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Agent Skill · 研究检索

bindingdb-database(绑定数据库)

用于辅助数据库表结构、查询语句、迁移脚本和数据维护任务。它适合让 Agent 分析 schema、编写 SQL、排查查询问题、整理索引或生成迁移建议。使用时需要明确数据库类型、连接环境和目标表,区分只读分析与写入变更;涉及删除、更新、迁移和批量导入时,应优先 dry-run、备份或事务保护,避免误操作。

bindingdb-database 是研究检索类 Agent Skill,可用宿主为 Codex、Claude、Cursor、Gemini CLI,通过GitHub 仓库获取,权限为需要联网;许可证信息还不明确,第三方扫描有提醒项,按安装量在研究检索类的 73,675 个 Skill 里排第 57,063。

总安装 441周安装 18GitHub Stars 19,667下载 143核验 2026-05-01

安装说明

本站只整理中文说明,不托管安装包,也不代用户安装。
GitHub
许可证
unknown

安装方式

通过对话安装

复制提示词发给支持本地命令或 Skills 的 AI 助手,先确认命令和权限,再让它执行。

请帮我安装这个 Agent Skill:bindingdb-database(绑定数据库)
来源仓库:https://github.com/k-dense-ai/claude-scientific-skills
仓库路径:skills/bindingdb-database
安装命令:
npx skills add https://github.com/k-dense-ai/claude-scientific-skills --skill bindingdb-database
安装前请先检查当前环境是否支持对应 CLI,并向我确认将要执行的命令、安装目录、联网范围和文件读写权限;确认后再执行。

命令行安装

复制命令到本机终端执行。该命令会通过 npx skills 从第三方来源获取 Skill;本站只展示命令,不托管安装包,也不自动执行。

skills.shnpx skills
npx skills add https://github.com/k-dense-ai/claude-scientific-skills --skill bindingdb-database

这个 Skill 是做什么的

研究检索类 Skill 主要解决「找资料、核对事实、把来源整理清楚」的问题,通常会让助手先检索再总结。

访问 BindingDB 公开的 Ki/Kd/IC50 数据,支持化合物与靶点检索。适合虚拟筛选、ADMET 预测与药物重定位研究,数据来源文献专利。提供 REST API 与批量下载选项,需注意调用频率与版权限制。建议使用标准化单位与物种注释,避免跨研究比较时的系统误差。

bindingdb-database 属于研究检索类 Skill,可作为该场景下的辅助能力补充。

来源仓库内路径:skills/bindingdb-database

上手步骤

4 步
  1. 1

    确认自己的宿主工具

    公开资料标注支持 Codex、Claude、Cursor、Gemini CLI;先确认自己用的是其中之一,再按对应工具的 Skills 目录放置。

  2. 2

    拿到安装命令

    可以直接复制的命令是 npx skills add https://github.com/k-dense-ai/claude-scientific-skills --skill bi…;命令里的占位符换成自己的路径或密钥再执行。

  3. 3

    安装后重启宿主

    命令执行完要完全退出宿主工具再打开,让新装的 Skill 被重新扫描到,否则列表里可能看不到。

  4. 4

    按最小权限试用

    它需要需要联网,先在测试目录或测试账号里跑,确认没问题再放到正式项目。

常见问题

6 条

bindingdb-database 怎么安装?

在终端执行 npx skills add https://github.com/k-dense-ai/claude-scientific-skills --skill bindingdb-da…。装完完全退出宿主工具再打开,让它重新扫描本地 Skill。

bindingdb-database 支持哪些 AI 工具?

公开资料标注支持 Codex、Claude、Cursor、Gemini CLI。其他工具只要能读取本地 Skill 目录,一般也能手动放进去,但要自己确认触发方式是否一致。

bindingdb-database 需要什么权限?

权限级别是需要联网。该 Skill 可能需要联网访问来源站点、仓库或外部 API;具体网络访问范围需要结合源码和 README 复核。

bindingdb-database 是免费的吗?

