File: obfragment.cpp

package info (click to toggle)
openbabel 2.3.2%2Bdfsg-2
  • links: PTS, VCS
  • area: main
  • in suites: jessie, jessie-kfreebsd
  • size: 75,308 kB
  • ctags: 41,952
  • sloc: cpp: 321,252; ansic: 89,228; python: 7,262; perl: 6,418; pascal: 793; sh: 194; xml: 97; ruby: 55; makefile: 47; java: 23
file content (255 lines) | stat: -rw-r--r-- 8,261 bytes parent folder | download | duplicates (4)
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
119
120
121
122
123
124
125
126
127
128
129
130
131
132
133
134
135
136
137
138
139
140
141
142
143
144
145
146
147
148
149
150
151
152
153
154
155
156
157
158
159
160
161
162
163
164
165
166
167
168
169
170
171
172
173
174
175
176
177
178
179
180
181
182
183
184
185
186
187
188
189
190
191
192
193
194
195
196
197
198
199
200
201
202
203
204
205
206
207
208
209
210
211
212
213
214
215
216
217
218
219
220
221
222
223
224
225
226
227
228
229
230
231
232
233
234
235
236
237
238
239
240
241
242
243
244
245
246
247
248
249
250
251
252
253
254
255
/**********************************************************************
obfragment - Generate coordinate database of ring fragments

Copyright (C) 2007 Geoffrey R. Hutchison
 
This file is part of the Open Babel project.
For more information, see <http://openbabel.org/>

This program is free software; you can redistribute it and/or modify
it under the terms of the GNU General Public License as published by
the Free Software Foundation version 2 of the License.
 
This program is distributed in the hope that it will be useful,
but WITHOUT ANY WARRANTY; without even the implied warranty of
MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE.  See the
GNU General Public License for more details.
***********************************************************************/

// used to set import/export for Cygwin DLLs
#ifdef WIN32
#define USING_OBDLL
#endif

#include <openbabel/babelconfig.h>
#include <openbabel/mol.h>
#include <openbabel/obconversion.h>

#if !HAVE_STRNCASECMP
extern "C" int strncasecmp(const char *s1, const char *s2, size_t n);
#endif

#include <stdio.h>
#include <iostream>
#include <fstream>

using namespace std;
using namespace OpenBabel;

string RewriteSMILES(const string smiles);

int main(int argc,char *argv[])
{
  // turn off slow sync with C-style output (we don't use it anyway).
  std::ios::sync_with_stdio(false);

  OBConversion conv;
  OBFormat *inFormat, *canFormat;
  OBMol mol;
  ifstream ifs;
  vector<OBMol> fragments;
  unsigned int fragmentCount = 0; // track how many in library -- give a running count
  map<string, int> index; // index of cansmi
  string currentCAN;
  unsigned int size;
  OBAtom *atom;
  OBBond *bond;
  bool nonRingAtoms, nonRingBonds;
  char buffer[BUFF_SIZE];

  canFormat = conv.FindFormat("can");
  conv.SetOutFormat(canFormat);

  if (argc < 2)
    {
      cout << "Usage: obfragment <file>" << endl;
      return(-1);
    }

  for (int i = 1; i < argc; i++) {
    cerr << " Reading file " << argv[i] << endl;

    inFormat = conv.FormatFromExt(argv[i]);
    if(inFormat==NULL || !conv.SetInFormat(inFormat))
      {
        cerr << " Cannot read file format for " << argv[i] << endl;
        continue; // try next file
      }
    
    ifs.open(argv[i]);
    
    if (!ifs)
      {
        cerr << "Cannot read input file: " << argv[i] << endl;
        continue;
      }
    
    
    while(ifs.peek() != EOF && ifs.good())
      {
        conv.Read(&mol, &ifs);
        if (!mol.Has3D()) continue; // invalid coordinates!
        mol.DeleteHydrogens(); // remove these before we do anything else
        
        do {
          nonRingAtoms = false;
          size = mol.NumAtoms();
          for (unsigned int i = 1; i <= size; ++i)
            {
              atom = mol.GetAtom(i);
              if (!atom->IsInRing()) {
                mol.DeleteAtom(atom);
                nonRingAtoms = true;
                break; // don't know how many atoms there are
              } 
              // Previously, we changed atoms to carbon here.
              // Now we perform this alchemy in terms of string-rewriting
              // once the canonical SMILES is generated
            }
        } while (nonRingAtoms);
        
        if (mol.NumAtoms() < 3)
          continue;
        
        if (mol.NumBonds() == 0)
          continue;
        
        do {
          nonRingBonds = false;
          size = mol.NumBonds();
          for (unsigned int i = 0; i < size; ++i)
            {
              bond = mol.GetBond(i);
              if (!bond->IsInRing()) {
                mol.DeleteBond(bond);
                nonRingBonds = true;
                break; // don't know how many bonds there are
              }
            }        
        } while (nonRingBonds);

