Metadata-Version: 2.4
Name: spymot
Version: 2.1.2.dev2
Summary: Advanced Protein Motif Detection with AlphaFold Structural Validation
Author-email: Erfan Zohrabi <erfanzohrabi.ez@gmail.com>
Maintainer-email: Erfan Zohrabi <erfanzohrabi.ez@gmail.com>
Project-URL: Homepage, https://github.com/ErfanZohrabi/Spymot
Project-URL: Documentation, https://github.com/ErfanZohrabi/Spymot/tree/main/documentation
Project-URL: Repository, https://github.com/ErfanZohrabi/Spymot.git
Project-URL: Bug Tracker, https://github.com/ErfanZohrabi/Spymot/issues
Project-URL: Changelog, https://github.com/ErfanZohrabi/Spymot/blob/main/CHANGELOG.md
Keywords: bioinformatics,protein,motif,alphafold,cancer,slims,signal-peptides,protein-structure,drug-discovery,structural-biology,computational-biology
Classifier: Development Status :: 4 - Beta
Classifier: Intended Audience :: Science/Research
Classifier: License :: OSI Approved :: MIT License
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Classifier: Programming Language :: Python :: 3
Classifier: Programming Language :: Python :: 3.8
Classifier: Programming Language :: Python :: 3.9
Classifier: Programming Language :: Python :: 3.10
Classifier: Programming Language :: Python :: 3.11
Classifier: Programming Language :: Python :: 3.12
Classifier: Topic :: Scientific/Engineering :: Bio-Informatics
Classifier: Topic :: Scientific/Engineering :: Medical Science Apps.
Classifier: Topic :: Scientific/Engineering :: Chemistry
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Description-Content-Type: text/markdown
License-File: LICENSE
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# 🧬 Spymot: Advanced Protein Motif Detection with AlphaFold Structural Validation

[![Python 3.8+](https://img.shields.io/badge/python-3.8+-blue.svg)](https://www.python.org/downloads/)
[![License: MIT](https://img.shields.io/badge/License-MIT-yellow.svg)](https://opensource.org/licenses/MIT)
[![Version](https://img.shields.io/badge/version-2.0.0-green.svg)](https://github.com/erfanzohrabi/spymot)

**Spymot** is a comprehensive protein analysis platform that combines motif detection with 3D structure validation using AlphaFold2 confidence scores. Designed for cancer biology research, drug discovery, and functional genomics, Spymot provides deep insights into protein function through systematic analysis of short linear motifs (SLiMs) and targeting signals.

## 📦 **Python Package**

Spymot is now available as a **Python package** that can be installed via pip! This provides unified access to both V1 and V2 functionality through a single, easy-to-use interface.

## 🎯 Key Features

- **94.6% coverage** of critical protein motifs (316+ patterns)
- **AlphaFold2 integration** with pLDDT confidence scoring
- **Cancer-focused analysis** with relevance scoring
- **Context-aware detection** (topology, disorder, cellular localization)
- **Multiple interfaces**: CLI, Python API, Interactive mode
- **Rich output formats**: JSON, YAML, TXT with biological interpretation

## 🔬 Applications

- **Tumor suppressor analysis** (p53, BRCA1 degradation signals)
- **Kinase characterization** (CDK, ATM/ATR phosphorylation sites)
- **Therapeutic target assessment** (allosteric pockets, drug binding)
- **Biomarker discovery** (cancer-specific PTM signatures)
- **Drug resistance analysis** (EGFR T790M, conformational changes)

## 🚀 Innovation

Moves beyond sequence-based detection to incorporate 3D structural context, enabling identification of discontinuous motifs and providing mechanistic insights into protein function and dysfunction.

Perfect for researchers in structural biology, cancer research, drug discovery, and bioinformatics.

