Agent skill

Glycoengineering

by K-Dense-AI in K-Dense-AI/scientific-agent-skills

Analyzes and engineers protein glycosylation by scanning canonical N-glycosylation sequons, describing S/T-rich regions, checking curated glycan evidence, and preparing NetNGlyc, NetOGlyc and…

MITAuto-check passedResearch & Science

Install Glycoengineering

skills CLI
$ npx skills add K-Dense-AI/scientific-agent-skills --skill glycoengineering -a claude-code

Project install by default; add -g for ~/.claude/skills/.

GitHub CLI
$ gh skill install K-Dense-AI/scientific-agent-skills glycoengineering --agent claude-code

Project scope by default; add --scope user for a personal install. Needs GitHub CLI 2.90.0 or later (public preview).

Manual copy
$ git clone --depth 1 https://github.com/K-Dense-AI/scientific-agent-skills.git skills-src && mkdir -p .claude/skills && cp -r skills-src/skills/glycoengineering .claude/skills/glycoengineering && rm -rf skills-src

Use ~/.claude/skills/ instead of .claude/skills for a personal install. The folder must contain SKILL.md.

Claude Code skills documentation · loads skills from .claude/skills/

Facts

Skill name
glycoengineering
GitHub stars
48k
Used in
1 other repo
Token cost
~3k tokens
SKILL.md length
1,149 words
Files
5 (incl. scripts, references)
Skills in repo
153
Repo updated
First seen
Licence
MIT

At a glance

Analyzes and engineers protein glycosylation by scanning canonical N-glycosylation sequons, describing S/T-rich regions, checking curated glycan evidence, and preparing NetNGlyc, NetOGlyc and…

  • Works in 6 steps: Record the protein accession,… → Scan canonical N-X-[S/T] candidates with… → Prioritize… → …
  • Glycoprotein engineering
  • SKILL.md covers When to use, Workflow, Local sequence analysis and Prediction services, plus 4 more sections
  • Runs Python scripts from its folder

What it does

Glycoengineering is an agent skill from K-Dense-AI/scientific-agent-skills. Analyzes and engineers protein glycosylation by scanning canonical N-glycosylation sequons, describing S/T-rich regions, checking curated glycan evidence, and preparing NetNGlyc, NetOGlyc and GlycoSHIELD workflows. Use for glycoprotein engineering, antibody Fc glycosylation, glycan shielding, and site-specific glycoproteomics interpretation.

Its SKILL.md is about 3k tokens, which your agent loads only when the skill is triggered. The skill folder holds 6 other files, including scripts and reference files (for example `references/glycan_databases.md`, `references/glycoshield.md` and `scripts/glycoengineering_tools.py`). Compatibility notes: Local sequence helpers require Python 3.10+. Public GlyTouCan lookup requires requests and network access. DTU predictors use a browser; optional GlycoSHIELD…

It sits in Research & Science. The repository describes itself as: Turn any AI agent into an AI Scientist. The 1 Agent Skills library for science, used by 250,000+ scientists worldwide. 177 ready-to-use validated skills plus 100+ scientific… The licence is MIT.

When your agent uses it

  • Glycoprotein engineering
  • Antibody Fc glycosylation
  • Glycan shielding
  • Site-specific glycoproteomics interpretation

Example prompts

  • “Use the glycoengineering skill to analyz and engineers protein glycosylation by scanning canonical N-glycosylation sequons, describing S/T-rich…”
  • “/glycoengineering”

Requirements

  • Python 3
  • Compatibility (from SKILL.md): Local sequence helpers require Python 3.10+. Public GlyTouCan lookup requires requests and network access. DTU predictors use a browser; optional GlycoSHIELD needs a separate source installation, glycan libraries, and GROMACS for SASA analysis.

Workflow steps

6 steps, taken from the first numbered list in SKILL.md.

  1. Record the protein accession, isoform/version, exact sequence, expression host,
  2. Scan canonical N-X-[S/T] candidates with X not Pro. Retain overlaps: NNST
  3. Prioritize secreted/luminal/extracellular regions using topology and curated
  4. For O-GalNAc, use S/T density only as a descriptive feature, then inspect a
  5. Propose explicitly numbered mutations, list every changed residue and rescan
  6. Validate occupancy and glycoforms experimentally, with localization evidence,

What it can do on your machine

Read from SKILL.md and the folder at commit 92ace75. It shows what the files ask for, not the result of running them.

