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Chemical Markup Language (cml, mrv)

An XML format for interchange of chemical information.

This format writes and reads CML XML files. To write CML1 format rather than the default CML2, use the -x1 option. To write the array form use -xa and to specify all hydrogens using the hydrogenCount attribute on atoms use -xh.

Crystal structures are written using the <crystal>, <xfract> (,...etc.) elements if the OBMol has a OBGenericDataType::UnitCell data.

All these forms are handled transparently during reading. Only a subset of CML elements and attributes are recognised, but these include most of those which define chemical structure, see below.

The following are read:

  • Elements:
    • molecule, atomArray, atom, bondArray, bond, atomParity, bondStereo
    • name, formula, crystal, scalar (contains crystal data)
    • string, stringArray, integer, integerArray, float floatArray, builtin
  • Attributes:
    • On <molecule>: id, title, ref(in CMLReact)
    • On <atom>: id, atomId, atomID, elementType, x2, y2, x3, y3, z3, xy2, xyz3, xFract, yFract, zFract, xyzFract, hydrogenCount, formalCharge, isotope, isotopeNumber, spinMultiplicity, radical(from Marvin), atomRefs4 (for atomParity)
    • On <bond>: atomRefs2, order, CML1: atomRef, atomRef1, atomRef2

Read Options

2 read 2D rather than 3D coordinates if both provided

Write Options

1 write CML1 (rather than CML2)
a write array format for atoms and bonds
A write aromatic bonds as such, not Kekule form
h use hydrogenCount for all hydrogens
m write metadata
x omit XML and namespace declarations
c continuous output: no formatting
p write properties
N <prefix> add namespace prefix to elements

Comments

In the absence of hydrogenCount and any explicit hydrogen on an atom, implicit hydrogen is assumed to be present appropriate to the radical or spinMultiplicity attributes on the atom or its normal valency if they are not present.

The XML formats require the XML text to be well formed but generally interpret it fairly tolerantly. Unrecognised elements and attributes are ignored and there are rather few error messages when any required structures are not found. This laxity allows, for instance, the reactant and product molecules to be picked out of a CML React file using CML. Each format has an element which is regarded as defining the object that OpenBabel will convert. For CML this is <molecule>. Files can have multiple objects and these can be treated the same as with other multiple object formats like SMILES and MDL Molfile. So conversion can start at the nth object using the -fn option and finish before the end using the -ln option. Multiple object XML files also can be indexed and searched using FastSearch, although this has not yet been extensively tested.