公开资料没有标注明确许可证,收费和商用限制都无法确认。正式使用前请到来源仓库核对授权说明。

bindingdb-database 用的人多吗?

公开数据是累计安装 441 次,近一周安装 18 次,下载 143 次,GitHub 19,667 星。这些数字来自第三方目录统计,只能当作热度参考,不代表质量或安全性。

bindingdb-database 安全吗?

第三方扫描有提醒项,说明存在需要人工确认的行为。安装前请打开源码看清它读了什么、联网到哪里。

值得选的地方和要先想清楚的地方

值得选的地方

  • 同时适配 4 种工具,换客户端不用重新找替代品。
  • 来源仓库有 19,667 星,维护活跃度相对可查。

先想清楚的地方

  • 许可证没有明确标注,能不能商用、能不能再分发都不确定。
  • 第三方扫描存在提醒项或未通过项,需要人工逐条确认。
  • 第三方目录整理,版本更新和行为细节以来源仓库为准。

适不适合你

更适合

  • 已经在用 Codex,想直接扩展它能力的人。
  • 需要处理研究检索类任务、又不想每次都手写提示词的人。

不太适合

  • 需要明确授权才能用到公司项目里的场景。
  • 需要厂商级技术支持和 SLA 的生产系统。

研究检索类 Skill 对比

6 个同类
Skill总安装GitHub 星权限许可证扫描
find-skills

寻找技能 · Codex、Claude

31,199,81316,486操作浏览器MIT有提醒
self-improving-agent

自我改进 Agent · OpenClaw

16,464,0023,396接触敏感数据MIT-0通过
soultrace

灵魂追踪 · Codex、Claude

7,588,94412需要联网未明确有提醒
self-improving

自我完善 · OpenClaw

6,829,2841,046需要联网MIT-0通过
microsoft-foundry

微软代工厂 · Codex、Claude

6,614,144764调用外部服务未明确有提醒
bindingdb-database

绑定数据库 · 本页

44119,667需要联网未明确有提醒

按安装量取同分类前几名;数字来自第三方目录统计,只作热度参考,不代表质量结论。

SKILL.md 原文

BindingDB Database

Overview

BindingDB (https://www.bindingdb.org/) is the primary public database of measured drug-protein binding affinities. It contains over 3 million binding data records for ~1.4 million compounds tested against ~9,200 protein targets, curated from scientific literature and patent literature. BindingDB stores quantitative binding measurements (Ki, Kd, IC50, EC50) essential for drug discovery, pharmacology, and computational chemistry research.

Key resources:

When to Use This Skill

Use BindingDB when:

  • Target-based drug discovery: What known compounds bind to a target protein? What are their affinities?
  • SAR analysis: How do structural modifications affect binding affinity for a series of analogs?
  • Lead compound profiling: What targets does a compound bind (selectivity/polypharmacology)?
  • Benchmark datasets: Obtain curated protein-ligand affinity data for ML model training
  • Repurposing analysis: Does an approved drug bind to an unintended target?
  • Competitive analysis: What is the best reported affinity for a target class?
  • Fragment screening: Find validated binding data for fragments against a target

Core Capabilities

1. BindingDB REST API

Base URL: https://www.bindingdb.org/axis2/services/BDBService

import requests

BASE_URL = "https://www.bindingdb.org/axis2/services/BDBService"

def bindingdb_query(method, params):
    """Query the BindingDB REST API."""
    url = f"{BASE_URL}/{method}"
    response = requests.get(url, params=params, headers={"Accept": "application/json"})
    response.raise_for_status()
    return response.json()

2. Query by Target (UniProt ID)

def get_ligands_for_target(uniprot_id, affinity_type="Ki", cutoff=10000, unit="nM"):
    """
    Get all ligands with measured affinity for a UniProt target.