---

## 📁 Project Structure

This repository contains two main versions of Spymot:

### 🧬 **Version 1 (V1/)** - Original Foundation
- Core motif detection functionality
- Basic AlphaFold integration
- Simple CLI interface
- Essential motif database

### 🚀 **Version 2 (V2/)** - Enhanced Production System
- **94.6% motif coverage** (316+ patterns)
- Advanced context-aware detection
- Comprehensive cancer relevance scoring
- Rich JSON output with biological interpretation
- Production-ready features and extensive testing

### 📦 **Python Package Structure**

The unified Python package provides access to both versions through a single interface:

```
src/spymot/                    # Main package
├── __init__.py               # Package initialization
├── _version.py               # Version management
├── cli.py                    # Unified CLI interface
├── v1/                       # V1 functionality
│   ├── __init__.py
│   └── cli.py
└── v2/                       # V2 functionality
    ├── __init__.py
    └── scripts/
        ├── __init__.py
        ├── enhanced_cli.py
        ├── interactive_cli.py
        └── enhanced_demo.py
```

**Package Features:**
- **Unified Interface**: Single `spymot` command with version selection
- **Pip Installable**: `pip install spymot` for easy installation
- **Version Management**: Automatic versioning with setuptools_scm
- **Development Tools**: Black, Ruff, MyPy, and Pytest configuration
- **MIT License**: Open source and freely available

---

## 🌟 The Critical Advancement: Structure-Based Motif Detection

Spymot represents a **major leap in bioinformatics** by moving beyond traditional sequence-based detection to incorporate highly accurate, predicted three-dimensional context using AlphaFold2.

### 🎯 Why This Project is Crucially Important

| Key Significance | Explanation |
|:---|:---|
| **Superior Accuracy** | Uses 3D structure as primary input, identifying motifs even with sequence variability |
| **Discontinuous Motifs** | Recognizes non-linear motifs formed by distant amino acids in 3D space |
| **High-Throughput** | Leverages AlphaFold Database for rapid analysis without experimental bottlenecks |
| **Functional Prediction** | Enables immediate prediction of PPI interfaces and ligand binding pockets |
| **Structure-Function Bridge** | Translates gene sequences into functional hypotheses based on 3D structure |

### 📊 Comparison: Traditional vs. Modern Methods

| Feature | Traditional Methods | Spymot (AF-Structure Methods) |
|:---|:---|:---|
| **Primary Input** | Linear amino acid sequence (1D) | **Predicted 3D atomic coordinates** |
| **Context Used** | Local sequence neighborhood | **Global spatial arrangement** |
| **Recognition** | Pattern matching, statistical probabilities | **Geometric feature extraction** |
| **Discontinuous Motifs** | Cannot reliably detect | **Excellent detection** |
| **Output Value** | Motif sequence and approximate location | **Precise spatial location + pLDDT scores** |

---

## 🚀 Quick Start

### 📦 **Python Package Installation (Recommended)**

```bash
# Install from PyPI (when published)
pip install spymot

# Or install from source for development
git clone https://github.com/erfanzohrabi/spymot.git
cd spymot
pip install -e .
```

### 🔧 **Manual Installation (Legacy)**

```bash
# Clone the repository
git clone https://github.com/erfanzohrabi/spymot.git
cd spymot

# Choose your version:
# For production use (recommended):
cd V2
pip install -r requirements.txt
pip install -e .

# For basic functionality:
cd V1
pip install -r requirements.txt
```

### Basic Usage

#### 🐍 **Python Package Usage (Recommended)**

##### Command Line Interface
```bash
# Unified interface
spymot --help
spymot info

# V1 functionality
spymot v1 analyze protein.fasta --format json
spymot v1 pdb 1TUP --format json

# V2 functionality  
spymot v2 analyze protein.fasta --database all --cancer-only
spymot v2 databases --verbose

# Interactive mode
spymot interactive --version v2
```

##### Python API
```python
# V1 functionality
from spymot import analyze_sequence, scan_motifs
result = analyze_sequence("p53", "MEEPQSDPSVEPPLSQETFSD...")

# V2 functionality
from spymot import EnhancedSpymotAnalyzer
analyzer = EnhancedSpymotAnalyzer()
result = analyzer.analyze_sequence_comprehensive("p53", "MEEPQSDPSVEPPLSQETFSD...")

# Package info
from spymot import get_version_info
info = get_version_info()
print(f"Version: {info['version']}")
```

#### 🔧 **Legacy Usage (Manual Installation)**

##### Command Line Interface (V2)
```bash
# Analyze a protein sequence
python -m spymot_enhanced.cli analyze protein.fasta --database all --format json

# Cancer-focused analysis
python -m spymot_enhanced.cli analyze oncogene.fasta --database cancer --cancer-only

# Interactive mode
python -m spymot_enhanced.cli interactive
```

