structural_homology_modeling
Structural Homology & Evolution Analysis - Analyze protein evolution: get gene tree from Ensembl, find homologs, compare sequences, and predict structure. Use this skill for evolutionary biology tasks involving get homology symbol get genetree member symbol calculate protein sequence properties pred protein structure esmfold. Combines 4 tools from 3 SCP server(s).
Best use case
structural_homology_modeling is best used when you need a repeatable AI agent workflow instead of a one-off prompt.
Structural Homology & Evolution Analysis - Analyze protein evolution: get gene tree from Ensembl, find homologs, compare sequences, and predict structure. Use this skill for evolutionary biology tasks involving get homology symbol get genetree member symbol calculate protein sequence properties pred protein structure esmfold. Combines 4 tools from 3 SCP server(s).
Teams using structural_homology_modeling should expect a more consistent output, faster repeated execution, less prompt rewriting.
When to use this skill
- You want a reusable workflow that can be run more than once with consistent structure.
When not to use this skill
- You only need a quick one-off answer and do not need a reusable workflow.
- You cannot install or maintain the underlying files, dependencies, or repository context.
Installation
Claude Code / Cursor / Codex
Manual Installation
- Download SKILL.md from GitHub
- Place it in
.claude/skills/structural_homology_modeling/SKILL.mdinside your project - Restart your AI agent — it will auto-discover the skill
How structural_homology_modeling Compares
| Feature / Agent | structural_homology_modeling | Standard Approach |
|---|---|---|
| Platform Support | Not specified | Limited / Varies |
| Context Awareness | High | Baseline |
| Installation Complexity | Unknown | N/A |
Frequently Asked Questions
What does this skill do?
Structural Homology & Evolution Analysis - Analyze protein evolution: get gene tree from Ensembl, find homologs, compare sequences, and predict structure. Use this skill for evolutionary biology tasks involving get homology symbol get genetree member symbol calculate protein sequence properties pred protein structure esmfold. Combines 4 tools from 3 SCP server(s).
Where can I find the source code?
You can find the source code on GitHub using the link provided at the top of the page.
SKILL.md Source
# Structural Homology & Evolution Analysis
**Discipline**: Evolutionary Biology | **Tools Used**: 4 | **Servers**: 3
## Description
Analyze protein evolution: get gene tree from Ensembl, find homologs, compare sequences, and predict structure.
## Tools Used
- **`get_homology_symbol`** from `ensembl-server` (streamable-http) - `https://scp.intern-ai.org.cn/api/v1/mcp/12/Origene-Ensembl`
- **`get_genetree_member_symbol`** from `ensembl-server` (streamable-http) - `https://scp.intern-ai.org.cn/api/v1/mcp/12/Origene-Ensembl`
- **`calculate_protein_sequence_properties`** from `server-2` (streamable-http) - `https://scp.intern-ai.org.cn/api/v1/mcp/2/DrugSDA-Tool`
- **`pred_protein_structure_esmfold`** from `server-3` (streamable-http) - `https://scp.intern-ai.org.cn/api/v1/mcp/3/DrugSDA-Model`
## Workflow
1. Find homologs via Ensembl
2. Get gene tree
3. Compare sequence properties
4. Predict structure for divergent homolog
## Test Case
### Input
```json
{
"gene_symbol": "BRCA1",
"species": "homo_sapiens"
}
```
### Expected Steps
1. Find homologs via Ensembl
2. Get gene tree
3. Compare sequence properties
4. Predict structure for divergent homolog
## Usage Example
> **Note:** Replace `sk-b04409a1-b32b-4511-9aeb-22980abdc05c` with your own SCP Hub API Key. You can obtain one from the [SCP Platform](https://scphub.intern-ai.org.cn).
