def calculate_physiochemical_features(temp_dict, sequence):
analyzed_seq = ProteinAnalysis(sequence)
charge_at_pH7 = analyzed_seq.charge_at_pH(7)
instability_index = analyzed_seq.instability_index()
molecular_weight = analyzed_seq.molecular_weight()
aromaticity = analyzed_seq.aromaticity()
molar_extinction_coefficient = analyzed_seq.molar_extinction_coefficient()
range_l, range_h = molar_extinction_coefficient
molar_extinction_coefficient = (float(range_l) + float(range_h)) / 2
gravy = analyzed_seq.gravy(
) #Grand Average Hyrdopathy - Higher value = More Hydrophobic
isoelectric_point = analyzed_seq.isoelectric_point()
helix_fraction, turn_fraction, sheet_fraction = analyzed_seq.secondary_structure_fraction(
)
physiochem_dict = {
"Charge at pH7": charge_at_pH7,
"Instability Index": instability_index,
"Molecular Wt": molecular_weight,
"Aromaticity": aromaticity,
"Molar Extinction Coeff": molar_extinction_coefficient,
"Gravy": gravy,
"Isoelectric pt": isoelectric_point,
"Helix Fraction": helix_fraction,
"Turn Fraction": turn_fraction,
"Sheet Fraction": sheet_fraction
}
temp_dict.update(physiochem_dict)
#Adding separately because get_amino_acids_percent() generates a dictionary on its own
aa_percent = analyzed_seq.get_amino_acids_percent()
temp_dict.update(aa_percent)
def _protein_parameters(self, sequence):
"""Calculates physicochemical properties for the amino acid sequence.
Args:
sequence: str, amino acid sequence.
Returns:
property_arr: np array, vector of properties.
"""
analysis = ProteinAnalysis(sequence)
property_arr = []
property_arr.append(analysis.molecular_weight())
property_arr.append(analysis.aromaticity())
property_arr.append(analysis.instability_index())
property_arr.append(analysis.gravy())
property_arr.append(analysis.isoelectric_point())
secondary = analysis.secondary_structure_fraction()
property_arr.append(secondary[0])
property_arr.append(secondary[1])
property_arr.append(secondary[2])
molar_extinction_coefficient = analysis.molar_extinction_coefficient()
property_arr.append(molar_extinction_coefficient[0])
property_arr.append(molar_extinction_coefficient[1])
property_arr.append(self._net_charge(sequence))
return np.array(property_arr)
def get_molar_extinction_coefficient(
self
): # [reduced, oxidized] # with reduced cysteines / # with disulfid bridges
"""
Calculates the molar extinction coefficient (2 values) from biopython
:return: dictionary with the value of reduced cysteins and oxidized (with disulfid bridges)
"""
res = {}
analysed_seq = ProteinAnalysis(self.ProteinSequence)
res['Molar_extinction_coefficient_reduced'] = analysed_seq.molar_extinction_coefficient(
)[0] # reduced
res['Molar_extinction_coefficient_oxidized'] = analysed_seq.molar_extinction_coefficient(
)[1] # cys cys bounds
return res
def phyChemProps(seq):
svv = [0 for x in range(10)]
X = ProteinAnalysis(seq)
svv[0] = X.aromaticity()
svv[1] = X.secondary_structure_fraction()[0]
svv[2] = X.secondary_structure_fraction()[1]
svv[3] = X.secondary_structure_fraction()[2]
svv[4] = X.gravy()
svv[5] = X.instability_index()
svv[6] = X.isoelectric_point()
svv[7] = X.molecular_weight()
svv[8] = X.molar_extinction_coefficient()[0]
svv[9] = X.molar_extinction_coefficient()[1]
return svv
def biopython_proteinanalysis_seq(seq, scaling=False):
res = ProteinAnalysis(seq)
d = {}
flex = np.array(res.flexibility())
d['flex:min'], d['flex:max'], d['flex:std'] = flex.min(), flex.max(
), flex.std()
d['gravy'] = res.gravy()
d['instability_index'] = res.instability_index()
d['isoelectric_point'] = res.isoelectric_point()
r, c = res.molar_extinction_coefficient()
d['molar_extinction_coefficient_reduced'], d[
'molar_extinction_coefficient_cysteines'] = r, c
d['molecular_weight'] = res.molecular_weight()
d['percent_helix_naive'], d['percent_turn_naive'], d[
