pdbaln.Rd
Create multiple sequences alignments from a list of PDB files returning aligned sequence and structure records.
pdbaln(files, fit = FALSE, pqr = FALSE, ncore = 1, nseg.scale = 1, progress = NULL, ...)
files | a character vector of PDB file names. Alternatively, a
list of |
---|---|
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.
|
nseg.scale | split input data into specified number of segments
prior to running multiple core calculation. See |
progress | progress bar for use with shiny web app. |
... | extra arguments passed to |
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.
Returns a list of class "pdbs"
with the following five
components:
numeric matrix of aligned C-alpha coordinates.
character matrix of aligned residue numbers.
numeric matrix of aligned B-factor values.
character matrix of aligned chain identifiers.
character vector of PDB sequence/structure names.
character matrix of aligned sequences.
the matched call.
Grant, B.J. et al. (2006) Bioinformatics 22, 2695--2696.
Barry Grant
See recommendation in details section above.
read.pdb
, pdbseq
, seqaln
,
read.fasta
,read.fasta.pdb
,
core.find
, fit.xyz
, read.all
,
pymol.pdbs
if (FALSE) { ##- 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) }