Write aligned or un-aligned sequences to a PIR format file.
write.pir(alignment=NULL, ids=NULL, seqs=alignment$ali,
pdb.file = NULL, chain.first = NULL, resno.first = NULL,
chain.last = NULL, resno.last = NULL, file, append = FALSE)
an alignment list object with id
and ali
components, similar to that generated by read.fasta
.
a vector of sequence names to serve as sequence identifers
an sequence or alignment character matrix or vector with a row per sequence
a vector of pdb filenames; For sequence, provide "".
a vector of chain id for the first residue.
a vector of residue number for the first residue.
a vector of chain id for the last residue.
a vector of residue number for the last residue.
name of output file.
logical, if TRUE output will be appended to
file
; otherwise, it will overwrite the contents of
file
.
Called for its effect.
Grant, B.J. et al. (2006) Bioinformatics 22, 2695--2696.
# NOT RUN {
# Needs MUSCLE installed - testing excluded
if(check.utility("muscle")) {
## Generate an input file for structural modeling of
## transducin G-alpha subunit using the template 3SN6_A
## Read transducin alpha subunit sequence
seq <- get.seq("P04695", db = "uniprot", outfile = tempfile())
## Read structure template
path = tempdir()
pdb.file <- get.pdb("3sn6_A", path = path, split = TRUE)
pdb <- read.pdb(pdb.file)
## Build an alignment between template and target
aln <- seqaln(seqbind(pdbseq(pdb), seq), id = c("3sn6_A", seq$id), outfile = tempfile())
## Write PIR format alignment file
outfile = file.path(tempdir(), "eg.pir")
write.pir(aln, pdb.file = c(pdb.file, ""), file = outfile)
invisible( cat("\nSee the output file:", outfile, sep = "\n") )
}
# }
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