'percent_strand_naive'] = res.secondary_structure_fraction()
aap = res.get_amino_acids_percent()
aas = sorted(aap.keys())
d.update({'percent:%s' % aa: aap[aa] for aa in aas})
d.update({
'prop_res_%s' % key: sum([aap.get(x, 0) for x in value])
for key, value in list(property_residues.items())
})
return d
def extract(self):
AA=["A","C","D","E","F","G","H","I","K","L","M","N","P","Q","R","S","T","V","W","Y"]
SC=["1","2","3","4","5","6","7"]
tri_pep = [''.join(i) for i in itertools.product(AA, repeat = 3)]
myseq="AILMVNQSTGPCHKRDEFWY"
trantab2=myseq.maketrans("AILMVNQSTGPCHKRDEFWY","11111222233455566777")
tetra_sc = [''.join(i) for i in itertools.product(SC, repeat = 4)]
total_fasta=self.g_total_fasta
sec_code=0
record_current=0
arr = numpy.empty((total_fasta,10409), dtype=numpy.float)
names = numpy.empty((total_fasta,1), dtype=object)
names_dic=dict()
for record in SeqIO.parse(self.infile, "fasta"):
data=(record_current/total_fasta) * 100
if (self.g_is_socket==1):
self.g_socketio.emit('set bar', {'data': data},room=self.g_sid)
else:
print('extracting features of seq ' + str(record_current+1) + ' of ' + str(total_fasta),end='\r')
#yield "event: update\ndata:" + str(data) + "\n\n"
record_current += 1
#job.meta['current']=record_current
#job.save_meta()
ll=len(record.seq)
seq_name=''
if not self.prot_check(str(record.seq)):
print("Warning: " + record.id + " is not a valid protein sequence")
continue
if record.id in names_dic:
seq_name= record.id + '_' + str(names_dic[record.id])
names_dic[record.id]=names_dic[record.id]+1
else:
seq_name= record.id
names_dic[record.id]=1
seqq=record.seq.__str__().upper()
seqqq=seqq.replace('X','A').replace('J','L').replace('*','A').replace('Z','E').replace('B','D')
# X = ProteinAnalysis(record.seq.__str__().upper().replace('X','A').replace('J','L').replace('*',''))
X = ProteinAnalysis(seqqq)
myseq=seqq.translate(trantab2)
tt= [X.isoelectric_point(), X.instability_index(),ll,X.aromaticity(),
X.molar_extinction_coefficient()[0],X.molar_extinction_coefficient()[1],
X.gravy(),X.molecular_weight()]
tt_n = numpy.asarray(tt,dtype=numpy.float)
tri_pep_count=[seqq.count(i)/(ll-2) for i in tri_pep]
tri_pep_count_n = numpy.asarray(tri_pep_count,dtype=numpy.float)
tetra_sc_count=[myseq.count(i)/(ll-3) for i in tetra_sc]
tetra_sc_count_n = numpy.asarray(tetra_sc_count,dtype=numpy.float)
cat_n= numpy.concatenate((tetra_sc_count_n,tri_pep_count_n,tt_n))
cat_n = cat_n.reshape((1,cat_n.shape[0]))
arr[sec_code,:]=cat_n
names[sec_code,0]=seq_name
sec_code += 1
if (self.g_is_socket==1):
self.g_socketio.emit('set bar', {'data': 100},room=self.g_sid)
self.g_socketio.emit('done features',1,room=self.g_sid)
print("\nDone")
return (names,arr)
def get_phanns_input(fasta_list, d2vmodel):
# d2vmodel = pickle.load(open('d2v_model1.p','rb'))
AA = [
"A", "C", "D", "E", "F", "G", "H", "I", "K", "L", "M", "N", "P", "Q",
"R", "S", "T", "V", "W", "Y"
]
SC = ["1", "2", "3", "4", "5", "6", "7"]
tri_pep = [''.join(i) for i in itertools.product(AA, repeat=3)]
tetra_sc = [''.join(i) for i in itertools.product(SC, repeat=4)]
prot_class = 0
myseq = "AILMVNQSTGPCHKRDEFWY"
trantab2 = myseq.maketrans("AILMVNQSTGPCHKRDEFWY", "11111222233455566777")
kmer_size = 3
this_prot = 0
vectors = []
classes = []
for file in fasta_list:
print('####################' + file)
# file_path = os.path.join(os.path.dirname(os.path.dirname(os.path.abspath("__file__"))),"fasta",file + "_all_clustered.fasta")
for record in SeqIO.parse(file, "fasta"):
ll = len(record.seq)
seqq = record.seq.__str__().upper()
seqqq = seqq.replace('X', 'A').replace('J', 'L').replace(
'*', 'A').replace('Z', 'E').replace('B', 'D')
X = ProteinAnalysis(seqqq)
tt = [
X.isoelectric_point(),
X.instability_index(), ll,
X.aromaticity(),
X.molar_extinction_coefficient()[0],
X.molar_extinction_coefficient()[1],
X.gravy(),
