@TestMethod("testCalculate_IAtomContainer")
public DescriptorValue calculate(IAtomContainer container) {
// removeHydrogens does a deep copy, so no need to clone
IAtomContainer localAtomContainer = AtomContainerManipulator.removeHydrogens(container);
CDKAtomTypeMatcher matcher = CDKAtomTypeMatcher.getInstance(container.getBuilder());
Iterator<IAtom> atoms = localAtomContainer.atoms().iterator();
while (atoms.hasNext()) {
IAtom atom = atoms.next();
IAtomType type;
try {
type = matcher.findMatchingAtomType(localAtomContainer, atom);
AtomTypeManipulator.configure(atom, type);
} catch (Exception e) {
return getDummyDescriptorValue(new CDKException("Error in atom typing: " + e.getMessage()));
}
}
CDKHydrogenAdder hAdder = CDKHydrogenAdder.getInstance(container.getBuilder());
try {
hAdder.addImplicitHydrogens(localAtomContainer);
} catch (CDKException e) {
return getDummyDescriptorValue(
new CDKException("Error in hydrogen addition: " + e.getMessage()));
}
List subgraph3 = order3(localAtomContainer);
List subgraph4 = order4(localAtomContainer);
List subgraph5 = order5(localAtomContainer);
List subgraph6 = order6(localAtomContainer);
double order3s = ChiIndexUtils.evalSimpleIndex(localAtomContainer, subgraph3);
double order4s = ChiIndexUtils.evalSimpleIndex(localAtomContainer, subgraph4);
double order5s = ChiIndexUtils.evalSimpleIndex(localAtomContainer, subgraph5);
double order6s = ChiIndexUtils.evalSimpleIndex(localAtomContainer, subgraph6);
double order3v, order4v, order5v, order6v;
try {
order3v = ChiIndexUtils.evalValenceIndex(localAtomContainer, subgraph3);
order4v = ChiIndexUtils.evalValenceIndex(localAtomContainer, subgraph4);
order5v = ChiIndexUtils.evalValenceIndex(localAtomContainer, subgraph5);
order6v = ChiIndexUtils.evalValenceIndex(localAtomContainer, subgraph6);
} catch (CDKException e) {
return getDummyDescriptorValue(
new CDKException("Error in substructure search: " + e.getMessage()));
}
DoubleArrayResult retval = new DoubleArrayResult();
retval.add(order3s);
retval.add(order4s);
retval.add(order5s);
retval.add(order6s);
retval.add(order3v);
retval.add(order4v);
retval.add(order5v);
retval.add(order6v);
return new DescriptorValue(
getSpecification(), getParameterNames(), getParameters(), retval, getDescriptorNames());
}
/**
* Place hydrogens connected to the provided atom <i>atom</i> using the specified
* <i>bondLength</i>.
*
* @param container atom container
* @param bondLength bond length to user
* @throws IllegalArgumentException thrown if the <i>atom</i> or <i>container</i> was null or the
* atom has connected atoms which have not been placed.
*/
@TestMethod("testNoConnections,testNullContainer,unplacedNonHydrogen")
public void placeHydrogens2D(IAtomContainer container, IAtom atom, double bondLength) {
if (container == null)
throw new IllegalArgumentException("cannot place hydrogens, no container provided");
if (atom.getPoint2d() == null)
throw new IllegalArgumentException("cannot place hydrogens on atom without coordinates");
logger.debug(
"placing hydrogens connected to atom ", atom.getSymbol(),
": ", atom.getPoint2d());
logger.debug("bond length", bondLength);
AtomPlacer atomPlacer = new AtomPlacer();
atomPlacer.setMolecule(container);
List<IAtom> connected = container.getConnectedAtomsList(atom);
IAtomContainer placed = container.getBuilder().newInstance(IAtomContainer.class);
IAtomContainer unplaced = container.getBuilder().newInstance(IAtomContainer.class);
// divide connected atoms into those which are have and haven't been placed
for (final IAtom conAtom : connected) {
if (conAtom.getPoint2d() == null) {
if (conAtom.getSymbol().equals("H")) {
unplaced.addAtom(conAtom);
} else {
throw new IllegalArgumentException(
"cannot place hydrogens, atom has connected" + " non-hydrogens without coordinates");
}
} else {
placed.addAtom(conAtom);
}
}
logger.debug("Atom placement before procedure:");
logger.debug("Centre atom ", atom.getSymbol(), ": ", atom.getPoint2d());
for (int i = 0; i < unplaced.getAtomCount(); i++) {
logger.debug("H-" + i, ": ", unplaced.getAtom(i).getPoint2d());
}
Point2d centerPlacedAtoms = GeometryTools.get2DCenter(placed);
atomPlacer.distributePartners(atom, placed, centerPlacedAtoms, unplaced, bondLength);
logger.debug("Atom placement after procedure:");
logger.debug("Centre atom ", atom.getSymbol(), ": ", atom.getPoint2d());
for (int i = 0; i < unplaced.getAtomCount(); i++) {
logger.debug("H-" + i, ": ", unplaced.getAtom(i).getPoint2d());
}
}
/**
* Returns the ring that is formed by the atoms in the given vector.
*
* @param vec The vector that contains the atoms of the ring
* @param mol The molecule this ring is a substructure of
* @return The ring formed by the given atoms
*/
private IRing prepareRing(List vec, IAtomContainer mol) {
// add the atoms in vec to the new ring
int atomCount = vec.size();
IRing ring = mol.getBuilder().newInstance(IRing.class, atomCount);
IAtom[] atoms = new IAtom[atomCount];
vec.toArray(atoms);
ring.setAtoms(atoms);
// add the bonds in mol to the new ring
try {
IBond b;
for (int i = 0; i < atomCount - 1; i++) {
b = mol.getBond(atoms[i], atoms[i + 1]);
if (b != null) {
ring.addBond(b);
} else {
logger.error("This should not happen.");
}
}
b = mol.getBond(atoms[0], atoms[atomCount - 1]);
if (b != null) {
ring.addBond(b);
} else {
logger.error("This should not happen either.");
}
} catch (Exception exc) {
logger.debug(exc);
}
logger.debug("found Ring ", ring);
return ring;
}
public String perceiveCDKAtomTypes(IMolecule mol)
throws InvocationTargetException {
ICDKMolecule cdkmol;
try {
cdkmol = cdk.asCDKMolecule(mol);
}
catch ( BioclipseException e ) {
e.printStackTrace();
throw new InvocationTargetException(
e, "Error while creating a ICDKMolecule" );
}
IAtomContainer ac = cdkmol.getAtomContainer();
CDKAtomTypeMatcher cdkMatcher
= CDKAtomTypeMatcher.getInstance(ac.getBuilder());
StringBuffer result = new StringBuffer();
int i = 1;
for (IAtom atom : ac.atoms()) {
IAtomType type = null;
try {
type = cdkMatcher.findMatchingAtomType(ac, atom);
}
catch ( CDKException e ) {}
result.append(i).append(':').append(
type != null ? type.getAtomTypeName() : "null"
).append('\n'); // FIXME: should use NEWLINE here
i++;
}
return result.toString();
}
private void atomLayout(IAtomContainer atomContainer) {
IMolecule mol = atomContainer.getBuilder().newInstance(IMolecule.class, atomContainer);
sdg.setMolecule(mol, false);
try {
sdg.generateCoordinates();
} catch (Exception e) {
e.printStackTrace();
}
}
private void processAtomsBlock(int lineCount, IAtomContainer container) throws IOException {
for (int i = 0; i < lineCount; i++) {
String line = input.readLine();
int atomicNumber = Integer.parseInt(line.substring(7, 10).trim());
IAtom atom = container.getBuilder().newAtom();
atom.setAtomicNumber(atomicNumber);
atom.setSymbol(Symbols.byAtomicNumber[atomicNumber]);
container.addAtom(atom);
}
}
/**
* Test to recognize if a IAtomContainer matcher correctly identifies the CDKAtomTypes.
*
* @param molecule The IAtomContainer to analyze
* @throws CDKException
*/
private void makeSureAtomTypesAreRecognized(IAtomContainer molecule) throws CDKException {
Iterator<IAtom> atoms = molecule.atoms().iterator();
CDKAtomTypeMatcher matcher = CDKAtomTypeMatcher.getInstance(molecule.getBuilder());
while (atoms.hasNext()) {
IAtom nextAtom = atoms.next();
Assert.assertNotNull(
"Missing atom type for: " + nextAtom, matcher.findMatchingAtomType(molecule, nextAtom));
}
}
/** A unit test for JUnit */
@Test
public void testAlanin() throws Exception {
HydrogenPlacer hydrogenPlacer = new HydrogenPlacer();
IAtomContainer mol1 = new AtomContainer();
SmilesGenerator sg = new SmilesGenerator();
mol1.addAtom(new Atom("N", new Point2d(1, 0)));
// 1
mol1.addAtom(new Atom("C", new Point2d(1, 2)));
// 2
mol1.addAtom(new Atom("F", new Point2d(1, 2)));
// 3
mol1.addAtom(new Atom("C", new Point2d(0, 0)));
// 4
mol1.addAtom(new Atom("C", new Point2d(1, 4)));
// 5
mol1.addAtom(new Atom("O", new Point2d(1, 5)));
// 6
mol1.addAtom(new Atom("O", new Point2d(1, 6)));
// 7
mol1.addBond(0, 1, IBond.Order.SINGLE);
// 1
mol1.addBond(1, 2, IBond.Order.SINGLE, IBond.Stereo.UP);
// 2
mol1.addBond(1, 3, IBond.Order.SINGLE, IBond.Stereo.DOWN);
// 3
mol1.addBond(1, 4, IBond.Order.SINGLE);
// 4
mol1.addBond(4, 5, IBond.Order.SINGLE);
// 5
mol1.addBond(4, 6, IBond.Order.DOUBLE);
// 6
addExplicitHydrogens(mol1);
hydrogenPlacer.placeHydrogens2D(mol1, 1.0);
IsotopeFactory ifac = IsotopeFactory.getInstance(mol1.getBuilder());
ifac.configureAtoms(mol1);
String smiles1 = null;
if (standAlone) {
display(mol1);
}
smiles1 = sg.createSMILES(mol1, true, new boolean[mol1.getBondCount()]);
if (standAlone) {
System.err.println("SMILES 1: " + smiles1);
}
Assert.assertNotNull(smiles1);
Assert.assertEquals("[H]OC(=O)[C@](F)(N([H])[H])C([H])([H])[H]", smiles1);
mol1.getBond(1).setStereo(IBond.Stereo.DOWN);
mol1.getBond(2).setStereo(IBond.Stereo.UP);
smiles1 = sg.createSMILES(mol1, true, new boolean[mol1.getBondCount()]);
if (standAlone) {
System.err.println("SMILES 1: " + smiles1);
}
Assert.assertNotNull(smiles1);
Assert.assertEquals("[H]OC(=O)[C@](F)(C([H])([H])[H])N([H])[H]", smiles1);
}
private void fixHydrogenIsotopes(IAtomContainer molecule, IsotopeFactory isotopeFactory) {
for (IAtom atom : AtomContainerManipulator.getAtomArray(molecule)) {
if (atom instanceof IPseudoAtom) {
IPseudoAtom pseudo = (IPseudoAtom) atom;
if ("D".equals(pseudo.getLabel())) {
IAtom newAtom = molecule.getBuilder().newInstance(IAtom.class, atom);
newAtom.setSymbol("H");
newAtom.setAtomicNumber(1);
isotopeFactory.configure(newAtom, isotopeFactory.getIsotope("H", 2));
AtomContainerManipulator.replaceAtomByAtom(molecule, atom, newAtom);
} else if ("T".equals(pseudo.getLabel())) {
IAtom newAtom = molecule.getBuilder().newInstance(IAtom.class, atom);
newAtom.setSymbol("H");
newAtom.setAtomicNumber(1);
isotopeFactory.configure(newAtom, isotopeFactory.getIsotope("H", 3));
AtomContainerManipulator.replaceAtomByAtom(molecule, atom, newAtom);
}
}
}
}
private void processBondsBlock(int lineCount, IAtomContainer container) throws IOException {
for (int i = 0; i < lineCount; i++) {
String line = input.readLine();
int atom1 = Integer.parseInt(line.substring(10, 13).trim()) - 1;
int atom2 = Integer.parseInt(line.substring(16, 19).trim()) - 1;
if (container.getBond(container.getAtom(atom1), container.getAtom(atom2)) == null) {
IBond bond =
container.getBuilder().newBond(container.getAtom(atom1), container.getAtom(atom2));
int order = Integer.parseInt(line.substring(23).trim());
bond.setOrder(BondManipulator.createBondOrder((double) order));
container.addBond(bond);
} // else: bond already present; CTX store the bonds twice
}
}
@Test
public void testNNMolecule_IAtomContainer() {
IAtomContainer acetone = new org.openscience.cdk.AtomContainer();
IAtom c1 = acetone.getBuilder().newAtom("C");
IAtom c2 = acetone.getBuilder().newAtom("C");
IAtom o = acetone.getBuilder().newAtom("O");
IAtom c3 = acetone.getBuilder().newAtom("C");
acetone.addAtom(c1);
acetone.addAtom(c2);
acetone.addAtom(c3);
acetone.addAtom(o);
IBond b1 = acetone.getBuilder().newBond(c1, c2, IBond.Order.SINGLE);
IBond b2 = acetone.getBuilder().newBond(c1, o, IBond.Order.DOUBLE);
IBond b3 = acetone.getBuilder().newBond(c1, c3, IBond.Order.SINGLE);
acetone.addBond(b1);
acetone.addBond(b2);
acetone.addBond(b3);
IMolecule m = new NNMolecule(acetone);
Assert.assertNotNull(m);
Assert.assertEquals(4, m.getAtomCount());
Assert.assertEquals(3, m.getBondCount());
}
/**
* Method that actually does the work of convert the atomContainer to IMolecularFormula given a
* IMolecularFormula.
