yunta 0.0.1.post1

Predicting protein-protein interactions and structures from multiple sequence alignments.

🍐 yunta

Predicting a pairwise protein-protein interactions and structures from multiple sequence alignments.

• Installation
• Credit
• Command-line usage
  • Generating multiple-sequence alignments
  • Calculating contact maps
  • [Predicting protein complex structures]
  • Command-line tools
• Python API
• Scaling up
• Issues, problems, suggestions
• Further help

yunta provides several implementations of protein-protein interaction evaluation. In increasing computational cost:

• GPU-accelerated direct coupling analysis (DCA) (in Tensorflow and PyTorch)
• RoseTTAFold-2track via the rf2t-micro package
• AlphaFold2 for protein-protein structure prediction

yunta has streamlined installation, a command-line interface, a Python API, and some resilience to GPU out-of-memory error (though CPU-fallback). It takes as input unpaired multiple-sequence alignments in A3M format (as generated by tools like hhblits), and outputs a matrix of inter-residue contacts.

Rough timings for a pair of ~200 amino-acid proteins (S. cerevisiae DHFR and WW domain-containing protein) on CPU:

• DCA: 5 seconds

• RosettaFold-2track: 10 seconds

• AlphaFold2: 1 hour

Note that these times will increase quadratically with the total length of the proteins.

Installation

Obtaining and setting up yunta is easy.

$ pip install yunta

If you want to enable GPU, use

$ pip install yunta[cuda12]

If you want to use a local CUDA installation instead, use

$ pip install yunta[cuda12_local]

Using the embedded model requires using the RoseTTAFold-2track and AlphaFold2 weights. These are automatically downloaded, but by using yunta you agree that the trained weights for RoseTTAFold are made available for non-commercial use only under the terms of the Rosetta-DL Software license and AlphaFold2's pretrained parameters fall under the CC BY 4.0 license.

Credit

yunta is a fork of SpeedPPI, which is itself inspired by FoldDock. This method used AlphaFold2 to evaluate 65,484 protein-protein interactions from the human proteome in Towards a structurally resolved human protein interaction network.

The idea of using DCA, RoseTTAFold-2track, and AlphaFold2 in a cascade of increasingly expensive and specific PPI detection methods has been explored in a series of papers from David Baker's lab:

• Cong et al., Protein interaction networks revealed by proteome coevolution. Science, 2019
• Humpreys et al., Computed structures of core eukaryotic protein complexes. Science, 2021
• Humpreys et al., Protein interactions in human pathogens revealed through deep learning. Nature Microbiology, 2024

yunta puts these algorithms in one place with easy installation, a command-line interface, and a Python API.

Command-line usage

You can always get more help by running

$ yunta --help
usage: yunta [-h] {dca-single,dca-many,rf2t-single,af2-single,af2-many} ...

Screening protein-protein interactions using DCA and AlphaFold2.

options:
  -h, --help            show this help message and exit

Sub-commands:
  {dca-single,dca-many,rf2t-single,af2-single,af2-many}
                        Use these commands to specify the tool you want to use.
    dca-single          Calculate DCA for one protein-protein interaction.
    dca-many            Calculate DCA between two sets of proteins, or all pairs in one set of proteins.
    rf2t-single         Calculate RF-2track contacts for between one protein and a series of others.
    af2-single          Model one protein-protein interaction.
    af2-many            Model all interactions between two sets of proteins, or all pairs in one set of proteins.

Generating multiple-sequence alignments

All the algorithms depend on pre-computed multiple-sequence alignments (MSAs) between a protein of interest and as many other proteins as possible. This allows computations to be sped up by separating out this phase of the calculation. You can generate MSAs using a dedicated tool like hhblits, which will speed up the process by using pre-clustered datasbes like UniClust. We typically use a command like:

hhblits -e 0.01 -v 3 -d /path/to/UniClust-database -i input.fasta -oa3m output-msa.a3m -o /dev/null -cov 60 -n 3 -realign -realign_max 10000

In our experience, this can take 1-40 min depending on the complexity of the query. Check the hhsuite documentation for more details.

Once you have your MSAs, you can use the information contained within them using tools in yunta to calculate contact maps and predict structures of protein complexes with AlphaFold2.

Calculating contact maps

Given two MSAs, yunta will calculate the contact map using DCA, RF2t, or AlphaFold2, and produce a summary table for each pair provided as input.

