def complex(**kwargs):
"""
Protocol:
Compare ECs for a complex to
3D structure
Parameters
----------
Mandatory kwargs arguments:
See list below in code where calling check_required
Returns
-------
outcfg : dict
Output configuration of the pipeline, including
the following fields:
* ec_file_compared_all
* ec_file_compared_all_longrange
* pdb_structure_hits
* distmap_monomer
* distmap_multimer
* contact_map_files
* remapped_pdb_files
"""
check_required(kwargs, [
"prefix", "ec_file", "min_sequence_distance", "pdb_mmtf_dir",
"atom_filter", "first_compare_multimer", "second_compare_multimer",
"distance_cutoff", "first_sequence_id", "second_sequence_id",
"first_sequence_file", "second_sequence_file", "first_segments",
"second_segments", "first_target_sequence_file",
"second_target_sequence_file", "scale_sizes"
])
prefix = kwargs["prefix"]
outcfg = {
# initialize output EC files
"ec_compared_all_file": prefix + "_CouplingScoresCompared_all.csv",
"ec_compared_longrange_file":
prefix + "_CouplingScoresCompared_longrange.csv",
"ec_compared_inter_file": prefix + "_CouplingScoresCompared_inter.csv",
# initialize output inter distancemap files
"distmap_inter": prefix + "_distmap_inter",
"inter_contacts_file": prefix + "_inter_contacts_file"
}
# Add PDB comparison files for first and second monomer
for monomer_prefix in ["first", "second"]:
outcfg = {
**outcfg,
monomer_prefix + "_pdb_structure_hits_file":
"{}_{}_structure_hits.csv".format(prefix, monomer_prefix),
monomer_prefix + "_pdb_structure_hits_unfiltered_file":
"{}_{}_structure_hits_unfitered.csv".format(
prefix, monomer_prefix),
monomer_prefix + "_distmap_monomer":
"{}_{}_distance_map_monomer".format(prefix, monomer_prefix),
monomer_prefix + "_distmap_multimer":
"{}_{}_distance_map_multimer".format(prefix, monomer_prefix),
}
# make sure EC file exists
verify_resources("EC file does not exist", kwargs["ec_file"])
# make sure output directory exists
create_prefix_folders(prefix)
# store auxiliary files here (too much for average user)
aux_prefix = insert_dir(prefix, "aux", rootname_subdir=False)
create_prefix_folders(aux_prefix)
# store auxiliary files here (too much for average user)
first_aux_prefix = insert_dir(aux_prefix,
"first_monomer",
rootname_subdir=False)
create_prefix_folders(first_aux_prefix)
# store auxiliary files here (too much for average user)
second_aux_prefix = insert_dir(aux_prefix,
"second_monomer",
rootname_subdir=False)
create_prefix_folders(second_aux_prefix)
# Step 1: Identify 3D structures for comparison
def _identify_monomer_structures(name_prefix, outcfg, aux_prefix):
# create a dictionary with kwargs for just the current monomer
# remove the "prefix" kwargs so that we can replace with the
# aux prefix when calling _identify_structures
# only replace first occurrence of name_prefix
monomer_kwargs = {
k.replace(name_prefix + "_", "", 1): v
for k, v in kwargs.items() if "prefix" not in k
}
# this field needs to be set explicitly else it gets overwritten by concatenated file
monomer_kwargs["alignment_file"] = kwargs[name_prefix +
"_alignment_file"]
monomer_kwargs["raw_focus_alignment_file"] = kwargs[
name_prefix + "_raw_focus_alignment_file"]
# identify structures for that monomer
sifts_map, sifts_map_full = _identify_structures(**monomer_kwargs,
prefix=aux_prefix)
# save selected PDB hits
sifts_map.hits.to_csv(outcfg[name_prefix + "_pdb_structure_hits_file"],
index=False)
# also save full list of hits
sifts_map_full.hits.to_csv(
outcfg[name_prefix + "_pdb_structure_hits_unfiltered_file"],
index=False)
return outcfg, sifts_map
outcfg, first_sifts_map = _identify_monomer_structures(
"first", outcfg, first_aux_prefix)
outcfg, second_sifts_map = _identify_monomer_structures(
"second", outcfg, second_aux_prefix)
# get the segment names from the kwargs
segment_list = kwargs["segments"]
# Make sure user provided exactly two segments
if len(segment_list) != 2:
raise InvalidParameterError(
"Compare stage for protein complexes requires exactly two segments"
)
first_segment_name = kwargs["segments"][0][0]
second_segment_name = kwargs["segments"][1][0]
# Step 2: Compute distance maps
def _compute_monomer_distance_maps(sifts_map, name_prefix, chain_name):