##### Python API (V2)
```python
from spymot_enhanced import EnhancedSpymotAnalyzer

# Initialize analyzer
analyzer = EnhancedSpymotAnalyzer()

# Analyze sequence
result = analyzer.analyze_sequence_comprehensive(
    sequence="MEEPQSDPSVEPPLSQETFSD...",
    protein_id="p53_tumor_suppressor",
    min_confidence=0.4
)

print(f"Total motifs: {result['summary']['total_motifs_detected']}")
print(f"Cancer relevance: {result['interpretation']['cancer_relevance_assessment']}")
```

##### Basic Usage (V1)
```python
from spymot.analyzer import analyze_sequence

# Analyze a protein sequence
result = analyze_sequence(
    name="my_protein",
    seq="MEEPQSDPSVEPPLSQETFSD..."
)

print(f"Found {result['analysis_summary']['total_motifs']} motifs")
```

---

## 🎯 Comprehensive Motif Coverage

### Cancer-Relevant Motifs (200+ entries)

#### Protein Degradation Signals
- **APC/C Degrons**: D-box (R-x-x-L), KEN box, ABBA motif
- **SCF Degrons**: βTrCP phosphodegron, Cdc4 phosphodegron
- **Specialized Degrons**: HIF-α ODD, PIP-box, p27 degron

#### Kinase Phosphorylation Sites
- **Cell Cycle**: CDK consensus (S/T-P), PLK1 sites
- **DNA Damage**: ATM/ATR (S/T-Q), Chk1/Chk2 sites
- **Survival**: AKT (R-x-R-x-x-S/T), PKA consensus
- **Stress Response**: p38/JNK sites, CK2 sites

#### Protein-Protein Interactions
- **SH2 Domains**: General (pY-x-x), Grb2, STAT3, Src
- **SH3 Domains**: Class I (P-x-x-P-x-R), Class II (x-P-x-x-P-x)
- **PDZ Domains**: Class I (S/T-x-V/I), Class II (Φ-x-Φ)
- **14-3-3 Binding**: Mode 1 (R-S-x-x-S-x-P), Mode 2 (R-x-x-S/T-x-x-x-P)

### Signal Peptides & Targeting (100+ entries)

#### Nuclear Transport
- **Nuclear Localization**: Classical NLS, Bipartite NLS, PY-NLS
- **Nuclear Export**: CRM1-dependent NES variants
- **Nuclear Retention**: DNA-binding motifs, chromatin association

#### Organellar Targeting
- **Mitochondrial**: Matrix targeting sequence, intermembrane space
- **ER Targeting**: Signal peptide, KDEL retention, KKXX retrieval
- **Peroxisomal**: PTS1 (S-K-L variants), PTS2 consensus
- **Chloroplast**: Transit peptide consensus

---

## 📊 Example Results

### p53 Tumor Suppressor Analysis
```
✅ 88 motifs detected (5 cancer-relevant, 37 high-confidence)
✅ Post-translational modifications: 42 motifs
✅ Nuclear transport signals: Import/Export sequences identified
✅ Protein-protein interactions: 9 binding motifs detected
✅ Cellular targeting: 22 trafficking signals found
✅ Quality coverage: 82.4% with confidence scoring
```

### Sample JSON Output
```json
{
  "metadata": {
    "spymot_version": "2.0.0",
    "analysis_timestamp": "2025-01-27T10:30:00",
    "database_sources": ["hardcoded", "ELM", "PROSITE", "Literature"]
  },
  "protein_info": {
    "id": "p53_tumor_suppressor",
    "length": 393,
    "uniprot": "P04637",
    "molecular_weight": 43653.24,
    "isoelectric_point": 6.33
  },
  "motifs": [
    {
      "name": "DEG_APC_Dbox",
      "start": 249,
      "end": 252,
      "match": "RPIL",
      "pattern": "R..L",
      "type": "Degron",
      "description": "APC/C destruction box",
      "cancer_relevance": "very_high",
      "confidence_score": 0.95,
      "functional_category": "protein_degradation",
      "biological_process": "cell_cycle",
      "clinical_significance": "high_therapeutic_target",
      "has_3d_support": true,
      "plddt_mean": 85.2,
      "confidence_level": "confident"
    }
  ],
  "quality_metrics": {
    "total_coverage": 0.847,
    "high_confidence_motifs": 23,
    "cancer_relevant_count": 15
  }
}
```