*
* <p>The hydrogens must be implicit.
*
* @param atomContainer IAtomContainer object
* @param formula IMolecularFormula molecularFormula to put the new Isotopes
* @return the filled AtomContainer
* @see #getMolecularFormula(IAtomContainer)
*/
public static IMolecularFormula getMolecularFormula(
IAtomContainer atomContainer, IMolecularFormula formula) {
int charge = 0;
IAtom hAtom = null;
for (IAtom iAtom : atomContainer.atoms()) {
formula.addIsotope(iAtom);
if (iAtom.getFormalCharge() != null) charge += iAtom.getFormalCharge();
if (iAtom.getImplicitHydrogenCount() != null && (iAtom.getImplicitHydrogenCount() > 0)) {
if (hAtom == null) hAtom = atomContainer.getBuilder().newInstance(IAtom.class, "H");
formula.addIsotope(hAtom, iAtom.getImplicitHydrogenCount());
}
}
formula.setCharge(charge);
return formula;
}
/**
* Helper method to generate 2d coordinates when JChempaint loads a molecule
* without 2D coordinates. Typically happens for SMILES strings.
*
* @param molecules
* @throws Exception
*/
private static void generate2dCoordinates(
final List<IAtomContainer> molecules) {
final StructureDiagramGenerator sdg = new StructureDiagramGenerator();
for (int atIdx = 0; atIdx < molecules.size(); atIdx++) {
final IAtomContainer mol = molecules.get(atIdx);
sdg.setMolecule(mol.getBuilder().newInstance(IAtomContainer.class,
mol));
try {
sdg.generateCoordinates();
} catch (final Exception e) {
e.printStackTrace();
}
final IAtomContainer ac = sdg.getMolecule();
for (int i = 0; i < ac.getAtomCount(); i++) {
mol.getAtom(i).setPoint2d(ac.getAtom(i).getPoint2d());
}
}
}
/**
* Returns the number of double bond equivalents in this molecule.
*
* @param formula The IMolecularFormula to calculate
* @return The number of DBEs
* @throws CDKException if DBE cannot be be evaluated
* @cdk.keyword DBE
* @cdk.keyword double bond equivalent
*/
public static double getDBE(IMolecularFormula formula) throws CDKException {
int valencies[] = new int[5];
IAtomContainer ac = getAtomContainer(formula);
AtomTypeFactory factory =
AtomTypeFactory.getInstance(
"org/openscience/cdk/config/data/structgen_atomtypes.xml", ac.getBuilder());
for (int f = 0; f < ac.getAtomCount(); f++) {
IAtomType[] types = factory.getAtomTypes(ac.getAtom(f).getSymbol());
if (types.length == 0)
throw new CDKException(
"Calculation of double bond equivalents not possible due to problems with element "
+ ac.getAtom(f).getSymbol());
// valencies[(int) (types[0].getBondOrderSum() + ac.getAtom(f).getFormalCharge())]++;
valencies[types[0].getBondOrderSum().intValue()]++;
}
return 1 + (valencies[4]) + (valencies[3] / 2) - (valencies[1] / 2);
}
/**
* Convert the input into a pcore molecule.
*
* @param input the compound being converted from
* @return pcore molecule
* @throws CDKException match failed
*/
private IAtomContainer getPharmacophoreMolecule(IAtomContainer input) throws CDKException {
// XXX: prepare query, to be moved
prepareInput(input);
IAtomContainer pharmacophoreMolecule =
input.getBuilder().newInstance(IAtomContainer.class, 0, 0, 0, 0);
final Set<String> matched = new HashSet<>();
final Set<PharmacophoreAtom> uniqueAtoms = new LinkedHashSet<>();
logger.debug("Converting [" + input.getProperty(CDKConstants.TITLE) + "] to a pcore molecule");
// lets loop over each pcore query atom
for (IAtom atom : pharmacophoreQuery.atoms()) {
final PharmacophoreQueryAtom qatom = (PharmacophoreQueryAtom) atom;
final String smarts = qatom.getSmarts();
// a pcore query might have multiple instances of a given pcore atom (say
// 2 hydrophobic groups separated by X unit). In such a case we want to find
// the atoms matching the pgroup SMARTS just once, rather than redoing the
// matching for each instance of the pcore query atom.
if (!matched.add(qatom.getSymbol())) continue;
// see if the smarts for this pcore query atom gets any matches
// in our query molecule. If so, then collect each set of
// matching atoms and for each set make a new pcore atom and
// add it to the pcore atom container object
int count = 0;
for (final IQueryAtomContainer query : qatom.getCompiledSmarts()) {
// create the lazy mappings iterator
final Mappings mappings = Pattern.findSubstructure(query).matchAll(input).uniqueAtoms();
for (final int[] mapping : mappings) {
uniqueAtoms.add(newPCoreAtom(input, qatom, smarts, mapping));
count++;
}
}
logger.debug("\tFound " + count + " unique matches for " + smarts);
}
pharmacophoreMolecule.setAtoms(uniqueAtoms.toArray(new IAtom[uniqueAtoms.size()]));
// now that we have added all the pcore atoms to the container
// we need to join all atoms with pcore bonds (i.e. distance constraints)
if (hasDistanceConstraints(pharmacophoreQuery)) {
int npatom = pharmacophoreMolecule.getAtomCount();
for (int i = 0; i < npatom - 1; i++) {
for (int j = i + 1; j < npatom; j++) {
PharmacophoreAtom atom1 = (PharmacophoreAtom) pharmacophoreMolecule.getAtom(i);
PharmacophoreAtom atom2 = (PharmacophoreAtom) pharmacophoreMolecule.getAtom(j);
PharmacophoreBond bond = new PharmacophoreBond(atom1, atom2);
pharmacophoreMolecule.addBond(bond);
}
}
}
// if we have angle constraints, generate only the valid
// possible angle relationships, rather than all possible
if (hasAngleConstraints(pharmacophoreQuery)) {
int nangleDefs = 0;
for (IBond bond : pharmacophoreQuery.bonds()) {
if (!(bond instanceof PharmacophoreQueryAngleBond)) continue;
IAtom startQAtom = bond.getAtom(0);
IAtom middleQAtom = bond.getAtom(1);
IAtom endQAtom = bond.getAtom(2);
// make a list of the patoms in the target that match
// each type of angle atom
List<IAtom> startl = new ArrayList<IAtom>();
List<IAtom> middlel = new ArrayList<IAtom>();
List<IAtom> endl = new ArrayList<IAtom>();
for (IAtom tatom : pharmacophoreMolecule.atoms()) {
if (tatom.getSymbol().equals(startQAtom.getSymbol())) startl.add(tatom);
if (tatom.getSymbol().equals(middleQAtom.getSymbol())) middlel.add(tatom);
if (tatom.getSymbol().equals(endQAtom.getSymbol())) endl.add(tatom);
}
// now we form the relevant angles, but we will
// have reversed repeats
List<IAtom[]> tmpl = new ArrayList<IAtom[]>();
for (IAtom middle : middlel) {
for (IAtom start : startl) {
if (middle.equals(start)) continue;
for (IAtom end : endl) {
if (start.equals(end) || middle.equals(end)) continue;
tmpl.add(new IAtom[] {start, middle, end});
}
}
}
// now clean up reversed repeats
List<IAtom[]> unique = new ArrayList<IAtom[]>();
for (int i = 0; i < tmpl.size(); i++) {
IAtom[] seq1 = tmpl.get(i);
boolean isRepeat = false;
for (int j = 0; j < unique.size(); j++) {
if (i == j) continue;
IAtom[] seq2 = unique.get(j);
if (seq1[1] == seq2[1] && seq1[0] == seq2[2] && seq1[2] == seq2[0]) {
isRepeat = true;
}
}
if (!isRepeat) unique.add(seq1);
}
// finally we can add the unique angle to the target
for (IAtom[] seq : unique) {
PharmacophoreAngleBond pbond =
new PharmacophoreAngleBond(
(PharmacophoreAtom) seq[0],
(PharmacophoreAtom) seq[1],
(PharmacophoreAtom) seq[2]);
pharmacophoreMolecule.addBond(pbond);
nangleDefs++;
}
}
logger.debug("Added " + nangleDefs + " defs to the target pcore molecule");
}
return pharmacophoreMolecule;
}
/**
* Method that actually does the work of convert the atomContainer to IMolecularFormula.
*
* <p>The hydrogens must be implicit.
*
* @param atomContainer IAtomContainer object
* @return a molecular formula object
* @see #getMolecularFormula(IAtomContainer,IMolecularFormula)
*/
public static IMolecularFormula getMolecularFormula(IAtomContainer atomContainer) {
IMolecularFormula formula = atomContainer.getBuilder().newInstance(IMolecularFormula.class);
return getMolecularFormula(atomContainer, formula);
}
/**
* Initiate process. It is needed to call the addExplicitHydrogensToSatisfyValency from the class
* tools.HydrogenAdder.
*
* @exception CDKException Description of the Exception
* @param reactants reactants of the reaction.