# prepare a sequence map to remap the structures we have found
verify_resources("Target sequence file does not exist",
kwargs[name_prefix + "_target_sequence_file"])
# create target sequence map for remapping structure
with open(kwargs[name_prefix + "_target_sequence_file"]) as f:
header, seq = next(read_fasta(f))
# create target sequence map for remapping structure
seq_id, seq_start, seq_end = parse_header(header)
seqmap = dict(zip(range(seq_start, seq_end + 1), seq))
# compute distance maps and save
# (but only if we found some structure)
if len(sifts_map.hits) > 0:
d_intra = intra_dists(sifts_map,
structures,
atom_filter=kwargs["atom_filter"],
output_prefix=aux_prefix + "_" +
name_prefix + "_distmap_intra")
d_intra.to_file(outcfg[name_prefix + "_distmap_monomer"])
# save contacts to separate file
outcfg[
name_prefix +
"_monomer_contacts_file"] = prefix + "_" + name_prefix + "_contacts_monomer.csv"
d_intra.contacts(kwargs["distance_cutoff"]).to_csv(
outcfg[name_prefix + "_monomer_contacts_file"], index=False)
# compute multimer distances, if requested;
# note that d_multimer can be None if there
# are no structures with multiple chains
if kwargs[name_prefix + "_compare_multimer"]:
d_multimer = multimer_dists(sifts_map,
structures,
atom_filter=kwargs["atom_filter"],
output_prefix=aux_prefix + "_" +
name_prefix + "_distmap_multimer")
else:
d_multimer = None
# if we have a multimer contact map, save it
if d_multimer is not None:
d_multimer.to_file(outcfg[name_prefix + "_distmap_multimer"])
outcfg[
name_prefix +
"_multimer_contacts_file"] = prefix + name_prefix + "_contacts_multimer.csv"
# save contacts to separate file
d_multimer.contacts(kwargs["distance_cutoff"]).to_csv(
outcfg[name_prefix + "_multimer_contacts_file"],
index=False)
else:
outcfg[name_prefix + "_distmap_multimer"] = None
# create remapped structures (e.g. for
# later comparison of folding results)
# remap structures, swap mapping index and filename in
# dictionary so we have a list of files in the dict keys
outcfg[name_prefix + "_remapped_pdb_files"] = {
filename: mapping_index
for mapping_index, filename in remap_chains(
sifts_map,
aux_prefix,
seqmap,
chain_name=chain_name,
raise_missing=kwargs["raise_missing"]).items()
}
else:
# if no structures, cannot compute distance maps
d_intra = None
d_multimer = None
outcfg[name_prefix + "_distmap_monomer"] = None
outcfg[name_prefix + "_distmap_multimer"] = None
outcfg[name_prefix + "remapped_pdb_files"] = None
return d_intra, d_multimer, seqmap
# load all structures for both monomers
all_structures = set(first_sifts_map.hits.pdb_id).union(
set(second_sifts_map.hits.pdb_id))
structures = load_structures(all_structures,
kwargs["pdb_mmtf_dir"],
raise_missing=False)
d_intra_i, d_multimer_i, seqmap_i = _compute_monomer_distance_maps(
first_sifts_map, "first", "A")
d_intra_j, d_multimer_j, seqmap_j = _compute_monomer_distance_maps(
second_sifts_map, "second", "B")
# compute inter distance map if sifts map for each monomer exists
if len(first_sifts_map.hits) > 0 and len(second_sifts_map.hits) > 0:
d_inter = inter_dists(first_sifts_map,
second_sifts_map,
raise_missing=kwargs["raise_missing"])
# if there were overlapping PDBs, save the results
if d_inter is not None:
d_inter.to_file(outcfg["distmap_inter"])
# save contacts to separate file
d_inter.contacts(kwargs["distance_cutoff"]).to_csv(
outcfg["inter_contacts_file"], index=False)
else:
outcfg["inter_contacts_file"] = None
d_inter = None
# # Step 3: Compare ECs to distance maps
ec_table = pd.read_csv(kwargs["ec_file"])
for out_file, min_seq_dist in [
("ec_compared_longrange_file", kwargs["min_sequence_distance"]),
("ec_compared_all_file", 0),
]:
# compare ECs only if we have an intra distance map
# for at least one monomer - inter can't exist unless
# we have both monomers
if (d_intra_i is not None) or (d_intra_j is not None):
# compare distances individually for each segment pair
ecs_intra_i = ec_table.query(
"segment_i == segment_j == @first_segment_name")
if d_intra_i is not None:
ecs_intra_i_compared = coupling_scores_compared(
ecs_intra_i,
d_intra_i,
d_multimer_i,
dist_cutoff=kwargs["distance_cutoff"],
output_file=None,
min_sequence_dist=min_seq_dist)
else:
# If no distance map, the distance is saved as np.nan
ecs_intra_i_compared = ecs_intra_i.assign(dist=np.nan)
ecs_intra_j = ec_table.query(
"segment_i == segment_j == @second_segment_name")
if d_intra_j is not None:
ecs_intra_j_compared = coupling_scores_compared(
ecs_intra_j,
d_intra_j,
d_multimer_j,
dist_cutoff=kwargs["distance_cutoff"],
output_file=None,
min_sequence_dist=min_seq_dist)
else:
ecs_intra_j_compared = ecs_intra_j.assign(dist=np.nan)
ecs_inter = ec_table.query("segment_i != segment_j")
if d_inter is not None:
ecs_inter_compared = coupling_scores_compared(
ecs_inter,
d_inter,
dist_map_multimer=None,
dist_cutoff=kwargs["distance_cutoff"],
output_file=None,
min_sequence_dist=
None # does not apply for inter-protein ECs
)
else:
ecs_inter_compared = ecs_inter.assign(dist=np.nan)
# combine the tables
ec_table_compared = pd.concat([
ecs_inter_compared, ecs_intra_i_compared, ecs_intra_j_compared
])
# rename the precision column to "segmentwise_precision"
# because we calculated precision for each segment independently
ec_table_compared = ec_table_compared.rename(
columns={"precision": "segmentwise_precision"})
# TODO: change "cn" to "score" eventually
ec_table_compared = ec_table_compared.sort_values("cn",
ascending=False)
# add the total precision
# TODO: implement different cutoffs for intra vs inter contacts
ec_table_compared = add_precision(
ec_table_compared, dist_cutoff=kwargs["distance_cutoff"])
# save to file
# all ecs
ec_table_compared.to_csv(outcfg[out_file])
# save the inter ECs to a file
ecs_inter_compared.to_csv(outcfg["ec_compared_inter_file"])
# create the inter-ecs line drawing script
if outcfg["ec_compared_inter_file"] is not None and kwargs[
"plot_highest_count"] is not None:
inter_ecs = ec_table.query("segment_i != segment_j")
outcfg[
"ec_lines_compared_pml_file"] = prefix + "_draw_ec_lines_compared.pml"
pairs.ec_lines_pymol_script(
inter_ecs.iloc[:kwargs["plot_highest_count"], :],
outcfg["ec_lines_compared_pml_file"],
distance_cutoff=kwargs["distance_cutoff"],
chain={
first_segment_name: "A",
second_segment_name: "B"
})
# Remap the complex crystal structures, if available
if len(first_sifts_map.hits) > 0 and len(second_sifts_map.hits) > 0:
outcfg["complex_remapped_pdb_files"] = {
filename: mapping_index
for mapping_index, filename in remap_complex_chains(
first_sifts_map,
second_sifts_map,
seqmap_i,
seqmap_j,
output_prefix=aux_prefix,
raise_missing=kwargs["raise_missing"]).items()
}
# Step 4: Make contact map plots
# if no structures available, defaults to EC-only plot
outcfg["contact_map_files"] = _make_complex_contact_maps(
ec_table, d_intra_i, d_multimer_i, d_intra_j, d_multimer_j, d_inter,
first_segment_name, second_segment_name, **kwargs)
return outcfg
def standard(**kwargs):
"""
Protocol:
Compare ECs for single proteins (or domains)
to 3D structure information
Parameters
----------
Mandatory kwargs arguments:
See list below in code where calling check_required
Returns
-------
outcfg : dict
Output configuration of the pipeline, including
the following fields:
* ec_file_compared_all
* ec_file_compared_all_longrange
* pdb_structure_hits
* distmap_monomer
* distmap_multimer
* contact_map_files
* remapped_pdb_files
"""
check_required(kwargs, [
"prefix",
"ec_file",
"min_sequence_distance",
"pdb_mmtf_dir",
"atom_filter",
"compare_multimer",
"distance_cutoff",
"target_sequence_file",
"scale_sizes",
])
prefix = kwargs["prefix"]
outcfg = {
"ec_compared_all_file": prefix + "_CouplingScoresCompared_all.csv",
"ec_compared_longrange_file":
prefix + "_CouplingScoresCompared_longrange.csv",
"pdb_structure_hits_file": prefix + "_structure_hits.csv",
"pdb_structure_hits_unfiltered_file":
prefix + "_structure_hits_unfiltered.csv",
# cannot have the distmap files end with "_file" because there are
# two files (.npy and .csv), which would cause problems with automatic
# checking if those files exist
"distmap_monomer": prefix + "_distance_map_monomer",
"distmap_multimer": prefix + "_distance_map_multimer",
}
# make sure EC file exists
verify_resources("EC file does not exist", kwargs["ec_file"])
# make sure output directory exists
create_prefix_folders(prefix)
