PluginBench
Skill
Review
Audit score 70

protein-sequence-similarity-search

google-deepmind/science-skills

Search for homologous protein sequences using MMseqs2 or BLAST to find matches and infer function.

What is protein-sequence-similarity-search?

Finds homologous protein sequences from a user-provided amino acid sequence or FASTA file using MMseqs2 (fast, default) or BLAST (comprehensive). Use this when you need to identify similar proteins, infer function from sequence similarity, or explore evolutionary relationships—but not for structure-based function inference.

  • Searches for sequence homologues using MMseqs2 (ColabFold API) by default or BLAST (EBI) on fallback or explicit request
  • Generates Markdown-formatted tables of top sequence matches with alignment metrics (E-value, query coverage, sequence identity)
  • Interprets key alignment statistics and summarizes inferred protein functions from homologue descriptions
  • Saves results as both JSON (for programmatic use) and Markdown (for human review) locally
  • Automatically falls back to BLAST if MMseqs2 hits rate limits or API errors

How to install protein-sequence-similarity-search

npx skills add https://github.com/google-deepmind/science-skills --skill protein-sequence-similarity-search
Prerequisites
  • Install and configure `uv` (Python package manager) on PATH
  • Check license terms at https://www.ebi.ac.uk/jdispatcher/sss/ncbiblast and https://colabfold.com; a notification file will be created in the workspace root on first use
  • Create or ensure a `.env` file exists in your home directory
  • (Recommended) Set `USER_EMAIL` environment variable for EBI BLAST job tracking; use the `credentials` skill to securely provide this
Claude Code
Cursor
Windsurf
Cline

How to use protein-sequence-similarity-search

  1. 1.Provide a protein sequence (raw string or path to a `.fasta` file) and specify whether you want a quick search, BLAST, or a specific database
  2. 2.The skill will run MMseqs2 by default; if it fails or you request BLAST explicitly, it will fall back to or use the EBI BLAST API
  3. 3.Wait for the search to complete (MMseqs2 typically takes under 2 minutes; BLAST can take up to 15 minutes)
  4. 4.Review the generated `.md` file containing the results table with top homologues, alignment metrics, and functional summaries
  5. 5.Use the generated `.json` file for downstream programmatic analysis or tool integration

Use cases

Good for
  • Find homologous proteins in UniProt or curated databases to infer the function of an uncharacterized sequence
  • Search for a protein sequence across specific taxonomic groups (e.g., bacteria, human) to understand evolutionary conservation
  • Retrieve top sequence matches with statistical confidence metrics to validate a newly discovered or predicted protein
  • Explore protein family relationships and functional diversity among homologues for a given query sequence
  • Quickly screen a sequence against public databases before running computationally expensive structural predictions
Who it's for
  • Bioinformaticians and computational biologists performing sequence analysis
  • Researchers inferring protein function from homology
  • Scientists validating newly discovered or predicted protein sequences
  • Structural biologists preparing sequences for downstream modeling

protein-sequence-similarity-search FAQ

When should I use MMseqs2 vs. BLAST?

MMseqs2 (default) is fast and suitable for general homologue searches. Use BLAST if you need a specific curated database (e.g., Swiss-Prot), explicit request, or if MMseqs2 fails due to rate limits.

What do the alignment metrics mean?

E-value indicates statistical significance (lower is better); Query Coverage (Q-Cov) shows what fraction of your sequence is matched; Sequence Identity reflects evolutionary distance between sequences.

Will the skill look up protein functions automatically?

If results include protein descriptions, functions are summarized directly. If only UniProt IDs are returned (common with MMseqs2), the skill will use the uniprot-database skill to fetch names and functions for top hits.

What databases can I search with BLAST?

Available databases include uniprotkb (full UniProt), uniprotkb_swissprot (manually curated), uniprotkb_reference_proteomes, uniprotkb_trembl, and others. The skill validates your choice against the allowed list.

What if the search returns no hits or fails?

The skill will clearly inform you of the failure and not invent results. Check that your sequence is valid and, if using BLAST, that your database choice is correct.

Full instructions (SKILL.md)

Source of truth, from google-deepmind/science-skills.


name: protein-sequence-similarity-search description: > Searches for homologous protein sequences using MMseqs2 (fast, default) or BLAST (comprehensive, fallback). Trigger this whenever the user provides a protein sequence or FASTA file and asks to find homologues, sequence matches, or wants to infer protein function based on sequence similarity, but not when the user wants to infer protein function based on structural similarity.