X.molecular_weight()
]
tt_n = np.asarray(tt, dtype=np.float)
myseq = seqq.translate(trantab2)
#count tripeptides
tri_pep_count = [seqq.count(i) / (ll - 2) for i in tri_pep]
tri_pep_count_n = np.asarray(tri_pep_count, dtype=np.float)
#count tetra side chains
tetra_sc_count = [myseq.count(i) / (ll - 3) for i in tetra_sc]
tetra_sc_count_n = np.asarray(tetra_sc_count, dtype=np.float)
#get embedding vector
vec = d2vmodel.infer_vector([
seqqq[k:k + kmer_size] for k in range(0, len(seqqq), kmer_size)
])
for s in range(1, kmer_size):
vec = vec + d2vmodel.infer_vector([
seqqq[k:k + kmer_size]
for k in range(s, len(seqqq), kmer_size)
])
vec = vec / kmer_size
cat_n = np.concatenate(
(tri_pep_count_n, tetra_sc_count_n, tt_n, vec))
vectors.append((cat_n, record))
this_prot += 1
if (this_prot % 500 == 0):
print("processing sequence # " + str(this_prot), end="\r")
prot_class += 1
this_prot = 0
return vectors
def main():
aa = [
'A', 'C', 'D', 'E', 'F', 'G', 'H', 'I', 'K', 'L', 'M', 'N', 'P', 'Q',
'R', 'S', 'T', 'V', 'W', 'Y'
]
dipeptide = [
'AA', 'AC', 'AD', 'AE', 'AF', 'AG', 'AH', 'AI', 'AK', 'AL', 'AM', 'AN',
'AP', 'AQ', 'AR', 'AS', 'AT', 'AV', 'AW', 'AY', 'CA', 'CC', 'CD', 'CE',
'CF', 'CG', 'CH', 'CI', 'CK', 'CL', 'CM', 'CN', 'CP', 'CQ', 'CR', 'CS',
'CT', 'CV', 'CW', 'CY', 'DA', 'DC', 'DD', 'DE', 'DF', 'DG', 'DH', 'DI',
'DK', 'DL', 'DM', 'DN', 'DP', 'DQ', 'DR', 'DS', 'DT', 'DV', 'DW', 'DY',
'EA', 'EC', 'ED', 'EE', 'EF', 'EG', 'EH', 'EI', 'EK', 'EL', 'EM', 'EN',
'EP', 'EQ', 'ER', 'ES', 'ET', 'EV', 'EW', 'EY', 'FA', 'FC', 'FD', 'FE',
'FF', 'FG', 'FH', 'FI', 'FK', 'FL', 'FM', 'FN', 'FP', 'FQ', 'FR', 'FS',
'FT', 'FV', 'FW', 'FY', 'GA', 'GC', 'GD', 'GE', 'GF', 'GG', 'GH', 'GI',
'GK', 'GL', 'GM', 'GN', 'GP', 'GQ', 'GR', 'GS', 'GT', 'GV', 'GW', 'GY',
'HA', 'HC', 'HD', 'HE', 'HF', 'HG', 'HH', 'HI', 'HK', 'HL', 'HM', 'HN',
'HP', 'HQ', 'HR', 'HS', 'HT', 'HV', 'HW', 'HY', 'IA', 'IC', 'ID', 'IE',
'IF', 'IG', 'IH', 'II', 'IK', 'IL', 'IM', 'IN', 'IP', 'IQ', 'IR', 'IS',
'IT', 'IV', 'IW', 'IY', 'KA', 'KC', 'KD', 'KE', 'KF', 'KG', 'KH', 'KI',
'KK', 'KL', 'KM', 'KN', 'KP', 'KQ', 'KR', 'KS', 'KT', 'KV', 'KW', 'KY',
'LA', 'LC', 'LD', 'LE', 'LF', 'LG', 'LH', 'LI', 'LK', 'LL', 'LM', 'LN',
'LP', 'LQ', 'LR', 'LS', 'LT', 'LV', 'LW', 'LY', 'MA', 'MC', 'MD', 'ME',
'MF', 'MG', 'MH', 'MI', 'MK', 'ML', 'MM', 'MN', 'MP', 'MQ', 'MR', 'MS',
'MT', 'MV', 'MW', 'MY', 'NA', 'NC', 'ND', 'NE', 'NF', 'NG', 'NH', 'NI',
'NK', 'NL', 'NM', 'NN', 'NP', 'NQ', 'NR', 'NS', 'NT', 'NV', 'NW', 'NY',
'PA', 'PC', 'PD', 'PE', 'PF', 'PG', 'PH', 'PI', 'PK', 'PL', 'PM', 'PN',
'PP', 'PQ', 'PR', 'PS', 'PT', 'PV', 'PW', 'PY', 'QA', 'QC', 'QD', 'QE',
'QF', 'QG', 'QH', 'QI', 'QK', 'QL', 'QM', 'QN', 'QP', 'QQ', 'QR', 'QS',
'QT', 'QV', 'QW', 'QY', 'RA', 'RC', 'RD', 'RE', 'RF', 'RG', 'RH', 'RI',
'RK', 'RL', 'RM', 'RN', 'RP', 'RQ', 'RR', 'RS', 'RT', 'RV', 'RW', 'RY',
'SA', 'SC', 'SD', 'SE', 'SF', 'SG', 'SH', 'SI', 'SK', 'SL', 'SM', 'SN',
'SP', 'SQ', 'SR', 'SS', 'ST', 'SV', 'SW', 'SY', 'TA', 'TC', 'TD', 'TE',
'TF', 'TG', 'TH', 'TI', 'TK', 'TL', 'TM', 'TN', 'TP', 'TQ', 'TR', 'TS',
'TT', 'TV', 'TW', 'TY', 'VA', 'VC', 'VD', 'VE', 'VF', 'VG', 'VH', 'VI',
'VK', 'VL', 'VM', 'VN', 'VP', 'VQ', 'VR', 'VS', 'VT', 'VV', 'VW', 'VY',
'WA', 'WC', 'WD', 'WE', 'WF', 'WG', 'WH', 'WI', 'WK', 'WL', 'WM', 'WN',
'WP', 'WQ', 'WR', 'WS', 'WT', 'WV', 'WW', 'WY', 'YA', 'YC', 'YD', 'YE',
'YF', 'YG', 'YH', 'YI', 'YK', 'YL', 'YM', 'YN', 'YP', 'YQ', 'YR', 'YS',
'YT', 'YV', 'YW', 'YY'
]
sequences = pandas.read_csv('protein_data.csv', header=None)
lengths = []
weights = []
for protein in sequences.itertuples():
protein_length = len(str(protein[1])) # length of protein sequence
lengths.append(protein_length)
analyzed_protein = ProteinAnalysis(str(protein[1]))
ambigious_match = re.findall("X+|Z+", protein[1])
if ambigious_match:
molecular_weight = "?"