* @param agents agents of the reaction (Must be in this case null).
*/
@TestMethod("testInitiate_IAtomContainerSet_IAtomContainerSet")
public IReactionSet initiate(IAtomContainerSet reactants, IAtomContainerSet agents)
throws CDKException {
logger.debug("initiate reaction: RearrangementRadicalReaction");
if (reactants.getAtomContainerCount() != 1) {
throw new CDKException("RearrangementRadicalReaction only expects one reactant");
}
if (agents != null) {
throw new CDKException("RearrangementRadicalReaction don't expects agents");
}
IReactionSet setOfReactions =
DefaultChemObjectBuilder.getInstance().newInstance(IReactionSet.class);
IAtomContainer reactant = reactants.getAtomContainer(0);
/* if the parameter hasActiveCenter is not fixed yet, set the active centers*/
IParameterReact ipr = super.getParameterClass(SetReactionCenter.class);
if (ipr != null && !ipr.isSetParameter()) setActiveCenters(reactant);
Iterator<IAtom> atoms = reactants.getAtomContainer(0).atoms().iterator();
while (atoms.hasNext()) {
IAtom atomi = atoms.next();
if (atomi.getFlag(CDKConstants.REACTIVE_CENTER)
&& reactant.getConnectedSingleElectronsCount(atomi) == 1) {
Iterator<IBond> bondis = reactant.getConnectedBondsList(atomi).iterator();
while (bondis.hasNext()) {
IBond bondi = bondis.next();
if (bondi.getFlag(CDKConstants.REACTIVE_CENTER)
&& bondi.getOrder() == IBond.Order.SINGLE) {
IAtom atomj = bondi.getConnectedAtom(atomi);
if (atomi.getFlag(CDKConstants.REACTIVE_CENTER)
&& (atomj.getFormalCharge() == CDKConstants.UNSET ? 0 : atomj.getFormalCharge())
== 0
&& reactant.getConnectedSingleElectronsCount(atomj) == 0) {
Iterator<IBond> bondjs = reactant.getConnectedBondsList(atomj).iterator();
while (bondjs.hasNext()) {
IBond bondj = bondjs.next();
if (bondj.equals(bondi)) continue;
if (bondj.getFlag(CDKConstants.REACTIVE_CENTER)
&& bondj.getOrder() == IBond.Order.DOUBLE) {
IAtom atomk = bondj.getConnectedAtom(atomj);
if (atomk.getFlag(CDKConstants.REACTIVE_CENTER)
&& (atomk.getFormalCharge() == CDKConstants.UNSET
? 0
: atomk.getFormalCharge())
== 0
&& reactant.getConnectedSingleElectronsCount(atomk) == 0) {
ArrayList<IAtom> atomList = new ArrayList<IAtom>();
atomList.add(atomi);
atomList.add(atomj);
atomList.add(atomk);
ArrayList<IBond> bondList = new ArrayList<IBond>();
bondList.add(bondi);
bondList.add(bondj);
IAtomContainerSet moleculeSet =
reactant.getBuilder().newInstance(IAtomContainerSet.class);
moleculeSet.addAtomContainer(reactant);
IReaction reaction = mechanism.initiate(moleculeSet, atomList, bondList);
if (reaction == null) continue;
else setOfReactions.addReaction(reaction);
}
}
}
}
}
}
}
}
return setOfReactions;
}
private static IAtomContainer change(
IAtomContainer ac,
int x1,
int y1,
int x2,
int y2,
double b11,
double b12,
double b21,
double b22) {
IAtom ax1 = null, ax2 = null, ay1 = null, ay2 = null;
IBond b1 = null, b2 = null, b3 = null, b4 = null;
try {
ax1 = ac.getAtom(x1);
ax2 = ac.getAtom(x2);
ay1 = ac.getAtom(y1);
ay2 = ac.getAtom(y2);
} catch (Exception exc) {
logger.debug(exc);
}
b1 = ac.getBond(ax1, ay1);
b2 = ac.getBond(ax1, ay2);
b3 = ac.getBond(ax2, ay1);
b4 = ac.getBond(ax2, ay2);
if (b11 > 0) {
if (b1 == null) {
logger.debug("no bond " + x1 + "-" + y1 + ". Adding it with order " + b11);
b1 = ac.getBuilder().newBond(ax1, ay1, BondManipulator.createBondOrder(b11));
ac.addBond(b1);
} else {
b1.setOrder(BondManipulator.createBondOrder(b11));
logger.debug("Setting bondorder for " + x1 + "-" + y1 + " to " + b11);
}
} else if (b1 != null) {
ac.removeBond(b1);
logger.debug("removing bond " + x1 + "-" + y1);
}
if (b12 > 0) {
if (b2 == null) {
logger.debug("no bond " + x1 + "-" + y2 + ". Adding it with order " + b12);
b2 = ac.getBuilder().newBond(ax1, ay2, BondManipulator.createBondOrder(b12));
ac.addBond(b2);
} else {
b2.setOrder(BondManipulator.createBondOrder(b12));
logger.debug("Setting bondorder for " + x1 + "-" + y2 + " to " + b12);
}
} else if (b2 != null) {
ac.removeBond(b2);
logger.debug("removing bond " + x1 + "-" + y2);
}
if (b21 > 0) {
if (b3 == null) {
logger.debug("no bond " + x2 + "-" + y1 + ". Adding it with order " + b21);
b3 = ac.getBuilder().newBond(ax2, ay1, BondManipulator.createBondOrder(b21));
ac.addBond(b3);
} else {
b3.setOrder(BondManipulator.createBondOrder(b21));
logger.debug("Setting bondorder for " + x2 + "-" + y1 + " to " + b21);
}
} else if (b3 != null) {
ac.removeBond(b3);
logger.debug("removing bond " + x2 + "-" + y1);
}
if (b22 > 0) {
if (b4 == null) {
logger.debug("no bond " + x2 + "-" + y2 + ". Adding it with order " + b22);
b4 = ac.getBuilder().newBond(ax2, ay2, BondManipulator.createBondOrder(b22));
ac.addBond(b4);
} else {
b4.setOrder(BondManipulator.createBondOrder(b22));
logger.debug("Setting bondorder for " + x2 + "-" + y2 + " to " + b22);
}
} else if (b4 != null) {
ac.removeBond(b4);
logger.debug("removing bond " + x2 + "-" + y2);
}
return ac;
}
/**
* Read an IAtomContainer from a file in MDL sd format
*
* @return The Molecule that was read from the MDL file.
*/
private IAtomContainer readAtomContainer(IAtomContainer molecule) throws CDKException {
logger.debug("Reading new molecule");
IAtomContainer outputContainer = null;
int linecount = 0;
int atoms = 0;
int bonds = 0;
int atom1 = 0;
int atom2 = 0;
int order = 0;
IBond.Stereo stereo = (IBond.Stereo) CDKConstants.UNSET;
int RGroupCounter = 1;
int Rnumber = 0;
String[] rGroup = null;
double x = 0.0;
double y = 0.0;
double z = 0.0;
double totalX = 0.0;
double totalY = 0.0;
double totalZ = 0.0;
String title = null;
String remark = null;
// int[][] conMat = new int[0][0];
// String help;
IAtom atom;
String line = "";
// A map to keep track of R# atoms so that RGP line can be parsed
Map<Integer, IPseudoAtom> rAtoms = new HashMap<Integer, IPseudoAtom>();
try {
IsotopeFactory isotopeFactory = Isotopes.getInstance();
logger.info("Reading header");
line = input.readLine();
linecount++;
if (line == null) {
return null;
}
logger.debug("Line " + linecount + ": " + line);
if (line.startsWith("$$$$")) {
logger.debug("File is empty, returning empty molecule");
return molecule;
}
if (line.length() > 0) {
title = line;
}
line = input.readLine();
linecount++;
logger.debug("Line " + linecount + ": " + line);
line = input.readLine();
linecount++;
logger.debug("Line " + linecount + ": " + line);
if (line.length() > 0) {
remark = line;
}
logger.info("Reading rest of file");
line = input.readLine();
linecount++;
logger.debug("Line " + linecount + ": " + line);
// if the line is empty we hav a problem - either a malformed
// molecule entry or just extra new lines at the end of the file
if (line.length() == 0) {
// read till the next $$$$ or EOF
while (true) {
line = input.readLine();
linecount++;
if (line == null) {
return null;
}
if (line.startsWith("$$$$")) {
return molecule; // an empty molecule
}
}
}
// check the CT block version
if (line.contains("V3000") || line.contains("v3000")) {
handleError("This file must be read with the MDLV3000Reader.");
} else if (!line.contains("V2000") && !line.contains("v2000")) {
handleError("This file must be read with the MDLReader.");
}
atoms = Integer.parseInt(line.substring(0, 3).trim());
List<IAtom> atomList = new ArrayList<IAtom>();
logger.debug("Atomcount: " + atoms);
bonds = Integer.parseInt(line.substring(3, 6).trim());
logger.debug("Bondcount: " + bonds);
List<IBond> bondList = new ArrayList<IBond>();
// used for applying the MDL valence model
int[] explicitValence = new int[atoms];
// read ATOM block
logger.info("Reading atom block");
atomsByLinePosition = new ArrayList<IAtom>();
atomsByLinePosition.add(null); // 0 is not a valid position
int atomBlockLineNumber = 0;
for (int f = 0; f < atoms; f++) {
line = input.readLine();
linecount++;
atomBlockLineNumber++;
Matcher trailingSpaceMatcher = TRAILING_SPACE.matcher(line);
if (trailingSpaceMatcher.find()) {
handleError(
"Trailing space found",
linecount,
trailingSpaceMatcher.start(),
trailingSpaceMatcher.end());
line = trailingSpaceMatcher.replaceAll("");
}
x = Double.parseDouble(line.substring(0, 10).trim());
y = Double.parseDouble(line.substring(10, 20).trim());
z = Double.parseDouble(line.substring(20, 30).trim());
// *all* values should be zero, not just the sum
totalX += Math.abs(x);
totalY += Math.abs(y);
totalZ += Math.abs(z);
logger.debug("Coordinates: " + x + "; " + y + "; " + z);
String element = line.substring(31, Math.min(line.length(), 34)).trim();
if (line.length() < 34) {
handleError(
"Element atom type does not follow V2000 format type should of length three"
+ " and padded with space if required",
linecount,
31,
34);
}
logger.debug("Atom type: ", element);
if (isotopeFactory.isElement(element)) {
atom = isotopeFactory.configure(molecule.getBuilder().newInstance(IAtom.class, element));
} else if ("A".equals(element)) {
atom = molecule.getBuilder().newInstance(IPseudoAtom.class, element);
} else if ("Q".equals(element)) {
atom = molecule.getBuilder().newInstance(IPseudoAtom.class, element);
} else if ("*".equals(element)) {
atom = molecule.getBuilder().newInstance(IPseudoAtom.class, element);
} else if ("LP".equals(element)) {
atom = molecule.getBuilder().newInstance(IPseudoAtom.class, element);
} else if ("L".equals(element)) {
atom = molecule.getBuilder().newInstance(IPseudoAtom.class, element);
} else if (element.equals("R") || (element.length() > 0 && element.charAt(0) == 'R')) {
logger.debug("Atom ", element, " is not an regular element. Creating a PseudoAtom.");
// check if the element is R
rGroup = element.split("^R");
atom = null;
if (rGroup.length > 1) {
try {
Rnumber = Integer.valueOf(rGroup[(rGroup.length - 1)]);
RGroupCounter = Rnumber;
element = "R" + Rnumber;
atom = molecule.getBuilder().newInstance(IPseudoAtom.class, element);
} catch (Exception ex) {
// This happens for atoms labeled "R#".
