def test_pad_positions(null_position_structure):
"""Make sure None values in cartesian_site_positions are converted to padding float value"""
positions, padded_position = pad_positions(
null_position_structure.attributes.cartesian_site_positions)
assert not any(value is None for vector in positions for value in vector)
assert padded_position
positions, padded_position = pad_positions(positions)
assert not any(value is None for vector in positions for value in vector)
assert not padded_position
def get_jarvis_atoms(optimade_structure: OptimadeStructure) -> Atoms:
""" Get jarvis Atoms from OPTIMADE structure
NOTE: Cannot handle partial occupancies
:param optimade_structure: OPTIMADE structure
:return: jarvis.core.Atoms
"""
if globals().get("Atoms", None) is None:
warn(JARVIS_NOT_FOUND)
return None
attributes = optimade_structure.attributes
# Cannot handle partial occupancies
if "disorder" in attributes.structure_features:
raise ConversionError(
"jarvis-tools cannot handle structures with partial occupancies."
)
cartesian_site_positions, _ = pad_positions(attributes.cartesian_site_positions)
return Atoms(
lattice_mat=attributes.lattice_vectors,
elements=[specie.name for specie in attributes.species],
coords=cartesian_site_positions,
cartesian=True,
)
def get_aiida_structure_data(
optimade_structure: OptimadeStructure) -> StructureData:
""" Get AiiDA StructureData from OPTIMADE structure
:param optimade_structure: OPTIMADE structure
:return: StructureData
"""
if globals().get("StructureData", None) is None:
warn(AIIDA_NOT_FOUND)
return None
attributes = optimade_structure.attributes
# Convert null/None values to float("nan")
lattice_vectors, adjust_cell = pad_cell(attributes.lattice_vectors)
structure = StructureData(cell=lattice_vectors)
# Add Kinds
for kind in attributes.species:
symbols = []
concentration = []
for index, chemical_symbol in enumerate(kind.chemical_symbols):
# NOTE: The non-chemical element identifier "X" is identical to how AiiDA handles this,
# so it will be treated the same as any other true chemical identifier.
if chemical_symbol == "vacancy":
# Skip. This is how AiiDA handles vacancies;
# to not include them, while keeping the concentration in a site less than 1.
continue
else:
symbols.append(chemical_symbol)
concentration.append(kind.concentration[index])
# AiiDA needs a definition for the mass, and for it to be > 0
# mass is OPTIONAL for OPTIMADE structures
mass = kind.mass if kind.mass else 1
structure.append_kind(
Kind(symbols=symbols,
weights=concentration,
mass=mass,
name=kind.name))
# Convert null/None values to float("nan")
cartesian_site_positions, _ = pad_positions(
attributes.cartesian_site_positions)
# Add Sites
for index in range(attributes.nsites):
# range() to ensure 1-to-1 between kind and site
structure.append_site(
Site(
kind_name=attributes.species_at_sites[index],
position=cartesian_site_positions[index],
))
if adjust_cell:
structure._adjust_default_cell(
pbc=[bool(dim.value) for dim in attributes.dimension_types])
return structure
def _get_molecule(optimade_structure: OptimadeStructure) -> Molecule:
"""Create pymatgen Molecule from OPTIMADE structure"""
attributes = optimade_structure.attributes
cartesian_site_positions, _ = pad_positions(
attributes.cartesian_site_positions)
return Molecule(
species=_pymatgen_species(
nsites=attributes.nsites,
species=attributes.species,
species_at_sites=attributes.species_at_sites,
),
coords=cartesian_site_positions,
)
def _get_structure(optimade_structure: OptimadeStructure) -> Structure:
"""Create pymatgen Structure from OPTIMADE structure"""
attributes = optimade_structure.attributes
cartesian_site_positions, _ = pad_positions(
attributes.cartesian_site_positions)
return Structure(
lattice=attributes.lattice_vectors,
species=_pymatgen_species(
nsites=attributes.nsites,
species=attributes.species,
species_at_sites=attributes.species_at_sites,
),
coords=cartesian_site_positions,
coords_are_cartesian=True,
)
def get_pdbx_mmcif( # pylint: disable=too-many-locals
optimade_structure: OptimadeStructure, ) -> str: # pragma: no cover
""" Write Protein Data Bank (PDB) structure in the PDBx/mmCIF format from OPTIMADE structure
Inspired by `ase.io.proteindatabank:write_proteindatabank()` in the ASE package,
as well as `ase.io.cif:write_cif()`.