else:
molecular_weight = analyzed_protein.molecular_weight()
weights.append(molecular_weight)
# remove bad amino acids from sequences
for i in range(len(sequences)):
sequences[0][i] = sequences[0][i].replace('B', '')
sequences[0][i] = sequences[0][i].replace('U', '')
sequences[0][i] = sequences[0][i].replace('X', '')
sequences[0][i] = sequences[0][i].replace('Z', '')
pandas.DataFrame(sequences).to_csv('updated_protein_data.csv',
index_label=None,
header=None,
index=None)
# use amino acid composition results from pfeature to generate most common amino acid and dipeptide
data = pandas.read_csv('updated_protein_data.csv', header=None)
data = numpy.asarray(data)
most_frequent_di = []
most_frequent = []
for i in range(len(data)):
max = 0
col = 0
for j in range(len(dipeptide)):
c = data[i][0].count(dipeptide[j])
if (c > max):
max = c
col = j
most_frequent_di.append(dipeptide[col])
for j in range(len(aa)):
c = data[i][0].count(aa[j])
if (c > max):
max = c
col = j
most_frequent.append(aa[col])
# more features
amino_acid = {}
first_aa = []
last_aa = []
arom = []
ii = []
ip = []
mec_rc = []
mec_db = []
ssf_helix = []
ssf_turn = []
ssf_sheet = []
gravy = []
ph_0 = []
ph_7 = []
ph_14 = []
A = []
C = []
D = []
E = []
F = []
G = []
H = []
I = []
K = []
L = []
M = []
N = []
P = []
Q = []
R = []
S = []
T = []
V = []
W = []
Y = []
classes = []
data = pandas.read_csv('updated_protein_data.csv', header=None)
for protein in data.itertuples():
analyzed_protein = ProteinAnalysis(str(protein[1]))
amino_acid = (analyzed_protein.count_amino_acids())
A.append(amino_acid.get('A'))
C.append(amino_acid.get('C'))
D.append(amino_acid.get('D'))
E.append(amino_acid.get('E'))
F.append(amino_acid.get('F'))
G.append(amino_acid.get('G'))
H.append(amino_acid.get('H'))
I.append(amino_acid.get('I'))
K.append(amino_acid.get('K'))
L.append(amino_acid.get('L'))
M.append(amino_acid.get('M'))
N.append(amino_acid.get('N'))
P.append(amino_acid.get('P'))
Q.append(amino_acid.get('Q'))
R.append(amino_acid.get('R'))
S.append(amino_acid.get('S'))
T.append(amino_acid.get('T'))
V.append(amino_acid.get('V'))
W.append(amino_acid.get('W'))
Y.append(amino_acid.get('Y'))
first_aa.append(str(protein[1])[0])
last_aa.append(str(protein[1])[-1])
arom.append(analyzed_protein.aromaticity())
ii.append(analyzed_protein.instability_index())
ip.append(analyzed_protein.isoelectric_point())
mec_rc.append(analyzed_protein.molar_extinction_coefficient()[0])
mec_db.append(analyzed_protein.molar_extinction_coefficient()[1])
ssf_helix.append(analyzed_protein.secondary_structure_fraction()[0])
ssf_turn.append(analyzed_protein.secondary_structure_fraction()[1])
ssf_sheet.append(analyzed_protein.secondary_structure_fraction()[2])
gravy.append(analyzed_protein.gravy())
ph_0.append(analyzed_protein.charge_at_pH(0.0))
ph_7.append(analyzed_protein.charge_at_pH(7.0))
ph_14.append(analyzed_protein.charge_at_pH(14.0))
classes.append(protein[2])
features = pandas.DataFrame()
features["LENGTH"] = lengths
#features["MOLECULAR WEIGHT"] = weights
features["most frequent aa"] = most_frequent
#features["first amino acids"] = first_aa
features["last amino acid"] = last_aa
features["most frequence dipeptide"] = most_frequent_di
features["aromaticity"] = arom
features["instability index"] = ii
features["isolectric point"] = ip
features["molecular extinction coefficient - reduced cysteines"] = mec_rc
features["molecular extinction coefficient - disulfid bridges"] = mec_db
features["secondary structure fraction helix"] = ssf_helix
features["secondary structure fraction turn"] = ssf_turn
features["secondary structure fraction sheet"] = ssf_sheet
features["gravy"] = gravy
features["charge at ph 0"] = ph_0
features["charge at ph 7"] = ph_7
features["charge at ph 14"] = ph_14
features['A'] = A
features['C'] = C
features['D'] = D
features['E'] = E
features['F'] = F
features['G'] = G
features['H'] = H
features['I'] = I
features['K'] = K
features['L'] = L
features['M'] = M
features['N'] = N
features['P'] = P
features['Q'] = Q
