# NOT RUN {
# PDB server connection required - testing excluded
## Read a PDB file
pdb <- read.pdb("1bg2")
## Extract sequence from PDB file
s <- aa321(pdb$seqres) # SEQRES
a <- aa321(pdb$atom[pdb$calpha,"resid"]) # ATOM
## Write simple fasta file
#write.fasta( seqs=seqbind(s,a), file="eg.fa")
#write.fasta( ids=c("seqres","atom"), seqs=seqbind(s,a), file="eg.fa" )
outfile1 = file.path(tempdir(), "eg.fa")
write.fasta(list( id=c("seqres"),ali=s ), file = outfile1)
write.fasta(list( id=c("atom"),ali=a ), file = outfile1, append=TRUE)
## Align seqres and atom records
#seqaln(seqbind(s,a))
## Read alignment
aln<-read.fasta(system.file("examples/kif1a.fa",package="bio3d"))
## Cut all but positions 130 to 245
aln$ali=aln$ali[,130:245]
outfile2 = file.path(tempdir(), "eg2.fa")
write.fasta(aln, file = outfile2)
invisible( cat("\nSee the output files:", outfile1, outfile2, sep="\n") )
# }
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