# store auxiliary files here (too much for average user)
aux_prefix = insert_dir(prefix, "aux", rootname_subdir=False)
create_prefix_folders(aux_prefix)
# Step 1: Identify 3D structures for comparison
sifts_map, sifts_map_full = _identify_structures(
**{
**kwargs,
"prefix": aux_prefix,
})
# save selected PDB hits
sifts_map.hits.to_csv(outcfg["pdb_structure_hits_file"], index=False)
# also save full list of hits
sifts_map_full.hits.to_csv(outcfg["pdb_structure_hits_unfiltered_file"],
index=False)
# Step 2: Compute distance maps
# load all structures at once
structures = load_structures(sifts_map.hits.pdb_id,
kwargs["pdb_mmtf_dir"],
raise_missing=False)
# compute distance maps and save
# (but only if we found some structure)
if len(sifts_map.hits) > 0:
d_intra = intra_dists(sifts_map,
structures,
atom_filter=kwargs["atom_filter"],
output_prefix=aux_prefix + "_distmap_intra")
d_intra.to_file(outcfg["distmap_monomer"])
# save contacts to separate file
outcfg["monomer_contacts_file"] = prefix + "_contacts_monomer.csv"
d_intra.contacts(kwargs["distance_cutoff"]).to_csv(
outcfg["monomer_contacts_file"], index=False)
# compute multimer distances, if requested;
# note that d_multimer can be None if there
# are no structures with multiple chains
if kwargs["compare_multimer"]:
d_multimer = multimer_dists(sifts_map,
structures,
atom_filter=kwargs["atom_filter"],
output_prefix=aux_prefix +
"_distmap_multimer")
else:
d_multimer = None
# if we have a multimer contact mapin the end, save it
if d_multimer is not None:
d_multimer.to_file(outcfg["distmap_multimer"])
outcfg[
"multimer_contacts_file"] = prefix + "_contacts_multimer.csv"
# save contacts to separate file
d_multimer.contacts(kwargs["distance_cutoff"]).to_csv(
outcfg["multimer_contacts_file"], index=False)
else:
outcfg["distmap_multimer"] = None
# at this point, also create remapped structures (e.g. for
# later comparison of folding results)
verify_resources("Target sequence file does not exist",
kwargs["target_sequence_file"])
# create target sequence map for remapping structure
with open(kwargs["target_sequence_file"]) as f:
header, seq = next(read_fasta(f))
seq_id, seq_start, seq_end = parse_header(header)
seqmap = dict(zip(range(seq_start, seq_end + 1), seq))
# remap structures, swap mapping index and filename in
# dictionary so we have a list of files in the dict keys
outcfg["remapped_pdb_files"] = {
filename: mapping_index
for mapping_index, filename in remap_chains(
sifts_map, aux_prefix, seqmap).items()
}
else:
# if no structures, can not compute distance maps
d_intra = None
d_multimer = None
outcfg["distmap_monomer"] = None
outcfg["distmap_multimer"] = None
outcfg["remapped_pdb_files"] = None
# Step 3: Compare ECs to distance maps
ec_table = pd.read_csv(kwargs["ec_file"])
# identify number of sites in EC model
num_sites = len(
set.union(set(ec_table.i.unique()), set(ec_table.j.unique())))
for out_file, min_seq_dist in [
("ec_compared_longrange_file", kwargs["min_sequence_distance"]),
("ec_compared_all_file", 0),
]:
# compare ECs only if we minimally have intra distance map
if d_intra is not None:
coupling_scores_compared(ec_table,
d_intra,
d_multimer,
dist_cutoff=kwargs["distance_cutoff"],
output_file=outcfg[out_file],
min_sequence_dist=min_seq_dist)
else:
outcfg[out_file] = None
# also create line-drawing script if we made the csv
if outcfg["ec_compared_longrange_file"] is not None:
ecs_longrange = pd.read_csv(outcfg["ec_compared_longrange_file"])
outcfg[
"ec_lines_compared_pml_file"] = prefix + "_draw_ec_lines_compared.pml"
pairs.ec_lines_pymol_script(ecs_longrange.iloc[:num_sites, :],
outcfg["ec_lines_compared_pml_file"],
distance_cutoff=kwargs["distance_cutoff"])
# Step 4: Make contact map plots
# if no structures available, defaults to EC-only plot
outcfg["contact_map_files"] = _make_contact_maps(ec_table, d_intra,
d_multimer, **kwargs)
return outcfg
def _postprocess_inference(ecs, kwargs, model, outcfg, prefix, generate_line_plot=False,
generate_enrichment=False, ec_filter="abs(i - j) >= {}", chain=None):
"""
Post-process inference result of all protocols
Parameters
----------
ecs : pandas.DataFrame
EC table with additional column "probability"
containing confidence measure
kwargs arguments:
See list in protocols.