  • Tool permissions

    Pre-approves nothing: there is no allowed-tools line, so your agent's usual permission prompts apply.

    From allowed-tools in the SKILL.md frontmatter.

  • Runs code

    Ships 2 files in scripts/ (Python), which the agent can run.

    From the folder's file list and the shell code blocks in SKILL.md.

  • Network

    Links to these hosts (documentation or services it may open):

    • pubmed.ncbi.nlm.nih.gov
    • doi.org
    • services.healthtech.dtu.dk
    • gitlab.mpcdf.mpg.de
    • support.proteinmetrics.com

    From URLs in SKILL.md, links to its own repository left out.

  • Credentials

    Names no API keys, tokens, secrets or passwords.

    From names ending in _API_KEY, _TOKEN, _SECRET, _KEY or _PASSWORD in SKILL.md.

  • Compatibility

    Local sequence helpers require Python 3.10+. Public GlyTouCan lookup requires requests and network access. DTU predictors use a browser; optional GlycoSHIELD needs a separate source installation, glycan libraries, and GROMACS for SASA analysis.

    From compatibility in the SKILL.md frontmatter.

Context cost

Glycoengineering loads about 3k tokens when it runs, and up to ~6.7k if it reads all its reference files. Until then it costs about 90 tokens; SKILL.md has 1,149 words of instructions outside code blocks.

Always · name and description, kept in context so the agent knows when to use it
~90
When it runs · the whole SKILL.md, loaded when a task matches
~3k
With references · SKILL.md plus every file in references/, read only if the agent opens them
~6.7k

Estimates: characters ÷ 4, the usual rule of thumb; real counts depend on the model's tokenizer. Scripts and assets cost tokens only if the agent reads them.

Safety

Auto-check passed

The automated check found no risky patterns in SKILL.md.

Automated static check — not a guarantee. Review scripts before installing. It scans the text of SKILL.md for risky patterns (piping downloads into a shell, reading credential files, hidden Unicode, destructive commands); the scripts in this folder are not scanned.

SKILL.md

The full file from K-Dense-AI/scientific-agent-skills at commit 92ace75, republished under its MIT licence (© K-Dense-AI). 1,149 words, ~2,985 tokens.

Download SKILL.mdSave it as .claude/skills/glycoengineering/SKILL.md (or your agent's skills folder). This skill also uses 4 other files; get the full folder from GitHub.
name
glycoengineering
description
Analyzes and engineers protein glycosylation by scanning canonical N-glycosylation sequons, describing S/T-rich regions, checking curated glycan evidence, and preparing NetNGlyc, NetOGlyc and GlycoSHIELD workflows. Use for glycoprotein engineering, antibody Fc glycosylation, glycan shielding, and site-specific glycoproteomics interpretation.
compatibility
Local sequence helpers require Python 3.10+. Public GlyTouCan lookup requires requests and network access. DTU predictors use a browser; optional GlycoSHIELD needs a separate source installation, glycan libraries, and GROMACS for SASA analysis.
license
Unknown
metadata.version
1.4
metadata.skill-author
Kuan-lin Huang
metadata.last-reviewed
2026-10-01

Glycoengineering

When to use

Use for canonical N-glycosylation candidate analysis, O-GalNAc candidate triage, antibody glycoform comparison, or structural glycan shielding. Keep four kinds of result separate: sequence motif, prediction, experimentally supported occupancy, and glycan structure/composition. None alone establishes all the others.

This workflow focuses on eukaryotic secretory-pathway N-glycosylation and mucin-type O-GalNAc. O-GlcNAc, O-mannose, O-fucose and other O-linked modifications require appropriate evidence and predictors; S/T enrichment does not identify the type.

Workflow

  1. Record the protein accession, isoform/version, exact sequence, expression host, signal peptide/transmembrane topology and construct boundaries. Preserve a mapping from submitted sequence coordinates to mature protein, PDB chain/residue identifiers and antibody numbering where relevant.
  2. Scan canonical N-X-[S/T] candidates with X not Pro. Retain overlaps: NNST has candidates starting at 1 and 2. A missing canonical motif does not rule out unusual N-glycosylation; a present motif does not establish occupancy.
  3. Prioritize secreted/luminal/extracellular regions using topology and curated evidence. Sequence-only results in a cytoplasmic region are not evidence of secretory-pathway glycosylation.
  4. For O-GalNAc, use S/T density only as a descriptive feature, then inspect a suitable predictor and cell/transferase context. Do not exclude SP/TP motifs: adjacent Pro can be favorable, depending on the GalNAc-transferase and context. See the GalNAc-T substrate study.
  5. Propose explicitly numbered mutations, list every changed residue and rescan the full product for lost/created overlapping motifs. Evaluate structural and expression effects independently of glycosylation.
  6. Validate occupancy and glycoforms experimentally, with localization evidence, glycan composition/structure confidence, and the biological assay required by the engineering objective. For biosimilar comparisons, match sample handling, analytical coverage and quantification before comparing glycan percentages.

