microprot is coded in Python 3.x

microprot clusters and annotates microbial metagenome sequences for the ultimate goal of predicting the 3-dimensional structure and function of these proteins.

Some of the tools and databases we're using were developed externally and cannot be automatically installed. We ask you to download them on your own, install and update appropriate paths in paths.yml

• PDB100 from PISCES PDB culling server (updated weekly)
• UniRef90 from EBI (the database is 10GB+; updated monthly)
• Uniclust30 (14GB+; updated every 3 months)
• PfamA for HH-suite (updated approx. every 6 months)

Tools requiring manual installation are listed and linked below:

• HH-suite 3.0
• metaPSICOV

All filenames are in the form: GenomeID_GeneID_ResiduesFrom-ResiduesTo and contain amino acid sequences.
For example, CP003179.1_3319 means gene 3319 from genome CP003179.1 (Sulfobacillus acidophilus DSM 10332), or CP003179.1_3319_1-60 means amino acids 1 to 60 from that gene.

• a3m
  An alignment file produced by HH-suite programs. It's a format similar to FASTA, but in sequence rows it contains additional information useful for the construction of HMMs (represented by [a-z]). A detailed description can be found in HH-suite user guide (section 6.1).

• out
  HH-suite output files reporting a list of hits for an input sequence, along with Probability, P-value, E-value and other parameters (hit list); as well as a set of pair-wise sequence alignments. A detailed description can be found in HH-suite user guide (section 5).

• match
  Internal microprot files showing which sub-sequence of the input sequence matched defined by config.yml criteria for any of E-value, P-value, Prob or minimum sequence length in the .out file. Multiple hits are possible. The file is reported in a FASTA format.

• non_match
  All sub-sequences longer than the minimum sequence length that do not meet the criteria for .match. Internal microprot file.

Gene CP00000.0_1 (CP00000.0_1.fasta) with 100 residues is run against HHsearch and it returns 2 outputs: CP00000.0_1.out and CP00000.0_1.a3m. Sequence split parameters are:

min_prob: 90.0
min_fragment_length: 10

and the hit list portion of CP00000.0_1.out is:

[7 lines of input parameters summary]

No Hit                             Prob E-value P-value  Score    SS Cols Query HMM  Template HMM
 1 1ABC_A Uncharacterized protein  91.5   0.001   0.001   24.3   0.0   20   10-30    211-231 (260)
 2 1BCD_A Uncharacterized protein  90.3   0.001   0.001   26.4   0.0   55   33-88    28-83  (149)
 3 1CDE_A Uncharacterized protein  85.3     0.2   0.001   26.4   0.0   55   43-98    28-83  (149)

According to our criteria, hits 1 and 2 are matches (probability >= 90.0 and fragment length (from Query_HMM) >= 10).
So CP00000.0_1.match file will contain sequences:

>CP00000.0_1_10-30
EXAMPLEEXAMPLEEXAMPL
>CP00000.0_1_33-88
EXAMPLEEXAMPLEEXAMPLEEXAMPLEEXAMPLEEXAMPLEEXAMPLEEXAMPL

and CP00000.0_1.non_match will contain sequence:

>CP00000.0_1_89-100
EXAMPLEEXAMP

Sub-sequences CP00000.0_1_1-9 and CP00000.0_1_31-33 will be dropped from subsequent analyses, as they did not match minimum fragment length criteria.