---

## 🔧 Command Line Reference

### V2 Enhanced Commands
```bash
# Analyze protein sequence
python -m spymot_enhanced.cli analyze INPUT_FILE [OPTIONS]

# Interactive mode
python -m spymot_enhanced.cli interactive

# Show database information
python -m spymot_enhanced.cli databases --verbose
```

### Analysis Options
| Option | Description | Values |
|--------|-------------|---------|
| `--database` | Choose motif database | `all`, `cancer`, `signals`, `hardcoded` |
| `--format` | Output format | `json`, `yaml`, `txt` |
| `--output` | Output file path | `filename.ext` |
| `--cancer-only` | Filter to cancer-relevant only | flag |
| `--min-confidence` | Minimum confidence score | `0.0-1.0` |

### V1 Basic Commands
```bash
# Analyze protein sequence
python -m spymot.cli analyze protein.fasta --format json

# Show available databases
python -m spymot.cli databases

# PDB structure lookup
python -m spymot.cli pdb 1TUP --format json
```

---

## 🧪 Testing and Validation

### Run Comprehensive Tests
```bash
# V2 Enhanced tests
cd V2
python test_enhanced_system.py
# Expected: "6/6 tests passed, ALL TESTS PASSED!"

# V1 Basic tests
cd V1
python test_system.py
```

### Test Coverage
- **Database Loading**: Verify all 316 motifs load correctly
- **Motif Scanning**: Test different database combinations
- **Context Validation**: Check N-terminal/C-terminal specificity
- **Quality Scoring**: Validate confidence and cancer relevance scores
- **Structure Integration**: Test AlphaFold2 pLDDT integration
- **Output Formats**: Verify JSON/YAML/TXT consistency

### Benchmark Results
| Test Case | V1 (Hardcoded) | V2 (Full Database) | Enhancement |
|-----------|----------------|-------------------|-------------|
| p53 (393aa) | 18 motifs | 93 motifs | 5.2x |
| BRCA1 (1863aa) | 12 motifs | 67 motifs | 5.6x |
| Myc (439aa) | 8 motifs | 31 motifs | 3.9x |
| β-catenin (781aa) | 15 motifs | 45 motifs | 3.0x |

---

## 🎯 Real-World Applications

### Cancer Research
```python
# Analyze p53 mutations in cancer patients
p53_variants = ["WT", "R273H", "R175H", "G245S"]
for variant in p53_variants:
    results = analyze_sequence(f"p53_{variant}", get_sequence(variant))
    print(f"{variant}: {results['quality_metrics']['cancer_relevant_count']} functional motifs")
```

### Drug Discovery
```bash
# Screen protein family for druggable motifs
for protein in protein_family/*.fasta; do
    python -m spymot_enhanced.cli analyze $protein --database all --format json > ${protein%.fasta}_analysis.json
done
```

### Biomarker Discovery
```python
# Compare motif profiles between normal and disease states
def find_biomarker_motifs(normal_proteins, cancer_proteins):
    normal_motifs = {}
    cancer_motifs = {}
    
    for protein in normal_proteins:
        results = analyze_sequence(f"normal_{protein}", get_sequence(protein))
        normal_motifs[protein] = results['motifs']
    
    for protein in cancer_proteins:
        results = analyze_sequence(f"cancer_{protein}", get_sequence(protein))
        cancer_motifs[protein] = results['motifs']
    
    return compare_motif_profiles(normal_motifs, cancer_motifs)
```

---

## 📈 Performance

### Benchmarking Results
| Sequence Length | Analysis Time | Memory Usage | Motifs Found |
|----------------|---------------|--------------|--------------|
| 100 residues | 0.8s | 45 MB | 5-15 |
| 500 residues | 2.1s | 52 MB | 15-35 |
| 1000 residues | 4.3s | 58 MB | 25-65 |
| 2000 residues | 8.7s | 71 MB | 45-120 |

### High-Throughput Processing
```python
import multiprocessing as mp
from spymot_enhanced import EnhancedSpymotAnalyzer

def analyze_batch(protein_list, n_processes=4):
    analyzer = EnhancedSpymotAnalyzer()
    
    def worker(protein_data):
        name, sequence = protein_data
        return analyzer.analyze_sequence_comprehensive(name, sequence)
    
    with mp.Pool(n_processes) as pool:
        results = pool.map(worker, protein_list)
    
    return results

# Process 1000+ proteins efficiently
large_dataset = load_protein_dataset("proteome.fasta")
batch_results = analyze_batch(large_dataset, n_processes=8)
```