model : CouplingsModel
The couplings model with the inferred parameters
outcfg : dict
Output configuration of the pipeline, including
the following fields:
* raw_ec_file
* model_file
* num_sites
* num_sequences
* effective_sequences
* focus_mode (passed through)
* focus_sequence (passed through)
* segments (passed through)
prefix : str
file path prefix
generate_line_plot : bool
Determines whether a line plot pymol structure will be generated
generate_enrichment : bool
Determines whether an EC enrichment file and pymol structure will be generated
ec_filter : str
String determining the ec distance filter (default: "abs(i - j) >= {}")
chain : dict
Dictionary to map different segments to their chains
Returns
-------
ext_outcfg : dict
Optional output configuration of the pipeline, including
the following fields:
* ec_longrange_file
* ec_lines_oml_file
* enrichmnet_file
* enrichment_pml_files
* evzoom_file
"""
ext_outcfg = {}
# write the sorted ECs table to csv file
ecs.to_csv(outcfg["ec_file"], index=False)
# also store longrange ECs as convenience output
if kwargs["min_sequence_distance"] is not None:
ext_outcfg["ec_longrange_file"] = prefix + "_CouplingScores_longrange.csv"
ecs_longrange = ecs.query(
ec_filter.format(kwargs["min_sequence_distance"])
)
ecs_longrange.to_csv(ext_outcfg["ec_longrange_file"], index=False)
if generate_line_plot:
ext_outcfg["ec_lines_pml_file"] = prefix + "_draw_ec_lines.pml"
L = outcfg["num_sites"]
ec_lines_pymol_script(
ecs_longrange.iloc[:L, :],
ext_outcfg["ec_lines_pml_file"],
chain=chain,
score_column="cn" # "di
)
# compute EC enrichment (for now, for single segments
# only since enrichment code cannot handle multiple segments)
if generate_enrichment:
ext_outcfg["enrichment_file"] = prefix + "_enrichment.csv"
ecs_enriched = pairs.enrichment(ecs, score="cn") # "di"
ecs_enriched.to_csv(ext_outcfg["enrichment_file"], index=False)
# create corresponding enrichment pymol scripts
ext_outcfg["enrichment_pml_files"] = []
for sphere_view, pml_suffix in [
(True, "_enrichment_spheres.pml"), (False, "_enrichment_sausage.pml")
]:
pml_file = prefix + pml_suffix
enrichment_pymol_script(ecs_enriched, pml_file, sphere_view=sphere_view)
ext_outcfg["enrichment_pml_files"].append(pml_file)
# output EVzoom JSON file if we have stored model file
if outcfg.get("model_file", None) is not None:
ext_outcfg["evzoom_file"] = prefix + "_evzoom.json"
with open(ext_outcfg["evzoom_file"], "w") as f:
# create JSON output and write to file
f.write(
evzoom_json(model) + "\n"
)
return ext_outcfg
def standard(**kwargs):
"""
Protocol:
Infer ECs from alignment using plmc.
.. todo::
1. make EC enrichment calculation segment-ready
2. explain meaning of parameters in detail.
Parameters
----------
Mandatory kwargs arguments:
See list below in code where calling check_required
Returns
-------
outcfg : dict
Output configuration of the pipeline, including
the following fields:
* raw_ec_file
* model_file
* num_sites
* num_sequences
* effective_sequences
* focus_mode (passed through)
* focus_sequence (passed through)
* segments (passed through)
"""
check_required(
kwargs,
[
"prefix", "alignment_file",
"focus_mode", "focus_sequence", "theta",
"alphabet", "segments", "ignore_gaps", "iterations",
"lambda_h", "lambda_J", "lambda_group",
"scale_clusters",
"cpu", "plmc", "reuse_ecs",
"min_sequence_distance", # "save_model",
]
)
prefix = kwargs["prefix"]
# for now disable option to not save model, since
# otherwise mutate stage will crash. To remove model
# file at end, use delete option in management section.
"""
if kwargs["save_model"]:
model = prefix + ".model"
else:
model = None
"""
model = prefix + ".model"
outcfg = {
"model_file": model,
"raw_ec_file": prefix + "_ECs.txt",
"ec_file": prefix + "_CouplingScores.csv",
# TODO: the following are passed through stage...
# keep this or unnecessary?
"focus_mode": kwargs["focus_mode"],
"focus_sequence": kwargs["focus_sequence"],
"segments": kwargs["segments"],
}
# make sure input alignment exists
verify_resources(
"Input alignment does not exist",
kwargs["alignment_file"]
)
# make sure output directory exists
create_prefix_folders(prefix)
# regularization strength on couplings J_ij
lambda_J = kwargs["lambda_J"]
segments = kwargs["segments"]
if segments is not None:
segments = [
mapping.Segment.from_list(s) for s in segments
]
# first determine size of alphabet;
# default is amino acid alphabet
if kwargs["alphabet"] is None:
alphabet = ALPHABET_PROTEIN
alphabet_setting = None
else:
alphabet = kwargs["alphabet"]
# allow shortcuts for protein, DNA, RNA
if alphabet in ALPHABET_MAP:
alphabet = ALPHABET_MAP[alphabet]
# if we have protein alphabet, do not set
# as plmc parameter since default parameter,
# has some implementation advantages for focus mode
if alphabet == ALPHABET_PROTEIN:
alphabet_setting = None
else:
alphabet_setting = alphabet
# scale lambda_J to proportionally compensate
# for higher number of J_ij compared to h_i?
if kwargs["lambda_J_times_Lq"]:
num_symbols = len(alphabet)
# if we ignore gaps, there is one character less
if kwargs["ignore_gaps"]:
num_symbols -= 1
# second, determine number of uppercase positions
# that are included in the calculation
with open(kwargs["alignment_file"]) as f:
seq_id, seq = next(read_fasta(f))
# gap character is by convention first char in alphabet
gap = alphabet[0]
uppercase = [
c for c in seq if c == c.upper() or c == gap
]
L = len(uppercase)
# finally, scale lambda_J
lambda_J *= (num_symbols - 1) * (L - 1)
# run plmc... or reuse pre-exisiting results from previous run
plm_outcfg_file = prefix + ".couplings_standard_plmc.outcfg"
# determine if to rerun, only possible if previous results
# were stored in ali_outcfg_file
if kwargs["reuse_ecs"] and valid_file(plm_outcfg_file):
plmc_result = read_config_file(plm_outcfg_file)
# check if the EC/parameter files are there
required_files = [outcfg["raw_ec_file"]]
if outcfg["model_file"] is not None:
required_files += [outcfg["model_file"]]
verify_resources(
"Tried to reuse ECs, but empty or "
"does not exist",
*required_files
)
else:
# run plmc binary
plmc_result = ct.run_plmc(
kwargs["alignment_file"],
outcfg["raw_ec_file"],
outcfg["model_file"],
focus_seq=kwargs["focus_sequence"],
alphabet=alphabet_setting,
theta=kwargs["theta"],
scale=kwargs["scale_clusters"],
ignore_gaps=kwargs["ignore_gaps"],
iterations=kwargs["iterations"],
lambda_h=kwargs["lambda_h"],
lambda_J=lambda_J,
lambda_g=kwargs["lambda_group"],
cpu=kwargs["cpu"],
binary=kwargs["plmc"],
)
# save iteration table to file
iter_table_file = prefix + "_iteration_table.csv"
plmc_result.iteration_table.to_csv(
iter_table_file
)
# turn namedtuple into dictionary to make
# restarting code nicer
plmc_result = dict(plmc_result._asdict())
# then replace table with filename so
# we can store results in config file
plmc_result["iteration_table"] = iter_table_file
# save results of search for possible restart
write_config_file(plm_outcfg_file, plmc_result)
# store useful information about model in outcfg
outcfg.update({
"num_sites": plmc_result["num_valid_sites"],
"num_sequences": plmc_result["num_valid_seqs"],
"effective_sequences": plmc_result["effective_samples"],
"region_start": plmc_result["region_start"],
})
# read and sort ECs
ecs = pairs.read_raw_ec_file(outcfg["raw_ec_file"])
# add mixture model probability
ecs = pairs.add_mixture_probability(ecs)
if segments is not None: # and (len(segments) > 1 or not kwargs["focus_mode"]):
# create index mapping
seg_mapper = mapping.SegmentIndexMapper(
kwargs["focus_mode"], outcfg["region_start"], *segments
)
# apply to EC table
ecs = mapping.segment_map_ecs(ecs, seg_mapper)
# write updated table to csv file
ecs.to_csv(outcfg["ec_file"], index=False)
# also store longrange ECs as convenience output
if kwargs["min_sequence_distance"] is not None:
outcfg["ec_longrange_file"] = prefix + "_CouplingScores_longrange.csv"
ecs_longrange = ecs.query(
"abs(i - j) >= {}".format(kwargs["min_sequence_distance"])
)
ecs_longrange.to_csv(outcfg["ec_longrange_file"], index=False)
# also create line-drawing script (for now, only for single segments)
if segments is None or len(segments) == 1:
outcfg["ec_lines_pml_file"] = prefix + "_draw_ec_lines.pml"
L = outcfg["num_sites"]
ec_lines_pymol_script(
ecs_longrange.iloc[:L, :],
outcfg["ec_lines_pml_file"]
)
# compute EC enrichment (for now, for single segments
# only since enrichment code cannot handle multiple segments)
if segments is None or len(segments) == 1:
outcfg["enrichment_file"] = prefix + "_enrichment.csv"
ecs_enriched = pairs.enrichment(ecs)
ecs_enriched.to_csv(outcfg["enrichment_file"], index=False)
# create corresponding enrichment pymol scripts
outcfg["enrichment_pml_files"] = []
for sphere_view, pml_suffix in [
(True, "_enrichment_spheres.pml"), (False, "_enrichment_sausage.pml")
]:
pml_file = prefix + pml_suffix
enrichment_pymol_script(ecs_enriched, pml_file, sphere_view=sphere_view)
outcfg["enrichment_pml_files"].append(pml_file)
# output EVzoom JSON file if we have stored model file
if outcfg.get("model_file", None) is not None:
outcfg["evzoom_file"] = prefix + "_evzoom.json"
with open(outcfg["evzoom_file"], "w") as f:
# load parameters
c = CouplingsModel(outcfg["model_file"])
# create JSON output and write to file
f.write(
evzoom_json(c) + "\n"
)
# dump output config to YAML file for debugging/logging
write_config_file(prefix + ".couplings_standard.outcfg", outcfg)
return outcfg
def mean_field(**kwargs):
"""
Protocol:
Infer ECs from alignment using mean field direct coupling analysis.
