#!/usr/bin/env Rscript
#' ---
#' title: Compilation of CORUM protein complexes.
#' description:
#' authors: Tyler W Bradshaw
#' ---
## Compile CORUM protein complexes.
identity_threshold <- 0.9
## Parameters:
script <- "043_CORUM-Complexes"
short_name <- "corum"
tags <- c("corum", "protein complex", "complexes", "database")
ref_url <- "https://www.ncbi.nlm.nih.gov/pubmed/30357367"
data_url <- "https://mips.helmholtz-muenchen.de/corum/download/coreComplexes.txt.zip"
# Load renv.
renv::load(getrd())
# Imports.
suppressPackageStartupMessages({
library(dplyr)
library(getPPIs)
library(TBmiscr)
library(data.table)
})
# Load functions in root/R.
load_all()
# Directories.
root <- getrd()
gmtdir <- file.path(root, "gmt")
datadir <- file.path(root, "data")
tabsdir <- file.path(root, "tables")
downdir <- file.path(root, "downloads")
# Download Chorum complexes.
zip_file <- file.path(downdir, basename(data_url))
myfile <- tools::file_path_sans_ext(zip_file)
message(paste("Downloading PPI Complexes from CORUM database..."))
download.file(data_url, zip_file, quiet = TRUE)
# Extract zipped file and remove temporary files.
unzip(zip_file, exdir = downdir)
data <- data.table::fread(myfile)
unlink(zip_file)
unlink(myfile)
## Clean-up the Corum data.
# We need to extract Entrez IDs associated with protein complexes.
# Split Entrez ID column.
data <- tidyr::separate_rows(data, "subunits(Entrez IDs)", sep = ";")
# Let's collect the relevant data columns.
cols <- c(
"ComplexID", "subunits(Entrez IDs)", "Organism", "PubMed ID",
"ComplexName", "Synonyms",
"Protein complex purification method", "Complex comment"
)
corum <- data %>% select(all_of(cols))
# Clean-up colnames.
colnames(corum) <- c(
"ComplexID", "Entrez", "Organism", "PMID", "Name",
"Synonym", "Method", "Comment"
)
# Map entrez ids to mouse homologs.
musEntrez <- getHomologs(corum$Entrez, species = "mouse")
# Add mouse homologs to data.
corum <- tibble::add_column(corum, musEntrez, .after = "Entrez")
# Summarize total number of proteins per complex as well as the number of mouse
# homologs per complex and PMIDs.
corum_complexes <- corum %>%
group_by(ComplexID) %>%
summarize(
Name = unique(Name),
nProts = length(unique(Entrez)),
nHomologs = sum(!is.na(unique(musEntrez))),
PMIDs = paste(unique(PMID), collapse = "; "),
Entrez = paste(unique(Entrez), collapse = "; "),
musEntrez = paste(unique(musEntrez[!is.na(musEntrez)]),
collapse = "; "
)
)
# Separate out mouse Entrez column again.
corum_complexes <- tidyr::separate_rows(corum_complexes, "musEntrez", sep = "; ")
# Add percent coverage.
p <- corum_complexes$nHomologs / corum_complexes$nProts
corum_complexes <- tibble::add_column(corum_complexes,
percentID = p, .after = "nHomologs"
)
# Subset the data: complete identity.
subdat <- corum_complexes %>% filter(percentID >= identity_threshold)
n <- length(unique(subdat$Name))
message(paste("Collected", formatC(n, big.mark = ","), "mouse complexes."))
# Split into gene list.
data_list <- subdat %>%
group_by(Name) %>%
group_split()
# Collect list of genes.
gene_list <- sapply(data_list, function(x) unique(x$musEntrez))
names(gene_list) <- sapply(data_list, function(x) unique(x$Name))
# Save as gmt, and then save as rda and generate documentation.
myfile <- file.path(gmtdir, script)
write_gmt(gene_list, ref_url, myfile)
documentDataset(myfile, short_name, Rdir = file.path(root, "R"), datadir)
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