221 lines
5.9 KiB
R
221 lines
5.9 KiB
R
#!/usr/bin/env Rscript
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source("~/git/LSHTM_analysis/config/gid.R")
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source("~/git/LSHTM_analysis/scripts/plotting/get_plotting_dfs.R")
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#########################################################
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# TASK: Replace B-factors in the pdb file with the mean
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# normalised affinity values
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#########################################################
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# working dir and loading libraries
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#source("~/git/LSHTM_analysis/scripts/Header_TT.R")
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library(bio3d)
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require("getopt", quietly = TRUE) # cmd parse arguments
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#========================================================
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#========================================================
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cat(gene)
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gene_match = paste0(gene,"_p."); cat(gene_match)
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cat(gene_match)
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#=============
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# directories
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#=============
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datadir = paste0("~/git/Data")
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indir = paste0(datadir, "/", drug, "/input")
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outdir = paste0("~/git/Data", "/", drug, "/output")
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#outdir_plots = paste0("~/git/Writing/thesis/images/results/", tolower(gene))
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#=======
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# output
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#=======
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outdir_images = paste0("~/git/Writing/thesis/images/results/", tolower(gene), "/")
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cat("plots will output to:", outdir_images)
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#======
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# input
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#======
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in_filename_pdb = paste0(tolower(gene), "_complex.pdb")
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infile_pdb = paste0(indir, "/", in_filename_pdb)
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cat(paste0("Input file:", infile_pdb) )
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#=======
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# output
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#=======
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#out_filename_duet_mspdb = paste0(tolower(gene), "_complex_bduet_ms.pdb")
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out_filename_lig_mspdb = paste0(tolower(gene), "_complex_b_lig_ms.pdb")
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outfile_lig_mspdb = paste0(outdir_images,out_filename_lig_mspdb)
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print(paste0("Output file:", outfile_lig_mspdb))
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#%%===============================================================
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#NOTE: duet here refers to the ensemble affinity values
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###########################
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# Read file: average affinity values
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# or mcsm_normalised file
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###########################
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my_df_raw = merged_df3[, c("position", "ligand_distance", "avg_lig_affinity_scaled", "avg_lig_affinity")]
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my_df_raw = my_df_raw[my_df_raw$ligand_distance<10,]
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# avg by position on the SCALED values
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my_df <- my_df_raw %>%
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group_by(position) %>%
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summarize(avg_ligaff_sc_pos = mean(avg_lig_affinity_scaled))
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max(my_df$avg_ligaff_sc_pos)
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min(my_df$avg_ligaff_sc_pos)
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#############
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# Read pdb
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#############
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# list of 8
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my_pdb = read.pdb(infile_pdb
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, maxlines = -1
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, multi = FALSE
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, rm.insert = FALSE
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, rm.alt = TRUE
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, ATOM.only = FALSE
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, hex = FALSE
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, verbose = TRUE)
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# assign separately for duet and ligand
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my_pdb_duet = my_pdb
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#=========================================================
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# Replacing B factor with mean affinity scores
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# within the respective dfs
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#==========================================================
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# extract atom list into a variable
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# since in the list this corresponds to data frame, variable will be a df
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#df_duet = my_pdb_duet[[1]]
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df_duet= my_pdb_duet[['atom']]
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# make a copy: required for downstream sanity checks
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d2_duet = df_duet
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# sanity checks: B factor
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max(df_duet$b); min(df_duet$b)
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#==================================================
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# histograms and density plots for inspection
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# 1: original B-factors
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# 2: original mean affinity values
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# 3: replaced B-factors with mean affinity values
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#==================================================
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# Set the margin on all sides
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par(oma = c(3,2,3,0)
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, mar = c(1,3,5,2)
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#, mfrow = c(3,2)
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#, mfrow = c(3,4))
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, mfrow = c(3,2))
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#=============
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# Row 1 plots: original B-factors
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# duet and affinity
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#=============
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hist(df_duet$b
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, xlab = ""
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, main = "Bfactor affinity")
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plot(density(df_duet$b)
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, xlab = ""
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, main = "Bfactor affinity")
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#=============
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# Row 2 plots: original mean affinity values
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# affinity
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#=============
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#hist(my_df$averaged_duet
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hist(my_df$avg_ligaff_sc_pos
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, xlab = ""
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, main = "mean affinity values")
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#plot(density(my_df$averaged_duet)
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plot(density(my_df$avg_ligaff_sc_pos)
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, xlab = ""
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, main = "mean affinity values")
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################################################################
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#=========
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# step 1_P1
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#=========
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df_duet$b = my_df$avg_ligaff_sc_pos[match(df_duet$resno, my_df$position)]
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#=========
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# step 2_P1
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#=========
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# count NA in Bfactor
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b_na_duet = sum(is.na(df_duet$b)) ; b_na_duet
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# count number of 0"s in Bactor
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sum(df_duet$b == 0)
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# replace all NA in b factor with 0
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na_rep = 2
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df_duet$b[is.na(df_duet$b)] = na_rep
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#=========
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# step 3_P1
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#=========
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# sanity check: dim should be same before reassignment
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if ( (dim(df_duet)[1] == dim(d2_duet)[1]) &
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(dim(df_duet)[2] == dim(d2_duet)[2])
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){
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print("PASS: Dims of both dfs as expected")
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} else {
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print ("FAIL: Dims mismatch")
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quit()}
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#=========
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# step 4_P1:
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# VERY important
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#=========
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# assign it back to the pdb file
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my_pdb_duet[['atom']] = df_duet
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max(df_duet$b); min(df_duet$b)
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table(df_duet$b)
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sum(is.na(df_duet$b))
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#=========
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# step 5_P1: OUTPUT
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#=========
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cat(paste0("output file duet mean affinity pdb:", outfile_lig_mspdb))
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write.pdb(my_pdb_duet, outfile_lig_mspdb)
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# OUTPUT: position file
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poscsvF = paste0(outdir_images, tolower(gene), "_ligaff_positions.csv")
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cat(paste0("output file duet mean NA affinity POSITIONS:", poscsvF))
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filtered_pos = toString(my_df$position)
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write.table(filtered_pos, poscsvF, row.names = F, col.names = F )
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#============================
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# Add the 3rd histogram and density plots for comparisons
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#============================
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# Plots continued...
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# Row 3 plots: hist and density of replaced B-factors with affinity values
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hist(df_duet$b
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, xlab = ""
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, main = "repalcedB duet")
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plot(density(df_duet$b)
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, xlab = ""
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, main = "replacedB duet")
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# graph titles
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mtext(text = "Frequency"
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, side = 2
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, line = 0
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, outer = TRUE)
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mtext(text = paste0(tolower(gene), ": affinity distribution")
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, side = 3
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, line = 0
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, outer = TRUE)
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#============================================
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