src/openbabel/typer.cpp

/**********************************************************************
typer.cpp - Open Babel atom typer.
 
Copyright (C) 1998-2001 by OpenEye Scientific Software, Inc.
Some portions Copyright (C) 2001-2005 by Geoffrey R. Hutchison
 
This file is part of the Open Babel project.
For more information, see <http://openbabel.sourceforge.net/>
 
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.
***********************************************************************/

#include "mol.hpp"
#include "typer.hpp"
#include "atomtyp.hpp"
#include "aromatic.hpp"

#ifdef WIN32
#pragma warning (disable : 4786)
#endif

using namespace std;

namespace OpenBabel
{

OBAromaticTyper  aromtyper;
OBAtomTyper      atomtyper;

/*! \class OBAtomTyper
    \brief Assigns atom types, hybridization, implicit valence and formal charges

The OBAtomTyper class is designed to read in a list of atom typing
rules and apply them to molecules. The code that performs atom
typing is not usually used directly as atom typing, hybridization
assignment, implicit valence assignment and charge are all done
automatically when their corresponding values are requested of
atoms:
\code
atom->GetType();
atom->GetFormalCharge();
atom->GetHyb();
\endcode
*/
OBAtomTyper::OBAtomTyper()
{
    _init = false;
    STR_DEFINE(_dir, FRC_PATH);
    _envvar = "FORCE_PARAM_PATH";
    _filename = "atomtyp.txt";
    _subdir = "data";
    _dataptr = AtomTypeData;
}

void OBAtomTyper::ParseLine(const char *buffer)
{
    vector<string> vs;
    OBSmartsPattern *sp;

    if (EQn(buffer,"INTHYB",6))
    {
        tokenize(vs,buffer);
        if (vs.empty() || vs.size() < 3)
          {
            obErrorLog.ThrowError(__func__, " Could not parse INTHYB line in atom type table from atomtyp.txt", obInfo);
            return;
          }

        sp = new OBSmartsPattern;
        if (sp->Init(vs[1]))
            _vinthyb.push_back(pair<OBSmartsPattern*,int> (sp,atoi((char*)vs[2].c_str())));
        else
        {
            delete sp;
            sp = NULL;
            obErrorLog.ThrowError(__func__, " Could not parse INTHYB line in atom type table from atomtyp.txt", obInfo);
            return;
        }
    }
    else if (EQn(buffer,"IMPVAL",6))
    {
        tokenize(vs,buffer);
        if (vs.empty() || vs.size() < 3)
          {
            obErrorLog.ThrowError(__func__, " Could not parse IMPVAL line in atom type table from atomtyp.txt", obInfo);
            return;
          }

        sp = new OBSmartsPattern;
        if (sp->Init(vs[1]))
            _vimpval.push_back(pair<OBSmartsPattern*,int> (sp,atoi((char*)vs[2].c_str())));
        else
        {
            obErrorLog.ThrowError(__func__, " Could not parse IMPVAL line in atom type table from atomtyp.txt", obInfo);
            delete sp;
            sp = NULL;
            return;
        }
    }
    else if (EQn(buffer,"EXTTYP",6))
    {
        tokenize(vs,buffer);
        if (vs.empty() || vs.size() < 3)
          {
            obErrorLog.ThrowError(__func__, " Could not parse EXTTYP line in atom type table from atomtyp.txt", obInfo);
            return;
          }
        sp = new OBSmartsPattern;
        if (sp->Init(vs[1]))
            _vexttyp.push_back(pair<OBSmartsPattern*,string> (sp,vs[2]));
        else
        {
            delete sp;
            sp = NULL;
            obErrorLog.ThrowError(__func__, " Could not parse EXTTYP line in atom type table from atomtyp.txt", obInfo);
            return;
        }
    }
}