features['R'] = R
features['S'] = S
features['T'] = T
features['V'] = V
features['W'] = W
features['Y'] = Y
features["CLASS"] = classes
features.to_csv('features.csv', index=None)
print('\nResults for record: {} ###'.format(record.id))
print(X.count_amino_acids()['A'])
print(X.count_amino_acids()['E'])
print("A percentage :%0.2f" % X.get_amino_acids_percent()['A'])
print("T percentage :%0.2f" % X.get_amino_acids_percent()['T'])
print("C percentage :%0.2f" % X.get_amino_acids_percent()['C'])
print("G percentage :%0.2f" % X.get_amino_acids_percent()['G'])
print("%0.2f" % X.molecular_weight())
print("%0.2f" % X.aromaticity())
print("%0.2f" % X.instability_index())
print("%0.2f" % X.isoelectric_point())
sec_struc = X.secondary_structure_fraction()
print("%0.2f" % sec_struc[0])
epsilon_prot = X.molar_extinction_coefficient()
print(epsilon_prot[0])
print(epsilon_prot[1])
composition1 = X.count_amino_acids()
print("*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*-*\nTCF7L2:")
for record in SeqIO.parse('TCF7L2.fasta', 'fasta'):
X = ProteinAnalysis(str(record.seq))
print('\nResults for record: {} ###'.format(record.id))
print(X.count_amino_acids()['A'])
print(X.count_amino_acids()['E'])
print("A percentage :%0.2f" % X.get_amino_acids_percent()['A'])
print("T percentage :%0.2f" % X.get_amino_acids_percent()['T'])
print("C percentage :%0.2f" % X.get_amino_acids_percent()['C'])
"Gravy index", "pI", "Molar exctinction coefficient"
]
with open(csvfilename, "w") as csvfile:
writer = csv.DictWriter(csvfile, fieldnames=field_names)
writer.writeheader()
for inputfile in inputfiles:
for record in SeqIO.parse(inputfile, "fasta"):
print(record.id)
protein = ProteinAnalysis(str(record.seq))
writer.writerow({
"Accession number":
record.id,
"Molecular Weight":
protein.molecular_weight(),
"Aromaticity":
protein.aromaticity(),
"Instability index":
protein.instability_index(),
"Gravy index":
protein.gravy(),
"pI":
protein.isoelectric_point(),
"Molar exctinction coefficient":
protein.molar_extinction_coefficient()[1]
})
print("%s %s %s %s %s %s" %
(protein.molecular_weight(), protein.aromaticity(),
protein.instability_index(), protein.gravy(),
protein.isoelectric_point(),
protein.molar_extinction_coefficient()[1]))
fasta = SeqIO.parse(fasta_file, "fasta")
header = [
"protein_id", "MW", "length", "aromaticity", "II", "GRAVY", "pI",
"helix", "turn", "sheet", "extinction"
]
out_file.write("\t".join(header) + "\n")
for rec in fasta:
sequence = (str(rec.seq).upper().replace("*", "").replace(
"X", "").replace("J", "L").replace("B",
"N").replace("Z", "Q").replace(
"U", "C").replace("O", "K"))
ID = rec.id.split("|")[-1]
length = len(sequence)
anal = ProteinAnalysis(sequence)
mw = anal.molecular_weight()
aro = anal.aromaticity()
insta = anal.instability_index()
grev = anal.gravy()
ie = anal.isoelectric_point()
sec = anal.secondary_structure_fraction()
helix = sec[0]
turn = sec[1]
sheet = sec[2]
ext = anal.molar_extinction_coefficient()[0]
row = [ID, mw, length, aro, insta, grev, ie, helix, turn, sheet, ext]
row = [str(n) for n in row]
out_file.write("\t".join(row) + "\n")
# število alaninskih ostankov
print('Število A:', analysis_seq.count_amino_acids()['A'])
# delež ostankov, ki jih predstavljajo alaninski ostanki
print('Delež A: %0.2f' % analysis_seq.get_amino_acids_percent()['A'])
# izoelektrična točka
print('Izoelektrična točka (pI): %0.2f' % analysis_seq.isoelectric_point())
# delež ak-ostankov, ki so preferenčno v določenem elementu sekundarne strukture [helix, turn, sheet]
sec_struc = analysis_seq.secondary_structure_fraction()
print('Delež alfa-vijačnic: %0.2f' % sec_struc[0])
# ekstinkcijski koeficient
excoeff_prot = analysis_seq.molar_extinction_coefficient()
# ekstinkcijski koeficient, vsi cisteinski ostanki reducirani (prosti)
print("Molarni ekstinkcijski koeficient, red. [1/(M cm)]:", excoeff_prot[0])
# ekstinkcijski koeficient, vsi cisteinski ostanki v obliki cistinov
print("Molarni ekstinkcijski koeficient, oks. [1/(M cm)]:", excoeff_prot[1])
