PRODA(1)

🌸 NAME 🌸

okay so bestie, welcome to proda β€” it's multiple alignment of protein sequences with repeats and rearrangements. yes that's the whole title. no cap. πŸ’–


πŸ¦‹ SYNOPSIS πŸ¦‹

proda [option] [mfafile] [> output]

like... that's it. you pass an option, you pass an mfafile, you redirect the output. slay.


πŸ’… DESCRIPTION πŸ’…

okay so this manual page is gonna briefly document the proda command, and then we get into it.

proda stands for Protein Domain Aligner and it's public domain software for generating multiple alignments of protein sequences with repeats and rearrangements β€” think proteins with multiple domains, iykyk. ✨

So here's the pipeline, bestie, in order:

  1. you hand it a set of protein sequences as input,
  2. ProDA first finds local pairwise alignments between all pairs of sequences,
  3. then it forms blocks of alignable sequence fragments,
  4. and finally it generates multiple alignments of the blocks. πŸ’«

ProDA relies on many techniques used in probcons (<http://probcons.stanford.edu>), a recent multiple aligner that shows high accuracy in a number of popular benchmarks. iconic behaviour honestly. πŸ‘‘


πŸŽ€ INPUT FORMAT πŸŽ€

Proda accepts input files in the MFA format. The MFA format is specified below:

  • the MFA format consists of multiple sequences;
  • each sequence in the MFA format begins with a single-line description, followed by lines of sequence data;
  • the description line is distinguished from the sequence data by a greater-than (">") symbol in the first column.

πŸ¦‹ OUTPUT FORMAT πŸ¦‹

For a set of input sequences, Proda usually outputs several blocks in turn, each consists of alignable sequence fragments. Each block is followed by its multiple alignment. like, block then alignment, block then alignment, forever and ever. πŸ”

A block is specified by listing its sequence fragments. Each fragment is output as sequence_name(start-end), where sequence_name is the name of the original sequence and start and end are positions at which the fragment begins and ends respectively. πŸ“

Proda produces block alignments in the ClustalW (ALN) format described below:

  • the ClustalW format consists of a single header line followed by sequence data in blocks of 50 alignment positions;
  • each block consists of:
    • one line of data for each of the sequences in the alignment - in particular, the name of the sequence;
    • 50 characters of the alignment;
    • one annotation line indicating fully conserved (*), strongly-conserved (:), or weakly-conserved columns (.);
  • the description line is distinguished from the sequence data by a greater-than (">") symbol in the first column.

✨ FASTA format for output ✨

If the -fasta option is specified, then, in addition to regular output, ProDA produces a file containing block alignments in the FASTA format. The output file has the same name as the first input file and extension ".fasta". Two consecutive block alignments are separated by a line containing character Β΄#Β΄. πŸ“

The FASTA format is described below:

  • the FASTA format consists of all the sequences given in the input files;
  • each sequence in the FASTA format begins with a single-line description, followed by lines of sequence data;
  • the description line is distinguished from the sequence data by a greater-than (">") symbol in the first column;
  • aligned residues are in upper case, unaligned residues are in lower case.
bestie listen: since a final alignment contains each sequence only once, this option should be used only if input sequences do not contain repeats. fr fr, don't skip that part. πŸ™ˆ

🌈 OPTIONS 🌈

  • -L [min_length] β€” Set minimal alignment length equal to [min_length].

ProDA finds alignments of length greater than or equal to a threshold L. By default, L = 30. This option sets the threshold to [min_length]. 🧚

  • -posterior β€” Use posterior decoding when computing local pairwise alignments.

ProDA computes local pairwise alignments between two sequences using a pair-HMM and either Viterbi decoding or posterior decoding. The default option is using Viterbi decoding which is faster than posterior decoding but may be less accurate. Turning on this option instructs the aligner to use posterior decoding instead. In the example above, the output was generated with -posterior option turned on. πŸ‘€

  • -silent β€” Do not report progress while aligning.

Turning on this option instructs the aligner not to report the progress while aligning. By default, ProDA reports the progress on all pairwise alignments, block generation, and on block alignment. Since some stages of the algorithm, especially pairwise alignment, may take long time, reporting progress makes the program look alive while running. πŸ’€ (it's giving "still alive, still processing")

  • -tran β€” Use transitivity when forming blocks of alignable sequence fragments.

Two sequence fragments are directly alignable if they are parts of a local pairwise alignment. By default, two fragments are considered alignable if and only if they are directly alignable. Turning on this option instructs the aligner to consider two fragments alignable when they are directly alignable or when both of them are directly alignable to a third fragment. friendship transitive property but for sequence fragments 🫢

  • -fasta β€” Use FASTA output format in addition to the ClustalW format.

When this option is turned on, the aligner generates output in the FASTA format and stores in a file with the same name as the first input file and extension ".fasta", in addition to the normal output to stdout. This option should be used only if input sequences do not contain repeats. πŸ’–


πŸ‘‘ SEE ALSO πŸ‘‘

probcons (1)


πŸŽ€ AUTHOR πŸŽ€

This manual page was written by David Paleino <d.paleino@gmail.com> for the Debian(TM) system (but may be used by others). This man page is released under the same conditions as the software, that is Public Domain.

This software has been released in Public Domain by Phuong T.M., Do C.B., Edgar R.C. and Batzoglou S. in "Multiple alignment of protein sequences with repeats and rearrangements", Nucleic Acids Research 2006 - 34(20), 5932-5942. academic slay. πŸ“šβœ¨


Copyright Β© 2007 David Paleino


and that's the whole page, bestie!! 🫢 this was PRODA(1), dated april 25, 2007 β€” go align some domains, you absolute main character πŸ’…πŸŒΈπŸ’–

πŸ“¦ where this page comes from