def __init__(self, params):
#
# Initialise
#
self.params = params
import pKaTool.pKaIO as pKaIO
self.pdbfile = self.params['pdb']
self.MCsteps = int(self.params['MCsteps'])
self.pHstep = float(self.params['pHstep'])
self.pHstart = float(self.params['pHstart'])
self.pHend = float(self.params['pHend'])
IO = pKaIO.pKaIO(self.pdbfile)
#
# Define the tmpdir for all our calcs
#
import os
self.topdir = os.path.split(self.pdbfile)[0]
self.topdir = os.path.join(
self.topdir, '%s_autonomy' % os.path.split(self.pdbfile)[1])
if not os.path.isdir(self.topdir):
os.mkdir(self.topdir)
#
# Did we find a completed pKa calculation for the PDB file
#
if IO.calculation_completed:
#
# All files found
#
print 'pKa calculation files found'
else:
print
print 'I could not find a completed pKa calculation for the specified PDB file'
print 'Please complete the pKa calculation first'
print
raise Exception()
#
# Get the wild type titration curves calculated with WHAT IF
#
import pKaTool.pKaIO
IO = pKaTool.pKaIO.pKaIO(self.pdbfile)
self.wt_titcurv = IO.read_titration_curve()
self.wt_pKas = IO.readpka()
#
# Recalculate titration curves with the CPP algorithm
#
import os
dirname = os.path.join(self.topdir, 'wt_recalc')
if not os.path.isdir(dirname):
os.mkdir(dirname)
filename = os.path.join(dirname, 'WT.DAT')
data = None
if os.path.isfile(filename):
try:
fd = open(filename)
import cPickle
data = cPickle.load(fd)
fd.close()
self.wtpkas = data['pkas']
self.wt_titcurv = data['titcurv']
print 'Loaded wild type recalculated titration curves'
print 'Loaded %d titration curves' % (len(
self.wt_titcurv.keys()))
except:
data = None
#
# If we don't have the data calculate it
#
if data is None:
import pKa_MC
print 'Recalculating wild type titration curves'
pKa_params = {
'pHstart': self.pHstart,
'pHstop': self.pHend,
'pHstep': self.pHstep,
'pKMCsteps': self.MCsteps,
'verbose': 1
}
self.pKaCALC = pKa_MC.pKa_calculation_class(self.pdbfile,
pKa_info=None,
params=pKa_params,
parent=self)
self.pKaCALC.set_MC_CPP()
self.pKaCALC.set_reporter_groups(self.wt_pKas.keys())
self.wtpkas, self.wt_titcurv = self.pKaCALC.calc_wt_pkas()
#
# Save the data
#
fd = open(filename, 'w')
import cPickle
data = cPickle.dump(
{
'pkas': self.wtpkas,
'titcurv': self.wt_titcurv
}, fd)
fd.close()
print 'done'
print
print 'Calculated %d titration curves' % (len(
self.wt_titcurv.keys()))
#
# Get the in_system energies
#
self.in_data = self.calculate_insystem_dpKas()
#
# Get the ex_data
#
self.ex_data = self.calculate_exsystem_dpKas()
return
def main():
#
# Do all the analyses we want
#
print
print 'Design_plots.py: Do all analyses of the Design_pKa runs'
print
print 'Usage Design_plots.py [files] <type>'
print
#
# dpKa vs. distance from active site & number of mutations
#
import sys
#
# Get the type
#
type=sys.argv[-1]
if type=='two':
#
# Analysing a single group
#
files=get_files(sys.argv[1:-2],type,sys.argv[-2])
else:
#
# Get the files
#
files=get_files(sys.argv[1:-1],type)
#
# If not files then exit
#
if files==[]:
print 'Error: Did not find any files to match criteria'
return
#
# Prepare the data matrix
#
raw_data={}
max_dist=25
max_muts=20
distance_range=range(max_dist+1)
nummuts_range=range(1,max_muts+1)
for num in nummuts_range:
raw_data[num]={}
for dist in distance_range:
raw_data[num][dist]=[0.0]
#
# Loop over all the files
#
added=0
big_dict={}
tot_target={}
for file in files:
if file[-5:]=='.lock':
continue
print 'Processing %s' %file
try:
import pickle
fd=open(file)
d=pickle.load(fd)
fd.close()
except:
continue
#
# Set the prefix
#
prefix=get_prefix(file)
#
# -----------------------------------
#
# Loop over all the design-data
#
targets=d.keys()