:param optimade_structure: OPTIMADE structure
:return: str
"""
if globals().get("np", None) is None:
warn(NUMPY_NOT_FOUND)
return None
cif = """#
# Created from an OPTIMADE structure.
#
# See https://www.optimade.org and/or
# https://github.com/Materials-Consortia/OPTIMADE for more information.
#
# CIF 2.0 format, specifically mmCIF (PDBx).
# See http://mmcif.wwpdb.org for more information.
#
"""
entry_id = f"{optimade_structure.type}{optimade_structure.id}"
cif += f"data_{entry_id}\n_entry.id {entry_id}\n#\n"
attributes = optimade_structure.attributes
# Do this only if there's three non-zero lattice vectors
if all(attributes.dimension_types):
a_vector, b_vector, c_vector, alpha, beta, gamma = cell_to_cellpar(
attributes.lattice_vectors)
cif += (f"_cell.entry_id {entry_id}\n"
f"_cell.length_a {a_vector:g}\n"
f"_cell.length_b {b_vector:g}\n"
f"_cell.length_c {c_vector:g}\n"
f"_cell.angle_alpha {alpha:g}\n"
f"_cell.angle_beta {beta:g}\n"
f"_cell.angle_gamma {gamma:g}\n"
"_cell.Z_PDB 1\n#\n")
cif += (f"_symmetry.entry_id {entry_id}\n"
"_symmetry.space_group_name_H-M 'P 1'\n"
"_symmetry.Int_Tables_number 1\n#\n")
# Since some structure viewers are having issues with cartesian coordinates,
# we calculate the fractional coordinates if this is a 3D structure and we have all the necessary information.
if not hasattr(attributes, "fractional_site_positions"):
sites, _ = pad_positions(attributes.cartesian_site_positions)
attributes.fractional_site_positions = fractional_coordinates(
cell=attributes.lattice_vectors, cartesian_positions=sites)
# TODO: The following lines are perhaps needed to create a "valid" PDBx/mmCIF file.
# However, at the same time, the information here is "default" and will for all structures "at this moment in time"
# be the same. I.e., no information is gained by adding this now.
# If it is found that they indeed are needed to create a "valid" PDBx/mmCIF file, they should be included in the output.
# cif += (
# "loop_\n"
# "_struct_asym.id\n"
# "_struct_asym.entity_id\n"
# "A 1\n#\n" # At this point, not using this feature.
# )
# cif += (
# "loop_\n"
# "_chem_comp.id\n"
# "X\n#\n" # At this point, not using this feature.
# )
# cif += (
# "loop_\n"
# "_entity.id\n"
# "1\n#\n" # At this point, not using this feature.
# )
# NOTE: This is otherwise a bit ahead of its time, since this OPTIMADE property is part of an open PR.
# See https://github.com/Materials-Consortia/OPTIMADE/pull/206
coord_type = ("fract" if hasattr(attributes, "fractional_site_positions")
else "Cartn")
cif += (
"loop_\n"
"_atom_site.group_PDB\n" # Always "ATOM"
"_atom_site.id\n" # number (1-counting)