// The Rnumber may be set later on, using RGP line
atom = molecule.getBuilder().newInstance(IPseudoAtom.class, "R");
rAtoms.put(atomBlockLineNumber, (IPseudoAtom) atom);
}
} else {
atom = molecule.getBuilder().newInstance(IPseudoAtom.class, element);
}
} else {
handleError(
"Invalid element type. Must be an existing " + "element, or one in: A, Q, L, LP, *.",
linecount,
32,
35);
atom = molecule.getBuilder().newInstance(IPseudoAtom.class, element);
atom.setSymbol(element);
}
// store as 3D for now, convert to 2D (if totalZ == 0.0) later
atom.setPoint3d(new Point3d(x, y, z));
// parse further fields
if (line.length() >= 36) {
String massDiffString = line.substring(34, 36).trim();
logger.debug("Mass difference: ", massDiffString);
if (!(atom instanceof IPseudoAtom)) {
try {
int massDiff = Integer.parseInt(massDiffString);
if (massDiff != 0) {
IIsotope major = Isotopes.getInstance().getMajorIsotope(element);
atom.setMassNumber(major.getMassNumber() + massDiff);
}
} catch (Exception exception) {
handleError("Could not parse mass difference field.", linecount, 35, 37, exception);
}
} else {
logger.error("Cannot set mass difference for a non-element!");
}
} else {
handleError("Mass difference is missing", linecount, 34, 36);
}
// set the stereo partiy
Integer parity = line.length() > 41 ? Character.digit(line.charAt(41), 10) : 0;
atom.setStereoParity(parity);
if (line.length() >= 51) {
String valenceString = removeNonDigits(line.substring(48, 51));
logger.debug("Valence: ", valenceString);
if (!(atom instanceof IPseudoAtom)) {
try {
int valence = Integer.parseInt(valenceString);
if (valence != 0) {
// 15 is defined as 0 in mol files
if (valence == 15) atom.setValency(0);
else atom.setValency(valence);
}
} catch (Exception exception) {
handleError(
"Could not parse valence information field", linecount, 49, 52, exception);
}
} else {
logger.error("Cannot set valence information for a non-element!");
}
}
if (line.length() >= 39) {
String chargeCodeString = line.substring(36, 39).trim();
logger.debug("Atom charge code: ", chargeCodeString);
int chargeCode = Integer.parseInt(chargeCodeString);
if (chargeCode == 0) {
// uncharged species
} else if (chargeCode == 1) {
atom.setFormalCharge(+3);
} else if (chargeCode == 2) {
atom.setFormalCharge(+2);
} else if (chargeCode == 3) {
atom.setFormalCharge(+1);
} else if (chargeCode == 4) {
} else if (chargeCode == 5) {
atom.setFormalCharge(-1);
} else if (chargeCode == 6) {
atom.setFormalCharge(-2);
} else if (chargeCode == 7) {
atom.setFormalCharge(-3);
}
} else {
handleError("Atom charge is missing", linecount, 36, 39);
}
try {
// read the mmm field as position 61-63
String reactionAtomIDString = line.substring(60, 63).trim();
logger.debug("Parsing mapping id: ", reactionAtomIDString);
try {
int reactionAtomID = Integer.parseInt(reactionAtomIDString);
if (reactionAtomID != 0) {
atom.setProperty(CDKConstants.ATOM_ATOM_MAPPING, reactionAtomID);
}
} catch (Exception exception) {
logger.error("Mapping number ", reactionAtomIDString, " is not an integer.");
logger.debug(exception);
}
} catch (Exception exception) {
// older mol files don't have all these fields...
logger.warn("A few fields are missing. Older MDL MOL file?");
}
// shk3: This reads shifts from after the molecule. I don't think this is an official
// format, but I saw it frequently 80=>78 for alk
if (line.length() >= 78) {
double shift = Double.parseDouble(line.substring(69, 80).trim());
atom.setProperty("first shift", shift);
}
if (line.length() >= 87) {
double shift = Double.parseDouble(line.substring(79, 87).trim());
atom.setProperty("second shift", shift);
}
atomList.add(atom);
atomsByLinePosition.add(atom);
}
// convert to 2D, if totalZ == 0
if (totalX == 0.0 && totalY == 0.0 && totalZ == 0.0) {
logger.info("All coordinates are 0.0");
if (atomList.size() == 1) {
atomList.get(0).setPoint2d(new Point2d(x, y));
} else {
for (IAtom atomToUpdate : atomList) {
atomToUpdate.setPoint3d(null);
}
}
} else if (totalZ == 0.0 && !forceReadAs3DCoords.isSet()) {
logger.info("Total 3D Z is 0.0, interpreting it as a 2D structure");
for (IAtom atomToUpdate : atomList) {
Point3d p3d = atomToUpdate.getPoint3d();
if (p3d != null) {
atomToUpdate.setPoint2d(new Point2d(p3d.x, p3d.y));
atomToUpdate.setPoint3d(null);
}
}
}
// read BOND block
logger.info("Reading bond block");
int queryBondCount = 0;
for (int f = 0; f < bonds; f++) {
line = input.readLine();
linecount++;
atom1 = Integer.parseInt(line.substring(0, 3).trim());
atom2 = Integer.parseInt(line.substring(3, 6).trim());
order = Integer.parseInt(line.substring(6, 9).trim());
if (line.length() >= 12) {
int mdlStereo =
line.length() > 12
? Integer.parseInt(line.substring(9, 12).trim())
: Integer.parseInt(line.substring(9).trim());
if (mdlStereo == 1) {
// MDL up bond
stereo = IBond.Stereo.UP;
} else if (mdlStereo == 6) {
// MDL down bond
stereo = IBond.Stereo.DOWN;
} else if (mdlStereo == 0) {
if (order == 2) {
// double bond stereo defined by coordinates
stereo = IBond.Stereo.E_Z_BY_COORDINATES;
} else {
// bond has no stereochemistry
stereo = IBond.Stereo.NONE;
}
} else if (mdlStereo == 3 && order == 2) {
// unknown E/Z stereochemistry
stereo = IBond.Stereo.E_OR_Z;
} else if (mdlStereo == 4) {
// MDL bond undefined
stereo = IBond.Stereo.UP_OR_DOWN;
}
} else {
handleError("Missing expected stereo field at line: ", linecount, 10, 12);
}
if (logger.isDebugEnabled()) {
logger.debug("Bond: " + atom1 + " - " + atom2 + "; order " + order);
}
// interpret CTfile's special bond orders
IAtom a1 = atomList.get(atom1 - 1);
IAtom a2 = atomList.get(atom2 - 1);
IBond newBond = null;
if (order >= 1 && order <= 3) {
IBond.Order cdkOrder = IBond.Order.SINGLE;
if (order == 2) cdkOrder = IBond.Order.DOUBLE;
if (order == 3) cdkOrder = IBond.Order.TRIPLE;
if (stereo != null) {
newBond = molecule.getBuilder().newInstance(IBond.class, a1, a2, cdkOrder, stereo);
} else {
newBond = molecule.getBuilder().newInstance(IBond.class, a1, a2, cdkOrder);
}
} else if (order == 4) {
// aromatic bond
if (stereo != null) {
newBond =
molecule.getBuilder().newInstance(IBond.class, a1, a2, IBond.Order.UNSET, stereo);
} else {
newBond = molecule.getBuilder().newInstance(IBond.class, a1, a2, IBond.Order.UNSET);
}
// mark both atoms and the bond as aromatic and raise the SINGLE_OR_DOUBLE-flag
newBond.setFlag(CDKConstants.SINGLE_OR_DOUBLE, true);
newBond.setFlag(CDKConstants.ISAROMATIC, true);
a1.setFlag(CDKConstants.ISAROMATIC, true);
a2.setFlag(CDKConstants.ISAROMATIC, true);
} else {
queryBondCount++;
newBond = new CTFileQueryBond(molecule.getBuilder());
IAtom[] bondAtoms = {a1, a2};
newBond.setAtoms(bondAtoms);
newBond.setOrder(null);
CTFileQueryBond.Type queryBondType = null;
switch (order) {
case 5:
queryBondType = CTFileQueryBond.Type.SINGLE_OR_DOUBLE;
break;
case 6:
queryBondType = CTFileQueryBond.Type.SINGLE_OR_AROMATIC;
break;
case 7:
queryBondType = CTFileQueryBond.Type.DOUBLE_OR_AROMATIC;
break;
case 8:
queryBondType = CTFileQueryBond.Type.ANY;
break;
}
((CTFileQueryBond) newBond).setType(queryBondType);
newBond.setStereo(stereo);
}
bondList.add((newBond));
// add the bond order to the explicit valence for each atom
if (newBond.getOrder() != null && newBond.getOrder() != IBond.Order.UNSET) {
explicitValence[atom1 - 1] += newBond.getOrder().numeric();
explicitValence[atom2 - 1] += newBond.getOrder().numeric();
} else {
explicitValence[atom1 - 1] = Integer.MIN_VALUE;
explicitValence[atom2 - 1] = Integer.MIN_VALUE;
}
}
if (queryBondCount == 0) outputContainer = molecule;
else {
outputContainer = new QueryAtomContainer(molecule.getBuilder());
}
outputContainer.setProperty(CDKConstants.TITLE, title);
outputContainer.setProperty(CDKConstants.REMARK, remark);
for (IAtom at : atomList) {
outputContainer.addAtom(at);
}
for (IBond bnd : bondList) {
outputContainer.addBond(bnd);
}
// read PROPERTY block
logger.info("Reading property block");
while (true) {
line = input.readLine();
linecount++;
if (line == null) {
handleError("The expected property block is missing!", linecount, 0, 0);
}
if (line.startsWith("M END")) break;
boolean lineRead = false;
if (line.startsWith("M CHG")) {
// FIXME: if this is encountered for the first time, all
// atom charges should be set to zero first!
int infoCount = Integer.parseInt(line.substring(6, 9).trim());
StringTokenizer st = new StringTokenizer(line.substring(9));
for (int i = 1; i <= infoCount; i++) {
String token = st.nextToken();
int atomNumber = Integer.parseInt(token.trim());
token = st.nextToken();
int charge = Integer.parseInt(token.trim());
outputContainer.getAtom(atomNumber - 1).setFormalCharge(charge);
}
} else if (line.matches("A\\s{1,4}\\d+")) {
// Reads the pseudo atom property from the mol file
// The atom number of the to replaced atom
int aliasAtomNumber =
Integer.parseInt(line.replaceFirst("A\\s{1,4}", "")) - RGroupCounter;
line = input.readLine();
linecount++;
String[] aliasArray = line.split("\\\\");
// name of the alias atom like R1 or R2 etc.