OBAtomTyper::~OBAtomTyper()
{
    vector<pair<OBSmartsPattern*,int> >::iterator i;
    for (i = _vinthyb.begin();i != _vinthyb.end();i++)
    {
        delete i->first;
        i->first = NULL;
    }
    for (i = _vimpval.begin();i != _vimpval.end();i++)
    {
        delete i->first;
        i->first = NULL;
    }

    vector<pair<OBSmartsPattern*,string> >::iterator j;
    for (j = _vexttyp.begin();j != _vexttyp.end();j++)
    {
        delete j->first;
        j->first = NULL;
    }

}

void OBAtomTyper::AssignTypes(OBMol &mol)
{
    if (!_init)
        Init();

    obErrorLog.ThrowError(__func__,
                          "Ran OpenBabel::AssignTypes", obAuditMsg);

    mol.SetAtomTypesPerceived();

    vector<vector<int> >::iterator j;
    vector<pair<OBSmartsPattern*,string> >::iterator i;

    for (i = _vexttyp.begin();i != _vexttyp.end();i++)
        if (i->first->Match(mol))
        {
            _mlist = i->first->GetMapList();
            for (j = _mlist.begin();j != _mlist.end();j++)
                mol.GetAtom((*j)[0])->SetType(i->second);
        }
}

void OBAtomTyper::AssignHyb(OBMol &mol)
{
    if (!_init)
        Init();

    aromtyper.AssignAromaticFlags(mol);

    mol.SetHybridizationPerceived();
    obErrorLog.ThrowError(__func__,
                          "Ran OpenBabel::AssignHybridization", obAuditMsg);

    OBAtom *atom;
    vector<OBNodeBase*>::iterator k;
    for (atom = mol.BeginAtom(k);atom;atom = mol.NextAtom(k))
        atom->SetHyb(0);

    vector<vector<int> >::iterator j;
    vector<pair<OBSmartsPattern*,int> >::iterator i;

    for (i = _vinthyb.begin();i != _vinthyb.end();i++)
        if (i->first->Match(mol))
        {
            _mlist = i->first->GetMapList();
            for (j = _mlist.begin();j != _mlist.end();j++)
                mol.GetAtom((*j)[0])->SetHyb(i->second);
        }
}

void OBAtomTyper::AssignImplicitValence(OBMol &mol)
{
    // FF Make sure that valence has not been perceived
    if(mol.HasImplicitValencePerceived())
        return;

    if (!_init)
        Init();

    mol.SetImplicitValencePerceived();
    obErrorLog.ThrowError(__func__,
                          "Ran OpenBabel::AssignImplicitValence", obAuditMsg);

    // FF Ensure that the aromatic typer will not be called
    int oldflags = mol.GetFlags(); // save the current state flags
    mol.SetAromaticPerceived();    // and set the aromatic perceived flag on

    OBAtom *atom;
    vector<OBNodeBase*>::iterator k;
    for (atom = mol.BeginAtom(k);atom;atom = mol.NextAtom(k))
        atom->SetImplicitValence(atom->GetValence());

    vector<vector<int> >::iterator j;
    vector<pair<OBSmartsPattern*,int> >::iterator i;

    for (i = _vimpval.begin();i != _vimpval.end();i++)
        if (i->first->Match(mol))
        {
            _mlist = i->first->GetMapList();
            for (j = _mlist.begin();j != _mlist.end();j++)
                mol.GetAtom((*j)[0])->SetImplicitValence(i->second);
        }

    if (!mol.HasAromaticCorrected())
        CorrectAromaticNitrogens(mol);

    for (atom = mol.BeginAtom(k);atom;atom = mol.NextAtom(k))
    {
        if (atom->GetImplicitValence() < atom->GetValence())
            atom->SetImplicitValence(atom->GetValence());
    }