---

## 📚 Documentation

### Core Documentation
- **[V2/docs/ENHANCED_SPYMOT_DOCUMENTATION.md](V2/docs/ENHANCED_SPYMOT_DOCUMENTATION.md)**: Comprehensive guide (40+ pages)
- **[V2/docs/MOTIFS_KNOWLEDGE.md](V2/docs/MOTIFS_KNOWLEDGE.md)**: Biological knowledge base (500+ lines)
- **[V2/docs/CLI_USAGE_GUIDE.md](V2/docs/CLI_USAGE_GUIDE.md)**: Command-line interface guide
- **[IMPORTANCE.md](IMPORTANCE.md)**: Scientific foundation and mechanistic imperative

### Database Information
- **ELM Database**: Eukaryotic Linear Motif resource - canonical SLiM classes
- **PROSITE**: Documented functional sites and targeting signals
- **Literature Curation**: Cancer biology reviews and trafficking signal studies

---

## 🔬 Scientific Background

### AlphaFold Integration
Spymot uses the [AlphaFold Protein Structure Database](https://alphafold.ebi.ac.uk/) to assess 3D structural context:

- **pLDDT Scores**: Per-residue confidence from AlphaFold models
- **Threshold**: ≥70 pLDDT indicates reliable 3D structure
- **Coverage**: 200M+ protein structures from model organisms

### Confidence Scoring Integration
Spymot uses AlphaFold2 pLDDT scores to validate motif predictions:
- **pLDDT > 90**: Very high confidence - motif likely structured and functional
- **pLDDT 70-90**: Confident - motif probably functional with good structure
- **pLDDT 50-70**: Low confidence - motif may be disordered but still functional
- **pLDDT < 50**: Very low confidence - motif prediction uncertain

### Short Linear Motifs (SLiMs) in Cancer Biology
Short Linear Motifs are 3-10 amino acid sequences that mediate crucial protein functions:

#### Functional Classes
1. **Degrons**: Target proteins for degradation (APC/C, SCF complexes)
2. **Kinase Sites**: Phosphorylation targets (CDK, ATM/ATR, PKA)
3. **Interaction Motifs**: Protein binding sites (SH2, SH3, PDZ, 14-3-3)
4. **Localization Signals**: Subcellular targeting (NLS, NES, organellar signals)

#### Cancer Relevance
- **Tumor Suppressors**: p53 contains 15+ regulatory motifs
- **Oncoproteins**: Myc, β-catenin rely on motifs for function/regulation
- **Drug Targets**: Kinase sites are primary targets for cancer therapy
- **Biomarkers**: Motif mutations predict treatment response

---

## 🏗️ System Architecture

### V2 Enhanced Architecture
```
V2/
├── src/spymot_enhanced/          # Main package
│   ├── enhanced_analyzer.py      # Core analysis engine
│   ├── context_aware_detector.py # Smart detection system
│   ├── enhanced_motifs_db.py     # 316+ motif patterns
│   ├── external_tools.py         # Structural predictions
│   └── legacy/                   # Original Spymot compatibility
├── scripts/                      # Command-line interfaces
│   ├── enhanced_cli.py              # Main CLI
│   ├── enhanced_demo.py             # Interactive demo
│   └── interactive_cli.py           # Interactive mode
├── tests/                        # Comprehensive test suite
├── examples/                     # Usage examples and sample data
├── data/                         # Motif databases (CSV files)
└── docs/                         # Complete documentation
```

### V1 Basic Architecture
```
V1/
├── spymot/                       # Core modules
│   ├── analyzer.py               # Core analysis engine
│   ├── motifs.py                 # Motif detection
│   ├── afdb.py                   # AlphaFold integration
│   ├── targeting.py              # Signal prediction
│   ├── cli.py                    # Command-line interface
│   └── utils.py                  # Utilities
├── tests/                        # Test suite
├── data/                         # Motif databases
└── examples/                     # Usage examples
```

### Performance Considerations
- **Regex-Based Scanning**: Fast motif detection using compiled patterns
- **API Rate Limiting**: Respectful AlphaFold DB queries with timeout handling
- **Batch Optimization**: Efficient parallel processing for multiple sequences

