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(__FUNCTION__,
"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<OBAtom*>::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 Come back to the initial flags
mol.SetFlags(oldflags);
return;
}
void OBAromaticTyper::AssignAromaticFlags(OBMol &mol)
{
if (!_init)
Init();
if (mol.HasAromaticPerceived())
return;
mol.SetAromaticPerceived();
obErrorLog.ThrowError(__FUNCTION__,
"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<OBAtom*>::iterator i;
vector<OBBond*>::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 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,14);
//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;
}