targets.sort()
for target in targets:
#if target!=':0231:ASP':
# continue
#
# pdbfile and wt_full are not interesting
#
if target=='pdbfile' or target=='wt_full':
continue
target_pka=d[target]
designs=target_pka.keys()
designs.sort()
if designs==['pKa out of range']:
continue
#
# Loop over each design (normally +20 and -20 for Design_dist_nummuts)
#
for design in designs:
#if design!='m20':
# continue
try:
nummuts=target_pka[design].keys()
except:
#print 'Skipping:',target_pka[design]
continue
nummuts.sort()
for num in nummuts:
dist_cutoffs=target_pka[design][num].keys()
for cutoff in dist_cutoffs:
#text='%15s %4s #muts: %2d, dist_co: %5.2f, sols:' %(target,design,num,float(cutoff))
#print text
#
# Make sure we have a bin for the this distance cutoff
#
#if not raw_data[num].has_key(cutoff):
# raw_data[num][cutoff]=[]
#
# Loop over all solutions and store the dpKa values
#
sol_dict=target_pka[design][num][cutoff]
solutions=sol_dict.keys()
#
# Loop over all the solutions
#
for sol in solutions:
if sol_dict[sol].has_key(type):
dpka=sol_dict[sol][type][target]
mutations=sol_dict[sol]['mutations']
#
# Count the number of mutations
#
nums=0
for mut in mutations:
if mut:
nums=nums+1
#
# Add the data to the array
#
# We skip all data points outside the range specified
# by max_muts and max_dist
#
skip=None
if not raw_data.has_key(nums):
skip=1
if not skip:
if not raw_data[nums].has_key(cutoff):
skip=1
if not skip:
raw_data[nums][cutoff].append(dpka)
#
# Add to the big dictionary
#
import os
tname=prefix+target
if not big_dict.has_key(tname):
big_dict[tname]=[]
clean_muts=[]
for mut in mutations:
if mut:
clean_muts.append(mut)
big_dict[tname].append([clean_muts,dpka])
#
# Keep track of how many we add
#
added=added+1
#print 'Adding: nummuts: %2d, cutoff: %4.1f, dpka: %4.2f' %(nums,cutoff,dpka)
#except:
# pass
#print '--------------------'
#
# Read the definition of the active site
#
act_site=read_actsit_def()
#
# Get properties from the PDB files/wt pKa calculation
#
import string, os
for file in files:
if file[-5:]=='.lock':
continue
prefix=get_prefix(file)
#
# Analysis
#
print 'Analysing for %s' %prefix
#
# Read the PDB file
#
pdbfile=os.path.join(basedir,prefix[:4],prefix)
import Protool
Z=Protool.structureIO()
Z.readpdb(pdbfile)
#
# Get the relative accs
#
import WI_tools
accs=WI_tools.relative_accessibility(pdbfile)
#
# Open the wt pKa calc
#
import pKaTool.pKaIO as pKaIO
X=pKaIO.pKaIO(pdbfile)
pkavals=X.readpka()
matrix=X.read_matrix()
for residue in pkavals.keys():
target=prefix+residue
if not tot_target.has_key(target):
tot_target[target]={}
tot_target[target]['pKa']=pkavals[residue]['pKa']
elecs=[]
for other_res in matrix[residue].keys():
elecs.append(matrix[residue][other_res][0])
tot_target[target]['elecs']=elecs[:]
#
# Insert number of aas
#
tot_target[target]['prot_aas']=len(Z.residues.keys())
#
# Is this target in the vicinity of the active site?
#
tot_target[target]['act_site']=None
target_res=target.split('pdb')[1]
target_res=':'+target_res.split(':')[1]
try:
target_atoms=Z.residues[target_res]
except:
print target_res
print Z.residues.keys()
stop
if act_site.has_key(prefix):
for act_res in act_site[prefix]:
r_act_res=':'+act_res.split(':')[1]
for atom2 in Z.residues[r_act_res]:
for target_atom in target_atoms:
#print 'Comparing',target_atom,atom2
if Z.distance(target_atom,atom2)<5.0:
tot_target[target]['act_site']='Yes'
#
# Insert rel. acc
#
if residue[-6:]==':CTERM':
residue=residue[:-6]
if residue[-6:]==':NTERM':
residue=residue[:-6]
#print accs[residue]['sum']
tot_target[target]['relacc']=accs[residue]['sum']['rel']
#print residue,accs[residue]
print
print ' All done'
