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EffectR is a brilliant package for identifying effectors.
I just had a question regarding the identification of proteins with custom motifs. For some reason, when I use a custom pattern, the resulting table does not give the domain numbers and positions. I was wondering if there is some way to fix this.
Thank you!
Best,
Savithri
The text was updated successfully, but these errors were encountered:
Thanks for you message. I tried doing what you said. For example I used the following commands with your test data
library(effectR)
fasta.file <- system.file("extdata", "test_infestans.fasta", package = "effectR")
ORF <- seqinr::read.fasta(fasta.file)
reg.pat <- "^\w{50,60}[w,v]"
REGEX <- regex.search(sequence = ORF, motif = "custom", reg.pat = reg.pat)
candidate.custom <- hmm.search(original.seq = fasta.file, regex.seq = REGEX)
custom.effectors <- effector.summary(candidate.custom, motif = "custom", reg.pat = reg.pat)
write.table(custom.effectors[["motif.table"]], file = "example.xls", append = FALSE, quote = FALSE, sep = "\t ", eol ="\r", na = "NA", dec = ".", row.names = TRUE, col.names = TRUE,qmethod = c("escape", "double"))
The custom motif position in the resulting table is a default 1 (file attached) example.txt
I tried the same with my data with the REGEX pattern "^\w{10,40}\w{1,96}Q\wLR\w{1,40}[ED][ED][RK]". It still gives '1' as the motif position and does not separate the positions and numbers of the QXLR and EER-like motifs like it does for the "RxLR" function.
Hi,
EffectR is a brilliant package for identifying effectors.
I just had a question regarding the identification of proteins with custom motifs. For some reason, when I use a custom pattern, the resulting table does not give the domain numbers and positions. I was wondering if there is some way to fix this.
Thank you!
Best,
Savithri
The text was updated successfully, but these errors were encountered: