# tocID <- "BIN-ALI-BLAST.R" # # Purpose: A Bioinformatics Course: # R code accompanying the BIN-ALI-BLAST unit. # # ============================================================================== # # Version: 1.3 # # Date: 2017-10 - 2020-09 # Author: Boris Steipe (boris.steipe@utoronto.ca) # # Versions: # 1.3 2020 Maintenance # 1.2 Change from require() to requireNamespace(), # use ::() idiom throughout # 1.1 Fixed parsing logic. # 1.0 First live version 2017. # 0.1 First code copied from 2016 material. # # # TODO: # # # == DO NOT SIMPLY source() THIS FILE! ======================================= # # If there are portions you don't understand, use R's help system, Google for an # answer, or ask your instructor. Don't continue if you don't understand what's # going on. That's not how it works ... # # ============================================================================== #TOC> ========================================================================== #TOC> #TOC> Section Title Line #TOC> --------------------------------------------------- #TOC> 1 Defining the APSES domain 45 #TOC> 2 Executing the BLAST search 75 #TOC> 3 Analysing results 97 #TOC> #TOC> ========================================================================== # = 1 Defining the APSES domain =========================================== # Load your protein database source("makeProteinDB.R") # Get the APSES domain sequence via your MBP1_MYSPE feature annotation. (You # have entered this data into your database in the # BIN-ALI-Optimal_sequence_alignment unit.) ( myOrth <- sprintf("MBP1_%s", biCode(MYSPE)) ) # If this is not the correct # name of the Mbp1 orthologue # of Mbp1 in your protein # database, DON'T continue. We # need to fix this problem. # Get in touch. (proID <- myDB$protein$ID[myDB$protein$name == myOrth]) (ftrID <- myDB$feature$ID[myDB$feature$name == "APSES fold"]) (fanID <- myDB$annotation$ID[myDB$annotation$proteinID == proID & myDB$annotation$featureID == ftrID]) (start <- myDB$annotation$start[myDB$annotation$ID == fanID]) (end <- myDB$annotation$end[myDB$annotation$ID == fanID]) (apses <- substr(myDB$protein$sequence[myDB$protein$ID == proID], start, end)) # The MYSPE "apses" sequence is the sequence that we will use for our reverse # BLAST search. # = 2 Executing the BLAST search ========================================== # The ./scripts/BLAST.R code defines two functions to access the BLAST interface # through its Web API, and to parse results. Have a look at the script, then # source it: source("./scripts/BLAST.R") # Use BLAST() to find the best match to the MYSPE APSES domain in Saccharomyces # cerevisiae: BLASTresults <- BLAST(apses, # MYSPE APSES domain sequence db = "refseq_protein", # database to search in nHits = 10, # E = 0.01, # limits = "txid559292[ORGN]") # S. cerevisiae S288c length(BLASTresults$hits) # There should be at least one hit there. Ask for # advice in case this step fails. # = 3 Analysing results =================================================== (topHit <- BLASTresults$hits[[1]]) # Get the top hit # What is the refseq ID of the top hit topHit$accession # If this is "NP_010227.1" you have confirmed the RBM of the MYSPE apses # domain. If it is not, ask me for advice. # [END]