#
# How many solutions in total?
#
print 'I added %5d solutions to the matrix' %added
#
# For each target, what's the maximum dpKa?
#
targets=big_dict.keys()
targets.sort()
max_dpkas=[]
all=[]
actsite_dpkas=[]
all_actsite_dpkas=[]
file_dpkas={}
for target in targets:
tmp_dpkas=[]
for solution,dpka in big_dict[target]:
tmp_dpkas.append(abs(dpka))
if not file_dpkas.has_key(target[:4]):
file_dpkas[target[:4]]={}
file_dpkas[target[:4]]['dpkas']=[]
file_dpkas[target[:4]]['num_target']=0
file_dpkas[target[:4]]['max_dpka']=0.0
#
# Add the new dpKa
#
file_dpkas[target[:4]]['dpkas'].append(abs(dpka))
avg,var,sdev=average(tmp_dpkas)
print 'Average pKa shift for %25s is %5.2f (%5.2f)' %(target,avg,sdev)
tmp_dpkas.sort()
max_dpka=tmp_dpkas[-1]
max_dpkas.append(max_dpka)
all=all+tmp_dpkas
#
# Store the average and max dpka for each target
#
tot_target[target]['avg_dpka']=avg
tot_target[target]['max_dpka']=max_dpka
#
# Set the aa size
#
file_dpkas[target[:4]]['prot_aas']=tot_target[target]['prot_aas']
#
# Increment the number of targets designed for this protein
#
file_dpkas[target[:4]]['num_target']=file_dpkas[target[:4]]['num_target']+1
#
# Is is an active site target?
#
if tot_target[target]['act_site']:
actsite_dpkas.append(max_dpka)
all_actsite_dpkas=all_actsite_dpkas+tmp_dpkas
#
# Write the PDB files
#
for file in files:
tf_max=[]
if file[-5:]=='.lock':
continue
prefix=get_prefix(file)
#
# Writing Yasara script
#
print 'Writing Yasara script for %s' %prefix
#
# Read the PDB file
#
fd=open('yasara.mcr','w')
pdbfile=os.path.join(basedir,prefix[:4],prefix)
fd.write('LoadPDB %s\n' %pdbfile)
fd.write('ColorAll 606060\n')
fd.write('Style Stick\n')
fd.write('HUD Off\n')
fd.write('HideRes Hoh\n')
import Protool
Z=Protool.structureIO()
Z.readpdb(pdbfile)
#
# Zero all B-factors
#
#for residue in Z.residues.keys():
# for atom in Z.residues[residue]:
# Z.atoms[atom]['B-factor']=0.0
#
# Loop over all targets and set the colour
#
colors={1.0:'Blue',
2.0:'Cyan',
3.0:'Green',
4.0:'Yellow',
5.0:'Red'}
for target in tot_target.keys():
#
# Collect stats on the max abs(dpka)
#
pos=target.find(prefix)
if pos!=-1:
if tot_target[target].has_key('max_dpka'):
tf_max.append(abs(tot_target[target]['max_dpka']))
#
# Write the PDB file
#
if pos!=-1:
resnum=target[pos+len(prefix):]
resnum=':'+resnum.split(':')[1]
if Z.residues.has_key(resnum):
if tot_target[target].has_key('max_dpka'):
col_cutoff=colors.keys()
col_cutoff.sort()
co=0.5
for col in col_cutoff:
co=col
if tot_target[target]['max_dpka']<col:
break
colour=colors[co]
fd.write('ColorRes %d,%s\n' %(int(resnum[1:]),colour))
else:
fd.write('ColorRes %d,%s\n' %(int(resnum[1:]),'aaaaaa'))
else:
raise 'Residue not found',target
#Z.writepdb('BF_dpKa')
print 'Number of max_pkas in %s is %d' %(prefix,len(tf_max))
avg,var,sdev=average(tf_max)
print '%s, average max dpKa %5.1f, sdev: %5.1f' %(prefix,avg,sdev)
#fd.write('exit\n')
fd.close()
#
# Print all the stats
#
print
print 'Number of targets designed is : %4d ' %(len(targets))
all_targets=len(tot_target.keys())