```python
import asyncio
import json
from contextlib import AsyncExitStack
from mcp import ClientSession
from mcp.client.streamable_http import streamablehttp_client
from mcp.client.sse import sse_client
SERVERS = {
"ensembl-server": "https://scp.intern-ai.org.cn/api/v1/mcp/12/Origene-Ensembl",
"server-2": "https://scp.intern-ai.org.cn/api/v1/mcp/2/DrugSDA-Tool",
"server-3": "https://scp.intern-ai.org.cn/api/v1/mcp/3/DrugSDA-Model"
}
async def connect(url, stack):
transport = streamablehttp_client(url=url, headers={"SCP-HUB-API-KEY": "sk-b04409a1-b32b-4511-9aeb-22980abdc05c"})
read, write, _ = await stack.enter_async_context(transport)
ctx = ClientSession(read, write)
session = await stack.enter_async_context(ctx)
await session.initialize()
return session
def parse(result):
try:
if hasattr(result, 'content') and result.content:
c = result.content[0]
if hasattr(c, 'text'):
try: return json.loads(c.text)
except: return c.text
return str(result)
except: return str(result)
async def main():
async with AsyncExitStack() as stack:
# Connect to required servers
sessions = {}
sessions["ensembl-server"] = await connect("https://scp.intern-ai.org.cn/api/v1/mcp/12/Origene-Ensembl", stack)
sessions["server-2"] = await connect("https://scp.intern-ai.org.cn/api/v1/mcp/2/DrugSDA-Tool", stack)
sessions["server-3"] = await connect("https://scp.intern-ai.org.cn/api/v1/mcp/3/DrugSDA-Model", stack)
# Execute workflow steps
# Step 1: Find homologs via Ensembl
result_1 = await sessions["ensembl-server"].call_tool("get_homology_symbol", arguments={})
data_1 = parse(result_1)
print(f"Step 1 result: {json.dumps(data_1, indent=2, ensure_ascii=False)[:500]}")
# Step 2: Get gene tree
result_2 = await sessions["ensembl-server"].call_tool("get_genetree_member_symbol", arguments={})
data_2 = parse(result_2)
print(f"Step 2 result: {json.dumps(data_2, indent=2, ensure_ascii=False)[:500]}")
# Step 3: Compare sequence properties
result_3 = await sessions["server-2"].call_tool("calculate_protein_sequence_properties", arguments={})
data_3 = parse(result_3)
print(f"Step 3 result: {json.dumps(data_3, indent=2, ensure_ascii=False)[:500]}")
# Step 4: Predict structure for divergent homolog
result_4 = await sessions["server-3"].call_tool("pred_protein_structure_esmfold", arguments={})
data_4 = parse(result_4)
print(f"Step 4 result: {json.dumps(data_4, indent=2, ensure_ascii=False)[:500]}")
# Cleanup
print("Workflow complete!")
if __name__ == "__main__":
asyncio.run(main())
```Related Skills
structural_pharmacogenomics
Structural Pharmacogenomics - Link structure to pharmacogenomics: variant effect, protein structure change, drug binding, and clinical data. Use this skill for pharmacogenomics tasks involving get vep hgvs pred protein structure esmfold boltz binding affinity get pharmacogenomics info by drug name. Combines 4 tools from 3 SCP server(s).
wind-site-assessment
Assess wind energy potential and perform site analysis using atmospheric science calculations.
web_literature_mining
Scientific Literature Mining - Mine scientific literature: PubMed search, arXiv search, web search, and Tavily deep search. Use this skill for scientific informatics tasks involving pubmed search search literature search web tavily search. Combines 4 tools from 2 SCP server(s).
virus_genomics
Virus Genomics Analysis - Analyze virus genomics: NCBI virus dataset, annotation, taxonomy, and literature search. Use this skill for virology tasks involving get virus dataset report get virus annotation report get taxonomy search literature. Combines 4 tools from 2 SCP server(s).
virtual_screening
Virtual Screening Pipeline - Virtual screening: search PubChem by substructure, compute similarity, filter by drug-likeness, and predict binding affinity. Use this skill for drug discovery tasks involving search pubchem by smiles calculate smiles similarity calculate mol drug chemistry boltz binding affinity. Combines 4 tools from 3 SCP server(s).
variant_pathogenicity
Variant Pathogenicity Assessment - Assess variant pathogenicity: Ensembl VEP prediction, ClinVar lookup, variation details, and gene phenotype associations. Use this skill for clinical genetics tasks involving get vep hgvs clinvar search get variation get phenotype gene. Combines 4 tools from 2 SCP server(s).
variant-population-frequency
Query gnomAD for variant allele frequency across populations. Uses FAVOR to convert rsID→variant_id first, then queries gnomAD.
variant-pharmacogenomics
Query PharmGKB (clinPGx) for pharmacogenomic clinical annotations — how a variant affects drug response, dosing, and adverse reactions.
variant-gwas-associations
Query EBI GWAS Catalog for GWAS statistical associations (p-value, effect size, risk allele) between a variant and traits/diseases.
variant-genomic-location
Query dbSNP + NCBI Gene to get variant genomic position (chromosome, coordinates, ref/alt alleles, mutation type) and associated gene coordinates.
variant-functional-prediction
Query FAVOR API for variant functional prediction scores (CADD, SIFT, PolyPhen, REVEL, etc.) and gene annotation.
variant-cross-database-ids
Query ClinGen Allele Registry to map variant rsID to identifiers in other databases (ClinVar, gnomAD, COSMIC, UniProtKB, OMIM, etc.).