    //FF moved to  OBMol::AssignSpinMultiplicity();
    //begin CM 18 Sept 2003
    //if there are any explicit Hs on an atom, then they consitute all the Hs
    //Any discrepancy with the expected atom valency is because it is a radical of some sort
    //Also adjust the ImplicitValence for radical atoms
    //for (atom = mol.BeginAtom(k);atom;atom = mol.NextAtom(k))
    //  {
    //    if (!atom->IsHydrogen() && atom->ExplicitHydrogenCount()!=0)
    //  {
    //    int diff=atom->GetImplicitValence() - (atom->GetHvyValence() + atom->ExplicitHydrogenCount());
    //    if (diff)
    //      atom->SetSpinMultiplicity(diff+1);//radicals =2; all carbenes =3
    //  }

    //    int mult=atom->GetSpinMultiplicity();
    //   if(mult) //radical or carbene
    //  atom->DecrementImplicitValence();
    //   if(mult==1 || mult==3) //e.g.singlet or triplet carbene
    //  atom->DecrementImplicitValence();
    //  }
    //end CM
    //FF end

    // FF Come back to the initial flags
    mol.SetFlags(oldflags);

    return;
}


void OBAtomTyper::CorrectAromaticNitrogens(OBMol &mol)
{
    if (!_init)
        Init();

    if (mol.HasAromaticCorrected())
        return;
    mol.SetAromaticCorrected();

    return;

//     int j;
//     OBAtom *atom,*nbr,*a;
//     vector<OBNodeBase*>::iterator i,m;
//     vector<OBEdgeBase*>::iterator k;
//     OBBitVec curr,used,next;
//     vector<OBNodeBase*> v_N,v_OS;

//     vector<bool> _aromNH;
//     _aromNH.clear();
//     _aromNH.resize(mol.NumAtoms()+1);

//     for (atom = mol.BeginAtom(i);atom;atom = mol.NextAtom(i))
//         if (atom->IsAromatic() && !atom->IsCarbon() && !used[atom->GetIdx()])
//         {
//             vector<OBNodeBase*> rsys;
//             rsys.push_back(atom);
//             curr |= atom->GetIdx();
//             used |= atom->GetIdx();

//             while (!curr.Empty())
//             {
//                 next.Clear();
//                 for (j = curr.NextBit(0);j != curr.EndBit();j = curr.NextBit(j))
//                 {
//                     atom = mol.GetAtom(j);
//                     for (nbr = atom->BeginNbrAtom(k);nbr;nbr = atom->NextNbrAtom(k))
//                     {
//                         if (!(*k)->IsAromatic())
//                             continue;
//                         if (used[nbr->GetIdx()])
//                             continue;

//                         rsys.push_back(nbr);
//                         next |= nbr->GetIdx();
//                         used |= nbr->GetIdx();
//                     }
//                 }

//                 curr = next;
//             }

//             //count number of electrons in the ring system
//             v_N.clear();
//             v_OS.clear();
//             int nelectrons = 0;

//             for (m = rsys.begin();m != rsys.end();m++)
//             {
//                 a = (OBAtom *)*m;

//                 int hasExoDoubleBond = false;
//                 for (nbr = a->BeginNbrAtom(k);nbr;nbr = a->NextNbrAtom(k))
//                     if ((*k)->GetBO() == 2 && !(*k)->IsInRing())
//                         if (nbr->IsOxygen() || nbr->IsSulfur() || nbr->IsNitrogen())
//                             hasExoDoubleBond = true;

//                 if (a->IsCarbon() && hasExoDoubleBond)
//                     continue;

//                 if (a->IsCarbon())
//                     nelectrons++;
//                 else
//                     if (a->IsOxygen() || a->IsSulfur())
//                     {
//                         v_OS.push_back(a);
//                         nelectrons += 2;
//                     }
//                     else
//                         if (a->IsNitrogen())
//                         {
//                             v_N.push_back(a); //store nitrogens
//                             nelectrons++;
//                         }
//             }

//             //calculate what the number of electrons should be for aromaticity
//             int naromatic = 2+4*((int)((double)(rsys.size()-2)*0.25+0.5));

