3. Selection commands
>>> kalp = universe.select_atoms("segid KALP")
select_atoms() method of a
AtomGroup or a
Universe returns a
AtomGroup, so you can use all the methods
defined for AtomGroups on them. Selections always return an
AtomGroup with atoms sorted according to their
index in the topology (this is to ensure that there are not any duplicates,
which can happen with complicated selections).
One can group subselections using parentheses:
>>> universe.select_atoms("segid DMPC and not (name H* or type OW)") <AtomGroup with 3420 atoms>
Almost all the basic CHARMM selections work.
It is also possible to export selections for external software packages with the help of Selection exporters.
By default, atoms are sorted by index in the output AtomGroup.
For example, the below code will return the first, second, and
sixth atom in
>>> ag = u.select_atoms("name N") >>> ag2 = ag[[5, 1, 0]] >>> ag3 = ag2.select_atoms("name N") >>> np.all(ag3.ix == ag2.ix) False
You can turn off sorting behavior with the
>>> ag = u.select_atoms("name N") >>> ag2 = ag[[5, 1, 0]] >>> ag3 = ag2.select_atoms("name N", sorted=False) >>> np.all(ag3.ix == ag2.ix) True
3.1. Selection Keywords
The following describes all selection keywords currently understood by the selection parser. The following applies to all selections:
Keywords are case sensitive.
Atoms are automatically sequentially ordered in a resulting selection (see notes below on Ordered selections for how to circumvent this if necessary).
Selections are parsed left to right and parentheses can be used for grouping.
You can use the singular name of any topology attribute as a selection keyword. Defined topology attributes are listed in the User Guide. Alternatively, you can define a
TopologyAttryourself, providing that the attribute
dtypeis one of
bool. However, the topology must contain this attribute information for the selection to work.
Selections of attributes that are integers or floats can use the syntax “myTopologyAttr 0 - 2”, “myTopologyAttr 0:2”, or “myTopologyAttr 0 to 2”, to select a range with both ends inclusive. Whitespace and negative numbers are allowed.
“myTopologyAttr 0” can be used to select all atoms matching the value; however, this can be tricky with floats because of precision differences and we recommend using a range like above when possible.
Boolean selections default to True, so “myTopologyAttr” and “myTopologyAttr True” both give all atoms with
myTopologyAttr == True.
3.1.1. Simple selections
This is a non-exhaustive list of the available selection keywords. As noted
in the dot point above, keywords will be automatically generated for any
TopologyAttr. A list of
Defined topology attributes is available in the User Guide.
- protein, backbone, nucleic, nucleicbackbone
selects all atoms that belong to a standard set of residues; a protein is identfied by a hard-coded set of residue names so it may not work for esoteric residues.
- segid seg-name
select by segid (as given in the topology), e.g.
- resid residue-number-range
resid can take a single residue number or a range of numbers. A range consists of two numbers separated by a colon (inclusive) such as
resid 1:5. A residue number (“resid”) is taken directly from the topology.
- resnum resnum-number-range
resnum is the canonical residue number; typically it is set to the residue id in the original PDB structure.
- resname residue-name
select by residue name, e.g.
- name atom-name
select by atom name (as given in the topology). Often, this is force field dependent. Example:
name CA(for Cα atoms) or
name OW(for SPC water oxygen)
- type atom-type
select by atom type; this is either a string or a number and depends on the force field; it is read from the topology file (e.g. the CHARMM PSF file contains numeric atom types). It has non-sensical values when a PDB or GRO file is used as a topology.
- atom seg-name residue-number atom-name
a selector for a single atom consisting of segid resid atomname, e.g.
DMPC 1 C2selects the C2 carbon of the first residue of the DMPC segment
- altLoc alternative-location
a selection for atoms where alternative locations are available, which is often the case with high-resolution crystal structures e.g.
resid 4 and resname ALA and altLoc Bselects only the atoms of ALA-4 that have an altLoc B record.
- chainID chain-name
a selection for atoms where chainIDs have been defined.
- element element-name
a selection for atoms where elements have been defined. e.g.
element H C
- moltype molecule-type
select by molecule type, e.g.
moltype Protein_A. At the moment, only the TPR format defines the molecule type.
- smarts SMARTS-query
select atoms using Daylight’s SMARTS queries, e.g.
smarts [#7;R]to find nitrogen atoms in rings. Requires RDKit. All matches (max 1000) are combined as a unique match.
