bio3d (version 2.3-0)

pdbaln: Sequence Alignment of PDB Files

Description

Create multiple sequences alignments from a list of PDB files returning aligned sequence and structure records.

Usage

pdbaln(files, fit = FALSE, pqr = FALSE, ncore = 1, nseg.scale = 1,  ...)

Arguments

files

a character vector of PDB file names. Alternatively, a list of pdb objects can be provided.

fit

logical, if TRUE coordinate superposition is performed on the input structures.

pqr

logical, if TRUE the input structures are assumed to be in PQR format.

ncore

number of CPU cores used to do the calculation. ncore>1 requires package ‘parallel’ installed.

nseg.scale

split input data into specified number of segments prior to running multiple core calculation. See fit.xyz.

...

extra arguments passed to seqaln function.

Value

Returns a list of class "pdbs" with the following five components:

Details

This wrapper function calls the underlying functions read.pdb, pdbseq, seqaln and read.fasta.pdb returning a list of class "pdbs" similar to that returned by read.fasta.pdb.

As these steps are often error prone it is recomended for most cases that the individual underlying functions are called in sequence with checks made on the valadity of their respective outputs to ensure sensible results.

References

Grant, B.J. et al. (2006) Bioinformatics 22, 2695--2696.

See Also

read.pdb, pdbseq, seqaln, read.fasta,read.fasta.pdb, core.find, fit.xyz, read.all, pymol.pdbs

Examples

## Not run: 
# ##- Align PDBs (from vector of filenames)
# #files <- get.pdb(c("4q21","5p21"), URLonly=TRUE)
# files <- get.pdb(c("4q21","5p21"), path=tempdir(), overwrite=TRUE)
# pdbaln(files)
# 
# 
# ##- Align PDBs (from list of existing PDB objects)
# pdblist <- list(read.pdb(files[1]), read.pdb(files[2]))
# pdbaln(pdblist)
# 
# ## End(Not run)