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 Ca.PLC_g

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
Ca.PLC_g participated asMoleculeSum total ofEnzymeSubstrate of an enzymeProduct of an enzymeSubstrate in ReactionProduct in Reaction
No. of occurrences1011002

Accession and Pathway Details
Accession NameAccession No.Accession TypePathway Link
  • Synaptic_
    Network
  • 16Network
    Shared_Object_Synaptic_Network PKC PLA2 
    PLCbeta Gq MAPK 
    Ras EGFR Sos 
    PLC_g CaMKII CaM 
    PP1 PP2B PKA 
    AC CaRegulation 
    This model is an annotated version of the synaptic signaling network.
    The primary reference is Bhalla US and Iyengar R. Science (1999) 283(5400):381-7 but several of the model pathways have been updated.
    Bhalla US Biophys J. 2002 Aug;83(2):740-52
    Bhalla US J Comput Neurosci. 2002 Jul-Aug;13(1):49-62

    Ca.PLC_g acting as a Molecule in  
    Synaptic_Network Network
    NameAccession NamePathway NameInitial Conc.
    (uM)
    Volume
    (fL)
    Buffered
    Ca.PLC_g
  • Synaptic_
    Network

    Accession No. : 16
  • PLC_g
    Pathway No. : 79
    01000No

    Ca.PLC_g acting as an Enzyme in  
    Synaptic_Network Network
    Enzyme Molecule /
    Enzyme Activity
    Accession NamePathway NameKm (uM)kcat (s^-1)RatioEnzyme TypeReagents
    Ca.PLC_g /
    PIP2_hydrolysis
  • Synaptic_
    Network

    Accession No. : 16
  • PLC_g
    Pathway No. : 79
    97.2222144Classical Michaelis-Menten
    V = Etot.S.Kcat/Km+S
    Substrate
    PIP2

    Product
    DAG
    IP3
    Wahl et al JBC 267(15) 10447-10456 1992. Homma et al JBC 263:14 1988 pp 6592. These parms are the Ca-stimulated form. This is close to Wahl's figure 7, which I am using as reference. Also see Nakanishi et al Biochem J 256 453-459 1998, Nishibe et al Science 250 :1253-1256 This model uses a rather low PIP2 of 10 uM.

    Ca.PLC_g acting as a Substrate for an Enzyme in  
    Synaptic_Network Network
    Enzyme Molecule /
    Enzyme Activity
    Accession NamePathway NameKm (uM)kcat (s^-1)RatioEnzyme TypeReagents
    L.EGFR  /
    phosph_PLC_g
  • Synaptic_
    Network

    Accession No. : 16
  • EGFR
    Pathway No. : 77
    0.3333330.24explicit E-S complexSubstrate
    Ca.PLC_g

    Product
    Ca.PLC_g*
    Hsu et al JBC 266:1 603-608 1991 Km = 385 +- 100 uM, Vm = 5.1 +-1 pmol/min/ug for PLC-771. Other sites have similar range, but are not stim as much by EGF. These rates are improbably slow and are for the intracellular domain of EGFR alone. Wahl et al JBC 267(15) 10447-10456 1992 reports a tau of 5min for activation of PLC-gamma in vivo. Also Sherrill and Kyte say turnover # for angiotensin II is 5/min for cell extt, and 2/min for placental. Also see Okada et al JBC 270(35) 20737-20741 1995 for Shc rates where Km = 0.7 and Vmax = 4.4 pmol/min To achieve these turnovers and time-courses, we may need to consider the membrane-plane action of the the receptor, but for now the rates are consistent with the Wahl et al reports.

    Ca.PLC_g acting as a Product in a reaction in  
    Synaptic_Network 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
    1Ca_act_PLC_g
  • Synaptic_
    Network

    Accession No. : 16
  • PLC_g
    Pathway No. : 79
    180
    (uM^-1 s^-1)
    10
    (s^-1)
    Kd(bf) = 0.0556(uM)-Substrate
    Ca
    PLC_g

    Product
    Ca.PLC_g
      Nice curves from Homma et al JBC 263:14 6592-6598 1988 Fig 5c. The activity falls above 10 uM, but that is too high to reach physiologically anyway, so we'll ignore the higher pts and match the lower ones only. Half-max at 1 uM. But Wahl et al JBC 267:15 10447-10456 1992 have half-max at 56 nM which is what I'll use.
    2dephosph_PLC_g
  • Synaptic_
    Network

    Accession No. : 16
  • PLC_g
    Pathway No. : 79
    0.05
    (s^-1)
    0
    (s^-1)
    --Substrate
    Ca.PLC_g*

    Product
    Ca.PLC_g
      This is a generic balancing dephosphorylation step for the PLC. Rates are determined by considering balance between phosph and non-phosph forms of PLC-gamma. Wahl et al JBC 267(15) 10447-10456 1992 put the ratio at 50% phosph form in cytoplasm, about 20% in membrane.



    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.