//             if (nelectrons > naromatic) //try to give one electron back to O or S
//                 for (m = v_OS.begin();m != v_OS.end();m++)
//                 {
//                     if (naromatic == nelectrons)
//                         break;
//                     if ((*m)->GetValence() == 2 && (*m)->GetHvyValence() == 2)
//                     {
//                         nelectrons--;
//                         ((OBAtom*)*m)->SetFormalCharge(1);
//                     }
//                 }

//             if (v_N.empty())
//                 continue; //no nitrogens found in ring

//             //check for protonated nitrogens
//             for (m = v_N.begin();m != v_N.end();m++)
//             {
//                 if (naromatic == nelectrons)
//                     break;
//                 if (((OBAtom*)*m)->GetValence() == 3 &&
//                         ((OBAtom*)*m)->GetHvyValence() == 2)
//                 {
//                     nelectrons++;
//                     _aromNH[((OBAtom*)*m)->GetIdx()] = true;
//                 }
//                 if (((OBAtom*)*m)->GetFormalCharge() == -1)
//                 {
//                     nelectrons++;
//                     _aromNH[((OBAtom*)*m)->GetIdx()] = false;
//                 }
//             }

//             //charge up tert nitrogens
//             for (m = v_N.begin();m != v_N.end();m++)
//                 if (((OBAtom*)*m)->GetHvyValence() == 3
//                         && ((OBAtom*)*m)->BOSum() < 5)
//                     ((OBAtom*)*m)->SetFormalCharge(1);

//             //try to uncharge nitrogens first
//             for (m = v_N.begin();m != v_N.end();m++)
//             {
//                 if (((OBAtom*)*m)->BOSum() > 4)
//                     continue; //skip n=O
//                 if (naromatic == nelectrons)
//                     break;
//                 if (((OBAtom*)*m)->GetHvyValence() == 3)
//                 {
//                     nelectrons++;
//                     ((OBAtom*)*m)->SetFormalCharge(0);
//                 }
//             }

//             if (naromatic == nelectrons)
//                 continue;

//             //try to protonate amides next
//             for (m = v_N.begin();m != v_N.end();m++)
//             {
//                 if (naromatic == nelectrons)
//                     break;
//                 if (((OBAtom*)*m)->IsAmideNitrogen() &&
//                         ((OBAtom*)*m)->GetValence() == 2 &&
//                         ((OBAtom*)*m)->GetHvyValence() == 2 &&
//                         !_aromNH[((OBAtom*)*m)->GetIdx()])
//                 {
//                     nelectrons++;
//                     _aromNH[((OBAtom*)*m)->GetIdx()] = true;
//                 }
//             }

//             if (naromatic == nelectrons)
//                 continue;

//             //protonate amines in 5 membered rings first - try to match kekule
//             for (m = v_N.begin();m != v_N.end();m++)
//             {
//                 if (naromatic == nelectrons)
//                     break;
//                 if (((OBAtom*)*m)->GetValence() == 2 &&
//                         !_aromNH[((OBAtom*)*m)->GetIdx()] &&
//                         ((OBAtom*)*m)->IsInRingSize(5) &&
//                         ((OBAtom*)*m)->BOSum() == 2)
//                 {
//                     nelectrons++;
//                     _aromNH[((OBAtom*)*m)->GetIdx()] = true;
//                 }
//             }

//             if (naromatic == nelectrons)
//                 continue;

//             //protonate amines in 5 membered rings first - no kekule restriction
//             for (m = v_N.begin();m != v_N.end();m++)
//             {
//                 if (naromatic == nelectrons)
//                     break;
//                 if ((*m)->GetValence() == 2 && !_aromNH[(*m)->GetIdx()] &&
//                         (*m)->IsInRingSize(5))
//                 {
//                     nelectrons++;
//                     _aromNH[(*m)->GetIdx()] = true;
//                 }
//             }

//             if (naromatic == nelectrons)
//                 continue;