Prerequisites

  1. uv: Read the uv skill and follow its Setup instructions to ensure uv is installed and on PATH.
  2. User Notification: If .licenses/protein_sequence_similarity_search_LICENSE.txt does not already exist in the workspace root directory then (1) prominently notify the user to check the terms at https://www.ebi.ac.uk/jdispatcher/sss/ncbiblast and https://colabfold.com, then (2) create the file recording the notification text and timestamp.
  3. .env file: Make sure the .env file exists in your home directory. Create one if it does not exist.
  4. USER_EMAIL (optional but recommended): Recommended by the EBI for BLAST job tracking, but the skill works without it. You MUST use the safe credentials protocol in the credentials skill to check for and request this credential if this skill looks relevant to the user's request.

Goal

Take a user-provided amino acid sequence (or a path to a .fasta file), search for sequence homologues using the fastest available method, generate a Markdown-formatted table of the top hits, interpret key alignment metrics, summarize the inferred protein functions, and save results locally for future programmatic analysis.

Core Rules

  • Strict Validation: For BLAST, only use database codes listed in the table below.
  • No Hallucinations: If a script throws an error or returns no hits, inform the user clearly. Do NOT invent sequence homologues.
  • Do Not Parse Output Files: Do not parse the JSON, a3m, or any other raw output files. Rely on the generated .md file for your summary. The JSON and other outputs are for subsequent tool use only.
  • Always State the Method: Every report must clearly state whether the search used the quick MMseqs2 (ColabFold API) or the slower EBI BLAST method.
  • Notification: If this skill is used, ensure this is mentioned in the output. Explicitly state that the corresponding program (MMSEQS2 or EBI BLAST) and Sequence Databases were used.

Search Method Selection

Choose the search method based on the user's request:

If the user says "quick search" or "fast search", no specific method requested / general homologue search, of if you are unsure: Run MMseqs2 (fast, default) using mmseqs2_search.py

If MMseqs2 fails (exit code 2: RATELIMIT or API error) or User explicitly requests "BLAST" or a specific BLAST database (e.g. uniprotkb_swissprot, pdb, uniprotkb_human): Run BLAST using uniprot_blast.py

Instructions

  1. Identify the query from the user. It can be a raw sequence string (e.g., "MKVLY...") or a path to a local file (e.g., "./data/sequence.fasta").

  2. Determine the search method using the list above.

Path A: MMseqs2 Search (Default)

  1. Generate File Names: Generate descriptive output file names based on the input (e.g., proteinA_mmseqs2.json and proteinA_mmseqs2.md).

  2. Execute the MMseqs2 script:

    • Default:
    uv run scripts/mmseqs2_search.py <SEQUENCE_OR_FILE> -o <generated-filename.md> -j <generated-filename.json>
    
    • With mgnify:
    uv run scripts/mmseqs2_search.py <SEQUENCE_OR_FILE> -o <generated-filename.md> -j <generated-filename.json> --include-mgnify
    
  3. The script will query the ColabFold MMseqs2 API and poll for completion. This is typically fast (under 2 minutes).

  4. If the script exits with code 2 (API failure, rate limit), automatically fall back to BLAST (Path B below). Inform the user: "MMseqs2 search failed, falling back to BLAST."

  5. Read the Results: Open and read the generated .md file.

Path B: BLAST Search (Explicit or Fallback)

  1. Database Selection & Validation: Determine the most appropriate database(s) based on the user's prompt.

    • Consult the Available BLAST Databases table below.
    • If the user specifies a taxonomic group (e.g., "Find homologues in microbes"), select the corresponding Database Code (e.g., uniprotkb_bacteria).
    • If the user explicitly requests curated hits, use uniprotkb_swissprot.
    • If no specific database is requested, do not specify --databases.
    • Validation: Ensure the database code exactly matches an entry in the table. If the user requests a database not on the list, do not proceed and provide the allowed list.
  2. Generate File Names: (e.g., proteinA_ebi_blast.json and proteinA_ebi_blast.md).

  3. This API requires the user email address to be set in the USER_EMAIL environment variable for inclusion in request header. You MUST use the safe credentials protocol in the credentials skill to check for and request this credential if this skill looks relevant to the user's request.