print 'Number of targets in total: : %4d ' %all_targets
print '%% designed : %5.2f' %(float(len(targets))/float(all_targets)*100.0)
print
print 'Number of active site targets : %5.2f' %(len(actsite_dpkas))
#
# Get average Delta pKas
#
avg,var,sdev=average(all)
print 'Average dpKa for all targets is : %5.2f (%5.2f)' %(avg,sdev)
avg,var,sdev=average(max_dpkas)
print 'Average MAX dpKa for all targets is :%5.2f (%5.2f)' %(avg,sdev)
# Max dpka for active sites
avg,var,sdev=average(actsite_dpkas)
print 'Average MAX dpKa for active site targets: %5.2f (%5.2f)' %(avg,sdev)
#
avg,var,sdev=average(all_actsite_dpkas)
print 'Average dpKa for actsit target :%5.2f (%5.2f)' %(avg,sdev)
print
print 'Average dpKa per protein'
prots=file_dpkas.keys()
prots.sort()
for prot in prots:
avg,var,sdev=average(file_dpkas[prot]['dpkas'])
num_target=file_dpkas[prot]['num_target']
aa_size=file_dpkas[prot]['prot_aas']
num_sol=len(file_dpkas[prot]['dpkas'])
print 'Average dpKa for %s is : %5.2f (%5.2f) [#targets %4d, #aas %4d, #sols/target %5.2f]' %(prot,avg,sdev,num_target,aa_size,float(num_sol)/float(num_target))
#
# Stats on the types of targets designed
#
designed={}
import pKarun
Y=pKarun.pKanalyse()
for target in big_dict.keys():
rtype=Y.get_residue_type(target)
if not designed.has_key(rtype):
designed[rtype]=0
designed[rtype]=designed[rtype]+1
des=designed.keys()
#
# Look at the targets not designed
#
not_designed={}
all_targets=tot_target.keys()
all_targets.sort()
import pKarun
Y=pKarun.pKanalyse()
for target in all_targets:
if not big_dict.has_key(target):
rtype=Y.get_residue_type(target)
if not not_designed.has_key(rtype):
not_designed[rtype]=0
not_designed[rtype]=not_designed[rtype]+1
#
# Stats
#
print
print 'Stats on types of groups designed'
types=['ASP','GLU','TYR','CYS','CTERM','NTERM','LYS','ARG','HIS']
types.sort()
for rtyp in types:
if designed.has_key(rtyp):
des=designed[rtyp]
else:
des=0
if not_designed.has_key(rtyp):
ndes=not_designed[rtyp]
else:
ndes=0
tot=ndes+des
if tot>0:
avg='%5.2f' %(float(des)/float(tot)*100.0)
else:
avg='NA'
print '%8s des: %3d notD: %3d, tot: %3d %% designed: %s' %(rtyp,des,ndes,tot,avg)
#
# Relation between average dpKa obtained and accessibility, type and electrostatic interactions.
#
print
#
# Plot of avg dpKa vs. sum of abs electrostatic interactions
#
avg_dpka=[]
max_dpka=[]
sum_elec=[]
acc=[]
for target in all_targets:
dpkas=[]
if big_dict.has_key(target):
for mutants,dpka in big_dict[target]:
dpkas.append(abs(dpka))
e_sum=[]
for elec in tot_target[target]['elecs']:
e_sum.append(elec)
#
max_dpka.append(max(dpkas))
#
avg,var,sdev=average(dpkas)
avg_dpka.append(avg)
#
avg,var,sdev=average(e_sum)
sum_elec.append(get_sum(e_sum))
#
# Accessibility
#
acc.append(tot_target[target]['relacc'])
else:
#print 'No design for',target
pass
import dislin_driver
file=dislin_driver.graf_mult2(acc,[avg_dpka,max_dpka],
title='Effect of solvent exposure',
x_legend='Relative accessibility of target',
y_legend='abs(dpKa)',
legends=['Avg. dpKa','Max. dpKa'])
#os.system('eog %s' %file)