//             //then others -- try to find an atom w/o a double bond first
//             for (m = v_N.begin();m != v_N.end();m++)
//             {
//                 if (naromatic == nelectrons)
//                     break;
//                 if (((OBAtom*)*m)->GetHvyValence() == 2 &&
//                         !_aromNH[((OBAtom*)*m)->GetIdx()] &&
//                         !((OBAtom*)*m)->HasDoubleBond())
//                 {
//                     nelectrons++;
//                     _aromNH[(*m)->GetIdx()] = true;
//                 }
//             }

//             for (m = v_N.begin();m != v_N.end();m++)
//             {
//                 if (naromatic == nelectrons)
//                     break;
//                 if ((*m)->GetHvyValence() == 2 && !_aromNH[(*m)->GetIdx()])
//                 {
//                     nelectrons++;
//                     _aromNH[(*m)->GetIdx()] = true;
//                 }
//             }
//         }

//     for (atom = mol.BeginAtom(i);atom;atom = mol.NextAtom(i))
//         if (_aromNH[atom->GetIdx()] && atom->GetValence() == 2)
//             atom->SetImplicitValence(3);
}

/*! \class OBAromaticTyper
  \brief Assigns aromatic typing to atoms and bonds
 
  The OBAromaticTyper class is designed to read in a list of 
  aromatic perception rules and apply them to molecules. The code 
  that performs typing is not usually used directly -- it is usually 
  done automatically when their corresponding values are requested of atoms 
  or bonds.
\code
  atom->IsAromatic();
  bond->IsAromatic();
  bond->IsDouble(); // needs to check aromaticity and define Kekule structures
\endcode
*/
OBAromaticTyper::OBAromaticTyper()
{
    _init = false;
    STR_DEFINE(_dir, FRC_PATH);
    _envvar = "FORCE_PARAM_PATH";
    _filename = "aromatic.txt";
    _subdir = "data";
    _dataptr = AromaticData;
}

void OBAromaticTyper::ParseLine(const char *buffer)
{
    OBSmartsPattern *sp;
    char temp_buffer[BUFF_SIZE];

    if (buffer[0] == '#')
        return;
    vector<string> vs;
    tokenize(vs,buffer);
    if (!vs.empty() && vs.size() == 3)
    {
        strcpy(temp_buffer,vs[0].c_str());
        sp = new OBSmartsPattern();
        if (sp->Init(temp_buffer))
        {
            _vsp.push_back(sp);
            _verange.push_back(pair<int,int>
                               (atoi((char*)vs[1].c_str()),
                                atoi((char*)vs[2].c_str())));
        }
        else
        {
            obErrorLog.ThrowError(__func__, " Could not parse line in aromatic typer from aromatic.txt", obInfo);
            delete sp;
            sp = NULL;
            return;
        }
    }
    else
      obErrorLog.ThrowError(__func__, " Could not parse line in aromatic typer from aromatic.txt", obInfo);
}

OBAromaticTyper::~OBAromaticTyper()
{
    vector<OBSmartsPattern*>::iterator i;
    for (i = _vsp.begin();i != _vsp.end();i++)
    {
        delete *i;
        *i = NULL;
    }
}

void OBAromaticTyper::AssignAromaticFlags(OBMol &mol)
{
    if (!_init)
        Init();

    if (mol.HasAromaticPerceived())
        return;
    mol.SetAromaticPerceived();
    obErrorLog.ThrowError(__func__,
                          "Ran OpenBabel::AssignAromaticFlags", obAuditMsg);

    _vpa.clear();
    _vpa.resize(mol.NumAtoms()+1);
    _velec.clear();
    _velec.resize(mol.NumAtoms()+1);
    _root.clear();
    _root.resize(mol.NumAtoms()+1);

    OBBond *bond;
    OBAtom *atom;
    vector<OBNodeBase*>::iterator i;
    vector<OBEdgeBase*>::iterator j;

    //unset all aromatic flags
    for (atom = mol.BeginAtom(i);atom;atom = mol.NextAtom(i))
        atom->UnsetAromatic();
    for (bond = mol.BeginBond(j);bond;bond = mol.NextBond(j))
        bond->UnsetAromatic();

    int idx;
    vector<vector<int> >::iterator m;
    vector<OBSmartsPattern*>::iterator k;

