Thursday, 9 November 2017

Using drawProteins with BioMart to draw schematic of human MAP kinases...

Update (5th April, 2018): 'unigene' is not a valid attribute(s) so I have changed the code here.

Last week, I submitted my drawProteins R package to Bioconductor. One of the recommended things to do as a Bioconductor developer is to ensure that the package can work with other Bioconductor packages.

I've created this blog post to show how it's possible to use bioMart to pull out the UniProt accession numbers for the Gene Ontology (GO) term, "MAP kinase activity". This has a GO number of GO:0004707.

My script borrows heavily on the biomaRt users guide written by Steffen Durinck, Wolfgang Huber, Mike Smith. My thanks to them.

Using the R script below, I created this protein schematic:

# install bioMart if you haven't used it before
# remove the hash tags...
# source(" ")
# biocLite()
# biocLite("biomaRt")

# steps
# 1 choose a Mart with useMart()
# 2 choose a dataset with useMart()
# 3. make query with getBM()
# with
# A. filter  -  restriction on the query
# e.g. Interpro ID(s) [e.g. IPR000001]
# e.g. chromosome_name
# B. attributes  -  values we are interested in to retrieve.
# C. values - values you want to

# from

# chosing a database = MART and a dataset - gets more focussed each step...
ensembl = useMart("ensembl",

# Retrieve all entrezgene identifiers and HUGO gene symbols of genes which have
# a “MAP kinase activity” GO term associated with it.
# this is the GO:0004707
getBM(attributes = c('entrezgene','hgnc_symbol'),
      filters = 'go',
      values = 'GO:0004707',
      mart = ensembl)

# this is 14 proteins....

# create output in a dataframe and add uniprotswissprot
# which is the UniProt ID
output <- getBM(attributes = c('uniprotswissprot',
                filters = 'go',
                values = 'GO:0004707',
                mart = ensembl)

# returns a dataframe... pull out uniprotIDs for drawing...
uniprotIDs <- output$uniprotswissprot
# get rid of blank entries - turn into NA
uniprotIDs[uniprotIDs==""] <- NA
# remove NA
uniprotIDs <- na.omit(uniprotIDs)
# make the IDs characters
uniprotIDs <- as.character(uniprotIDs)
# just the unique ones
uniprotIDs <- unique(uniprotIDs)
# combine into one element
uniprotIDs <- paste(uniprotIDs, collapse = " ")
# this can now be used in drawProteins

# now get features from Uniprot

# install drawProteins from Github
# devtools::install_github("brennanpincardiff/drawProteins")

uniprotIDs %>%
  drawProteins::get_features() %>%
  drawProteins::feature_to_dataframe() ->
# data frame with 722 observations

# basic drawing
p <- draw_canvas(prot_data)
p <- draw_chains(p, prot_data)
p <- draw_domains(p, prot_data)
draw_repeat(p, prot_data)

p <- draw_motif(p, prot_data)
p <- draw_phospho(p, prot_data, size = 4)

# background and y-axis
p <- p + theme_bw(base_size = 20) +  # white background and change text size
    panel.grid.major=element_blank()) +
  theme(axis.ticks = element_blank(),
    axis.text.y = element_blank()) +
  theme(panel.border = element_blank())

# add titles
p <- p + labs(title = "Schematic of human MAP kinases",
  subtitle = "circles = phosphorylation sites\nsource:Uniprot")

# move legend to top
p <- p + theme(legend.position="top") + labs(fill="")

# AND it works!!


Resources and citations:

No comments:

Post a Comment

Comments and suggestions are welcome.