- chiral R | S
select a particular stereocenter. e.g.
name C and chirality Sto select only S-chiral carbon atoms. Only
Swill be possible options but other values will not raise an error.
3.1.2. Pattern matching
The pattern matching notation described below is used to specify
patterns for matching strings (based on
Is a pattern that will match any single character. For example,
resname T?Rselects residues named “TYR” and “THR”.
Is a pattern that will match multiple characters. For example,
GL*selects all strings that start with “GL” such as “GLU”, “GLY”, “GLX29”, “GLN”.
Would match any character in seq. For example, “resname GL[NY]” selects all residues named “GLN” or “GLY” but would not select “GLU”.
Would match any character not in seq. For example, “resname GL[!NY]” would match residues named “GLU” but would not match “GLN” or “GLY”.
all atoms not in the selection, e.g.
not proteinselects all atoms that aren’t part of a protein
- and, or
combine two selections according to the rules of boolean algebra, e.g.
protein and not (resname ALA or resname LYS)selects all atoms that belong to a protein, but are not in a lysine or alanine residue
- around distance selection
selects all atoms a certain cutoff away from another selection, e.g.
around 3.5 proteinselects all atoms not belonging to protein that are within 3.5 Angstroms from the protein
- sphlayer innerRadius externalRadius selection
selects all atoms within a spherical layer centered in the center of geometry (COG) of a given selection, e.g.,
sphlayer 2.4 6.0 ( protein and ( resid 130 or resid 80 ) )selects the center of geometry of protein, resid 130, resid 80 and creates a spherical layer of inner radius 2.4 and external radius 6.0 around the COG.
- sphzone externalRadius selection
selects all atoms within a spherical zone centered in the center of geometry (COG) of a given selection, e.g.
sphzone 6.0 ( protein and ( resid 130 or resid 80 ) )selects the center of geometry of protein, resid 130, resid 80 and creates a sphere of radius 6.0 around the COG.
- cylayer innerRadius externalRadius zMax zMin selection
selects all atoms within a cylindric layer centered in the center of geometry (COG) of a given selection, e.g.
cylayer 5 10 10 -8 proteinselects the center of geometry of protein, and creates a cylindrical layer of inner radius 5, external radius 10 centered on the COG. In z, the cylinder extends from 10 above the COG to 8 below. Positive values for zMin, or negative ones for zMax, are allowed.
- cyzone externalRadius zMax zMin selection
selects all atoms within a cylindric zone centered in the center of geometry (COG) of a given selection, e.g.
cyzone 15 4 -8 protein and resid 42selects the center of geometry of protein and resid 42, and creates a cylinder of external radius 15 centered on the COG. In z, the cylinder extends from 4 above the COG to 8 below. Positive values for zMin, or negative ones for zMax, are allowed.
Changed in version 0.10.0: keywords cyzone and cylayer now take zMax and zMin to be relative to the COG of selection, instead of absolute z-values in the box.
- point x y z distance
selects all atoms within a cutoff of a point in space, make sure coordinate is separated by spaces, e.g.
point 5.0 5.0 5.0 3.5selects all atoms within 3.5 Angstroms of the coordinate (5.0, 5.0, 5.0)
- prop [abs] property operator value
selects atoms based on position, using property x, y, or z coordinate. Supports the abs keyword (for absolute value) and the following operators: <, >, <=, >=, ==, !=. For example,
prop z >= 5.0selects all atoms with z coordinate greater than 5.0;
prop abs z <= 5.0selects all atoms within -5.0 <= z <= 5.0.
By default periodicity is taken into account with geometric
selections, i.e. selections will find atoms that are in different
To control this behaviour, use the boolean
3.1.5. Similarity and connectivity
- same subkeyword as selection
selects all atoms that have the same subkeyword value as any atom in selection. Allowed subkeyword values are the atom properties:
name, type, resname, resid, segid, mass, charge, radius, bfactor, resnum, the groups an atom belong to:
residue, segment, fragment, and the atom coordinates
x, y, z.
- byres selection
selects all atoms that are in the same segment and residue as selection, e.g. specify the subselection after the byres keyword.
byresis a shortcut to
same residue as
- bonded selection
selects all atoms that are bonded to selection eg:
select name H and bonded name Oselects only hydrogens bonded to oxygens
- bynum index-range
selects all atoms within a range of (1-based) inclusive indices, e.g.
bynum 1selects the first atom in the universe;
bynum 5:10selects atoms 5 through 10 inclusive. All atoms in the
MDAnalysis.Universeare consecutively numbered, and the index runs from 1 up to the total number of atoms.