    //mark atoms as potentially aromatic
    for (idx=0,k = _vsp.begin();k != _vsp.end();k++,idx++)
        if ((*k)->Match(mol))
        {
            _mlist = (*k)->GetMapList();
            for (m = _mlist.begin();m != _mlist.end();m++)
            {
                _vpa[(*m)[0]] = true;
                _velec[(*m)[0]] = _verange[idx];
            }
        }

    //sanity check - exclude all 4 substituted atoms and sp centers
    for (atom = mol.BeginAtom(i);atom;atom = mol.NextAtom(i))
    {
        if (atom->GetImplicitValence() > 3)
        {
            _vpa[atom->GetIdx()] = false;
            continue;
        }

        switch(atom->GetAtomicNum())
        {
            //phosphorus and sulfur may be initially typed as sp3
        case 6:
        case 7:
        case 8:
            if (atom->GetHyb() != 2)
                _vpa[atom->GetIdx()] = false;
            break;
        }
    }

    //propagate potentially aromatic atoms
    for (atom = mol.BeginAtom(i);atom;atom = mol.NextAtom(i))
        if (_vpa[atom->GetIdx()])
            PropagatePotentialAromatic(atom);

    //select root atoms
    SelectRootAtoms(mol);

    ExcludeSmallRing(mol); //remove 3 membered rings from consideration

    //loop over root atoms and look for 5-6 membered aromatic rings
    _visit.clear();
    _visit.resize(mol.NumAtoms()+1);
    for (atom = mol.BeginAtom(i);atom;atom = mol.NextAtom(i))
        if (_root[atom->GetIdx()])
            CheckAromaticity(atom,6);

    for (atom = mol.BeginAtom(i);atom;atom = mol.NextAtom(i))
        if (_root[atom->GetIdx()])
            CheckAromaticity(atom,20);

    //for (atom = mol.BeginAtom(i);atom;atom = mol.NextAtom(i))
    //    if (atom->IsAromatic())
    //            cerr << "aro = " <<atom->GetIdx()  << endl;

    //for (bond = mol.BeginBond(j);bond;bond = mol.NextBond(j))
    //if (bond->IsAromatic())
    //cerr << bond->GetIdx() << ' ' << bond->IsAromatic() << endl;
}

bool OBAromaticTyper::TraverseCycle(OBAtom *root, OBAtom *atom, OBBond *prev, 
                                    std::pair<int,int> &er,int depth)
{
    if (atom == root)
    {
        int i;
        for (i = er.first;i <= er.second;i++)
            if (i%4 == 2 && i > 2)
                return(true);

        return(false);
    }

    if (!depth || !_vpa[atom->GetIdx()] || _visit[atom->GetIdx()])
        return(false);

    bool result = false;

    depth--;
    er.first  += _velec[atom->GetIdx()].first;
    er.second += _velec[atom->GetIdx()].second;

    _visit[atom->GetIdx()] = true;
    OBAtom *nbr;
    vector<OBEdgeBase*>::iterator i;
    for (nbr = atom->BeginNbrAtom(i);nbr;nbr = atom->NextNbrAtom(i))
        if (*i != prev && (*i)->IsInRing() && _vpa[nbr->GetIdx()])
        {
            if (TraverseCycle(root,nbr,(OBBond*)(*i),er,depth))
            {
                result = true;
                ((OBBond*) *i)->SetAromatic();
            }
        }

