in ReactionProduct in Reaction
No. of occurrences1110001

Accession and Pathway Details
Accession NameAccession No.Accession TypePathway Link
  • mkp1_feedback_
    effects
  • 4Network
    Shared_Object_mkp1_feedback_effects Sos PKC 
    MAPK PLA2 Ras 
    PDGFR 
    This is a network involving the MAPK-PKC feedback loop with input from the PDGFR in the synapse. The distinctive feature of this model is that it includes MKP-1 induction by MAPK, and the consequent inhibitory regulation of MAPK and the feedback loop. Lots of interesting dynamics arise from this. This link provides supplementary material for the paper Bhalla US et al. Science (2002) 297(5583):1018-23. In the form of several example simulations and demos for the figures in the paper.

    nuc_MAPK* acting as a Molecule in  
    mkp1_feedback_effects Network
    NameAccession NamePathway NameInitial Conc.
    (uM)
    Volume
    (fL)
    Buffered
    nuc_MAPK*
  • mkp1_feedback_
    effects

    Accession No. : 4
  • MAPK
    Pathway No. : 35
    0200No
    Cytoplasmic MAPK declines 20%, nuclear MAPK rises 100%. Furuno et al J Immunol 166:4416 (2001) Assume nuc vol 1/5 that of cytoplasm so nuc vol = 2e-16 Note therefore that the concentrations here will be higher for the same number of molecules.

    nuc_MAPK* acting as a Summed Molecule in  
    mkp1_feedback_effects Network
    Accession NamePathway NameTargetInput
  • mkp1_feedback_
    effects

    Accession No. : 4
  • Shared_Object_
    mkp1_feedback_
    effects

    Pathway No. : 32
  • tot_MAPKMAPK*
    nuc_MAPK*
    Total available active MAPK. This sums the levels of the cytosolic and nuclear localized forms.

    nuc_MAPK* acting as an Enzyme in  
    mkp1_feedback_effects Network
    Enzyme Molecule /
    Enzyme Activity
    Accession NamePathway NameKm (uM)kcat (s^-1)RatioEnzyme TypeReagents
    nuc_MAPK* /
  • act_
    transcription
  • mkp1_feedback_
    effects

    Accession No. : 4
  • MAPK
    Pathway No. : 35
    4.000020.00084explicit E-S complexSubstrate
    Nucleotides

    Product
    MKP1-RNA
    This is a 'black box' representation of a lot of steps. Constraint provided by determining rate of formation of MKP-1.

    nuc_MAPK* acting as a Product in a reaction in  
    mkp1_feedback_effects 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.
    NameAccession NamePathway NameKfKbKdtauReagents
    translocation
  • mkp1_feedback_
    effects

    Accession No. : 4
  • MAPK
    Pathway No. : 35
    0.01
    (#^-1 s^-1)
    0.005
    (s^-1)
    Not applicable**-Substrate
    MAPK*
    MAPK*

    Product
    nuc_MAPK*
    A nuclear translocation step. This lumps in all sorts of processes into a single set of rates constrained by time courses. Furuno et al J Immunol 166:4416-4421 (2001): In within 6 min, out within 7. The outgoing path is dephosphorylated MAPK so this reac will be one-way. Kf=0.01, Kb=0.005. The reaction is 2nd order in MAPK*, to represent dimerization of transcription factors.
    ** This is a trasport reation between compartments of different volumes. Therefore Kd is not applicable. Please Note Kf, Kb units are in number of molecules instead of concentration



    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.