- index index-range
selects all atoms within a range of (0-based) inclusive indices, e.g.
index 0selects the first atom in the universe;
index 5:10selects atoms 6 through 11 inclusive. All atoms in the
MDAnalysis.Universeare consecutively numbered, and the index runs from 0 up to the total number of atoms - 1.
3.1.7. Preexisting selections and modifiers
- group group-name
selects the atoms in the
AtomGrouppassed to the function as an argument named group-name. Only the atoms common to group-name and the instance
select_atoms()was called from will be considered, unless
groupis preceded by the
globalkeyword. group-name will be included in the parsing just by comparison of atom indices. This means that it is up to the user to make sure the group-name group was defined in an appropriate
- global selection
by default, when issuing
AtomGroup, selections and subselections are returned intersected with the atoms of that instance. Prefixing a selection term with
globalcauses its selection to be returned in its entirety. As an example, the
globalkeyword allows for
lipids.select_atoms("around 10 global protein")— where
lipidsis a group that does not contain any proteins. Were
globalabsent, the result would be an empty selection since the
proteinsubselection would itself be empty. When issuing
Changed in version 1.0.0: The
fullgroup selection has now been removed. Please use the equivalent
global group selection.
3.2. Dynamic selections
select_atoms() returns an
AtomGroup, in which the list of atoms is
constant across trajectory frame changes. If
select_atoms() is invoked with named
updating set to
UpdatingAtomGroup instance will be returned
instead. It behaves just like an
object, with the difference that the selection expressions are re-evaluated
every time the trajectory frame changes (this happens lazily, only when the
UpdatingAtomGroup object is accessed so that
there is no redundant updating going on):
# A dynamic selection of corner atoms: >>> ag_updating = universe.select_atoms("prop x < 5 and prop y < 5 and prop z < 5", updating=True) >>> ag_updating <UpdatingAtomGroup with 9 atoms> >>> universe.trajectory.next() >>> ag_updating <UpdatingAtomGroup with 14 atoms>
group selection keyword for
preexisting-selections, one can
make updating selections depend on
AtomGroup, or even other
Likewise, making an updating selection from an already updating group will
cause later updates to also reflect the updating of the base group:
>>> chained_ag_updating = ag_updating.select_atoms("resid 1:1000", updating=True) >>> chained_ag_updating <UpdatingAtomGroup with 3 atoms> >>> universe.trajectory.next() >>> chained_ag_updating <UpdatingAtomGroup with 7 atoms>
>>> static_ag = ag_updating.select_atoms("resid 1:1000") >>> static_ag <UpdatingAtomGroup with 3 atoms> >>> universe.trajectory.next() >>> static_ag <UpdatingAtomGroup with 3 atoms>
3.3. Ordered selections
select_atoms() sorts the atoms
AtomGroup by atom index before
returning them (this is to eliminate possible duplicates in the
selection). If the ordering of atoms is crucial (for instance when
describing angles or dihedrals) or if duplicate atoms are required
then one has to concatenate multiple AtomGroups, which does not sort
The most straightforward way to concatentate two AtomGroups is by using the
>>> ordered = u.select_atoms("segid DMPC and resid 3 and name P") + u.select_atoms("segid DMPC and resid 2 and name P") >>> print list(ordered) [< Atom 570: name 'P' of type '180' of resid 'DMPC', 3 and 'DMPC'>, < Atom 452: name 'P' of type '180' of resid 'DMPC', 2 and 'DMPC'>]
A shortcut is to provide two or more selections to
select_atoms(), which then
does the concatenation automatically:
>>> print list(universe.select_atoms("segid DMPC and resid 3 and name P", "segid DMPC and resid 2 and name P")) [< Atom 570: name 'P' of type '180' of resid 'DMPC', 3 and 'DMPC'>, < Atom 452: name 'P' of type '180' of resid 'DMPC', 2 and 'DMPC'>]
Just for comparison to show that a single selection string does not work as one might expect:
# WRONG! >>> print list(universe.select_atoms("segid DMPC and ( resid 3 or resid 2 ) and name P")) [< Atom 452: name 'P' of type '180' of resid 'DMPC', 2 and 'DMPC'>, < Atom 570: name 'P' of type '180' of resid 'DMPC', 3 and 'DMPC'>]