#
# Any difference for active site targets?
#
#
# Plot it
#
nummuts={}
nums=raw_data.keys()
nums.sort()
for num in nums:
for co in raw_data[num].keys():
max_val=-1.0
sum=0.0
count=0
for dpka in raw_data[num][co]:
if abs(dpka)>max_val:
max_val=abs(dpka)
if dpka>0.01:
sum=sum+abs(dpka)
count=count+1
#
# Sort as function of number of mutations for other stat
#
if not nummuts.has_key(num):
nummuts[num]=[]
nummuts[num].append(abs(dpka))
if count==0:
raw_data[num][co]=0
else:
raw_data[num][co]=float(sum)/float(count)
#raw_data[num][co]=max_val
import dislin_driver
#dislin_driver.colour_2D(raw_data,'','','# of mutations','distance from target (A)','abs(dpKa)','dpka.tif')
import os
#os.system('gimp dpka.tif')
#
# Get dpKa as a function of # of mutants
#
#nums=nummuts.keys()
#nums.sort()
#x=[]
#y=[]
#for num in nums:
# for dpka in nummuts[num]:
# x.append(num)
# y.append(dpka)
#file=dislin_driver.graf_mult2(x,[y],
# title='dpKa, number of mutations',
# x_legend='Number of mutations',
# y_legend='abs(dpKa)')
#os.system('gimp %s' %file)
#
# Save bigdict
#
fd=open('/home/nielsen/pKa-design/done_distnummuts/bigdict','w')
import pickle
pickle.dump(big_dict,fd)
fd.close()
def __init__(self,params):
#
# Initialise
#
self.params=params
import pKaTool.pKaIO as pKaIO
self.pdbfile=self.params['pdb']
self.MCsteps=int(self.params['MCsteps'])
self.pHstep=float(self.params['pHstep'])
self.pHstart=float(self.params['pHstart'])
self.pHend=float(self.params['pHend'])
IO=pKaIO.pKaIO(self.pdbfile)
#
# Define the tmpdir for all our calcs
#
import os
self.topdir=os.path.split(self.pdbfile)[0]
self.topdir=os.path.join(self.topdir,'%s_autonomy' %os.path.split(self.pdbfile)[1])
if not os.path.isdir(self.topdir):
os.mkdir(self.topdir)
#
# Did we find a completed pKa calculation for the PDB file
#
if IO.calculation_completed:
#
# All files found
#
print 'pKa calculation files found'
else:
print
print 'I could not find a completed pKa calculation for the specified PDB file'
print 'Please complete the pKa calculation first'
print
raise Exception()
#
# Get the wild type titration curves calculated with WHAT IF
#
import pKaTool.pKaIO
IO=pKaTool.pKaIO.pKaIO(self.pdbfile)
self.wt_titcurv=IO.read_titration_curve()
self.wt_pKas=IO.readpka()
#
# Recalculate titration curves with the CPP algorithm
#
import os
dirname=os.path.join(self.topdir,'wt_recalc')
if not os.path.isdir(dirname):
os.mkdir(dirname)
filename=os.path.join(dirname,'WT.DAT')
data=None
if os.path.isfile(filename):
try:
fd=open(filename)
import cPickle
data=cPickle.load(fd)
fd.close()
self.wtpkas=data['pkas']
self.wt_titcurv=data['titcurv']
print 'Loaded wild type recalculated titration curves'
print 'Loaded %d titration curves' %(len(self.wt_titcurv.keys()))
except:
data=None
#
# If we don't have the data calculate it
#
if data is None:
import pKa_MC
print 'Recalculating wild type titration curves'
pKa_params={'pHstart':self.pHstart,'pHstop':self.pHend,'pHstep':self.pHstep,'pKMCsteps':self.MCsteps,'verbose':1}
self.pKaCALC=pKa_MC.pKa_calculation_class(self.pdbfile,pKa_info=None,params=pKa_params,parent=self)
self.pKaCALC.set_MC_CPP()
self.pKaCALC.set_reporter_groups(self.wt_pKas.keys())
self.wtpkas,self.wt_titcurv=self.pKaCALC.calc_wt_pkas()
#
# Save the data
#
fd=open(filename,'w')
import cPickle
data=cPickle.dump({'pkas':self.wtpkas,'titcurv':self.wt_titcurv},fd)
fd.close()
print 'done'
print
print 'Calculated %d titration curves' %(len(self.wt_titcurv.keys()))
#
# Get the in_system energies
#
self.in_data=self.calculate_insystem_dpKas()
#
# Get the ex_data
#
self.ex_data=self.calculate_exsystem_dpKas()
return
