func main() {
flag.BoolVar(&flagAllFragments, "all-fragments", flagAllFragments,
"When set, all fragments will be shown, even if the best fragment\n"+
"of each ATOM set is the same.")
util.FlagParse(
"fraglib align.{fasta,ali,a2m,a3m} pdb-file out-csv",
"Writes a CSV file to out-csv containing the best matching fragment\n"+
"for each pairwise contiguous set of alpha-carbon atoms of the\n"+
"first two proteins in the alignment and PDB file.")
util.AssertNArg(4)
flib := util.StructureLibrary(util.Arg(0))
aligned := util.MSA(util.Arg(1))
pentry := util.PDBRead(util.Arg(2))
outcsv := util.CreateFile(util.Arg(3))
csvWriter := csv.NewWriter(outcsv)
csvWriter.Comma = '\t'
defer csvWriter.Flush()
pf := func(record ...string) {
util.Assert(csvWriter.Write(record), "Problem writing to '%s'", outcsv)
}
pf("start1", "end1", "start2", "end2", "frag1", "frag2", "frag_rmsd")
iter := newContiguous(
flib.FragmentSize(),
aligned.GetFasta(0), aligned.GetFasta(1),
pentry.Chains[0], pentry.Chains[1])
for iter.next() {
best1 := flib.BestStructureFragment(iter.atoms1)
best2 := flib.BestStructureFragment(iter.atoms2)
if !flagAllFragments && best1 == best2 {
continue
}
bestRmsd := structure.RMSD(flib.Atoms(best1), flib.Atoms(best2))
pf(
fmt.Sprintf("%d", iter.s1()),
fmt.Sprintf("%d", iter.e1()),
fmt.Sprintf("%d", iter.s2()),
fmt.Sprintf("%d", iter.e2()),
fmt.Sprintf("%d", best1),
fmt.Sprintf("%d", best2),
fmt.Sprintf("%f", bestRmsd),
)
}
}
// RMSDChains is the same as RMSD, except it uses *Chain values directly.
func RMSDChains(chain1 *Chain, start1, end1 int,
chain2 *Chain, start2, end2 int) (float64, error) {
// In order to fetch the appropriate carbon-alpha atoms, we need to
// traverse each chain's carbon-alpha atom slice and pick only the carbon
// alpha atoms with residue indices in the range specified.
struct1 := chain1.SequenceCaAtomSlice(start1-1, end1)
struct2 := chain2.SequenceCaAtomSlice(start2-1, end2)
// Verify that neither of the atom sets is 0.
if struct1 == nil || len(struct1) == 0 {
return 0.0, fmt.Errorf("The range '%d-%d' (for chain %c in %s) does "+
"not correspond to any carbon-alpha ATOM records.",
start1, end1, chain1.Ident, chain1.Entry.Path)
}
if struct2 == nil || len(struct2) == 0 {
return 0.0, fmt.Errorf("The range '%d-%d' (for chain %c in %s) does "+
"not correspond to any carbon-alpha ATOM records.",
start2, end2, chain2.Ident, chain2.Entry.Path)
}
// If we don't have the same number of atoms from each chain, we can't
// compute RMSD.
if len(struct1) != len(struct2) {
return 0.0, fmt.Errorf("The range '%d-%d' (%d ATOM records for chain "+
"%c in %s) does not correspond to the same number of carbon-alpha "+
"atoms as the range '%d-%d' (%d ATOM records for chain %c in %s). "+
"It is possible that the PDB file does not contain a carbon-alpha "+
"atom for every residue index in the ranges.",
start1, end1, len(struct1), chain1.Ident, chain1.Entry.Path,
start2, end2, len(struct2), chain2.Ident, chain2.Entry.Path)
}
// We're good to go...
return structure.RMSD(struct1, struct2), nil
}
func main() {
fmapPath := util.Arg(0)
fmap := util.FmapRead(fmapPath)
qchain := getPdbChain(fmapPath)
stats := newSequenceStats(qchain.Sequence)
total, trueps := 0, 0
qcorrupt, tcorrupt := 0, 0
for _, frags := range fmap.Segments {
for _, frag := range frags.Frags {
hit := frag.Hit
if frag.IsCorrupt() {
tcorrupt += 1
stats.incTCorrupt(hit)
continue
}
qatoms := qchain.SequenceCaAtomSlice(hit.QueryStart-1, hit.QueryEnd)
if qatoms == nil {
qcorrupt += 1
stats.incQCorrupt(hit)
continue
}
if len(qatoms) != len(frag.CaAtoms) {
util.Fatalf("Uncomparable lengths. Query is (%d, %d) while "+
"template is (%d, %d). Length of query CaAtoms: %d, "+
"length of template CaAtoms: %d",
hit.QueryStart, hit.QueryEnd,
hit.TemplateStart, hit.TemplateEnd,
len(qatoms), len(frag.CaAtoms))
}
if structure.RMSD(qatoms, frag.CaAtoms) <= flagRmsd {
trueps += 1
stats.incTruePs(hit)
}
total += 1
stats.incTotal(hit)
}
}
coveredResidues := 0
for _, resStats := range stats {
if resStats.trueps >= 1 {
coveredResidues += 1
}
}
coverage := float64(coveredResidues) / float64(len(qchain.Sequence))
fmt.Printf("RMSDThreshold: %f\n", flagRmsd)
fmt.Printf("TotalFragments: %d\n", total)
fmt.Printf("TruePositives: %d\n", trueps)
fmt.Printf("Precision: %f\n", float64(trueps)/float64(total))
fmt.Printf("CorruptQuery: %d\n", qcorrupt)
fmt.Printf("CorruptTemplate: %d\n", tcorrupt)
fmt.Printf("TotalResidues: %d\n", len(qchain.Sequence))
fmt.Printf("CoveredResidues: %d\n", coveredResidues)
fmt.Printf("Coverage: %f\n", coverage)
}
