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tooluniverse-protein-therapeutic-design

AI-guided de novo protein design — RFdiffusion backbone generation, ProteinMPNN sequence design, structure validation (pLDDT, pTM, MPNN scores). Use for designing therapeutic protein binders, novel scaffolds, enzyme variants, and miniprotein/protein-interface design before experimental validation.

66

Quality

79%

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SecuritybySnyk

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tessl review fix ./plugin/skills/tooluniverse-protein-therapeutic-design/SKILL.md
SKILL.md
Quality
Evals
Security

Quality

Content

71%Weight 40%Scale 1-5

Reviews the quality of instructions and guidance provided to agents. Good implementation is clear, handles edge cases, and produces reliable results.

A well-structured, information-dense skill body with correct/incorrect parameter tables, a clear six-phase workflow with embedded validation and a checklist, and explicit evidence-grading tiers. The main problems are the missing reference files the whole depth of the skill depends on, and notable redundancy in the repeated NVIDIA_API_KEY annotations.

Suggestions

Add the referenced files (DESIGN_PROCEDURES.md, TOOLS_REFERENCE.md, EXAMPLES.md, CHECKLIST.md, design_templates.md) to the bundle — or inline the essential per-phase code examples — since progressive_disclosure currently points at files that do not exist.

State the API-key requirement once (in the NVIDIA NIM Requirements section) and drop the '(requires NVIDIA_API_KEY...)' parenthetical repeated in every table row.

Merge or trim the 'Common Parameter Mistakes' table, since the primary tool table already states the correct parameter for each tool.

DimensionReasoningScore

Conciseness

Largely lean, table-driven content with no explanations of concepts Claude already knows, but there is trimmable redundancy: '(requires NVIDIA_API_KEY env var; free key at build.nvidia.com)' is repeated in every relevant row of two tables and then again in a dedicated 'NVIDIA NIM Requirements' section, and the 'Common Parameter Mistakes' table partially restates the key parameters from the tool table. This fits the level-4 anchor (efficient with minor over-explanation) rather than 5, where every token earns its place.

4 / 5

Actionability

Gives executable specifics: exact tool names, the correct parameter for each ('diffusion_steps (NOT num_steps)', 'pdb_string (NOT pdb)'), rate limits ('40 RPM'), thresholds, and minimum counts ('>= 5 backbones', '>= 8 sequences per backbone'). Not a 5 because the body contains no actual runnable call/code examples — those are deferred to reference files — and 'write and run Python code via Bash' is direction rather than instruction.

4 / 5

Workflow Clarity

The six-phase workflow is clearly sequenced with an explicit validation phase ('Predict structure, compare to backbone, assess pLDDT/pTM'), tiered acceptance criteria (T1–T4), and a completeness checklist with pass gates ('>= 3 passing'). Not a 5 because error-recovery/fallback loops are only promised in the (missing) DESIGN_PROCEDURES.md rather than stated, and per-phase execution detail is entirely external.

4 / 5

Progressive Disclosure

The body ends with a clearly signaled, well-annotated one-level-deep reference list (five files with one-line descriptions), which is the right structure. However, none of the referenced files (DESIGN_PROCEDURES.md, TOOLS_REFERENCE.md, EXAMPLES.md, CHECKLIST.md, design_templates.md) exist in the bundle — there is no references/ directory at all — so the disclosure structure is asserted but not actually realized, leaving navigation broken.

3 / 5

Total

15

/

20

Passed

Description

87%Weight 40%Scale 1-5

Based on the skill's description, can an agent find and select it at the right time? Clear, specific descriptions lead to better discovery.

A strong description: it states concrete tool-backed capabilities with validation metrics, uses third person, and carries an explicit 'Use for...' clause covering binder, scaffold, enzyme, and miniprotein design. Its only weaknesses are unmentioned workflow phases (target characterization, developability) and missing common synonyms like antibody/nanobody design.

DimensionReasoningScore

Specificity

Names three concrete, tool-anchored actions — 'RFdiffusion backbone generation, ProteinMPNN sequence design, structure validation (pLDDT, pTM, MPNN scores)' — with specific metrics. Not a 5 because the workflow the skill actually covers includes target characterization and developability assessment, which the description omits (minor coverage gaps fitting the level-4 anchor).

4 / 5

Completeness

Explicitly answers both questions: what it does ('RFdiffusion backbone generation, ProteinMPNN sequence design, structure validation') and when to use it ('Use for designing therapeutic protein binders, novel scaffolds, enzyme variants, and miniprotein/protein-interface design before experimental validation'), matching the level-5 anchor with concrete trigger phrases.

5 / 5

Trigger Term Quality

Includes natural phrases users would say — 'de novo protein design', 'therapeutic protein binders', 'novel scaffolds', 'enzyme variants', 'protein-interface design'. Not a 5 because common synonyms and phrasings users actually use (antibody/nanobody design, binder design, protein engineering) are absent.

4 / 5

Distinctiveness Conflict Risk

A clear niche (AI-guided de novo therapeutic protein design) with distinct tool and domain triggers (RFdiffusion, ProteinMPNN, pLDDT, pTM) that virtually no other skill would share, matching the level-5 'clear niche with distinct triggers' anchor. Voice is third-person throughout, so no specificity penalty applies.

5 / 5

Total

18

/

20

Passed

Validation

100%

Checks the skill against the spec for correct structure and formatting. All validation checks must pass before discovery and implementation can be scored.

Validation — 16 / 16 Passed

Validation for skill structure

No warnings or errors.

Repository
mims-harvard/ToolUniverse
Reviewed

Table of Contents

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