Version 2.1.5¶
OEChem TK 2.1.5¶
New features¶
New
OEHasExplicitHydrogenExpression
andOEHasImplicitHydrogenExpression
functions have been added.The
OEPrepareSearch
function now takes a parameter that determines whether to adjust the hydrogen of a target molecule based on the presence or absence of implicit and explicit hydrogens on the query molecule of the substructure search.Both
OEGetSubtree
andOEGetSmallestSubtree
functions now take an optional max depth parameter that allows partial traversal of subtrees. For example, the parameter allows identification of the subtree of a proline residue without traversing back onto the main chain. Similarly, it is possible to get the subtree of a cysteine residue involved in a disulfide without traversing across the disulfide bond and back on the main chain.Two new constants,
OEIFlavor.MDL.SuppressImp2ExpENHSTE
andOEOFlavor.MDL.SuppressImp2ExpENHSTE
, have been added with related MDL input and output formats (e.g., SDF, RDF) to allow suppression of explicit MDL stereogroup generation for implied stereocollection membership. By default, marked stereocenters not explicitly included in stereocollections are added to their implied stereocollection membership based on the chiral flag setting.A new
OEGroupType.UserDefined
type has been added to OEGroupBase to support serialization and deserialization via theOEB
format.A new OEIsBridgeHead functor has been added to identify bridge head atoms in a molecule.
A new
OERingBondCount
function has been added that returns the number of bonds connected to an atom that are part of a ring.
Major bug fixes¶
The FASTA reader has been fixed to support reading multiline FASTA strings.
Generic data attached to OEGroupBase is no longer lost when the molecule is copied.
Generic data attached to OEGroupBase is no longer lost when the molecule is added to another molecule by invoking the
OEAddMols
function.Relative stereo (e.g., 1,4-disubstituted cyclohexanes) information is now preserved on input, ensuring that the conformers generated will respect the input stereochemistry. Previously, such relative stereocenters would be cleared during activities to clear other illegally marked stereochemistry.
The V3000 MDL format readers called by
OEReadMolecule
now support noncontiguous object indices. It previously had been assumed that such indices were contiguous, but recent third-party writers have demonstrated that this assumption is no longer valid.
Minor bug fixes¶
The
OEGenerate2DCoordinates
function now returnsfalse
when it fails to generate coordinates that are consistent with the atom/bond stereo of a molecule.A memory corruption issue in the InChI generation code that previously required a check for hydrogen isotopes beyond
[3H]
will no longer generate InChI for these unrealistic hydrogen isotopes.Malformed SD bond lines that lacked both atom endpoints had previously been ignored.
OEReadMolecule
now fails for these types of format errors.OEUniMolecularRxn internal validations have been relaxed to allow reaction transformations that create a bond between two separate fragments.
OEGetHybridization
has been repaired to returnOEHybridization.sp3d
andOEHybridization.sp3d2
for high valence halogens. Previously, this function had only returnedOEHybridization.sp3
for these cases.OEUncolorMol
has been augmented to remove stereogroups when stripping atom stereochemistry. Additionally, a new option,OEUncolorStrategy.RemoveGroupStereo
, has been added to support the explicit stripping of stereogroups.OEAnd and OEOr have been augmented to support using OEGroupBase types to allow a more complex selection of MDL stereogroup types via custom predicates.
A new copy constructor and new assignment operator have been added to OERotMatrix.
Python-specific changes¶
Type comparisons between
OEBase
and non-OEBase
objects have been fixed to ensure that an exception is longer thrown.A new
__str__()
function has been added to OEResidue to provide a convenient string representation.
Java-specific changes¶
A new
OELibExtractor.GetTmpDirName()
method has been added to return the temporary directory used for the extraction of native libraries from the JarFile and the extraction lock file. This directory location can potentially be used to clean up extraction locks that have been left behind due to inadvertent or explicit Java process kill activities.
Documentation changes¶
The documentation for
OESMILESFlag.Hydrogens
has been clarified.The porphyrin footnote in the aromaticity table in the Aromaticity Perception section has been clarified.
OEBio TK 2.1.5¶
New features¶
The following APIs have been added to perform Ramachandran analyses on protein structures:
OERamachandranAnalysis class
OEGetRamachandranTypeName
andOEGetRamachandranCategoryName
functionsOERamaType
andOERamaCategory
namespaces
A new
OERotamerLibrary.Richardson_2016
constant has been added to provide rotamers from the ultimate rotamer library [Hintze-2016] . This new rotamer library is now the default.The following atom predicates have been added to identify RNA atoms:
A new
OESetRotamer
overload has been added that takes a residue atom.
Minor bug fixes¶
It is now possible to set an alternative rotamer on proline residues.
C++-specific changes¶
OEBio TK now depends on OEGrid TK. As result, CMake files might need to be modified to reflect this library dependency.
Java-specific changes¶
The Java wrapping of the following predicates has been fixed:
C#-specific changes¶
The C# wrapping of the following predicates has been fixed:
OEPlatform TK 2.1.5¶
Minor internal improvements have been made.
OESystem TK 2.1.5¶
The
OEWriteSettings
function now takes a 4th argument that specifies the name of an optimized parameter set for OpenEye’s applications.