How to do Direct Coupling Analysis

Background

Direct Coupling Analysis (DCA) tells you highly correlated residue pairs in a given protein sequence by means of synchronized (coupled) mutations during evolution.

Existing Online Server

EVcoupling

Do it from scratch

Build your sequence library

Choose existing sequence libraries with reference to HHsuite [1]

UniRef30 is definitely a good start: [2]

Untar it and you will get a >200G folder

Multisequence alignment

1. Install HHsuite (using conda)
2. Using hhblits and reformat.pl (provided by hhsuite) to get an MSA result (.fas)

hhblits -i prot.seq -d ../database/UniRef30_2020_06 -o $PREFIX.hhr -n 2 -oa3m $PREFIX.a3m -cov $COV
reformat.pl a3m fas $PREFIX.a3m $PREFIX.fas

Structure-based filtering

Then filter the residue pairs based on structural info

cat > TCL << 'EOF'
set THRES 0.2
set SHIFT 314
set infile [open "tmp" r]
set outfile [open "tmppairs" w]
set outlog [open "LOG" w]
set nn 0
while {[gets $infile line] >= 0} {
   lassign [regexp -inline -all {\S+} $line] ii jj kk
   if {$kk > $THRES} {
       puts $outfile "$ii $jj $kk"
       incr nn
   }
} 
puts $outlog "No. of Pairs (DCA score > $THRES): $nn"
close $infile
close $outfile

mol new ../pdb_monomer.pdb
draw delete all
set sel [atomselect top "name CA"]
set rr [measure rgyr $sel]
puts $outlog "Radius of gyration of the monomer: $rr"
set infile [open "tmppairs" r]
set outfile [open "tmppairs_clearmissing" w]
set nn 0
while {[gets $infile line] >= 0} {
   lassign [regexp -inline -all {\S+} $line] ii jj kk
   set ii [expr $ii + $SHIFT]
   set jj [expr $jj + $SHIFT]
   set sel [atomselect top "resid $ii $jj and name CA"]
   set sel1 [atomselect top "resid $ii and name CA"]
   set sel2 [atomselect top "resid $jj and name CA"]
   if {[llength [$sel get index]] != 2} {
       puts $outlog "Missing pair: $ii $jj"
   } elseif {[measure bond [$sel get index]] > [expr $rr * 1]} {
       puts [measure bond [$sel get index]]
       draw cylinder [measure center $sel1] [measure center $sel2] radius $kk 
       puts $outfile "$ii $jj $kk"
       incr nn
   }
} 
puts $outlog "No. of Pairs (Distance > rgyr): $nn"
close $infile
close $outfile

mol new ../pdb_dimer.pdb
draw delete all
draw color white
set sel [atomselect top "name CA"]
set selall [atomselect top all]
set selcenter [atomselect 0 "name CA"]
$selall moveby [vecsub [measure center $sel] [measure center $selcenter]]
set sela [atomselect top "chain A and name CA"]
set selb [atomselect top "chain B and name CA"]
set rr [vecdist [measure center $sela] [measure center $selb]] 
puts $rr
set infile [open "tmppairs_clearmissing" r]
set outfile [open "pairs_draw" w]
set nn 0
while {[gets $infile line] >= 0} {
   lassign [regexp -inline -all {\S+} $line] ii jj kk
   set sela [atomselect top "chain A and resid $ii and name CA or chain B and resid $jj and name CA"]
   set selb [atomselect top "chain B and resid $ii and name CA or chain A and resid $jj and name CA"]
   if {[measure bond [$sela get index]] < [measure bond [$selb get index]]} {
       set sel1 [atomselect top "chain A and resid $ii and name CA"]
       set sel2 [atomselect top "chain B and resid $jj and name CA"]
       draw cylinder [measure center $sel1] [measure center $sel2] radius [expr $kk * 10]
       puts $outfile "$ii $jj $kk"
   } else {
       set sel1 [atomselect top "chain B and resid $ii and name CA"]
       set sel2 [atomselect top "chain A and resid $jj and name CA"]
       draw cylinder [measure center $sel1] [measure center $sel2] radius [expr $kk * 10]
       puts $outfile "$jj $ii $kk"
   }
} 
close $infile
close $outfile

close $outlog
EOF