  4. Execute the BLAST script:

    • Default (uniprotkb):
    uv run scripts/uniprot_blast.py <SEQUENCE_OR_FILE> -o <generated-filename.md> -j <generated-filename.json>
    
    • Custom database:
    uv run scripts/uniprot_blast.py <SEQUENCE_OR_FILE> -o <generated-filename.md> -j <generated-filename.json> --databases <db1,db2>
    
  5. The script will query the EBI BLAST API and poll the server. Note: This can take up to 15 minutes; wait patiently.

  6. Read the Results: Open and read the generated .md file.

Common Steps (Both Methods)

  1. Interpret the Metrics: Summarize the top 3 to 5 sequence homologues. Assess match quality using:
    • Q-Cov (Query Coverage): High percentages mean the match covers most of the query sequence.
    • E-value: Lower E-values (e.g., 1e-50) indicate extreme statistical significance.
    • Seq Identity: Provides evolutionary context (highly conserved vs. distant homologue).
  2. Perform Functional Analysis:
    • If the results table includes protein descriptions, analyze them directly: report specific protein names/functions of the top homologues and summarize the variety of functions, domains, or protein families found.
    • If the results contain only UniProt accession IDs without descriptions (common with MMseqs2), look up the protein names and functions for the top 3–5 hits using the uniprot-database skill or other appropriate methods before summarizing.
  3. Inform the user of both newly created files (.json and .md) and their locations.

Available BLAST Databases

  • uniprotkb – UniProt Knowledgebase (The UniProt Knowledgebase includes UniProtKB/Swiss-Prot and UniProtKB/TrEMBL): The UniProt Knowledgebase (UniProtKB) is the central access point for extensive curated protein information, including function, classification, and cross-references. Search UniProtKB to retrieve "everything that is known" about a particular sequence
  • uniprotkb_swissprot – UniProtKB/Swiss-Prot (The manually annotated section of UniProtKB): The manually curated subsection of the UniProt Knowledgebase
  • uniprotkb_swissprotsv – UniProtKB/Swiss-Prot isoforms (The manually annotated isoforms of UniProtKB/Swiss-Prot): The isoform sequences for the manually curated subsection of the UniProt Knowledgebase
  • uniprotkb_reference_proteomes – UniProtKB Reference Proteomes: Taxonomic subset of the UniProtKB Reference Proteomes
  • uniprotkb_trembl – UniProtKB/TrEMBL (The automatically annotated section of UniProtKB): Subsection of the UniProt Knowledgebase derived from ENA Sequence (formerly EMBL-Bank) coding sequence translations with annotation produced by an automated process
  • uniprotkb_refprotswissprot – UniProtKB Reference Proteomes plus Swiss-Prot: UniProtKB Reference Proteomes plus Swiss-Prot
  • uniprotkb_archaea – UniProtKB Archaea: Taxonomic subset of the UniProt Knowledgebase for archaea
  • uniprotkb_arthropoda – UniProtKB Arthropoda: Taxonomic subset of the UniProt Knowledgebase for arthropoda
  • uniprotkb_bacteria – UniProtKB Bacteria: Taxonomic subset of the UniProt Knowledgebase for bacteria
  • uniprotkb_complete_microbial_proteomes – UniProtKB Complete Microbial Proteomes: Taxonomic subset of the UniProt Knowledgebase for complete microbial proteomes
  • uniprotkb_eukaryota – UniProtKB Eukaryota: Taxonomic subset of the UniProt Knowledgebase for eukaryota
  • uniprotkb_fungi – UniProtKB Fungi: Taxonomic subset of the UniProt Knowledgebase for fungi
  • uniprotkb_human – UniProtKB Human: Taxonomic subset of the UniProt Knowledgebase for human
  • uniprotkb_mammals – UniProtKB Mammals: Taxonomic subset of the UniProt Knowledgebase for mammals
  • uniprotkb_nematoda – UniProtKB Nematoda: Taxonomic subset of the UniProt Knowledgebase for nematoda
  • uniprotkb_rodents – UniProtKB Rodents: Taxonomic subset of the UniProt Knowledgebase for rodents
  • uniprotkb_vertebrates – UniProtKB Vertebrates: Taxonomic subset of the UniProt Knowledgebase for vertebrates
  • uniprotkb_viridiplantae – UniProtKB Viridiplantae: Taxonomic subset of the UniProt Knowledgebase for viridiplantae
  • uniprotkb_viruses – UniProtKB Viruses: Taxonomic subset of the UniProt Knowledgebase for viruses
  • uniprotkb_enzyme – UniProtKB Enzyme: Taxonomic subset of the UniProt Knowledgebase for enzymes
  • uniprotkb_covid19 – UniProtKB COVID-19: Taxonomic subset of the UniProt Knowledgebase for COVID-19
  • uniref100 – UniProt Clusters 100% (UniRef100): The UniProt Reference Clusters (UniRef) containing sequences which are 100% identical.
  • uniref90 – UniProt Clusters 90% (UniRef90): The UniProt Reference Clusters (UniRef) containing sequences which are 90% identical.
  • uniref50 – UniProt Clusters 50% (UniRef50): The UniProt Reference Clusters (UniRef) containing sequences which are 50% identical.
  • pdb – Protein Structure Sequences (PDBe protein structure sequences): Protein sequences from structures described in the Brookhaven Protein Data Bank (PDB)