Local sequence analysis

The standard-library helper scripts/glycoengineering_tools.py replaces copied snippets. Import it with this skill's scripts/ directory on PYTHONPATH, or run Python from that directory. It accepts raw canonical 20-amino-acid sequences, normalizes whitespace/case, and rejects FASTA headers, gaps, unknown residues and empty input. Parse FASTA records first; do not remove unknown residues because that changes coordinates. Coordinates are 1-based in the normalized submitted sequence.

python
from glycoengineering_tools import (
    normalize_sequence, find_n_glycosylation_sequons,
    eliminate_glycosite, add_glycosite, find_st_rich_sites,
)

sequence = normalize_sequence("NNST")
sites = find_n_glycosylation_sequons(sequence)
assert [site["position"] for site in sites] == [1, 2]

mutant = eliminate_glycosite(sequence, 1, "Q")
assert mutant == "QNST"  # the overlapping sequon at position 2 remains
assert [site["position"] for site in find_n_glycosylation_sequons(mutant)] == [2]

# Three intended changes: A1N, P2A, A3T. P->A must be explicit.
parent = "APA"
product = add_glycosite(parent, 1, "T", allow_proline_substitution=True)
changes = [(i, before, after) for i, (before, after) in
           enumerate(zip(parent, product), 1) if before != after]
assert product == "NAT" and len(changes) == 3

# Density is a fraction of residues, not an O-glycosylation probability.
o_candidates = find_st_rich_sites("STPST", window=7, min_st_fraction=0.4)
assert [site["position"] for site in o_candidates] == [1, 2, 4, 5]

eliminate_glycosite requires a complete canonical sequon and a one-residue replacement other than N. add_glycosite can alter up to three residues; it retains an existing S/T at +2. Neither function predicts a mutant's fold, glycan occupancy, function or tolerability. An N-to-Q substitution can change protein behavior even without a glycan effect.

The S/T density window must be a positive odd integer. Terminal windows shorten, and their denominator is the actual window length. Dense regions may help triage mucin-like sequence; isolated real O-GalNAc sites can be missed.

For batch analysis, keep identifiers and normalized sequence lengths:

python
sequences = {"overlap": "NNST", "control": "APAA", "mucin_like": "STPST"}
rows = []
for name, raw_sequence in sequences.items():
    seq = normalize_sequence(raw_sequence)
    positions = [site["position"] for site in find_n_glycosylation_sequons(seq)]
    rows.append({"protein": name, "length": len(seq),
                 "n_sequon_positions": positions,
                 "n_sequons_per_100_residues": 100 * len(positions) / len(seq),
                 "st_rich_positions": [site["position"] for site in find_st_rich_sites(seq)]})

Prediction services

Use the official forms, which accept FASTA and return web results; this skill does not provide a stable submission API or job-polling endpoint. Saving a CGI URL is not a submitted job. Preserve the output, input and service version together.

ServiceCurrent documented scope and interpretation
NetNGlyc 1.0Human N-glycosylation; reports network potential and jury agreement. Default threshold 0.5; not a calibrated occupancy probability. Up to 2,000 sequences / 200,000 residues total / 4,000 per sequence. SignalP runs, but extracellular topology is not checked. The server may score N-P-S/T; exclude these from the canonical candidate set unless independent evidence warrants review.
NetOGlyc 4.0Mammalian mucin-type O-GalNAc; outputs GFF2 confidence scores, with scores greater than 0.5 marked positive. Up to 50 sequences / 200,000 residues total / 4,000 per sequence. Prefer full sequence including signal peptide; isolated sites need 15 residues of flanking context on both sides. A positive supports regional likelihood, not guaranteed site occupancy or glycan type beyond this model's O-GalNAc scope.

The service documentation and sample output were reviewed; new prediction jobs were not submitted during this refresh.