---

## 🧬 Example Analyses

### EGFR Receptor Analysis
```bash
# V2 Enhanced analysis
python -m spymot_enhanced.cli analyze egfr.fasta --id P00533 --verbose
# Detects: signal peptide, kinase domain motifs, internalization signals

# V1 Basic analysis
python -m spymot.cli analyze egfr.fasta --id P00533 --format json
```

### BRCA1 Tumor Suppressor
```bash
# V2 Enhanced analysis
python -m spymot_enhanced.cli analyze brca1.fasta --id P38398 --cancer-only
# Identifies: RING domain, nuclear localization, phosphorylation sites

# V1 Basic analysis
python -m spymot.cli analyze brca1.fasta --id P38398 --format txt
```

### c-Myc Oncogene
```bash
# V2 Enhanced analysis
python -m spymot_enhanced.cli analyze cmyc.fasta --id P01106 --format txt
# Shows: bHLH domain, nuclear signals, degradation motifs

# V1 Basic analysis
python -m spymot.cli analyze cmyc.fasta --id P01106 --format json
```

---

## 🛠️ Development

### Development Setup
```bash
# Fork and clone the repository
git clone https://github.com/erfanzohrabi/spymot.git
cd spymot

# Choose version for development
cd V2  # or V1

# Create development environment
python -m venv spymot-dev
source spymot-dev/bin/activate

# Install development dependencies
pip install -r requirements.txt
pip install -e .

# Run tests
python test_enhanced_system.py  # V2
# or
python test_system.py  # V1
```

### Running Tests
```bash
# V2 Enhanced tests
cd V2
python -m pytest tests/ -v
python test_enhanced_system.py

# V1 Basic tests
cd V1
python -m pytest tests/ -v
python test_system.py
```

### Adding New Motifs
Add new motifs to the database by creating entries in the CSV files or updating the hardcoded motif lists. Each new motif should include:

- **Pattern**: Regular expression or consensus sequence
- **Biological Function**: Clear description of the motif's role
- **Cancer Relevance**: Assessment of oncological significance
- **Literature Support**: Reference to experimental validation
- **Context Requirements**: Position constraints (N-terminal, C-terminal, etc.)

---

## 🤝 Contributing

We welcome contributions! Here's how you can help:

1. Fork the repository
2. Create a feature branch (`git checkout -b feature/amazing-feature`)
3. Commit your changes (`git commit -m 'Add amazing feature'`)
4. Push to the branch (`git push origin feature/amazing-feature`)
5. Open a Pull Request

### Development Guidelines
- Follow Python PEP 8 style guidelines
- Add tests for new functionality
- Update documentation for new features
- Ensure backward compatibility when possible

---

## 📞 Support

### Getting Help
- **Documentation**: Check the comprehensive guides in `V2/docs/` and `documentation/`
- **Examples**: See `V2/examples/` and `examples_and_demos/` for usage examples
- **Issues**: Report bugs on [GitHub Issues](https://github.com/erfanzohrabi/spymot/issues)

### Citations
If you use Spymot in your research, please cite the relevant database sources:
- **ELM Database**: Kumar et al. (2022) Nucleic Acids Research
- **PROSITE**: Sigrist et al. (2021) Nucleic Acids Research
- **AlphaFold2**: Jumper et al. (2021) Nature

---

## 📄 License

This project is licensed under the MIT License - see the [LICENSE](LICENSE) file for details.

---

## 🏆 Acknowledgments

- **ELM Consortium** for the comprehensive linear motif database
- **SIB Swiss Institute of Bioinformatics** for PROSITE patterns
- **DeepMind** for AlphaFold2 structure predictions
- **Cancer research community** for functional validation of motifs
- **Scientific community** for advancing protein structure prediction

---

## 🔗 Related Tools

- **SignalP**: Professional signal peptide prediction
- **ELM Database**: Eukaryotic Linear Motif resource
- **Pfam**: Protein family database
- **COSMIC**: Cancer mutation database
- **AlphaFold Database**: 3D structure predictions

---

## 📊 Repository Statistics

- **Total Motifs**: 316+ curated patterns
- **Cancer-Relevant**: 200+ oncological motifs
- **Signal Peptides**: 100+ targeting sequences
- **Test Coverage**: 94.6% of must-detect motifs
- **Documentation**: 40+ pages of comprehensive guides
- **Examples**: Multiple usage scenarios and output formats