"_atom_site.type_symbol\n" # species.chemical_symbols
"_atom_site.label_atom_id\n" # species.checmical_symbols symbol + number
# For these next keys, see the comment above.
# "_atom_site.label_asym_id\n" # Will be set to "A" _struct_asym.id above
# "_atom_site.label_comp_id\n" # Will be set to "X" _chem_comp.id above
# "_atom_site.label_entity_id\n" # Will be set to "1" _entity.id above
# "_atom_site.label_seq_id\n"
"_atom_site.occupancy\n" # species.concentration
f"_atom_site.{coord_type}_x\n" # cartesian_site_positions
f"_atom_site.{coord_type}_y\n" # cartesian_site_positions
f"_atom_site.{coord_type}_z\n" # cartesian_site_positions
"_atom_site.thermal_displace_type\n" # Set to 'Biso'
"_atom_site.B_iso_or_equiv\n" # Set to 1.0:f
)
if coord_type == "fract":
sites, _ = pad_positions(attributes.fractional_site_positions)
else:
sites, _ = pad_positions(attributes.cartesian_site_positions)
species: Dict[str, OptimadeStructureSpecies] = {
species.name: species
for species in attributes.species
}
for site_number in range(attributes.nsites):
species_name = attributes.species_at_sites[site_number]
site = sites[site_number]
current_species = species[species_name]
for index, symbol in enumerate(current_species.chemical_symbols):
if symbol == "vacancy":
continue
label = f"{species_name.upper()}{site_number + 1}"
if len(current_species.chemical_symbols) > 1:
if ("vacancy" in current_species.chemical_symbols
and len(current_species.chemical_symbols) == 2):
pass
else:
label = f"{symbol.upper()}{index + 1}"
cif += (
f"ATOM {site_number + 1:5d} {symbol} {label:8} "
f"{current_species.concentration[index]:6.4f} {site[0]:8.5f} "
f"{site[1]:8.5f} {site[2]:8.5f} {'Biso':4} {'1.000':6}\n")
return cif
def get_pdb( # pylint: disable=too-many-locals
optimade_structure: OptimadeStructure, ) -> str:
""" Write Protein Data Bank (PDB) structure in the old PDB format from OPTIMADE structure
Inspired by `ase.io.proteindatabank.write_proteindatabank()` in the ASE package.
:param optimade_structure: OPTIMADE structure
:return: str
"""
if globals().get("np", None) is None:
warn(NUMPY_NOT_FOUND)
return None
pdb = ""
attributes = optimade_structure.attributes
rotation = None
if all(attributes.dimension_types):
currentcell = np.asarray(attributes.lattice_vectors)
cellpar = cell_to_cellpar(currentcell)
exportedcell = cellpar_to_cell(cellpar)
rotation = np.linalg.solve(currentcell, exportedcell)
# Setting Z-value = 1 and using P1 since we have all atoms defined explicitly
Z = 1
spacegroup = "P 1"
pdb += (
f"CRYST1{cellpar[0]:9.3f}{cellpar[1]:9.3f}{cellpar[2]:8.3f}"
f"{cellpar[3]:7.2f}{cellpar[4]:7.2f}{cellpar[5]:7.2f} {spacegroup:11s}{Z:4d}\n"
)
for i, vector in enumerate(scaled_cell(currentcell)):
pdb += f"SCALE{i + 1} {vector[0]:10.6f}{vector[1]:10.6f}{vector[2]:10.6f} {0:10.5f}\n"
# There is a limit of 5 digit numbers in this field.
pdb_maxnum = 100000
bfactor = 1.0
pdb += "MODEL 1\n"
species: Dict[str, OptimadeStructureSpecies] = {
species.name: species
for species in attributes.species
}
cartesian_site_positions, _ = pad_positions(
attributes.cartesian_site_positions)
sites = np.asarray(cartesian_site_positions)
if rotation is not None:
sites = sites.dot(rotation)
for site_number in range(attributes.nsites):
species_name = attributes.species_at_sites[site_number]
site = sites[site_number]
current_species = species[species_name]
for index, symbol in enumerate(current_species.chemical_symbols):
if symbol == "vacancy":
continue
label = species_name
if len(current_species.chemical_symbols) > 1:
if ("vacancy" in current_species.chemical_symbols
and len(current_species.chemical_symbols) == 2):
pass
else:
label = f"{symbol}{index + 1}"
pdb += (
f"ATOM {site_number % pdb_maxnum:5d} {label:4} MOL 1 "
f"{site[0]:8.3f}{site[1]:8.3f}{site[2]:8.3f}"
f"{current_species.concentration[index]:6.2f}"
f"{bfactor:6.2f} {symbol.upper():2} \n")
pdb += "ENDMDL\n"
return pdb
def get_cif( # pylint: disable=too-many-locals,too-many-branches
optimade_structure: OptimadeStructure,
) -> str:
""" Get CIF file as string from OPTIMADE structure
Based on `ase.io.cif:write_cif()`.