For now, mean field DCA can only be run in focus mode, gaps
included.
Parameters
----------
Mandatory kwargs arguments:
See list below in code where calling check_required.
Returns
-------
outcfg : dict
Output configuration of the pipeline, including
the following fields:
* raw_ec_file
* model_file
* num_sites
* num_sequences
* effective_sequences
* focus_mode (passed through)
* focus_sequence (passed through)
* segments (passed through)
"""
check_required(
kwargs,
[
"prefix", "alignment_file", "segments",
"focus_mode", "focus_sequence", "theta",
"pseudo_count", "alphabet",
"min_sequence_distance", # "save_model",
]
)
if not kwargs["focus_mode"]:
raise InvalidParameterError(
"For now, mean field DCA can only be run in focus mode."
)
prefix = kwargs["prefix"]
# option to save model disabled
"""
if kwargs["save_model"]:
model = prefix + ".model"
else:
model = None
"""
model = prefix + ".model"
outcfg = {
"model_file": model,
"raw_ec_file": prefix + "_ECs.txt",
"ec_file": prefix + "_CouplingScores.csv",
# TODO: the following are passed through stage...
# keep this or unnecessary?
"focus_mode": kwargs["focus_mode"],
"focus_sequence": kwargs["focus_sequence"],
"segments": kwargs["segments"],
}
# make sure input alignment exists
alignment_file = kwargs["alignment_file"]
verify_resources(
"Input alignment does not exist",
kwargs["alignment_file"]
)
# make sure output directory exists
create_prefix_folders(prefix)
segments = kwargs["segments"]
if segments is not None:
segments = [
mapping.Segment.from_list(s) for s in segments
]
# determine alphabet
# default is protein
if kwargs["alphabet"] is None:
alphabet = ALPHABET_PROTEIN
else:
alphabet = kwargs["alphabet"]
# allow shortcuts for protein, DNA, RNA
if alphabet in ALPHABET_MAP:
alphabet = ALPHABET_MAP[alphabet]
# read in a2m alignment
with open(alignment_file) as f:
input_alignment = Alignment.from_file(
f, alphabet=alphabet,
format="fasta"
)
# init mean field direct coupling analysis
mf_dca = MeanFieldDCA(input_alignment)
# run mean field approximation
model = mf_dca.fit(
theta=kwargs["theta"],
pseudo_count=kwargs["pseudo_count"]
)
# write ECs to file
model.to_raw_ec_file(
outcfg["raw_ec_file"]
)
# write model file
if outcfg["model_file"] is not None:
model.to_file(
outcfg["model_file"],
file_format="plmc_v2"
)
# store useful information about model in outcfg
outcfg.update({
"num_sites": model.L,
"num_sequences": model.N_valid,
"effective_sequences": float(round(model.N_eff, 1)),
"region_start": int(model.index_list[0]),
})
# read and sort ECs
ecs = pd.read_csv(
outcfg["raw_ec_file"], sep=" ",
# for now, call the last two columns
# "fn" and "cn" to prevent compare
# stage from crashing
names=["i", "A_i", "j", "A_j", "fn", "cn"]
# names=["i", "A_i", "j", "A_j", "mi", "di"]
).sort_values(
by="cn",
ascending=False
)
# write the sorted ECs table to csv file
ecs.to_csv(outcfg["ec_file"], index=False)
# also store longrange ECs as convenience output
if kwargs["min_sequence_distance"] is not None:
outcfg["ec_longrange_file"] = prefix + "_CouplingScores_longrange.csv"
ecs_longrange = ecs.query(
"abs(i - j) >= {}".format(kwargs["min_sequence_distance"])
)
ecs_longrange.to_csv(outcfg["ec_longrange_file"], index=False)
# also create line-drawing script (for now, only for single segments)
if segments is None or len(segments) == 1:
outcfg["ec_lines_pml_file"] = prefix + "_draw_ec_lines.pml"
L = outcfg["num_sites"]
ec_lines_pymol_script(
ecs_longrange.iloc[:L, :],
outcfg["ec_lines_pml_file"],
score_column="cn" # "di
)
# compute EC enrichment (for now, for single segments
# only since enrichment code cannot handle multiple segments)
if segments is None or len(segments) == 1:
outcfg["enrichment_file"] = prefix + "_enrichment.csv"
ecs_enriched = pairs.enrichment(ecs, score="cn") # "di"
ecs_enriched.to_csv(outcfg["enrichment_file"], index=False)
# create corresponding enrichment pymol scripts
outcfg["enrichment_pml_files"] = []
for sphere_view, pml_suffix in [
(True, "_enrichment_spheres.pml"), (False, "_enrichment_sausage.pml")
]:
pml_file = prefix + pml_suffix
enrichment_pymol_script(ecs_enriched, pml_file, sphere_view=sphere_view)
outcfg["enrichment_pml_files"].append(pml_file)
# output EVzoom JSON file if we have stored model file
if outcfg.get("model_file", None) is not None:
outcfg["evzoom_file"] = prefix + "_evzoom.json"
with open(outcfg["evzoom_file"], "w") as f:
# create JSON output and write to file
f.write(
evzoom_json(model) + "\n"
)
# dump output config to YAML file for debugging/logging
write_config_file(prefix + ".couplings_standard.outcfg", outcfg)
return outcfg
def _postprocess_inference(ecs, kwargs, model, outcfg, prefix, generate_line_plot=False,
generate_enrichment=False, ec_filter="abs(i - j) >= {}",
chain=None, score="cn"):
"""
Post-process inference result of all protocols
Parameters
----------
ecs : pandas.DataFrame
EC table with additional column "probability"
containing confidence measure
kwargs arguments:
See list in protocols.
