#
# This file is automatically generated with 
# the System Biology Format Converter (http://sbfc.sourceforge.net/)
# from an SBML file.
#
# The conversion system has the following limitations:
#  - You may have to re order some reactions and Assignment Rules definition
#  - Delays are not taken into account
#  - You should change the lsode parameters (start, end, steps) to get better results
#

#
# The following line is there to be sure that Octave think that this file 
# is a script and not function file
#
1;

#
# Model name = Lavrentovich2008_Ca_Oscillations
#
# is urn:miriam:biomodels.db:BIOMD0000000184
# is urn:miriam:biomodels.db:MODEL9223106020
# isDescribedBy urn:miriam:pubmed:18275973
#
function z=pow(x,y),z=x^y;endfunction
function z=root(x,y),z=y^(1/x);endfunction
function z = piecewise(varargin)
	numArgs = nargin;
	result = 0;
	foundResult = 0;
	for k=1:2: numArgs-1
		if varargin{k+1} == 1
			result = varargin{k};
			foundResult = 1;
			break;
		endif
	end
	if foundResult == 0
		result = varargin{numArgs};
	endif
z = result;
endfunction

function xdot=f(x,t)
# Compartment: id = compartment, name = Cytoplasm, constant
	compartment_compartment=1.0;
# Compartment: id = ER, name = Endoplasmic Reticulum, constant
	compartment_ER=1.0;
# Parameter:   id =  vin, name = vin
	global_par_vin=0.05;
# Parameter:   id =  kout, name = kout
	global_par_kout=0.5;
# Parameter:   id =  vM3, name = vM3
	global_par_vM3=40.0;
# Parameter:   id =  k_CaA, name = k_CaA
	global_par_k_CaA=0.15;
# Parameter:   id =  n, name = n
	global_par_n=2.02;
# Parameter:   id =  k_CaI, name = k_CaI
	global_par_k_CaI=0.15;
# Parameter:   id =  m, name = m
	global_par_m=2.2;
# Parameter:   id =  kip3, name = kip3
	global_par_kip3=0.1;
# Parameter:   id =  vM2, name = vM2
	global_par_vM2=15.0;
# Parameter:   id =  k2, name = k2
	global_par_k2=0.1;
# Parameter:   id =  kf, name = kf
	global_par_kf=0.5;
# Parameter:   id =  vp, name = vp
	global_par_vp=0.05;
# Parameter:   id =  kp, name = kp
	global_par_kp=0.3;
# Parameter:   id =  kdeg, name = kdeg
	global_par_kdeg=0.08;
# Reaction: id = R1, name = vin


	reaction_R1=compartment_compartment*global_par_vin;
# Reaction: id = R2, name = Calcium export from cell


	reaction_R2=compartment_compartment*global_par_kout*x(1);
# Reaction: id = R3, name = CICR


	reaction_R3=compartment_ER*4*global_par_vM3*global_par_k_CaA^global_par_n*x(1)^global_par_n/((x(1)^global_par_n+global_par_k_CaA^global_par_n)*(x(1)^global_par_n+global_par_k_CaI^global_par_n))*x(3)^global_par_m/(x(3)^global_par_m+global_par_kip3^global_par_m)*(x(2)-x(1));
# Reaction: id = R4, name = serca


	reaction_R4=compartment_compartment*global_par_vM2*x(1)^2/(x(1)^2+global_par_k2^2);
# Reaction: id = R5, name = Leak flux


	reaction_R5=compartment_ER*global_par_kf*(x(2)-x(1));
# Reaction: id = R6, name = PLC


	reaction_R6=compartment_compartment*global_par_vp*x(1)^2/(x(1)^2+global_par_kp^2);
# Reaction: id = R7, name = IP3 degradation


	reaction_R7=compartment_compartment*global_par_kdeg*x(3);
	xdot=zeros(3,1);
	# Species:   id = X, name = Cytoplasmic Calcium, affected by kineticLaw

	xdot(1) = (1/(compartment_compartment))*(( 1.0 * reaction_R1) + (-1.0 * reaction_R2) + ( 1.0 * reaction_R3) + (-1.0 * reaction_R4) + ( 1.0 * reaction_R5));

	# Species:   id = Y, name = Calcium in ER, affected by kineticLaw

	xdot(2) = (1/(compartment_ER))*((-1.0 * reaction_R3) + ( 1.0 * reaction_R4) + (-1.0 * reaction_R5));

	# Species:   id = Z, name = IP3, affected by kineticLaw

	xdot(3) = (1/(compartment_compartment))*(( 1.0 * reaction_R6) + (-1.0 * reaction_R7));

endfunction

#Initial conditions vector
x0=zeros(3,1);
x0(1) = 0.1;
x0(2) = 1.5;
x0(3) = 0.1;


#Creating linespace
t=linspace(0,90,100);

#Solving equations
x=lsode("f",x0,t);

#ploting the results
plot(t,x);