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Carbohydrate Active eNzyme Domain analYsis tool (CANDy) - automated analysis of domain architectures in carbohydrate-active enzymes

CANDy is a fast, FAIR and seamless protein domain analysis tool for any CAZy family.

CANDy is available as an installable Python package (CLI + Python API), replacing the original Google Colab / Jupyter Notebook implementation. The previous notebook (archive/CANDy v2.0.ipynb) is kept in this repository for reference, and the original is on Google Colab.

Installation

pip install candy-cazyme

That's it for most users -- CANDy's default toolchain is fully bundled:

  • Clustering: MMseqs2 -- auto-downloaded and cached on first use (no conda needed). On Linux/macOS this just works. On Windows, MMseqs2's clustering workflows internally need a POSIX shell; the official Windows build handles this itself by installing a small helper (busybox) the first time it runs, which may ask for administrator permission once -- never again after that. (This mirrors upstream: MMseqs2's own docs list WSL as the recommended Windows path and this static build as the fallback for anyone who can't use WSL.)

  • MSA: FAMSA via pyfamsa -- a real pip dependency, runs in-process, no download needed.

  • Phylogenetics: VeryFastTree via veryfasttree -- also a real pip dependency, no download needed.

    Apple Silicon (M1/M2/M3/M4) users: make sure you're using a native arm64 Python (e.g. Homebrew installed at /opt/homebrew, not an older Intel-only install at /usr/local). FAMSA and VeryFastTree ship native SIMD code, and running an x86_64 Python under Rosetta 2 translation is a known cause of a silent illegal hardware instruction crash during --tree. CANDy detects this at startup and logs a warning, but installing natively avoids it entirely.

If you'd rather use the original CD-HIT/MAFFT/FastTree tools instead (e.g. to reproduce results bit-for-bit against the published notebook), a conda environment with those is still provided:

conda env create -f environment.yml   # only needed for CD-HIT as a clustering alternative to MMseqs2
conda activate candy

and pass --clustering-software cd-hit / build a PipelineConfig with alignment_tool="mafft", tree_tool="fasttree".

To also enable automated Gemini-based domain-name curation, see Domain-name curation below.

If you'd rather not have CANDy download anything automatically (e.g. air-gapped environments), set CANDY_NO_AUTO_DOWNLOAD=1 -- clustering will then require mmseqs/cd-hit already on PATH.

Usage

Command line

# Query a CAZy family directly -- TARGET is auto-detected as a family code or a file path
candy GH173 --email you@example.com --tree

# Restrict to a taxonomic subset, and use a stricter clustering cutoff
candy GH173 --email you@example.com --taxonomy Bacteria --cluster-identity 90

# Reprioritize which InterPro database wins when two disagree on a domain boundary
# (only the databases you name move; everything else keeps its default order)
candy GH173 --email you@example.com --db-preference PFAM,SMART

# Analyse your own FASTA file instead
candy my_sequences.fasta --tree

--email falls back to the CANDY_EMAIL environment variable, then an interactive prompt, so export CANDY_EMAIL=you@example.com once and just run candy GH173 from then on. Run candy --help for the full list of options.

Domain-name curation

Partway through a run, CANDy needs to decide which raw InterPro domain names (often several near-duplicates from different member databases) should be grouped under one umbrella name. By default (--curation-backend manual) it asks you interactively: it prints a numbered list of the domain names still to curate, then prompts twice --

  1. Domain name: -- type the umbrella name you want to use (e.g. Catalytic domain)
  2. Includes: -- type the comma-separated numbers of the domains that belong under it (e.g. 0,2)

It repeats this until every domain is grouped; type STOP at the Domain name: prompt at any point to leave all remaining domains as their own individual groups.

To skip this entirely, use Gemini to curate automatically instead:

  1. Install the extra: pip install "candy-cazyme[gemini]" (the quotes matter in zsh, macOS's default shell -- without them, [gemini] is parsed as a glob pattern)
  2. Get a free API key at aistudio.google.com/app/api-keys
  3. Run with --curation-backend gemini --curation-api-key YOUR_KEY, or set it once via $env:GOOGLE_API_KEY="YOUR_KEY" (PowerShell) / export GOOGLE_API_KEY=YOUR_KEY (bash) and just pass --curation-backend gemini

If this step appears to hang with nothing printing (v3.0.2+): CANDy now logs before and after the Gemini request, and bounds each attempt to a 60-second timeout, so a multi-minute wait during retries is visible and finite rather than silent. On an older version, this step had no request timeout at all and could hang indefinitely on a stalled connection with zero output -- if you hit this, Ctrl+C, upgrade (pip install --upgrade candy-cazyme), and rerun.

Python API

from candy.config import CAZyFamilyInput, PipelineConfig, Taxonomy
from candy.pipeline import run_pipeline

config = PipelineConfig(
    input=CAZyFamilyInput(enzyme_class="GH", family_number=5, email="you@example.com", taxonomy=Taxonomy.ALL),
    jobname="my_gh5_run",
    output_dir="results",
    build_tree=True,
)
result = run_pipeline(config)
print(result.database_path, result.tree_path)

Output

Results are written to {output_dir}/{jobname}/:

  • FASTA files for each processing stage
  • A SQLite database ({jobname}_db.db) containing the domain annotations -- open it with DB Browser for SQLite
  • A protein domain co-occurrence network ({jobname}_domain_cooccurence_network.graphml) -- open it in Cytoscape (yFiles Organic Layout recommended)
  • If --tree/build_tree=True: a FAMSA alignment, a VeryFastTree phylogenetic tree (Newick), and iTOL annotation files for the domain architecture and (for CAZy family queries) characterized-enzyme activity

Acknowledgements

CANDy communicates with and/or references the following separate libraries, packages and tools:

Citation

If you find CANDy useful, please cite it as:

Windels A, Franceus J, Pleiss J, Desmet T. CANDy: Automated analysis of domain architectures in carbohydrate-active enzymes. PLoS One. 2024 Jul 11;19(7):e0306410. doi: 10.1371/journal.pone.0306410. PMID: 38990885; PMCID: PMC11238990.

Legal terms

License and Disclaimer

CANDy is licensed under MIT.

CANDy and other information provided is for theoretical utilisation only, caution should be exercised in its use. It is provided 'as-is' without any warranty of any kind, whether expressed or implied. Information is not intended to be a substitute for professional medical advice, diagnosis, or treatment, and does not constitute medical or other professional advice.

Third-party software

Use of the third-party software, libraries or code referred to in the Acknowledgements section in the CANDy README may be governed by separate terms and conditions or license provisions. Your use of the third-party software, libraries or code is subject to any such terms and you should check that you can comply with any applicable restrictions or terms and conditions before use.

Databases

The following databases are used by CANDy, and are available with reference to the following:

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CANDy allows the domain detection and annotation of protein sequences from any CAZy family.

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