:param optimade_structure: OPTIMADE structure
:param formatting: What formatting to use for the CIF file data keys.
Can be either "mp" or "default".
:param encoding: Encoding used for the string. CIF files use "latin-1" as standard.
If encoding is "str", a Python str object will be returned.
:return: str
"""
# NumPy is needed for calculations
if globals().get("np", None) is None:
warn(NUMPY_NOT_FOUND)
return None
cif = """#
# Created from an OPTIMADE structure.
#
# See https://www.optimade.org and/or
# https://github.com/Materials-Consortia/OPTIMADE for more information.
#
"""
cif += f"data_{optimade_structure.id}\n\n"
attributes = optimade_structure.attributes
# Do this only if there's three non-zero lattice vectors
# NOTE: This also negates handling of lattice_vectors with null/None values
if all(attributes.dimension_types):
a_vector, b_vector, c_vector, alpha, beta, gamma = cell_to_cellpar(
attributes.lattice_vectors
)
cif += (
f"_cell_length_a {a_vector:g}\n"
f"_cell_length_b {b_vector:g}\n"
f"_cell_length_c {c_vector:g}\n"
f"_cell_angle_alpha {alpha:g}\n"
f"_cell_angle_beta {beta:g}\n"
f"_cell_angle_gamma {gamma:g}\n\n"
)
cif += (
"_symmetry_space_group_name_H-M 'P 1'\n"
"_symmetry_int_tables_number 1\n\n"
"loop_\n"
" _symmetry_equiv_pos_as_xyz\n"
" 'x, y, z'\n\n"
)
# Since some structure viewers are having issues with cartesian coordinates,
# we calculate the fractional coordinates if this is a 3D structure and we have all the necessary information.
if not hasattr(attributes, "fractional_site_positions"):
sites, _ = pad_positions(attributes.cartesian_site_positions)
attributes.fractional_site_positions = fractional_coordinates(
cell=attributes.lattice_vectors, cartesian_positions=sites
)
# NOTE: This is otherwise a bit ahead of its time, since this OPTIMADE property is part of an open PR.
# See https://github.com/Materials-Consortia/OPTIMADE/pull/206
coord_type = (
"fract" if hasattr(attributes, "fractional_site_positions") else "Cartn"
)
cif += (
"loop_\n"
" _atom_site_type_symbol\n" # species.chemical_symbols
" _atom_site_label\n" # species.name + unique int
" _atom_site_occupancy\n" # species.concentration
f" _atom_site_{coord_type}_x\n" # cartesian_site_positions
f" _atom_site_{coord_type}_y\n" # cartesian_site_positions
f" _atom_site_{coord_type}_z\n" # cartesian_site_positions
" _atom_site_thermal_displace_type\n" # Set to 'Biso'
" _atom_site_B_iso_or_equiv\n" # Set to 1.0:f
)
if coord_type == "fract":
sites, _ = pad_positions(attributes.fractional_site_positions)
else:
sites, _ = pad_positions(attributes.cartesian_site_positions)
species: Dict[str, OptimadeStructureSpecies] = {
species.name: species for species in attributes.species
}
symbol_occurences = {}
for site_number in range(attributes.nsites):
species_name = attributes.species_at_sites[site_number]
site = sites[site_number]
current_species = species[species_name]
for index, symbol in enumerate(current_species.chemical_symbols):
if symbol == "vacancy":
continue
if symbol in symbol_occurences:
symbol_occurences[symbol] += 1
else:
symbol_occurences[symbol] = 1
label = f"{symbol}{symbol_occurences[symbol]}"
cif += (
f" {symbol} {label} {current_species.concentration[index]:6.4f} {site[0]:8.5f} "
f"{site[1]:8.5f} {site[2]:8.5f} {'Biso':4} {'1.000':6}\n"
)
return cif
