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library(pureseqtmr)
library(testthat)
library(knitr)
pureseqtmr
is a package to call PureseqTM from R. PureseqTM predicts the topology of a membrane protein, where the topology can be either inside, or not inside the membrane.
To be able to call PureseqTM, it needs to be installed:
pureseqtmr::install_pureseqtm()
Note that this code is not actually run, to comply with CRAN guidelines.
PureseqTM supplies some example files. Use get_example_filenames
to get the path to all these files:
if (is_pureseqtm_installed()) {
get_example_filenames()
}
In this example, 1bhaA.fasta
will be used. To obtain the full path, use get_example_filename
. get_example_filename
will give an error if the file is not found.
if (is_pureseqtm_installed()) {
get_example_filename("1bhaA.fasta")
fasta_filename <-head(readLines(fasta_filename))
}
Getting the topology of this protein:
if (is_pureseqtm_installed()) {
predict_topology(fasta_filename)
topology <-kable(topology)
}
Or show the topology as a plot:
if (is_pureseqtm_installed()) {
plot_topology(topology)
}
One needs the exact same code for a full proteome. Here we use a pureseqtmr
example file, which is the COVID-19 reference proteome, as downloaded from https://www.uniprot.org/proteomes/UP000464024
.
system.file(
fasta_filename <-"extdata",
"UP000464024.fasta",
package = "pureseqtmr"
)expect_true(file.exists(fasta_filename))
Show the (top of the) proteome:
head(readLines(fasta_filename))
#> [1] ">sp|P0DTC7|NS7A_SARS2 Protein 7a OS=Severe acute respiratory syndrome coronavirus 2 OX=2697049 GN=7a PE=3 SV=1"
#> [2] "MKIILFLALITLATCELYHYQECVRGTTVLLKEPCSSGTYEGNSPFHPLADNKFALTCFS"
#> [3] "TQFAFACPDGVKHVYQLRARSVSPKLFIRQEEVQELYSPIFLIVAAIVFITLCFTLKRKT"
#> [4] "E"
#> [5] ">sp|P0DTD1|R1AB_SARS2 Replicase polyprotein 1ab OS=Severe acute respiratory syndrome coronavirus 2 OX=2697049 GN=rep PE=1 SV=1"
#> [6] "MESLVPGFNEKTHVQLSLPVLQVRDVLVRGFGDSVEEVLSEARQHLKDGTCGLVEVEKGV"
Getting the topology of this protein:
if (is_pureseqtm_installed()) {
predict_topology(fasta_filename)
topology <- }
Instead of directly showing the raw data, the protein names are shortened first:
if (is_pureseqtm_installed()) {
$name <- stringr::str_match(
topologystring = topology$name,
pattern = "..\\|.*\\|(.*)_SARS2"
2]
)[, }
Show the topology as a plot:
if (is_pureseqtm_installed()) {
plot_topology(topology)
}
And tally the number of transmembrane helices per protein:
if (is_pureseqtm_installed()) {
kable(tally_tmhs(topology))
}
These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.