# Gre za podobno analizo, ki jo izvede spletna storitev ProtParam na naslovu https://web.expasy.org/protparam/.
# ---
# ## Analiza zaporedja z drsečim oknom
#
# Za primer bomo analizirali hidrofobnost proteina in sicer bomo narisali hidrofobni profil. Pri tovrstnih analizah ponavadi uporabljamo drseče okno ustrezne velikosti, pri čemer nek parameter povprečimo po tem oknu in ga pripišemo aminokislinskemu ostanki v sredini tega okna. Zato, da je določitev ak-ostanka v sredini okna nedvoumna, uporabljamo kot velikost okna liho število ak-ostankov.
#
# O analizi z uporabo drsečega okna smo že govorili na predavanjih:
# 
def extract_all(fasta_list):
d = {'seq_description': [], 'seq_id': [], "sec_code": []}
sec_code = 0
df = pd.DataFrame(data=d)
total_fasta = 0
for file in fasta_list:
for record in SeqIO.parse(file, "fasta"):
total_fasta += 1
AA = [
"A", "C", "D", "E", "F", "G", "H", "I", "K", "L", "M", "N", "P", "Q",
"R", "S", "T", "V", "W", "Y"
]
SC = ["1", "2", "3", "4", "5", "6", "7"]
di_pep = [''.join(i) for i in itertools.product(AA, repeat=2)]
tri_pep = [''.join(i) for i in itertools.product(AA, repeat=3)]
di_sc = [''.join(i) for i in itertools.product(SC, repeat=2)]
tri_sc = [''.join(i) for i in itertools.product(SC, repeat=3)]
tetra_sc = [''.join(i) for i in itertools.product(SC, repeat=4)]
prot_class = 0
myseq = "AILMVNQSTGPCHKRDEFWY"
trantab2 = myseq.maketrans("AILMVNQSTGPCHKRDEFWY", "11111222233455566777")
arr = numpy.empty((total_fasta, 11201), dtype=numpy.float)
class_arr = numpy.empty((total_fasta), dtype=numpy.int)
group_arr = numpy.empty((total_fasta), dtype=numpy.int)
id_arr = numpy.empty((total_fasta), dtype=numpy.int)
this_prot = 0
for file in fasta_list:
print('####################' + file)
for record in SeqIO.parse(file, "fasta"):
ll = len(record.seq)
seqq = record.seq.__str__().upper()
seqqq = seqq.replace('X', 'A').replace('J', 'L').replace(
'*', 'A').replace('Z', 'E').replace('B', 'D')
X = ProteinAnalysis(seqqq)
tt = [
X.isoelectric_point(),
X.instability_index(), ll,
X.aromaticity(),
X.molar_extinction_coefficient()[0],
X.molar_extinction_coefficient()[1],
X.gravy(),
X.molecular_weight()
]
tt_n = numpy.asarray(tt, dtype=numpy.float)
myseq = seqq.translate(trantab2)
di_pep_count = [seqq.count(i) / (ll - 1) for i in di_pep]
di_pep_count_n = numpy.asarray(di_pep_count, dtype=numpy.float)
tri_pep_count = [seqq.count(i) / (ll - 2) for i in tri_pep]
tri_pep_count_n = numpy.asarray(tri_pep_count, dtype=numpy.float)
di_sc_count = [myseq.count(i) / (ll - 1) for i in di_sc]
di_sc_count_n = numpy.asarray(di_sc_count, dtype=numpy.float)
tri_sc_count = [myseq.count(i) / (ll - 2) for i in tri_sc]
tri_sc_count_n = numpy.asarray(tri_sc_count, dtype=numpy.float)
tetra_sc_count = [myseq.count(i) / (ll - 3) for i in tetra_sc]
tetra_sc_count_n = numpy.asarray(tetra_sc_count, dtype=numpy.float)
cat_n = numpy.concatenate(
(di_pep_count_n, tri_pep_count_n, di_sc_count_n,
tri_sc_count_n, tetra_sc_count, tt_n))
#print(cat_n.shape)
cat_n = cat_n.reshape((1, cat_n.shape[0]))
#arr = numpy.append(arr,cat_n , axis=0)
#class_arr = numpy.append(class_arr,prot_class)
#id_arr = numpy.append(id_arr,sec_code)
arr[sec_code, :] = cat_n
class_arr[sec_code] = prot_class % 11
group_arr[sec_code] = prot_class // 11
id_arr[sec_code] = sec_code
data_row = [record.description, record.id, int(sec_code)]
# df=df.append(pd.Series(data_row,index=df.columns),sort=False,ignore_index=True)
sec_code += 1
this_prot += 1
if (this_prot % 500 == 0):
print("processing sequence # " + str(this_prot), end="\r")
prot_class += 1
this_prot = 0
return (arr, class_arr, group_arr, id_arr, df)
def featurise(self, data):
"""
Featurise the data.
