% B1AR module function [k_kinetic, N_cT] = kinetic_parameters(M, include_type2_reactions, num_cols) % Set the kinetic rate constants. % original model had reactions that omitted enzymes as substrates e.g. BARK % convert unit from 1/s to 1/uM.s by dividing by conc of enzyme % all reactions were irreversible, made reversible by letting kr ~= 0 % CONVERT TO fM % oncentration of BARK = 0.6uM (crude approx from litsearch, for GRK) bigNum = 1e6; fastKineticConstant = bigNum; smallReverse = fastKineticConstant/(bigNum^2); u_to_f = 1e9; cBARK = 0.6*u_to_f; %uM kB11p = 1.1e-3; % 1/s % creation of LRG - Type 2 reactions vK_mSig = [33, 0.285, 0.062, 0.285]; % uM vkSigm = zeros(4,1); vkSigm = zeros(4,1); for i= 1:4 vkSigm(i) = fastKineticConstant; %1/uM.s vkSigp(i) = vkSigm(i)/vK_mSig(i); %1/s end kB11p = kB11p / cBARK; % 1/fM.s kB11m = 2.2e-3; % 1/s kB12p = fastKineticConstant;%1/s kB12m = smallReverse; % 1/fM.s kB21p = kB11p; % 1/fM.s kB21m = kB11m; % 1/s kB22p = fastKineticConstant;%1/s kB22m = smallReverse; % 1/fM.s kP1p = 2.2e-3; % 1/s kP1m = 3.6e-3/u_to_f; % 1/fM.s kP2p = fastKineticConstant; % 1/s kP2m = smallReverse; % 1/fM.s kAct1p = 16; % 1/s kAct1m = smallReverse; % 1/fM.s kAct2m = 16; % 1/s kAct2p = smallReverse; % 1/fM.s kHydp = 0.8; % 1/s kHydm = smallReverse; % 1/s kReassocp = 1.21e3/u_to_f; % 1/fM.s kReassocm = kReassocp/bigNum; % 1/s k_kinetic = [ kB11p, kB12p, kB21p, kB22p, kP1p, kP2p, kAct1p, kAct2p, kHydp, kReassocp, ... kB11m, kB12m, kB21m, kB22m, kP1m, kP2m, kAct1m, kAct2m, kHydm, kReassocm ]'; % CONSTRAINTS N_cT = zeros(3,size(M,2)); % substrate LR/LRG is in eqlm with product B1ARd N_cT(1,num_cols + 1) = 1; N_cT(1,num_cols + 2) = -1; N_cT(2,num_cols + 5) = 1; N_cT(2,num_cols + 2) = -1; % substrate B1ARp is in eqlm with product B1ARtot N_cT(3,num_cols + 7) = 1; N_cT(3,num_cols + 8) = -1; return