model : CouplingsModel
The couplings model with the inferred parameters
outcfg : dict
Output configuration of the pipeline, including
the following fields:
* raw_ec_file
* model_file
* num_sites
* num_sequences
* effective_sequences
* focus_mode (passed through)
* focus_sequence (passed through)
* segments (passed through)
prefix : str
file path prefix
generate_line_plot : bool
Determines whether a line plot pymol structure will be generated
generate_enrichment : bool
Determines whether an EC enrichment file and pymol structure will be generated
ec_filter : str
String determining the ec distance filter (default: "abs(i - j) >= {}")
chain : dict
Dictionary to map different segments to their chains
score : str, optional (default: "cn")
Score column to use for postprocessing
Returns
-------
ext_outcfg : dict
Optional output configuration of the pipeline, including
the following fields:
* ec_longrange_file
* ec_lines_oml_file
* enrichmnet_file
* enrichment_pml_files
* evzoom_file
"""
ext_outcfg = {}
# write the sorted ECs table to csv file
ecs.to_csv(outcfg["ec_file"], index=False)
# if maximum coupling score is 0, bail out... will crash downstream calculations
if ecs[score].max() <= 0:
raise BailoutException("couplings: No couplings identified")
# also store longrange ECs as convenience output
if kwargs["min_sequence_distance"] is not None:
ext_outcfg["ec_longrange_file"] = prefix + "_CouplingScores_longrange.csv"
ecs_longrange = ecs.query(
ec_filter.format(kwargs["min_sequence_distance"])
)
ecs_longrange.to_csv(ext_outcfg["ec_longrange_file"], index=False)
if generate_line_plot:
ext_outcfg["ec_lines_pml_file"] = prefix + "_draw_ec_lines.pml"
L = outcfg["num_sites"]
ec_lines_pymol_script(
ecs_longrange.iloc[:L, :],
ext_outcfg["ec_lines_pml_file"],
chain=chain,
score_column=score
)
# compute EC enrichment (for now, for single segments
# only since enrichment code cannot handle multiple segments)
if generate_enrichment:
ext_outcfg["enrichment_file"] = prefix + "_enrichment.csv"
min_seqdist = kwargs["min_sequence_distance"]
if min_seqdist is None:
min_seqdist = 0
ecs_enriched = pairs.enrichment(
ecs, score=score, min_seqdist=min_seqdist
)
ecs_enriched.to_csv(ext_outcfg["enrichment_file"], index=False)
# create corresponding enrichment pymol scripts
ext_outcfg["enrichment_pml_files"] = []
for sphere_view, pml_suffix in [
(True, "_enrichment_spheres.pml"), (False, "_enrichment_sausage.pml")
]:
pml_file = prefix + pml_suffix
enrichment_pymol_script(ecs_enriched, pml_file, sphere_view=sphere_view)
ext_outcfg["enrichment_pml_files"].append(pml_file)
# output EVzoom JSON file if we have stored model file
if outcfg.get("model_file", None) is not None:
ext_outcfg["evzoom_file"] = prefix + "_evzoom.json"
# automatically determine reordering of alphabet for EVzoom output
# (proteins only)
alphabet = "".join(model.alphabet)
if alphabet == ALPHABET_PROTEIN_NOGAP:
reorder = ALPHABET_PROTEIN_NOGAP_ORDERED
elif alphabet == ALPHABET_PROTEIN:
reorder = ALPHABET_PROTEIN_ORDERED
else:
reorder = None
with open(ext_outcfg["evzoom_file"], "w") as f:
# create JSON output and write to file
# TODO: note that this will by default use CN scores as generated
# TODO: by CouplingsModel; at the moment there is no easy way
# TODO: around this limitation so just use CN score for now
f.write(
evzoom_json(model, reorder=reorder) + "\n"
)
return ext_outcfg