Parameters:
-----------
data : `list` of `Bio.SeqRecord.SeqRecord`
The data to be featurised.
Returns:
-------
featurised_data : `pandas.DataFrame`
(num_data, features) The featurised data.
"""
# Get features of data
features = collections.defaultdict(list)
# Featurise the data
for i, example in enumerate(data):
# Convert Bio.SeqRecord.SeqRecord object to string for Bio.SeqUtils.ProtParam.ProteinAnalysis
analysed_example = ProteinAnalysis(str(example.seq))
first50_analysed_example = ProteinAnalysis(str(example.seq)[:50])
last50_analysed_example = ProteinAnalysis(str(example.seq)[-50:])
features["length"].append(analysed_example.length)
features["molecular_weight"].append(
analysed_example.molecular_weight())
features["isoelectric_point"].append(
analysed_example.isoelectric_point())
features["aromaticity"].append(analysed_example.aromaticity())
features["instability_index"].append(
analysed_example.instability_index())
features["gravy"].append(analysed_example.gravy())
reduced, oxidised = analysed_example.molar_extinction_coefficient()
features["reduced"].append(reduced)
features["oxidised"].append(oxidised)
helix, turn, sheet = analysed_example.secondary_structure_fraction(
)
features["helix"].append(helix)
features["turn"].append(turn)
features["sheet"].append(sheet)
features["charge_at_ph1"].append(analysed_example.charge_at_pH(1))
# features["charge_at_ph2"].append(analysed_example.charge_at_pH(2))
# features["charge_at_ph3"].append(analysed_example.charge_at_pH(3))
# features["charge_at_ph4"].append(analysed_example.charge_at_pH(4))
features["charge_at_ph7"].append(analysed_example.charge_at_pH(7))
features["charge_at_ph12"].append(
analysed_example.charge_at_pH(12))
features["hydrophobicity"].append(
np.mean(
analysed_example.protein_scale(self.dicts['kd'],
window=5,
edge=1.0)))
features["flexibility"].append(
np.mean(
analysed_example.protein_scale(self.dicts['flex'],
window=5,
edge=1.0)))
features["hydrophilicity"].append(
np.mean(
analysed_example.protein_scale(self.dicts['hw'],
window=5,
edge=1.0)))
features["surface_accessibility"].append(
np.mean(
analysed_example.protein_scale(self.dicts['em'],
window=5,
edge=1.0)))
features["janin"].append(
np.mean(
analysed_example.protein_scale(self.dicts['ja'],
window=5,
edge=1.0)))
# features["dipeptide_dg "].append(np.mean(analysed_example.protein_scale(self.dicts['diwv'], window=5, edge=1.0)))
features["first50_hydrophobicity"].append(
np.mean(
first50_analysed_example.protein_scale(self.dicts['kd'],
window=5,
edge=1.0)))
features["first50_flexibility"].append(
np.mean(
first50_analysed_example.protein_scale(self.dicts['flex'],
window=5,
edge=1.0)))
features["first50_hydrophilicity"].append(
np.mean(
first50_analysed_example.protein_scale(self.dicts['hw'],
window=5,
edge=1.0)))
features["first50_surface_accessibility"].append(
np.mean(
first50_analysed_example.protein_scale(self.dicts['em'],
window=5,
edge=1.0)))
features["first50_janin"].append(
np.mean(
first50_analysed_example.protein_scale(self.dicts['ja'],
window=5,
edge=1.0)))
features["last50_hydrophobicity"].append(
np.mean(
last50_analysed_example.protein_scale(self.dicts['kd'],
window=5,
edge=1.0)))
features["last50_flexibility"].append(
np.mean(
last50_analysed_example.protein_scale(self.dicts['flex'],
window=5,
edge=1.0)))
features["last50_hydrophilicity"].append(
np.mean(
last50_analysed_example.protein_scale(self.dicts['hw'],
window=5,
edge=1.0)))
features["last50_surface_accessibility"].append(
np.mean(
last50_analysed_example.protein_scale(self.dicts['em'],
window=5,
edge=1.0)))
features["last50_janin"].append(
np.mean(
last50_analysed_example.protein_scale(self.dicts['ja'],
window=5,
edge=1.0)))
for key, val in analysed_example.get_amino_acids_percent().items():
features[key].append(val * 5)
for key, val in first50_analysed_example.get_amino_acids_percent(
).items():
features["first_50_" + str(key)].append(val * 5)
for key, val in last50_analysed_example.get_amino_acids_percent(
).items():
features["last_50_" + str(key)].append(val * 5)
return pd.DataFrame.from_dict(features)
class ProteinFeatureExtractor:
"""
Feature extraction from protein sequence for
Machine Learning classification or deeper analysis
Example usage:
from features.extractors.proteins import ProteinFeatureExtractor
