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Package rdkit :: Package Chem :: Package Fraggle :: Module FraggleSim
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Module FraggleSim

source code


Fragmentation algorithm
-----------------------

identify acyclic bonds
enumerate all single cuts
make sure you chop off more that 1 atom
keeps bits which are >60% query mol
enumerate all double cuts
keeps bits with 1 attachment point (i.e throw middle bit away)
need to be >60% query mol

identify exocyclic bonds
enumerate all single "ring" cuts
Check if it results in more that one component
keep correct bit if >40% query mol

enumerate successful "rings" cuts with an acyclic cut
Check if it results in more that one component
keep correct if >60% query mol
Functions [hide private]
 
delete_bonds(mol, bonds, ftype, hac)
Fragment molecule on bonds and reduce to fraggle fragmentation SMILES.		 source code
 
select_fragments(fragments, ftype, hac) source code
 
isValidRingCut(mol)
to check is a fragment is a valid ring cut, it needs to match the...		 source code
 
generate_fraggle_fragmentation(mol, verbose=False)
Create all possible fragmentations for molecule...		 source code
 
atomContrib(subs, mol, tverskyThresh=0.8)
atomContrib algorithm generate fp of query_substructs (qfp)		 source code
 
compute_fraggle_similarity_for_subs(inMol, qMol, qSmi, qSubs, tverskyThresh=0.8) source code
 
GetFraggleSimilarity(queryMol, refMol, tverskyThresh=0.8)
return the Fraggle similarity between two molecules		 source code
 
_runDoctests(verbose=None) source code
Variables [hide private]
  rdkitFpParams = {'fpSize': 1024, 'maxPath': 5, 'nBitsPerHash': 2}
  FTYPE_ACYCLIC = 'acyclic'
  FTYPE_CYCLIC = 'cyclic'
  FTYPE_CYCLIC_ACYCLIC = 'cyclic_and_acyclic'
  ACYC_SMARTS = Chem.MolFromSmarts("[*]!@!=!#[*]")
  CYC_SMARTS = Chem.MolFromSmarts("[R1,R2]@[r;!R1]")
  cSma1 = Chem.MolFromSmarts("[#0][r].[r][#0]")
  cSma2 = Chem.MolFromSmarts("[#0][r][#0]")
  dummyAtomQuery = rdqueries.AtomNumEqualsQueryAtom(0)
  modified_query_fps = {}
  __package__ = 'rdkit.Chem.Fraggle'

Imports: combinations, sys, Chem, DataStructs, rdqueries


Function Details [hide private]

delete_bonds(mol, bonds, ftype, hac)

source code  
Fragment molecule on bonds and reduce to fraggle fragmentation SMILES.
If none exists, returns None

isValidRingCut(mol)

source code  
to check is a fragment is a valid ring cut, it needs to match the
SMARTS: [$([#0][r].[r][#0]),$([#0][r][#0])]

generate_fraggle_fragmentation(mol, verbose=False)

source code  
Create all possible fragmentations for molecule
>>> q = Chem.MolFromSmiles('COc1cc(CN2CCC(NC(=O)c3cncc(C)c3)CC2)c(OC)c2ccccc12')
>>> fragments = generate_fraggle_fragmentation(q)
>>> fragments = sorted(['.'.join(sorted(s.split('.'))) for s in fragments])
>>> fragments
 ['[*]C(=O)NC1CCN(Cc2cc(OC)c3ccccc3c2OC)CC1',
  '[*]C(=O)c1cncc(C)c1.[*]C1CCN(Cc2cc(OC)c3ccccc3c2OC)CC1',
  '[*]C(=O)c1cncc(C)c1.[*]Cc1cc(OC)c2ccccc2c1OC',
  '[*]C(=O)c1cncc(C)c1.[*]c1cc(OC)c2ccccc2c1OC',
  '[*]C1CCN(Cc2cc(OC)c3ccccc3c2OC)CC1',
  '[*]C1CCN(Cc2cc(OC)c3ccccc3c2OC)CC1.[*]c1cncc(C)c1',
  '[*]Cc1cc(OC)c2ccccc2c1OC.[*]NC(=O)c1cncc(C)c1',
  '[*]Cc1cc(OC)c2ccccc2c1OC.[*]c1cncc(C)c1',
  '[*]N1CCC(NC(=O)c2cncc(C)c2)CC1.[*]c1cc(OC)c2ccccc2c1OC',
  '[*]NC(=O)c1cncc(C)c1.[*]c1cc(OC)c2ccccc2c1OC',
  '[*]NC1CCN(Cc2cc(OC)c3ccccc3c2OC)CC1',
  '[*]NC1CCN(Cc2cc(OC)c3ccccc3c2OC)CC1.[*]c1cncc(C)c1',
  '[*]c1c(CN2CCC(NC(=O)c3cncc(C)c3)CC2)cc(OC)c2ccccc12',
  '[*]c1c(OC)cc(CN2CCC(NC(=O)c3cncc(C)c3)CC2)c(OC)c1[*]',
  '[*]c1cc(CN2CCC(NC(=O)c3cncc(C)c3)CC2)c(OC)c2ccccc12',
  '[*]c1cc(OC)c2ccccc2c1OC.[*]c1cncc(C)c1']

atomContrib(subs, mol, tverskyThresh=0.8)

source code  
atomContrib algorithm
generate fp of query_substructs (qfp)

loop through atoms of smiles
  For each atom
  Generate partial fp of the atom (pfp)
  Find Tversky sim of pfp in qfp
  If Tversky < 0.8, mark atom in smiles

Loop through marked atoms
  If marked atom in ring - turn all atoms in that ring to * (aromatic) or Sc (aliphatic)
  For each marked atom
    If aromatic turn to a *
    If aliphatic turn to a Sc

Return modified smiles

GetFraggleSimilarity(queryMol, refMol, tverskyThresh=0.8)

source code  
return the Fraggle similarity between two molecules

>>> q = Chem.MolFromSmiles('COc1cc(CN2CCC(NC(=O)c3cncc(C)c3)CC2)c(OC)c2ccccc12')
>>> m = Chem.MolFromSmiles('COc1cc(CN2CCC(NC(=O)c3ccccc3)CC2)c(OC)c2ccccc12')
>>> sim,match = GetFraggleSimilarity(q,m)
>>> sim
0.980...
>>> match
'[*]C1CCN(Cc2cc(OC)c3ccccc3c2OC)CC1'

>>> m = Chem.MolFromSmiles('COc1cc(CN2CCC(Nc3nc4ccccc4s3)CC2)c(OC)c2ccccc12')
>>> sim,match = GetFraggleSimilarity(q,m)
>>> sim
0.794...
>>> match
'[*]C1CCN(Cc2cc(OC)c3ccccc3c2OC)CC1'

>>> q = Chem.MolFromSmiles('COc1ccccc1')
>>> sim,match = GetFraggleSimilarity(q,m)
>>> sim
0.347...
>>> match
'[*]c1ccccc1'

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