    _visit[atom->GetIdx()] = false;
    if (result)
        atom->SetAromatic();

    er.first  -= _velec[atom->GetIdx()].first;
    er.second -= _velec[atom->GetIdx()].second;

    return(result);
}

void OBAromaticTyper::CheckAromaticity(OBAtom *atom,int depth)
{
    OBAtom *nbr;
    vector<OBEdgeBase*>::iterator i;

    pair<int,int> erange;
    for (nbr = atom->BeginNbrAtom(i);nbr;nbr = atom->NextNbrAtom(i))
      if ((*i)->IsInRing()) // check all rings, regardless of assumed aromaticity
        {
            erange = _velec[atom->GetIdx()];

            if (TraverseCycle(atom,nbr,(OBBond *)*i,erange,depth-1))
            {
                atom->SetAromatic();
                ((OBBond*) *i)->SetAromatic();
            }
        }
}

void OBAromaticTyper::PropagatePotentialAromatic(OBAtom *atom)
{
    int count = 0;
    OBAtom *nbr;
    vector<OBEdgeBase*>::iterator i;

    for (nbr = atom->BeginNbrAtom(i);nbr;nbr = atom->NextNbrAtom(i))
        if ((*i)->IsInRing() && _vpa[nbr->GetIdx()])
            count++;

    if (count < 2)
    {
        _vpa[atom->GetIdx()] = false;
        if (count == 1)
            for (nbr = atom->BeginNbrAtom(i);nbr;nbr = atom->NextNbrAtom(i))
                if ((*i)->IsInRing() && _vpa[nbr->GetIdx()])
                    PropagatePotentialAromatic(nbr);
    }
}

/**
 * Select the root atoms for traversing atoms in rings.
 *
 * Picking only the begin atom of a closure bond can cause
 * difficulties when the selected atom is an inner atom
 * with three neighbour ring atoms. Why ? Because this atom
 * can get trapped by the other atoms when determining aromaticity,
 * because a simple visited flag is used in the
 * OBAromaticTyper::TraverseCycle() method.
 *
 * Ported from JOELib, copyright Joerg Wegner, 2003 under the GPL version 2
 *
 * @param mol the molecule
 * @param avoidInnerRingAtoms inner closure ring atoms with more than 2 neighbours will be avoided
 *
 */
void OBAromaticTyper::SelectRootAtoms(OBMol &mol, bool avoidInnerRingAtoms)
{
    OBBond *bond;
    OBAtom *atom, *nbr, *nbr2;
    OBRing *ring;
//    vector<OBNodeBase*>::iterator i;
    vector<OBEdgeBase*>::iterator j, l, nbr2Iter;
    vector<OBRing*> sssRings = mol.GetSSSR();
    vector<OBRing*>::iterator k;

    int rootAtom;
    int ringNbrs;
    int heavyNbrs;
    int newRoot = -1;
    vector<int> tmpRootAtoms;
    vector<int> tmp;

    for (bond = mol.BeginBond(j);bond;bond = mol.NextBond(j))
        if (bond->IsClosure())
            tmpRootAtoms.push_back(bond->GetBeginAtomIdx());

    for (bond = mol.BeginBond(j);bond;bond = mol.NextBond(j))
        if (bond->IsClosure())
        {
            // BASIC APPROACH
            // pick beginning atom at closure bond
            // this is really ready, isn't it ! ;-)
            rootAtom = bond->GetBeginAtomIdx();
            _root[rootAtom] = true;

            // EXTENDED APPROACH
            if (avoidInnerRingAtoms)
            {
                // count the number of neighbor ring atoms
                atom = mol.GetAtom(rootAtom);
                ringNbrs = heavyNbrs = 0;

                for (nbr = atom->BeginNbrAtom(l);nbr;nbr = atom->NextNbrAtom(l))
                {
                    // we can get this from atom->GetHvyValence()
                    // but we need to find neighbors in rings too
                    // so let's save some time
                    if (!nbr->IsHydrogen())
                    {
                        heavyNbrs++;
                        if (nbr->IsInRing())
                            ringNbrs++;
                    }

                    // if this atom has more than 2 neighbor ring atoms
                    // we could get trapped later when traversing cycles
                    // which can cause aromaticity false detection
                    newRoot = -1;

                    if (ringNbrs > 2)
                    {
                        // try to find another root atom
                        for (k = sssRings.begin();k != sssRings.end();k++)
                        {
                            ring = (*k);
                            tmp = ring->_path;