pfe = ProteinFeatureExtractor(protein_sequence='MAKINELLRESTTTNSNSIGRPNLVALTRATTKLIYSDIVATQRTNQPVAA')
pfe.get_features()
"""
FEATURE_NAMES = [
"protein_length",
"gravy",
"molecular_weight",
"aromaticity",
"instability_index",
"isoelectric_point",
"flexibility",
"mec_cysteines",
"mec_cystines",
"ssf_helix",
"ssf_turn",
"ssf_sheet",
]
def __init__(self, protein_sequence: str):
self.protein_sequence = self._normalize(protein_sequence)
self.protein_analysis = ProteinAnalysis(self.protein_sequence)
@staticmethod
def _normalize(source: Union[str, SeqRecord]) -> str:
"""
Normalize each protein sequence
to uppercase and without blank chars
"""
# If source is a string
if isinstance(source, str):
entry = source
# If source is a BioPython object with seq field
else:
entry = source.seq
return str(entry).upper().strip()
def _get_protein_length(self) -> int:
"""
Protein length
"""
return len(self.protein_sequence)
def _calculate_gravy(self) -> float:
"""
GRAVY (Grand Average of Hydropathy) index score
is calculated by adding the hydropathy value for
each residue and then dividing by the length of
the protein sequence
Negative GRAVY value indicates that the protein
is non-polar and Positive value indicates that
the protein is polar
"""
return self.protein_analysis.gravy()
def _calculate_molecular_weight(self) -> float:
"""
Molecular Weight is calculated as the sum
of atomic masses of all atoms in the molecul
"""
return self.protein_analysis.molecular_weight()
def _calculate_aromaticity(self) -> float:
"""
Aromaticity is used to describe a planar, cyclic
molecule with a ring of resonance bonds which is
more stable when compared to other connective or
geometric arrangements consisting of the same set
of atoms
"""
return self.protein_analysis.aromaticity()
def _calculate_instability_index(self) -> float:
"""
Instability index gives an estimate of the stability
of the protein in a test tube
Any value above 40 means that the protein is unstable
(has a short half life)
"""
return self.protein_analysis.instability_index()
def _calculate_isoelectric_point(self) -> float:
"""
Isoelectric point (pI) is the pH at which net charge of
the protein is zero. Isoelectric point is widely useful
for choosing a buffer system for purification and
crystallisation of a given protein
"""
return self.protein_analysis.isoelectric_point()
def _calculate_flexibility(self) -> float:
"""
Flexibility is of overwhelming importance for protein function,
because of the changes in protein structure during interactions
with binding partners
"""
return sum(self.protein_analysis.flexibility())
def _calculate_molar_extinction_coefficient(self) -> Mapping[str, float]:
"""
Molar extinction coefficient of a protein sequence can be calculated
from the molar extension coefficient of amino acids which are
Cystine, Tyrosine and Tryptophan
"""
cysteines, cystines = self.protein_analysis.molar_extinction_coefficient()
residues = {self.FEATURE_NAMES[7]: cysteines, self.FEATURE_NAMES[8]: cystines}
return residues
def _calculate_secondary_structure_fraction(self) -> Mapping[str, float]:
"""
This function returns a list of the fraction of amino acids which
tend to be in Helix, Turn or Sheet
Amino acids present in Turn are:
Asparagine (N), Proline (P), Glycine (G), Serine (S)
Amino acids present in Sheets are:
Glutamic acid (E), Methionine (M), Alanine (A), Leucine (L)
"""
helix, turn, sheet = self.protein_analysis.secondary_structure_fraction()
fractions = {
self.FEATURE_NAMES[9]: helix,
self.FEATURE_NAMES[10]: turn,
self.FEATURE_NAMES[11]: sheet,
}
return fractions
def get_features(self) -> Mapping[str, Union[int, float, None]]:
"""
Return full feature space for single protein as Python dict
"""
features = {
self.FEATURE_NAMES[0]: self._get_protein_length(),
self.FEATURE_NAMES[1]: self._calculate_gravy(),
self.FEATURE_NAMES[2]: self._calculate_molecular_weight(),
self.FEATURE_NAMES[3]: self._calculate_aromaticity(),
self.FEATURE_NAMES[4]: self._calculate_instability_index(),
self.FEATURE_NAMES[5]: self._calculate_isoelectric_point(),
self.FEATURE_NAMES[6]: self._calculate_flexibility(),
}
features.update(self._calculate_molar_extinction_coefficient())
features.update(self._calculate_secondary_structure_fraction())
return features