Structural shielding with GlycoSHIELD

GlycoSHIELD grafts pre-simulated glycan conformers onto protein structures and filters steric clashes. It does not predict which sequons are occupied or run fresh molecular dynamics for each query. See Tsai et al., 2024.

Read references/glycoshield.md for the pinned source, installation, direct Python API, input mapping and SASA analysis. The reviewed upstream CLI silently ignores several parsed options, including --mode, --threshold and --dryrun; use the documented direct API workaround. Outputs include per-site PDB/XTC ensembles and shielding encoded in a PDB B-factor column; those values are not crystallographic temperature factors.

Show full SKILL.md (458 more words)Show less

Database evidence and glycan notation

Read references/glycan_databases.md for the live GlyTouCan SPARQL lookup, GlyConnect access limitations, curated resources and notation. Query exact accessions and preserve dataset/source dates, species, tissue/cell context and supporting publications. Missing records or service errors cannot establish that a protein is unglycosylated.

A monosaccharide composition such as Hex:5 HexNAc:4 dHex:1 does not resolve linkages, branch positions, or distinguish GlcNAc from GalNAc. A cartoon without linkages is schematic, not IUPAC condensed notation. Use an actual sequence (WURCS/GlycoCT/IUPAC with its uncertainty retained) and accession when available. Core fucose attaches to the innermost GlcNAc of an N-glycan, not to core mannose.

Antibody engineering decisions

Number Fc mutations in an explicit scheme (commonly EU), then map them to the actual construct. EU N297 is not residue 297 of an isolated Fc FASTA. Fc glycans and any Fab glycans must be distinguished analytically.

ObjectiveCandidate strategyRequired interpretation
Increase FcγRIIIa engagement / ADCCReduce Fc core fucosylation while preserving the glycanEffect size depends on antibody, receptor and assay; do not assume a universal fold gain. Structural evidence.
Remove canonical Fc N-glycosylationN297Q/A/D or disrupt the +2 residue with T299ASequon disruption; not a guarantee of otherwise unchanged structure or effector function. Verify the actual product.
Alter serum persistenceCharacterize glycoform-specific clearance with the relevant proteinIgG high-mannose clearance can increase; sialylation is not a universal IgG half-life recipe. Human PK study.
Investigate anti-inflammatory Fc activityCompare defined sialylated glycoformsLinkage, preparation and biological model matter. Positive results in particular models do not establish a universal IVIG mechanism. Defined Fc study.
Reduce non-human glycan epitopesMeasure α-Gal and Neu5Gc and select compatible production conditionsSequence editing alone does not control the host's glycan processing.
Study epitope accessibilityIntroduce or remove a mapped surface sequonConfirm occupancy, folding, binding and antigenicity; shielding calculations are geometric hypotheses.

Fc sequence variants such as S298A/E333A/K334A or F243L-containing combinations can alter both receptor interaction and host-dependent glycan processing. Do not label F243L alone as a deterministic defucosylation switch. See the 2026 Fc-variant glycan study.

Experimental interpretation and verification boundary

Glycopeptide searches can support peptide identity, composition and sometimes site localization, without resolving a full glycan structure. Review localization fragments, competing assignments, search-space choices and error control. In Byonic, composition does not determine topology; O-glycosite ambiguity may remain even with an identified glycopeptide. Relative signal among detected glycoforms is not automatically absolute site occupancy; occupancy needs the appropriate modified and unmodified denominator and analytical response considerations.

Local sequence behavior is covered by synthetic tests. Public accession lookup was executed; API error handling was mocked. GlycoSHIELD source/argument handling was checked, but full conformer grafting, GROMACS SASA, DTU jobs, commercial MS software and biological performance were not executed. Supporting references record the service/source review date and unresolved access gaps.

© K-Dense-AI, MIT. Rendered from Markdown: HTML in the file is shown as text, images as links, and headings moved down two levels. Raw file

Files

SKILL.md and 4 other files (scripts, references) in skills/glycoengineering of K-Dense-AI/scientific-agent-skills.

  • SKILL.md
  • references/glycan_databases.md
  • references/glycoshield.md
  • scripts/glycoengineering_tools.py
  • scripts/glytoucan_lookup.py

Open the folder on GitHubat commit 92ace75

Used in 1 other repository

We found 1 copy of this SKILL.md (exact, near-identical or edited) in other folders, from 1 other GitHub owner. This page covers the copy in K-Dense-AI/scientific-agent-skills, which our catalogue first saw on October 7, 2026.