String alias = "";
for (int i = 0; i < aliasArray.length; i++) {
alias += aliasArray[i];
}
IAtom aliasAtom = outputContainer.getAtom(aliasAtomNumber);
// skip if already a pseudoatom
if (aliasAtom instanceof IPseudoAtom) {
((IPseudoAtom) aliasAtom).setLabel(alias);
continue;
}
IAtom newPseudoAtom = molecule.getBuilder().newInstance(IPseudoAtom.class, alias);
if (aliasAtom.getPoint2d() != null) {
newPseudoAtom.setPoint2d(aliasAtom.getPoint2d());
}
if (aliasAtom.getPoint3d() != null) {
newPseudoAtom.setPoint3d(aliasAtom.getPoint3d());
}
outputContainer.addAtom(newPseudoAtom);
List<IBond> bondsOfAliasAtom = outputContainer.getConnectedBondsList(aliasAtom);
for (int i = 0; i < bondsOfAliasAtom.size(); i++) {
IBond bondOfAliasAtom = bondsOfAliasAtom.get(i);
IAtom connectedToAliasAtom = bondOfAliasAtom.getConnectedAtom(aliasAtom);
IBond newBond = bondOfAliasAtom.getBuilder().newInstance(IBond.class);
newBond.setAtoms(new IAtom[] {connectedToAliasAtom, newPseudoAtom});
newBond.setOrder(bondOfAliasAtom.getOrder());
outputContainer.addBond(newBond);
outputContainer.removeBond(aliasAtom, connectedToAliasAtom);
}
outputContainer.removeAtom(aliasAtom);
RGroupCounter++;
} else if (line.startsWith("M ISO")) {
try {
String countString = line.substring(6, 10).trim();
int infoCount = Integer.parseInt(countString);
StringTokenizer st = new StringTokenizer(line.substring(10));
for (int i = 1; i <= infoCount; i++) {
int atomNumber = Integer.parseInt(st.nextToken().trim());
int absMass = Integer.parseInt(st.nextToken().trim());
if (absMass != 0) {
IAtom isotope = outputContainer.getAtom(atomNumber - 1);
isotope.setMassNumber(absMass);
}
}
} catch (NumberFormatException exception) {
String error =
"Error ("
+ exception.getMessage()
+ ") while parsing line "
+ linecount
+ ": "
+ line
+ " in property block.";
logger.error(error);
handleError(
"NumberFormatException in isotope information.", linecount, 7, 11, exception);
}
} else if (line.startsWith("M RAD")) {
try {
String countString = line.substring(6, 9).trim();
int infoCount = Integer.parseInt(countString);
StringTokenizer st = new StringTokenizer(line.substring(9));
for (int i = 1; i <= infoCount; i++) {
int atomNumber = Integer.parseInt(st.nextToken().trim());
int spinMultiplicity = Integer.parseInt(st.nextToken().trim());
MDLV2000Writer.SPIN_MULTIPLICITY spin = MDLV2000Writer.SPIN_MULTIPLICITY.NONE;
if (spinMultiplicity > 0) {
IAtom radical = outputContainer.getAtom(atomNumber - 1);
switch (spinMultiplicity) {
case 1:
spin = MDLV2000Writer.SPIN_MULTIPLICITY.DOUBLET;
break;
case 2:
spin = MDLV2000Writer.SPIN_MULTIPLICITY.SINGLET;
break;
case 3:
spin = MDLV2000Writer.SPIN_MULTIPLICITY.TRIPLET;
break;
default:
logger.debug("Invalid spin multiplicity found: " + spinMultiplicity);
break;
}
for (int j = 0; j < spin.getSingleElectrons(); j++) {
outputContainer.addSingleElectron(
molecule.getBuilder().newInstance(ISingleElectron.class, radical));
}
}
}
} catch (NumberFormatException exception) {
String error =
"Error ("
+ exception.getMessage()
+ ") while parsing line "
+ linecount
+ ": "
+ line
+ " in property block.";
logger.error(error);
handleError(
"NumberFormatException in radical information", linecount, 7, 10, exception);
}
} else if (line.startsWith("G ")) {
try {
String atomNumberString = line.substring(3, 6).trim();
int atomNumber = Integer.parseInt(atomNumberString);
// String whatIsThisString = line.substring(6,9).trim();
String atomName = input.readLine();
// convert Atom into a PseudoAtom
IAtom prevAtom = outputContainer.getAtom(atomNumber - 1);
IPseudoAtom pseudoAtom = molecule.getBuilder().newInstance(IPseudoAtom.class, atomName);
if (prevAtom.getPoint2d() != null) {
pseudoAtom.setPoint2d(prevAtom.getPoint2d());
}
if (prevAtom.getPoint3d() != null) {
pseudoAtom.setPoint3d(prevAtom.getPoint3d());
}
AtomContainerManipulator.replaceAtomByAtom(molecule, prevAtom, pseudoAtom);
} catch (NumberFormatException exception) {
String error =
"Error ("
+ exception.toString()
+ ") while parsing line "
+ linecount
+ ": "
+ line
+ " in property block.";
logger.error(error);
handleError("NumberFormatException in group information", linecount, 4, 7, exception);
}
} else if (line.startsWith("M RGP")) {
StringTokenizer st = new StringTokenizer(line);
// Ignore first 3 tokens (overhead).
st.nextToken();
st.nextToken();
st.nextToken();
// Process the R group numbers as defined in RGP line.
while (st.hasMoreTokens()) {
Integer position = new Integer(st.nextToken());
Rnumber = new Integer(st.nextToken());
IPseudoAtom pseudoAtom = rAtoms.get(position);
if (pseudoAtom != null) {
pseudoAtom.setLabel("R" + Rnumber);
}
}
}
if (line.startsWith("V ")) {
Integer atomNumber = new Integer(line.substring(3, 6).trim());
IAtom atomWithComment = outputContainer.getAtom(atomNumber - 1);
atomWithComment.setProperty(CDKConstants.COMMENT, line.substring(7));
}
if (!lineRead) {
logger.warn("Skipping line in property block: ", line);
}
}
if (interpretHydrogenIsotopes.isSet()) {
fixHydrogenIsotopes(molecule, isotopeFactory);
}
// note: apply the valence model last so that all fixes (i.e. hydrogen
// isotopes) are in place
for (int i = 0; i < atoms; i++) {
applyMDLValenceModel(outputContainer.getAtom(i), explicitValence[i]);
}
} catch (CDKException exception) {
String error =
"Error while parsing line " + linecount + ": " + line + " -> " + exception.getMessage();
logger.error(error);
logger.debug(exception);
throw exception;
} catch (Exception exception) {
exception.printStackTrace();
String error =
"Error while parsing line " + linecount + ": " + line + " -> " + exception.getMessage();
logger.error(error);
logger.debug(exception);
handleError("Error while parsing line: " + line, linecount, 0, 0, exception);
}
return outputContainer;
}
public String perceiveSybylAtomTypes(IMolecule mol)
throws InvocationTargetException {
ICDKMolecule cdkmol;
try {
cdkmol = cdk.asCDKMolecule(mol);
}
catch (BioclipseException e) {
System.out.println("Error converting cdk10 to cdk");
e.printStackTrace();
throw new InvocationTargetException(e);
}
IAtomContainer ac = cdkmol.getAtomContainer();
CDKAtomTypeMatcher cdkMatcher
= CDKAtomTypeMatcher.getInstance(ac.getBuilder());
AtomTypeMapper mapper
= AtomTypeMapper.getInstance(
"org/openscience/cdk/dict/data/cdk-sybyl-mappings.owl" );
IAtomType[] sybylTypes = new IAtomType[ac.getAtomCount()];
int atomCounter = 0;
int a=0;
for (IAtom atom : ac.atoms()) {
IAtomType type;
try {
type = cdkMatcher.findMatchingAtomType(ac, atom);
}
catch (CDKException e) {
type = null;
}
if (type==null) {
// logger.debug("AT null for atom: " + atom);
type = atom.getBuilder().newAtomType(atom.getSymbol());
type.setAtomTypeName("X");
}
AtomTypeManipulator.configure(atom, type);
a++;
}
try {
CDKHueckelAromaticityDetector.detectAromaticity(ac);
// System.out.println("Arom: "
// + CDKHueckelAromaticityDetector.detectAromaticity(ac) );
}
catch (CDKException e) {
logger.debug("Failed to perceive aromaticity: " + e.getMessage());
}
for (IAtom atom : ac.atoms()) {
String mappedType = mapper.mapAtomType(atom.getAtomTypeName());
if ("C.2".equals(mappedType)
&& atom.getFlag(CDKConstants.ISAROMATIC)) {
mappedType = "C.ar";
}
else if ("N.pl3".equals(mappedType)
&& atom.getFlag(CDKConstants.ISAROMATIC)) {
mappedType = "N.ar";
}
try {
sybylTypes[atomCounter] = factory.getAtomType(mappedType);
}
catch (NoSuchAtomTypeException e) {
// yes, setting null's here is important
sybylTypes[atomCounter] = null;
}
atomCounter++;
}
StringBuffer result = new StringBuffer();
// now that full perception is finished, we can set atom type names:
for (int i = 0; i < sybylTypes.length; i++) {
if (sybylTypes[i] != null) {
ac.getAtom(i).setAtomTypeName(sybylTypes[i].getAtomTypeName());
}
else {
ac.getAtom(i).setAtomTypeName("X");
}
result.append(i).append(':').append(ac.getAtom(i).getAtomTypeName())
/*.append("\n")*/;
}
return result.toString();
}
/** A unit test for JUnit */
@Test
public void testCisResorcinol() throws Exception {
HydrogenPlacer hydrogenPlacer = new HydrogenPlacer();
IAtomContainer mol1 = new AtomContainer();
SmilesGenerator sg = new SmilesGenerator();
mol1.addAtom(new Atom("O", new Point2d(3, 1)));
// 1
mol1.addAtom(new Atom("H", new Point2d(2, 0)));
// 2
mol1.addAtom(new Atom("C", new Point2d(2, 1)));
// 3
mol1.addAtom(new Atom("C", new Point2d(1, 1)));
// 4
mol1.addAtom(new Atom("C", new Point2d(1, 4)));
// 5
mol1.addAtom(new Atom("C", new Point2d(1, 5)));
// 6
mol1.addAtom(new Atom("C", new Point2d(1, 2)));
// 7
mol1.addAtom(new Atom("C", new Point2d(2, 2)));
// 1
mol1.addAtom(new Atom("O", new Point2d(3, 2)));
// 2
mol1.addAtom(new Atom("H", new Point2d(2, 3)));
// 3
mol1.addBond(0, 2, IBond.Order.SINGLE, IBond.Stereo.DOWN);
// 1
mol1.addBond(1, 2, IBond.Order.SINGLE, IBond.Stereo.UP);
// 2
mol1.addBond(2, 3, IBond.Order.SINGLE);
// 3
mol1.addBond(3, 4, IBond.Order.SINGLE);
// 4
mol1.addBond(4, 5, IBond.Order.SINGLE);
// 5
mol1.addBond(5, 6, IBond.Order.SINGLE);
// 6
mol1.addBond(6, 7, IBond.Order.SINGLE);
// 3
mol1.addBond(7, 8, IBond.Order.SINGLE, IBond.Stereo.UP);
// 4
mol1.addBond(7, 9, IBond.Order.SINGLE, IBond.Stereo.DOWN);
// 5
mol1.addBond(7, 2, IBond.Order.SINGLE);
// 6
try {
addExplicitHydrogens(mol1);
hydrogenPlacer.placeHydrogens2D(mol1, 1.0);
IsotopeFactory ifac = IsotopeFactory.getInstance(mol1.getBuilder());
ifac.configureAtoms(mol1);
} catch (IOException ex) {
} catch (ClassNotFoundException ex) {
}
String smiles1 = null;
if (standAlone) {
display(mol1);
}
try {
smiles1 = sg.createSMILES(mol1, true, new boolean[mol1.getBondCount()]);
} catch (Exception exc) {
System.out.println(exc);
if (!standAlone) {
Assert.fail();
}
}
if (standAlone) {
System.err.println("SMILES 1: " + smiles1);
}
Assert.assertNotNull(smiles1);
Assert.assertEquals(
"[H]O[C@]1(C([H])([H])C([H])([H])C([H])([H])C([H])([H])[C@]1(O[H])([H]))([H])", smiles1);
mol1 = AtomContainerManipulator.removeHydrogens(mol1);
try {
smiles1 = sg.createSMILES(mol1);
} catch (Exception exc) {
System.out.println(exc);
if (!standAlone) {
Assert.fail();
}
}
if (standAlone) {
System.err.println("SMILES 1: " + smiles1);
}
Assert.assertNotNull(smiles1);
Assert.assertEquals("OC1CCCCC1(O)", smiles1);
}
/**
* Process spectra in the following way: Fragment each hit in KEGG starting with the lowest
* collision energy If hits were found they are used for the next measurement as input and the
* original molecule is not used.