                            bool checkThisRing = false;
                            int rootAtomNumber=0;
                            int idx=0;
                            // avoiding two root atoms in one ring !
                            for (unsigned int j = 0; j < tmpRootAtoms.size(); j++)
                            {
                                idx= tmpRootAtoms[j];
                                if(ring->IsInRing(idx))
                                {
                                    rootAtomNumber++;
                                    if(rootAtomNumber>=2)
                                        break;
                                }
                            }
                            if(rootAtomNumber<2)
                            {
                                for (unsigned int j = 0; j < tmp.size(); j++)
                                {
                                    // find critical ring
                                    if (tmp[j] == rootAtom)
                                    {
                                        checkThisRing = true;
                                    }
                                    else
                                    {
                                        // second root atom in this ring ?
                                        if (_root[tmp[j]] == true)
                                        {
                                            // when there is a second root
                                            // atom this ring can not be
                                            // used for getting an other
                                            // root atom
                                            checkThisRing = false;

                                            break;
                                        }
                                    }
                                }
                            }

                            // check ring for getting another
                            // root atom to avoid aromaticity typer problems
                            if (checkThisRing)
                            {
                                // check if we can find another root atom
                                for (unsigned int m = 0; m < tmp.size(); m++)
                                {
                                    ringNbrs = heavyNbrs = 0;
                                    for (nbr2 = (mol.GetAtom(tmp[m]))->BeginNbrAtom(nbr2Iter);
                                            nbr2;nbr2 = (mol.GetAtom(tmp[m]))->NextNbrAtom(nbr2Iter))
                                    {
                                        if (!nbr2->IsHydrogen())
                                        {
                                            heavyNbrs++;

                                            if (nbr2->IsInRing())
                                                ringNbrs++;
                                        }
                                    }

                                    // if the number of neighboured heavy atoms is also
                                    // the number of neighboured ring atoms, the aromaticity
                                    // typer could be stuck in a local traversing trap
                                    if (ringNbrs <= 2 && ring->IsInRing((mol.GetAtom(tmp[m])->GetIdx())))
                                    {
                                        newRoot = tmp[m];
                                    }
                                }
                            }
                        }

                        if ((newRoot != -1) && (rootAtom != newRoot))
                        {
                            // unset root atom
                            _root[rootAtom] = false;

                            // pick new root atom
                            _root[newRoot] = true;
                        }
                    } // if (ringNbrs > 2)

                } // end for
            } // if (avoid)
        } // if (bond.IsClosure())
}

void OBAromaticTyper::ExcludeSmallRing(OBMol &mol)
{
    OBAtom *atom,*nbr1,*nbr2;
    vector<OBNodeBase*>::iterator i;
    vector<OBEdgeBase*>::iterator j,k;

    for (atom = mol.BeginAtom(i);atom;atom = mol.NextAtom(i))
        if (_root[atom->GetIdx()])
            for (nbr1 = atom->BeginNbrAtom(j);nbr1;nbr1 = atom->NextNbrAtom(j))
                if ((*j)->IsInRing() && _vpa[nbr1->GetIdx()])
                    for (nbr2 = nbr1->BeginNbrAtom(k);nbr2;nbr2 = nbr1->NextNbrAtom(k))
                        if (nbr2 != atom && (*k)->IsInRing() && _vpa[nbr2->GetIdx()])
                            if (atom->IsConnected(nbr2))
                                _root[atom->GetIdx()] = false;
}

} //namespace OpenBabel;

//! \file typer.cpp
//! \brief Open Babel atom and aromaticity typer.
Revision:	2518
Committed:	Fri Dec 16 21:52:50 2005 UTC (18 years, 6 months ago) by tim
File size:	30847 byte(s)
Log Message:	changed __FUNCTION__ to __func__ to match C99 standard, and then added an autoconf test to check for __func__ usability. Changed some default compile flags for the Sun architecture