Using DCA or RF2t will produce a table like this:

$ yunta dca-single test/inputs/DYR_YEAST.a3m -2 test/inputs/CAPZA_YEAST.a3m -o test/outputs/dca-single.tsv --apc

ID	uniprot_id_1	uniprot_id_2	seq_len	chain_a_len	chain_b_len	msa1_depth	msa2_depth	msa_depth	n_eff	apc	mean	median	maximum	minimum
O13297-D6VTK4	O13297	D6VTK4	980	549	431	14246	1546	670	2	False	0.01830857	0.014683756	0.07428725	2.284808e-06

If you also give the --plot option, then the contact maps for the entore complex and only the inter-chain contacts will be saved, along with CSV files containing the numerical values as matrix. For example,

$ yunta dca-single test/inputs/DYR_YEAST.a3m -2 test/inputs/CAPZA_YEAST.a3m -o test/outputs/dca-single.tsv --apc --plot test/outputs/DYR_YEAST-CAPZA_YEAST

0	1	2	...	420	421
-0.0	0.0009014737	0.0010275221	...	0.0005961701	-1.9190367e-05
...

Predicting protein complex structures

yunta can also feed your MSAs into the AlphaFold2 model to predict structures of binary protein complexes.

$ yunta af2-single test/inputs/DYR_YEAST.a3m -2 test/inputs/CAPZA_YEAST.a3m -o test/outputs/af2-single

This will also generate a table

Using --plot will generate the contact maps as with the other commands.

$ yunta af2-single test/inputs/DYR_YEAST.a3m -2 test/inputs/CAPZA_YEAST.a3m -o test/outputs/af2-single --plot test/outputs/af2-single-plot

Command-line tools

You can run 1-vs-many with the *-single commands. For example:

$ yunta dca-single --help
usage: yunta dca-single [-h] [--msa2 [MSA2 ...]] [--list-file] [--output [OUTPUT]] [--plot PLOT] [--apc] [msa1]

positional arguments:
  msa1                  MSA file. Default: STDIN.

options:
  -h, --help            show this help message and exit
  --msa2 [MSA2 ...], -2 [MSA2 ...]
                        Second MSA file(s). Default: if not provided, all pairwise from msa1.
  --list-file, -l       Treat inputs as plain-text list of MSA files, rather than MSA filenames. Default: treat as MSA filenames.
  --output [OUTPUT], -o [OUTPUT]
                        Output filename. Default: STDOUT.
  --plot PLOT, -p PLOT  Directory for saving plots. Default: don't plot.
  --apc, -a             Whether to use APC correction in DCA. Default: don't apply correction.

If one MSA is provided, then homodimeric interactions are probed. For convenience, you can use the --list-file option to provide a single file containing a list of MSA files (one per line).

You can run many-vs-many with the *-many commands. For example:

$ yunta af2-many --help
usage: yunta af2-many [-h] [--msa2 [MSA2 ...]] [--list-file] --output OUTPUT [--params PARAMS] [--recycles RECYCLES] [--plot PLOT] [msa1 ...]

positional arguments:
  msa1                  MSA file(s). Default: "<_io.TextIOWrapper name='<stdin>' mode='r' encoding='utf-8'>".

options:
  -h, --help            show this help message and exit
  --msa2 [MSA2 ...], -2 [MSA2 ...]
                        Second MSA file(s). Default: if not provided, all pairwise from msa1.
  --list-file, -l       Treat inputs as plain-text list of MSA files, rather than MSA filenames. Default: treat as MSA filenames.
  --output OUTPUT, -o OUTPUT
                        Output directory. Required.
  --params PARAMS, -w PARAMS
                        Path to AlphaFold2 params file (.npz).
  --recycles RECYCLES, -x RECYCLES
                        Maximum number of recyles through the model. Default: "10".
  --plot PLOT, -p PLOT  Directory for saving plots. Default: don't plot.

Python API

We provide an API for using MSAs in your own programs.

>>> from yunta.structs.msa import *
>>> msa = MSA.from_file("my-msa-file.a3m")
>>> msa.neff()
6

We also provide a reusable GPU-accelerated Tensorflow implementation of DCA (adapted from Humpreys, Science, 2021).

>>> from yunta.dca import calculate_dca
>>> from yunta.structs.msa import *
>>> paired_msa = PairedMSA.from_file("my-msa-file1.a3m", "my-msa-file2.a3m")
>>> calculate_dca(paired_msa, apc=True, gpu=False)

In case you prefer, you can also import a PyTorch implementation (which anecdotally is faster on both CPU and GPU).

>>> from yunta.dca_torch import calculate_dca
>>> from yunta.structs.msa import *
>>> paired_msa = PairedMSA.from_file("my-msa-file1.a3m", "my-msa-file2.a3m")
>>> calculate_dca(paired_msa, apc=True, gpu=False)

(More documentation coming soon!)

... if you want to scale up

While the *-many commands can deal with processing multiple possible protein-protein interactions, if you want to screen more than a few and have access to a HPC cluster then using our nf-ggi Nextflow pipeline will be more efficient.

Issues, problems, suggestions

Add to the issue tracker.

Further help

• RoseTTAFold
• AlphaFold2
• rf2t-micro
• hhblits