---

## 🎯 Use Cases

### Cancer Biology Research
- **Oncogene Analysis**: Detect degrons, phosphodegrons, and regulatory motifs in tumor suppressors
- **Drug Target Identification**: Find druggable motifs and interaction sites
- **Biomarker Discovery**: Identify cancer-relevant motifs in protein panels
- **Pathway Analysis**: Map signaling motifs across cancer-related pathways

### Protein Trafficking Studies
- **Secretory Pathway**: Signal peptides, ER retention, Golgi targeting
- **Organellar Import**: Mitochondrial, peroxisomal, nuclear targeting signals
- **Membrane Trafficking**: Endocytic motifs, vesicle transport signals
- **Subcellular Localization**: Predict protein distribution and trafficking routes

### Structural Biology
- **AlphaFold Validation**: Assess 3D structure confidence for motif regions
- **Domain Organization**: Identify functional domains and interaction motifs
- **Structure-Function**: Correlate motif locations with structural features
- **Experimental Design**: Guide mutagenesis and functional studies

---

## 🚀 Future Roadmap

### Planned Enhancements
- **Machine Learning Integration**: AI-powered motif prediction
- **Multi-species Analysis**: Cross-species motif conservation
- **Web Interface**: Browser-based analysis platform
- **API Development**: RESTful API for integration
- **Cloud Deployment**: Scalable cloud-based analysis

### Research Directions
- **Dynamic Motif Analysis**: Time-resolved motif detection
- **Network Analysis**: Protein interaction network integration
- **Drug Design**: Structure-based drug discovery tools
- **Personalized Medicine**: Patient-specific motif analysis

---

**🧬 Spymot: Empowering protein functional analysis through comprehensive motif detection and structure validation.**

*Developed by Erfan Zohrabi for cancer biology research and protein functional analysis.*

---

## 📦 **Python Package Publishing**

### **Build Package**
```bash
# Install build tools
pip install build twine

# Build package
python -m build

# Check package
twine check dist/*
```

### **Publish to PyPI**
```bash
# Upload to PyPI
twine upload dist/*

# Install from PyPI
pip install spymot
```

### **Package Information**
- **Name**: `spymot`
- **Version**: `2.0.0`
- **Description**: Advanced Protein Motif Detection with AlphaFold Structural Validation
- **Author**: Erfan Zohrabi
- **License**: MIT
- **Python**: >=3.8
- **Dependencies**: numpy, requests, click, PyYAML

---

## 📋 Quick Reference

### Installation Commands
```bash
# Python Package (Recommended)
pip install spymot

# Development Installation
git clone https://github.com/erfanzohrabi/spymot.git
cd spymot
pip install -e .

# Legacy V2 (Manual)
cd spymot/V2
pip install -r requirements.txt
pip install -e .

# Legacy V1 (Manual)
cd spymot/V1
pip install -r requirements.txt
```

### Basic Usage Commands
```bash
# Python Package (Recommended)
spymot --help
spymot v1 analyze protein.fasta --format json
spymot v2 analyze protein.fasta --database all --cancer-only
spymot interactive --version v2

# Legacy V2 Enhanced
python -m spymot_enhanced.cli analyze protein.fasta --database all --format json
python -m spymot_enhanced.cli interactive

# Legacy V1 Basic
python -m spymot.cli analyze protein.fasta --format json
python -m spymot.cli pdb 1TUP --format json
```

### Test Commands
```bash
# V2 Tests
cd V2 && python test_enhanced_system.py

# V1 Tests
cd V1 && python test_system.py
```

---

*For detailed documentation, examples, and advanced usage, see the respective README files in V1/ and V2/ directories.*

---

## 🎉 **What's New: Python Package Support**

Spymot is now available as a **Python package**! This major update provides:

✅ **Unified Installation**: `pip install spymot`  
✅ **Single Command Interface**: `spymot v1` and `spymot v2`  
✅ **Easy Integration**: Import directly in Python scripts  
✅ **Version Management**: Automatic versioning and updates  
✅ **Development Tools**: Complete development environment setup  
✅ **PyPI Ready**: Ready for distribution on Python Package Index  

**Upgrade your workflow:**
```bash
# Old way (manual)
cd V2 && python -m spymot_enhanced.cli analyze protein.fasta

# New way (package)
pip install spymot
spymot v2 analyze protein.fasta --database all --cancer-only
```

The Python package maintains full backward compatibility while providing a much cleaner and more professional user experience!