*
* @param folder the folder
* @param file the file
*/
private void processSpectra(String folder, String file, int treeDepth) {
this.scoreMap = new HashMap<Integer, ArrayList<String>>();
if (blackList.contains(file)) {
completeLog += "Blacklisted Molecule: " + file;
histogramReal += "\n" + file + "\tBLACKLIST\t";
histogram += "\n" + file + "\tBLACKLIST\t";
histogramCompare += "\n" + file + "\tBLACKLIST\t";
return;
}
double exactMass = spectra.get(0).getExactMass();
// timing
long timeStart = System.currentTimeMillis();
HashMap<Double, Vector<String>> realScoreMap = new HashMap<Double, Vector<String>>();
int mode = spectra.get(0).getMode();
// instantiate and read in CID-KEGG.txt
String keggIdentifier = spectra.get(0).getKEGG();
completeLog +=
"\n\n============================================================================";
completeLog +=
"\nFile: " + spectra.get(0).getTrivialName() + " (KEGG Entry: " + keggIdentifier + ")";
// get candidates from kegg webservice...with with a given mzppm and mzabs
Vector<String> candidates =
KeggWebservice.KEGGbyMass(exactMass, (mzabs + PPMTool.getPPMDeviation(exactMass, mzppm)));
try {
GetKEGGIdentifier keggID = new GetKEGGIdentifier(folder + "CID-KEGG/CID-KEGG.txt");
// now find the corresponding KEGG entry
if (keggID.existInKEGG(spectra.get(0).getCID()))
keggIdentifier = keggID.getKEGGID(spectra.get(0).getCID());
} catch (IOException e) {
System.out.println(e.getMessage());
completeLog += "Error! Message: " + e.getMessage();
}
// comparison histogram
if (keggIdentifier.equals("none"))
histogramCompare += "\n" + file + "\t" + keggIdentifier + "\t\t" + exactMass;
else
histogramCompare +=
"\n" + file + "\t" + keggIdentifier + "\t" + candidates.size() + "\t" + exactMass;
// list of peaks which are contained in the real molecule
Vector<Peak> listOfPeaksCorresponding = new Vector<Peak>();
// list of peaks which are not contained in the real molecule
Vector<Peak> listOfPeaks = new Vector<Peak>();
// loop over all hits
for (int c = 0; c < candidates.size(); c++) {
this.foundHits = new Vector<IAtomContainer>();
// get mol file from kegg....remove "cpd:"
String candidate = KeggWebservice.KEGGgetMol(candidates.get(c).substring(4), this.keggPath);
IAtomContainer molecule = null;
try {
// write string to disk
new File(folder + file + "_Mol").mkdir();
File outFile = new File(folder + file + "_Mol/" + candidates.get(c).substring(4) + ".mol");
FileWriter out = new FileWriter(outFile);
out.write(candidate);
out.close();
// now fragment the retrieved molecule
molecule = Molfile.Read(folder + file + "_Mol/" + candidates.get(c).substring(4) + ".mol");
// now create a new folder to write the .mol files into
new File(folder + file).mkdir();
boolean status = new File(folder + file + "/" + candidates.get(c).substring(4)).mkdir();
} catch (IOException e) {
completeLog += "Error: " + candidates.get(c).substring(4) + " Message: " + e.getMessage();
} catch (CDKException e) {
completeLog += "Error: " + candidates.get(c).substring(4) + " Message: " + e.getMessage();
}
try {
// add hydrogens
CDKAtomTypeMatcher matcher = CDKAtomTypeMatcher.getInstance(molecule.getBuilder());
for (IAtom atom : molecule.atoms()) {
IAtomType type = matcher.findMatchingAtomType(molecule, atom);
AtomTypeManipulator.configure(atom, type);
}
CDKHydrogenAdder hAdder = CDKHydrogenAdder.getInstance(molecule.getBuilder());
hAdder.addImplicitHydrogens(molecule);
AtomContainerManipulator.convertImplicitToExplicitHydrogens(molecule);
}
// there is a bug in cdk?? error happens when there is a S or Ti in the molecule
catch (IllegalArgumentException e) {
completeLog += "Error: " + candidates.get(c).substring(4) + " Message: " + e.getMessage();
// skip it
continue;
} catch (CDKException e) {
completeLog += "Error: " + candidates.get(c).substring(4) + " Message: " + e.getMessage();
// skip it
continue;
}
// get peak list....it is reset if this is not the first run
Vector<Peak> peakList = spectra.get(0).getPeakList();
// create a new instance
Fragmenter fragmenter =
new Fragmenter(
(Vector<Peak>) peakList.clone(),
mzabs,
mzppm,
mode,
breakAromaticRings,
quickRedundancy,
false,
false);
double combinedScore = 0;
int combinedHits = 0;
int combinedPeakCount = 0;
String peaks = "";
combinedPeakCount = peakList.size();
int count = 0;
boolean first = true;
// loop over the different collision energies
for (WrapperSpectrum spectrum : spectra) {
List<IAtomContainer> l = null;
long start = System.currentTimeMillis();
try {
if (first) {
try {
l = fragmenter.generateFragmentsInMemory(molecule, true, treeDepth);
count++;
} catch (OutOfMemoryError e) {
System.out.println("OUT OF MEMORY ERROR! " + candidates.get(c).substring(4));
completeLog +=
"Error: " + candidates.get(c).substring(4) + " Message: " + e.getMessage();
continue;
}
first = false;
} else {
peakList = spectrum.getPeakList();
combinedPeakCount += peakList.size();
// set the current peak list...
fragmenter.setPeakList((Vector<Peak>) peakList.clone());
try {
// l = fragmenter.generateFragmentsHierarchical(foundHits, true);
System.err.println("REMOVED....no improvement!");
System.exit(1);
count++;
} catch (OutOfMemoryError e) {
System.out.println("OUT OF MEMORY ERROR! " + candidates.get(c).substring(4));
completeLog +=
"Error: " + candidates.get(c).substring(4) + " Message: " + e.getMessage();
continue;
}
}
long time = System.currentTimeMillis() - start;
System.out.println("Benötigte Zeit: " + time);
System.out.println("Got " + l.size() + " fragments");
System.out.println("Needed " + fragmenter.getNround() + " calls to generateFragments()");
new File(
folder
+ file
+ "/"
+ candidates.get(c).substring(4)
+ "/"
+ spectrum.getCollisionEnergy())
.mkdir();
for (int i = 0; i < l.size(); i++) {
try {
// write fragments to disk
FileWriter w =
new FileWriter(
new File(
folder
+ file
+ "/"
+ candidates.get(c).substring(4)
+ "/"
+ spectrum.getCollisionEnergy()
+ "/frag_"
+ i
+ ".mol"));
MDLWriter mw = new MDLWriter(w);
mw.write(new Molecule(l.get(i)));
mw.close();
} catch (IOException e) {
System.out.println("IOException: " + e.toString());
completeLog +=
"Error: " + candidates.get(c).substring(4) + " Message: " + e.getMessage();
} catch (Exception e) {
System.out.println(e.toString());
completeLog +=
"Error: " + candidates.get(c).substring(4) + " Message: " + e.getMessage();
}
}
// Draw molecule and its fragments
if (showDiagrams) Render.Draw(molecule, l, "Original Molecule");
if (pdf) {
// Create PDF Output
l.add(0, molecule);
DisplayStructure ds1 = null;
// create pdf subfolder
new File(folder + file + "/" + candidates.get(c) + "pdf/").mkdir();
ds1 =
new WritePDFTable(
true,
300,
300,
0.9,
2,
false,
false,
folder + file + "/" + candidates.get(c) + "pdf/");
for (int i = 0; i < l.size(); i++) {
// ds = new displayStructure(false, 300, 300, 0.9, false, "PDF",
// "/home/basti/WorkspaceJava/TandemMSLookup/fragmenter/Test");
assert ds1 != null;
ds1.drawStructure(l.get(i), i);
}
if (ds1 != null) ds1.close();
}
// now read the saved mol files
List<IAtomContainer> fragments =
Molfile.Readfolder(
folder
+ file
+ "/"
+ candidates.get(c).substring(4)
+ "/"
+ spectrum.getCollisionEnergy());
List<IAtomContainer> fragmentsList = new ArrayList<IAtomContainer>();
for (int i = 0; i < fragments.size(); i++) {
fragmentsList.add(fragments.get(i));
}
// get the original peak list again
// spectrum = new SpectrumWrapper(folder + file + ".txt");
peakList = (Vector<Peak>) spectrum.getPeakList().clone();
// clean up peak list
CleanUpPeakList cList = new CleanUpPeakList(peakList);
Vector<Peak> cleanedPeakList = cList.getCleanedPeakList(spectrum.getExactMass());
// now find corresponding fragments to the mass
AssignFragmentPeak afp = new AssignFragmentPeak();
afp.setHydrogenTest(hydrogenTest);
afp.assignFragmentPeak(
fragments, cleanedPeakList, mzabs, mzppm, spectrum.getMode(), false);
Vector<PeakMolPair> hits = afp.getHits();
Vector<PeakMolPair> hitsAll = afp.getAllHits();
// add them to the list of already found fragments....they were found in the previous run
// with a smaller collission energy
for (PeakMolPair peakMolPair : hitsAll) {
foundHits.add(peakMolPair.getFragment());
}
combinedHits += ((combinedHits + hits.size()) - combinedHits);
// Render.Draw(molecule, foundHits, "Found Hits");
// now "real" scoring
Scoring score = new Scoring(cleanedPeakList);
double currentScore = score.computeScoring(afp.getHitsMZ());
combinedScore += currentScore;
// check for last run and create the data for the log file
if (count == spectra.size()) {
// save score in hashmap...if there are several hits with the same score --> vector of
// strings
if (realScoreMap.containsKey(combinedScore)) {
Vector<String> tempList = realScoreMap.get(combinedScore);
tempList.add(candidates.get(c).substring(4));
realScoreMap.put(combinedScore, tempList);
} else {
Vector<String> temp = new Vector<String>();
temp.add(candidates.get(c).substring(4));
realScoreMap.put(combinedScore, temp);
}
// save score in hashmap...if there are several hits with the same
// amount of identified peaks --> ArrayList
if (scoreMap.containsKey(combinedHits)) {
ArrayList<String> tempList = scoreMap.get(combinedHits);
