> ## Documentation Index
> Fetch the complete documentation index at: https://docs.boltz.bio/llms.txt
> Use this file to discover all available pages before exploring further.

# Overview

> Collaborative workspaces for protein binder design

<Note>
  Design Projects are shared workspaces where team members within an organization can collaborate on protein binder design projects. They facilitate hypothesis-driven phases of a research project and provide a space to collate knowledge, designs and predictions in an organized and accessible hierarchy. By default, all work is visible to everyone within your organization.
</Note>

## Project Hierarchy

<CardGroup cols={2}>
  <Card title="Design Project">
    Worked on by a team of scientists, optimizing protein binders against one or more **Targets**. Contains **Experiments** as sequential or parallel phases of the design cycle.
  </Card>

  <Card title="Target">
    The protein structure you want to design binders against. Can be defined by sequence or uploaded structure.
  </Card>

  <Card title="Binder Specifications">
    Defines the protein binder specifications (e.g., nanobody, antibody, peptide) and design motifs.
  </Card>

  <Card title="Experiment">
    A hypothesis-driven collection of **Virtual Screens** used to assess binding poses and affinity scores.
  </Card>
</CardGroup>

## Home

<Frame>
  <img src="https://mintcdn.com/boltzpbc/EKeBMCVOgldAcowK/images/user-guide/protein-design/protein-design-23.png?fit=max&auto=format&n=EKeBMCVOgldAcowK&q=85&s=b7ca2098e34586e4eaac819234ba3b71" alt="Boltz platform home page showing organization overview and projects list" width="2994" height="940" data-path="images/user-guide/protein-design/protein-design-23.png" />
</Frame>

Your home directory is the main point of entry, where you have access to:

1. **Organization:** Your organization account where you invite members, set up billing, etc.
2. **Sandbox:** A private workspace to test hypotheses and explore protein structures before scaling up.
3. **CLI:** Submit and manage prediction jobs using our command-line interface.
4. **Projects:** All your design projects are listed here.

### Project Cards

Each project card displays:

* **Project title** and **category** (Protein/Small Molecule)
* **Last updated** timestamp
* **Metrics:** Number of targets, experiments, and candidates

Click any project card to navigate to the project dashboard.

## Project Dashboard

<Frame>
  <img src="https://mintcdn.com/boltzpbc/EKeBMCVOgldAcowK/images/user-guide/protein-design/protein-design-24.png?fit=max&auto=format&n=EKeBMCVOgldAcowK&q=85&s=8e1161fd8d58af0eba2aec2aa5630221" alt="Project dashboard showing targets, libraries, tags, and experiments" width="1741" height="866" data-path="images/user-guide/protein-design/protein-design-24.png" />
</Frame>

The project dashboard provides access to:

* **Targets:** List of protein targets added to the project
* **Binder Specifications:** Defines what proteins you want to design (modality, structure, design regions)
* **Tags:** Labels used to organize and categorize candidates
* **Experiments:** All experiments conducted in this project

### Getting Started Workflow

New projects include a guided workflow (typically 4 steps):

1. **Add your first target** - Create a target to start your project
2. **Add your binder specification** - Define what proteins you want to design
3. **Create your experiment** - Set up an experiment to run virtual screens
4. **Add/generate candidates** - Add candidates to your experiment

## Experiment Examples

Good experiment hypotheses are specific and actionable:

<Tabs>
  <Tab title="Hit Discovery">
    **Name:** Designing a de novo protein binder for Pocket A of Target X

    **Hypothesis:** Identified Pocket A on target X as having potential for blocking target X activity through high-affinity protein binder engagement. Screening 60,000 generated molecules to find the initial hit for a drug discovery campaign.
  </Tab>

  <Tab title="Lead Optimization">
    **Name:** Antibody lead optimization targeting Epitope B on Target X

    **Hypothesis:** Identified Epitope B on Target X as a functional site for pathway blockade, and hypothesized that optimizing the lead antibody's CDR interactions with this epitope would increase binding affinity and inhibitory activity.
  </Tab>
</Tabs>