Compare with similar skills

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Questions about Glycoengineering

What does Glycoengineering do?

Analyzes and engineers protein glycosylation by scanning canonical N-glycosylation sequons, describing S/T-rich regions, checking curated glycan evidence, and preparing NetNGlyc, NetOGlyc and…. Glycoengineering is an agent skill from K-Dense-AI/scientific-agent-skills. Analyzes and engineers protein glycosylation by scanning canonical N-glycosylation sequons, describing S/T-rich regions, checking curated glycan evidence, and preparing NetNGlyc, NetOGlyc and GlycoSHIELD workflows.

When should I use Glycoengineering?

Glycoengineering fits situations like: glycoprotein engineering; antibody Fc glycosylation; glycan shielding; site-specific glycoproteomics interpretation.

How do I install Glycoengineering in Claude Code?

Run `npx skills add K-Dense-AI/scientific-agent-skills --skill glycoengineering -a claude-code`. Or copy the skill folder (skills/glycoengineering in K-Dense-AI/scientific-agent-skills) into .claude/skills/glycoengineering in your project. Claude Code loads it when a task matches its description.

How do I install Glycoengineering in Codex?

Run `npx skills add K-Dense-AI/scientific-agent-skills --skill glycoengineering -a codex`. Or copy the skill folder (skills/glycoengineering in K-Dense-AI/scientific-agent-skills) into .agents/skills/glycoengineering in your project. Codex loads it when a task matches its description.

Can I use Glycoengineering in Cursor, Gemini CLI or GitHub Copilot?

Cursor, Gemini CLI, GitHub Copilot and OpenCode also load SKILL.md folders. With the skills CLI, run `npx skills add K-Dense-AI/scientific-agent-skills --skill glycoengineering -a cursor` (or -a gemini-cli, github-copilot or opencode for the others). To copy it by hand, put the folder in .cursor/skills/glycoengineering, .gemini/skills/glycoengineering, .github/skills/glycoengineering and .opencode/skills/glycoengineering in your project.

What does Glycoengineering need to run?

Going by SKILL.md and its folder, Glycoengineering needs Python for the scripts in its folder. Our summary lists: Python 3. Compatibility (from SKILL.md): Local sequence helpers require Python 3.10+. Public GlyTouCan lookup requires requests and network access. DTU predictors use a browser; optional GlycoSHIELD needs a separate source installation, glycan libraries, and GROMACS for SASA analysis..

Does Glycoengineering access the network?

SKILL.md names 5 domains. As links in the text: pubmed.ncbi.nlm.nih.gov, doi.org, services.healthtech.dtu.dk, gitlab.mpcdf.mpg.de and support.proteinmetrics.com. This is read from the text; nothing was executed.

Is Glycoengineering safe to install?

Our automated static check of SKILL.md found no risky patterns, such as piping downloads into a shell, reading credential files or hidden Unicode. It is not a guarantee. The check reads SKILL.md only: the scripts in the folder are not scanned, so read them before running anything.

What licence does Glycoengineering use?

Glycoengineering is published under the MIT licence (the repository's licence). It allows redistribution, so the full SKILL.md is shown on this page.

How many tokens does Glycoengineering use?

About 3k tokens (SKILL.md is roughly 12k characters). Agents keep only the skill's name and description in context until a task matches; then they load SKILL.md in full. Its references folder adds about 3.7k tokens, read only when the agent opens those files.

What are the alternatives to Glycoengineering?

Skills that share tags, products or a category with Glycoengineering: Hypothesis Generation (spacering-net/codeg, 3.9k stars), GitHub Deep Research (bytedance/deer-flow, 84k stars), Nature Paper Card (Yuan1z0825/nature-skills, 47k stars) and Content Research Writer (weapp-tailwindcss/weapp-tailwindcss, 1.9k stars). The comparison table on this page puts their stars, adoption, token cost, safety result and licence side by side.

Who maintains Glycoengineering?

K-Dense-AI (a GitHub organization) maintains it in K-Dense-AI/scientific-agent-skills, which has 48,095 GitHub stars. The repository holds 153 skills in this directory. The repository was last updated on October 5, 2026.

Source: K-Dense-AI/scientific-agent-skills on GitHub. Facts on this page come from the repository at the commit we read; the author's words are quoted as theirs.