tempList.add(candidates.get(c).substring(4));
scoreMap.put(combinedHits, tempList);
} else {
ArrayList<String> temp = new ArrayList<String>();
temp.add(candidates.get(c).substring(4));
scoreMap.put(combinedHits, temp);
}
}
// get all the identified peaks
for (int i = 0; i < hits.size(); i++) {
peaks += hits.get(i).getPeak().getMass() + " ";
listOfPeaks.add(hits.get(i).getPeak());
if (keggIdentifier.equals(candidates.get(c).substring(4)))
listOfPeaksCorresponding.add(hits.get(i).getPeak());
}
List<IAtomContainer> hitsListTest = new ArrayList<IAtomContainer>();
for (int i = 0; i < hits.size(); i++) {
List<IAtomContainer> hitsList = new ArrayList<IAtomContainer>();
hitsList.add(AtomContainerManipulator.removeHydrogens(hits.get(i).getFragment()));
hitsListTest.add(hits.get(i).getFragment());
// Render.Highlight(AtomContainerManipulator.removeHydrogens(molecule), hitsList ,
// Double.toString(hits.get(i).getPeak()));
}
if (showDiagrams)
Render.Draw(molecule, hitsListTest, "Fragmente von: " + candidates.get(c));
} catch (CDKException e) {
System.out.println("CDK error!" + e.getMessage());
completeLog += "CDK Error! " + e.getMessage() + "File: " + candidates.get(c).substring(4);
} catch (FileNotFoundException e) {
System.out.println("File not found" + e.getMessage());
completeLog +=
"File not found error! " + e.getMessage() + "File: " + candidates.get(c).substring(4);
} catch (IOException e) {
System.out.println("IO error: " + e.getMessage());
completeLog += "IO Error! " + e.getMessage() + "File: " + candidates.get(c).substring(4);
} catch (Exception e) {
System.out.println("Error" + e.getMessage());
completeLog += "Error! " + e.getMessage() + "File: " + candidates.get(c).substring(4);
} catch (OutOfMemoryError e) {
System.out.println("Out of memory: " + e.getMessage() + "\n" + e.getStackTrace());
System.gc();
completeLog +=
"Out of memory! " + e.getMessage() + "File: " + candidates.get(c).substring(4);
}
}
// write things to log file
foundPeaks += combinedHits;
allPeaks += combinedPeakCount;
completeLog +=
"\nFile: "
+ candidates.get(c).substring(4)
+ "\t #Peaks: "
+ combinedPeakCount
+ "\t #Found: "
+ combinedHits;
completeLog += "\tPeaks: " + peaks;
}
// easy scoring
Integer[] keylist = new Integer[scoreMap.keySet().size()];
Object[] keys = scoreMap.keySet().toArray();
for (int i = 0; i < keys.length; i++) {
keylist[i] = Integer.parseInt(keys[i].toString());
}
Arrays.sort(keylist);
String scoreList = "";
int rank = 0;
for (int i = keylist.length - 1; i >= 0; i--) {
boolean check = false;
for (int j = 0; j < scoreMap.get(keylist[i]).size(); j++) {
scoreList += "\n" + keylist[i] + " - " + scoreMap.get(keylist[i]).get(j);
if (keggIdentifier.equals(scoreMap.get(keylist[i]).get(j))) {
check = true;
}
// worst case: count all which are better or have a equal position
rank++;
}
if (check) {
histogram += "\n" + file + "\t" + keggIdentifier + "\t" + rank + "\t" + exactMass;
}
}
if (keggIdentifier.equals("none")) {
histogram += "\n" + file + "\t" + keggIdentifier + "\t\t" + exactMass;
}
completeLog += "\n\n*****************Scoring*****************************";
completeLog += "Supposed to be: " + keggIdentifier;
completeLog += scoreList;
completeLog += "\n*****************************************************\n\n";
// easy scoring end
// real scoring
Double[] keysScore = new Double[realScoreMap.keySet().size()];
keysScore = realScoreMap.keySet().toArray(keysScore);
Arrays.sort(keysScore);
String scoreListReal = "";
rank = 0;
for (int i = keysScore.length - 1; i >= 0; i--) {
boolean check = false;
for (int j = 0; j < realScoreMap.get(keysScore[i]).size(); j++) {
scoreListReal += "\n" + keysScore[i] + " - " + realScoreMap.get(keysScore[i]).get(j);
if (keggIdentifier.compareTo(realScoreMap.get(keysScore[i]).get(j)) == 0) {
check = true;
}
// worst case: count all which are better or have a equal position
rank++;
}
if (check) {
histogramReal += "\n" + file + "\t" + keggIdentifier + "\t" + rank + "\t" + exactMass;
}
}
if (keggIdentifier.equals("none")) {
histogramReal += "\n" + file + "\t" + keggIdentifier + "\t\t" + exactMass;
}
// timing
long timeEnd = System.currentTimeMillis() - timeStart;
sumTime += timeEnd;
completeLog += "\n\n*****************Scoring(Real)*****************************";
completeLog += "Supposed to be: " + keggIdentifier;
completeLog += "\nTime: " + timeEnd;
completeLog += scoreListReal;
completeLog += "\n*****************************************************\n\n";
// write the data for peak histogram to log file
for (int i = 0; i < listOfPeaks.size(); i++) {
histogramPeaksAll += listOfPeaks.get(i) + "\n";
}
// filter the peaks which are contained in the all peaks list. (exclusive)
for (int i = 0; i < listOfPeaksCorresponding.size(); i++) {
for (int j = 0; j < listOfPeaks.size(); j++) {
Double valueA = listOfPeaks.get(j).getMass();
Double valueB = listOfPeaksCorresponding.get(i).getMass();
if (valueA.compareTo(valueB) == 0) {
listOfPeaks.remove(j);
}
}
}
for (int i = 0; i < listOfPeaks.size(); i++) {
histogramPeaks += listOfPeaks.get(i) + " ";
}
for (int i = 0; i < listOfPeaksCorresponding.size(); i++) {
histogramPeaksReal += listOfPeaksCorresponding.get(i) + " ";
}
}
/*
* this is a test contributed by mario baseda / see bug #1610997
* @cdk.bug 1610997
*/
@Test
public void testModel3D_bug_1610997() throws Exception {
Assume.assumeTrue(runSlowTests());
boolean notCalculatedResults = false;
List inputList = new ArrayList();
////////////////////////////////////////////////////////////////////////////////////////////
// generate the input molecules. This are molecules without x, y, z coordinats
String[] smiles =
new String[] {
"CC",
"OCC",
"O(C)CCC",
"c1ccccc1",
"C(=C)=C",
"OCC=CCc1ccccc1(C=C)",
"O(CC=C)CCN",
"CCCCCCCCCCCCCCC",
"OCC=CCO",
"NCCCCN"
};
SmilesParser sp = new SmilesParser(NoNotificationChemObjectBuilder.getInstance());
IAtomContainer[] atomContainer = new IAtomContainer[smiles.length];
for (int i = 0; i < smiles.length; i++) {
atomContainer[i] = sp.parseSmiles(smiles[i]);
inputList.add(atomContainer[i]);
}
System.out.println(inputList.size());
///////////////////////////////////////////////////////////////////////////////////////////
// Generate 2D coordinats for the input molecules with the Structure Diagram Generator
StructureDiagramGenerator str;
List resultList = new ArrayList();
for (Iterator iter = inputList.iterator(); iter.hasNext(); ) {
IAtomContainer molecules = (IAtomContainer) iter.next();
str = new StructureDiagramGenerator();
str.setMolecule((IMolecule) molecules);
str.generateCoordinates();
resultList.add(str.getMolecule());
}
inputList = resultList;
/////////////////////////////////////////////////////////////////////////////////////////////
// Delete x and y coordinats
for (Iterator iter = inputList.iterator(); iter.hasNext(); ) {
IAtomContainer molecules = (IAtomContainer) iter.next();
for (Iterator atom = molecules.atoms().iterator(); atom.hasNext(); ) {
Atom last = (Atom) atom.next();
last.setPoint2d(null);
}
}
////////////////////////////////////////////////////////////////////////////////////////////////////
// Test for the method Model3DBuildersWithMM2ForceField
ModelBuilder3D mb3d = ModelBuilder3D.getInstance();
for (Iterator iter = inputList.iterator(); iter.hasNext(); ) {
IAtomContainer molecules = (IAtomContainer) iter.next();
IMolecule mol = molecules.getBuilder().newInstance(IMolecule.class, molecules);
mol = mb3d.generate3DCoordinates(mol, false);
System.out.println("Calculation done");
}
for (Iterator iter = inputList.iterator(); iter.hasNext(); ) {
IAtomContainer molecule = (IAtomContainer) iter.next();
checkAverageBondLength(molecule);
for (Iterator atom = molecule.atoms().iterator(); atom.hasNext(); ) {
Atom last = (Atom) atom.next();
if (last.getPoint3d() == null) notCalculatedResults = true;
}
}
Assert.assertFalse(notCalculatedResults);
}
/**
* Finds the Smallest Set of Smallest Rings.
*
* @param mol the molecule to be searched for rings
* @return a RingSet containing the rings in molecule
*/
public IRingSet findSSSR(IAtomContainer mol) {
IBond brokenBond = null;
IChemObjectBuilder builder = mol.getBuilder();
IRingSet sssr = builder.newInstance(IRingSet.class);
IAtomContainer molecule = builder.newInstance(IAtomContainer.class);
molecule.add(mol);
IAtom smallest;
int smallestDegree, nodesToBreakCounter, degree;
IAtom[] rememberNodes;
IRing ring;
// Two Vectors - as defined in the article. One to hold the
// full set of atoms in the structure and on to store the numbers
// of the nodes that have been trimmed away.
// Furhter there is a Vector nodesN2 to store the number of N2 nodes
List<IAtom> fullSet = new ArrayList<IAtom>();
List<IAtom> trimSet = new ArrayList<IAtom>();
List<IAtom> nodesN2 = new ArrayList<IAtom>();
initPath(molecule);
logger.debug("molecule.getAtomCount(): " + molecule.getAtomCount());
// load fullSet with the numbers of our atoms
for (int f = 0; f < molecule.getAtomCount(); f++) {
fullSet.add(molecule.getAtom(f));
}
logger.debug("fullSet.size(): " + fullSet.size());
do {
// Add nodes of degree zero to trimset.
// Also add nodes of degree 2 to nodesN2.