        fragments = mol.Separate();
        for (unsigned int i = 0; i < fragments.size(); ++i)
          {
            if (fragments[i].NumAtoms() < 3) // too small to care
              continue;
              
            currentCAN = conv.WriteString(&fragments[i], true);
            currentCAN = RewriteSMILES(currentCAN); // change elements to "a/A" for compression
            if (index.find(currentCAN) != index.end()) { // already got this
              index[currentCAN] += 1; // add to the count for bookkeeping
              continue;
            }

            index[currentCAN] = 1; // don't ever write this ring fragment again

            // OK, now retrieve the canonical ordering for the fragment
            vector<string> canonical_order;
            if (fragments[i].HasData("Canonical Atom Order")) {
              OBPairData *data = (OBPairData*)fragments[i].GetData("Canonical Atom Order");
              tokenize(canonical_order, data->GetValue().c_str());
            }

            // Write out an XYZ-style file with the CANSMI as the title
            cout << fragments[i].NumAtoms() << '\n';
            cout << currentCAN << '\n'; // endl causes a flush

            vector<string>::iterator can_iter;
            unsigned int order;
            OBAtom *atom;

            fragments[i].Center();
            fragments[i].ToInertialFrame();

            for (unsigned int index = 0; index < canonical_order.size(); 
                 ++index) {
              order = atoi(canonical_order[index].c_str());
              atom = fragments[i].GetAtom(order);
              
              snprintf(buffer, BUFF_SIZE, "C%8.3f%8.3f%8.3f\n",
                       atom->x(), atom->y(), atom->z());
              cout << buffer;
            }

          }
        fragments.clear();
        if (index.size() > fragmentCount) {
          fragmentCount = index.size();
          cerr << " Fragments: " << fragmentCount << endl;
        }

      } // while reading molecules (in this file)
    ifs.close();
    ifs.clear();
  } // while reading files

  // loop through the map and output frequencies
  map<string, int>::const_iterator indexItr;
  for (indexItr = index.begin(); indexItr != index.end(); ++indexItr) {
    cerr << (*indexItr).second << " INDEX " << (*indexItr).first << "\n";
  }
    
  return(0);
}

// Replace all instances of a string pattern with another
// (This should be part of the STL, but isn't, sadly.)
void FindAndReplace( string &source, const string find, const string replace )
 {
	 size_t j;
	 for ( ; (j = source.find( find )) != string::npos ; ) {
		 source.replace( j, find.length(), replace );
	 }
 }

string RewriteSMILES(const string smiles)
{
  string fragment = smiles;
  
  // This is a bit tedious -- we must place all atom types here
  // It would be much easier with a regex

  // NOTE: You must replace the two-letter elements first
  // (since the one-letter elements would match too, e.g. C replacing Cl)
  FindAndReplace(fragment, "[Cl]", "A");
  FindAndReplace(fragment, "[Se]", "A");
  FindAndReplace(fragment, "[Br]", "A");
  FindAndReplace(fragment, "[Al]", "A");
  FindAndReplace(fragment, "[Si]", "A");
  FindAndReplace(fragment, "[As]", "A");
  FindAndReplace(fragment, "[Li]", "A");
  FindAndReplace(fragment, "[Na]", "A");
  FindAndReplace(fragment, "[Mg]", "A");
  FindAndReplace(fragment, "[Ca]", "A");
  FindAndReplace(fragment, "[Cr]", "A");
  FindAndReplace(fragment, "[Mn]", "A");
  FindAndReplace(fragment, "[Fe]", "A");
  FindAndReplace(fragment, "[Co]", "A");
  FindAndReplace(fragment, "[Ni]", "A");
  FindAndReplace(fragment, "[Zn]", "A");
  FindAndReplace(fragment, "[Cu]", "A");
  FindAndReplace(fragment, "B", "A");
  FindAndReplace(fragment, "C", "A");
  FindAndReplace(fragment, "N", "A");
  FindAndReplace(fragment, "O", "A");
  FindAndReplace(fragment, "F", "A");
  FindAndReplace(fragment, "P", "A");
  FindAndReplace(fragment, "S", "A");
  FindAndReplace(fragment, "I", "A");
  FindAndReplace(fragment, "K", "A");
  
  // And now some aromatics
  FindAndReplace(fragment, "[si]", "a");
  FindAndReplace(fragment, "[se]", "a");
  FindAndReplace(fragment, "b", "a");
  FindAndReplace(fragment, "c", "a");
  FindAndReplace(fragment, "n", "a");
  FindAndReplace(fragment, "o", "a");
  FindAndReplace(fragment, "p", "a");
  FindAndReplace(fragment, "s", "a");
  
  // There are probably other elements which might be ignored, but these are rare
  // (i.e., unlikely to be top ring fragment hits)
  
  return fragment;
}