// In the same run, check, which node has the lowest degree
// greater than zero.
smallestDegree = 7;
smallest = null;
nodesN2.clear();
for (int f = 0; f < molecule.getAtomCount(); f++) {
IAtom atom = molecule.getAtom(f);
degree = molecule.getConnectedBondsCount(atom);
if (degree == 0) {
if (!trimSet.contains(atom)) {
logger.debug("Atom of degree 0");
trimSet.add(atom);
}
}
if (degree == 2) {
nodesN2.add(atom);
}
if (degree < smallestDegree && degree > 0) {
smallest = atom;
smallestDegree = degree;
}
}
if (smallest == null) break;
// If there are nodes of degree 1, trim them away
if (smallestDegree == 1) {
trimCounter++;
trim(smallest, molecule);
trimSet.add(smallest);
}
// if there are nodes of degree 2, find out of which rings
// they are part of.
else if (smallestDegree == 2) {
rememberNodes = new IAtom[nodesN2.size()];
nodesToBreakCounter = 0;
for (int f = 0; f < nodesN2.size(); f++) {
ring = getRing((IAtom) nodesN2.get(f), molecule);
if (ring != null) {
// check, if this ring already is in SSSR
if (!RingSetManipulator.ringAlreadyInSet(ring, sssr)) {
sssr.addAtomContainer(ring);
rememberNodes[nodesToBreakCounter] = (IAtom) nodesN2.get(f);
nodesToBreakCounter++;
}
}
}
if (nodesToBreakCounter == 0) {
nodesToBreakCounter = 1;
rememberNodes[0] = (IAtom) nodesN2.get(0);
}
for (int f = 0; f < nodesToBreakCounter; f++) {
breakBond(rememberNodes[f], molecule);
}
if (brokenBond != null) {
molecule.addBond(brokenBond);
brokenBond = null;
}
}
// if there are nodes of degree 3
else if (smallestDegree == 3) {
ring = getRing(smallest, molecule);
if (ring != null) {
// check, if this ring already is in SSSR
if (!RingSetManipulator.ringAlreadyInSet(ring, sssr)) {
sssr.addAtomContainer(ring);
}
brokenBond = checkEdges(ring, molecule);
molecule.removeElectronContainer(brokenBond);
}
}
} while (trimSet.size() < fullSet.size());
logger.debug("fullSet.size(): " + fullSet.size());
logger.debug("trimSet.size(): " + trimSet.size());
logger.debug("trimCounter: " + trimCounter);
// molecule.setProperty(CDKConstants.SMALLEST_RINGS, sssr);
return sssr;
}
/** A unit test for JUnit */
@Test
public void testCisTransDecalin() throws Exception {
HydrogenPlacer hydrogenPlacer = new HydrogenPlacer();
IAtomContainer mol1 = new AtomContainer();
SmilesGenerator sg = new SmilesGenerator();
mol1.addAtom(new Atom("H", new Point2d(1, 0)));
// 1
mol1.addAtom(new Atom("C", new Point2d(1, 2)));
// 2
mol1.addAtom(new Atom("C", new Point2d(1, 2)));
// 3
mol1.addAtom(new Atom("C", new Point2d(0, 0)));
// 4
mol1.addAtom(new Atom("C", new Point2d(1, 4)));
// 5
mol1.addAtom(new Atom("C", new Point2d(1, 5)));
// 6
mol1.addAtom(new Atom("C", new Point2d(1, 6)));
// 7
mol1.addAtom(new Atom("H", new Point2d(1, 0)));
// 1
mol1.addAtom(new Atom("C", new Point2d(1, 2)));
// 2
mol1.addAtom(new Atom("C", new Point2d(1, 2)));
// 3
mol1.addAtom(new Atom("C", new Point2d(1, 2)));
// 2
mol1.addAtom(new Atom("C", new Point2d(1, 2)));
// 3
mol1.addBond(0, 1, IBond.Order.SINGLE, IBond.Stereo.DOWN);
// 1
mol1.addBond(1, 2, IBond.Order.SINGLE);
// 2
mol1.addBond(2, 3, IBond.Order.SINGLE);
// 3
mol1.addBond(3, 4, IBond.Order.SINGLE);
// 4
mol1.addBond(4, 5, IBond.Order.SINGLE);
// 5
mol1.addBond(5, 6, IBond.Order.SINGLE);
// 6
mol1.addBond(6, 7, IBond.Order.SINGLE, IBond.Stereo.DOWN);
// 3
mol1.addBond(6, 8, IBond.Order.SINGLE);
// 4
mol1.addBond(8, 9, IBond.Order.SINGLE);
// 5
mol1.addBond(9, 10, IBond.Order.SINGLE);
// 6
mol1.addBond(10, 11, IBond.Order.SINGLE);
// 6
mol1.addBond(11, 1, IBond.Order.SINGLE);
// 6
mol1.addBond(1, 6, IBond.Order.SINGLE);
// 6
try {
addExplicitHydrogens(mol1);
hydrogenPlacer.placeHydrogens2D(mol1, 1.0);
IsotopeFactory ifac = IsotopeFactory.getInstance(mol1.getBuilder());
ifac.configureAtoms(mol1);
} catch (IOException ex) {
} catch (ClassNotFoundException ex) {
}
String smiles1 = null;
if (standAlone) {
display(mol1);
}
try {
smiles1 = sg.createSMILES(mol1, true, new boolean[mol1.getBondCount()]);
} catch (Exception exc) {
System.out.println(exc);
if (!standAlone) {
Assert.fail();
}
}
if (standAlone) {
System.err.println("SMILES 1: " + smiles1);
}
Assert.assertNotNull(smiles1);
Assert.assertEquals(
"[H]C1([H])(C([H])([H])C([H])([H])C\\2([H])(C([H])([H])C([H])([H])C([H])([H])C([H])([H])C\\2([H])(C1([H])([H]))))",
smiles1);
mol1.getBond(6).setStereo(IBond.Stereo.UP);
String smiles3 = null;
try {
smiles3 = sg.createSMILES(mol1, true, new boolean[mol1.getBondCount()]);
} catch (Exception exc) {
System.out.println(exc);
if (!standAlone) {
Assert.fail();
}
}
Assert.assertNotSame(smiles3, smiles1);
}
/** A unit test for JUnit */
@Test
public void testDoubleBondConfiguration() throws Exception {
HydrogenPlacer hydrogenPlacer = new HydrogenPlacer();
IAtomContainer mol1 = new AtomContainer();
SmilesGenerator sg = new SmilesGenerator();
mol1.addAtom(new Atom("S", new Point2d(0, 0)));
// 1
mol1.addAtom(new Atom("C", new Point2d(1, 1)));
// 2
mol1.addAtom(new Atom("F", new Point2d(2, 0)));
// 3
mol1.addAtom(new Atom("C", new Point2d(1, 2)));
// 4
mol1.addAtom(new Atom("F", new Point2d(2, 3)));
// 5
mol1.addAtom(new Atom("S", new Point2d(0, 3)));
// 1
mol1.addBond(0, 1, IBond.Order.SINGLE);
// 1
mol1.addBond(1, 2, IBond.Order.SINGLE);
// 2
mol1.addBond(1, 3, IBond.Order.DOUBLE);
// 3
mol1.addBond(3, 4, IBond.Order.SINGLE);
// 4
mol1.addBond(3, 5, IBond.Order.SINGLE);
// 4
try {
IsotopeFactory ifac = IsotopeFactory.getInstance(mol1.getBuilder());
ifac.configureAtoms(mol1);
} catch (IOException ex) {
}
String smiles1 = null;
if (standAlone) {
display(mol1);
}
boolean[] bool = new boolean[mol1.getBondCount()];
bool[2] = true;
try {
smiles1 = sg.createSMILES(mol1, true, bool);
} catch (Exception exc) {
System.out.println(exc);
if (!standAlone) {
Assert.fail();
}
}
if (standAlone) {
System.err.println("SMILES 1: " + smiles1);
}
Assert.assertNotNull(smiles1);
Assert.assertEquals("F/C(=C/(F)S)S", smiles1);
mol1.getAtom(4).setPoint2d(new Point2d(0, 3));
mol1.getAtom(5).setPoint2d(new Point2d(2, 3));
try {
smiles1 = sg.createSMILES(mol1, true, bool);
} catch (Exception exc) {
System.out.println(exc);
if (!standAlone) {
Assert.fail();
}
}
if (standAlone) {
System.err.println("SMILES 1: " + smiles1);
}
Assert.assertNotNull(smiles1);
Assert.assertEquals("F/C(=C\\(F)S)S", smiles1);
try {
addExplicitHydrogens(mol1);
hydrogenPlacer.placeHydrogens2D(mol1, 1.0);
} catch (IOException ex) {
} catch (ClassNotFoundException ex) {
}
bool = new boolean[mol1.getBondCount()];
bool[2] = true;
try {
smiles1 = sg.createSMILES(mol1, true, bool);
} catch (Exception exc) {
System.out.println(exc);
if (!standAlone) {
Assert.fail();
}
}
Assert.assertEquals("[H]S/C(F)=C/(F)S[H]", smiles1);
mol1.getAtom(5).setPoint2d(new Point2d(0, 3));
mol1.getAtom(4).setPoint2d(new Point2d(2, 3));
try {
smiles1 = sg.createSMILES(mol1, true, bool);
} catch (Exception exc) {
System.out.println(exc);
if (!standAlone) {
Assert.fail();
}
}
Assert.assertEquals("[H]S/C(F)=C\\(F)S[H]", smiles1);
}
/**
* Calculates the 3 MI's, 3 ration and the R_gyr value.
*
* <p>The molecule should have hydrogens
*
* @param container Parameter is the atom container.
* @return An ArrayList containing 7 elements in the order described above
*/
@TestMethod("testCalculate_IAtomContainer")
public DescriptorValue calculate(IAtomContainer container) {
if (!GeometryTools.has3DCoordinates(container))
return getDummyDescriptorValue(new CDKException("Molecule must have 3D coordinates"));
IAtomContainer clone;
IsotopeFactory factory;
try {
clone = (IAtomContainer) container.clone();
factory = IsotopeFactory.getInstance(container.getBuilder());
factory.configureAtoms(clone);
} catch (Exception e) {
logger.debug(e);
return getDummyDescriptorValue(e);
}
DoubleArrayResult retval = new DoubleArrayResult(7);
double ccf = 1.000138;
double eps = 1e-5;
double[][] imat = new double[3][3];
Point3d centerOfMass = GeometryTools.get3DCentreOfMass(clone);
double xdif;
double ydif;
double zdif;
double xsq;
double ysq;
double zsq;
for (int i = 0; i < clone.getAtomCount(); i++) {
IAtom currentAtom = clone.getAtom(i);
double mass = factory.getMajorIsotope(currentAtom.getSymbol()).getExactMass();
xdif = currentAtom.getPoint3d().x - centerOfMass.x;
ydif = currentAtom.getPoint3d().y - centerOfMass.y;
zdif = currentAtom.getPoint3d().z - centerOfMass.z;
xsq = xdif * xdif;
ysq = ydif * ydif;
zsq = zdif * zdif;
imat[0][0] += mass * (ysq + zsq);
imat[1][1] += mass * (xsq + zsq);
imat[2][2] += mass * (xsq + ysq);
imat[1][0] += -1 * mass * ydif * xdif;
imat[0][1] = imat[1][0];
imat[2][0] += -1 * mass * xdif * zdif;
imat[0][2] = imat[2][0];
imat[2][1] += -1 * mass * ydif * zdif;
imat[1][2] = imat[2][1];
}
// diagonalize the MI tensor
Matrix tmp = new Matrix(imat);
EigenvalueDecomposition eigenDecomp = tmp.eig();
double[] eval = eigenDecomp.getRealEigenvalues();
retval.add(eval[2]);
retval.add(eval[1]);
retval.add(eval[0]);
double etmp = eval[0];
eval[0] = eval[2];
eval[2] = etmp;
if (Math.abs(eval[1]) > 1e-3) retval.add(eval[0] / eval[1]);
else retval.add(1000);
if (Math.abs(eval[2]) > 1e-3) {
retval.add(eval[0] / eval[2]);
retval.add(eval[1] / eval[2]);
} else {
retval.add(1000);
retval.add(1000);
}
// finally get the radius of gyration
double pri;
IMolecularFormula formula = MolecularFormulaManipulator.getMolecularFormula(clone);
if (Math.abs(eval[2]) > eps) pri = Math.pow(eval[0] * eval[1] * eval[2], 1.0 / 3.0);
else pri = Math.sqrt(eval[0] * ccf / MolecularFormulaManipulator.getTotalExactMass(formula));
retval.add(
Math.sqrt(
Math.PI * 2 * pri * ccf / MolecularFormulaManipulator.getTotalExactMass(formula)));
return new DescriptorValue(
getSpecification(), getParameterNames(), getParameters(), retval, getDescriptorNames());
}