    Args:
        uniprot_id: UniProt accession (e.g., "P00519" for ABL1)
        affinity_type: "Ki", "Kd", "IC50", "EC50"
        cutoff: Maximum affinity value to return (in nM)
        unit: "nM" or "uM"
    """
    params = {
        "uniprot_id": uniprot_id,
        "affinity_type": affinity_type,
        "affinity_cutoff": cutoff,
        "response": "json"
    }
    return bindingdb_query("getLigandsByUniprotID", params)

# Example: Get all compounds binding ABL1 (imatinib target)
ligands = get_ligands_for_target("P00519", affinity_type="Ki", cutoff=100)

3. Query by Compound Name or SMILES

def search_by_name(compound_name, limit=100):
    """Search BindingDB for compounds by name."""
    params = {
        "compound_name": compound_name,
        "response": "json",
        "max_results": limit
    }
    return bindingdb_query("getAffinitiesByCompoundName", params)

def search_by_smiles(smiles, similarity=100, limit=50):
    """
    Search BindingDB by SMILES string.

    Args:
        smiles: SMILES string of the compound
        similarity: Tanimoto similarity threshold (1-100, 100 = exact)
    """
    params = {
        "SMILES": smiles,
        "similarity": similarity,
        "response": "json",
        "max_results": limit
    }
    return bindingdb_query("getAffinitiesByBEI", params)

# Example: Search for imatinib binding data
result = search_by_name("imatinib")

4. Download-Based Analysis (Recommended for Large Queries)

For comprehensive analyses, download BindingDB data directly:

import pandas as pd

def load_bindingdb(filepath="BindingDB_All.tsv"):
    """
    Load BindingDB TSV file.
    Download from: https://www.bindingdb.org/bind/chemsearch/marvin/Download.jsp
    """
    # Key columns
    usecols = [
        "BindingDB Reactant_set_id",
        "Ligand SMILES",
        "Ligand InChI",
        "Ligand InChI Key",
        "BindingDB Target Chain  Sequence",
        "PDB ID(s) for Ligand-Target Complex",
        "UniProt (SwissProt) Entry Name of Target Chain",
        "UniProt (SwissProt) Primary ID of Target Chain",
        "UniProt (TrEMBL) Primary ID of Target Chain",
        "Ki (nM)",
        "IC50 (nM)",
        "Kd (nM)",
        "EC50 (nM)",
        "kon (M-1-s-1)",
        "koff (s-1)",
        "Target Name",
        "Target Source Organism According to Curator or DataSource",
        "Number of Protein Chains in Target (>1 implies a multichain complex)",
        "PubChem CID",
        "PubChem SID",
        "ChEMBL ID of Ligand",
        "DrugBank ID of Ligand",
    ]

    df = pd.read_csv(filepath, sep="\t", usecols=[c for c in usecols if c],
                     low_memory=False, on_bad_lines='skip')

    # Convert affinity columns to numeric
    for col in ["Ki (nM)", "IC50 (nM)", "Kd (nM)", "EC50 (nM)"]:
        if col in df.columns:
            df[col] = pd.to_numeric(df[col], errors='coerce')

    return df

def query_target_affinity(df, uniprot_id, affinity_types=None, max_nm=10000):
    """Query loaded BindingDB for a specific target."""
    if affinity_types is None:
        affinity_types = ["Ki (nM)", "IC50 (nM)", "Kd (nM)"]

    # Filter by UniProt ID
    mask = df["UniProt (SwissProt) Primary ID of Target Chain"] == uniprot_id
    target_df = df[mask].copy()

    # Filter by affinity cutoff
    has_affinity = pd.Series(False, index=target_df.index)
    for col in affinity_types:
        if col in target_df.columns:
            has_affinity |= target_df[col] <= max_nm

    result = target_df[has_affinity][["Ligand SMILES"] + affinity_types +
                                      ["PubChem CID", "ChEMBL ID of Ligand"]].dropna(how='all')
    return result.sort_values(affinity_types[0])

5. SAR Analysis

import pandas as pd

def sar_analysis(df, target_uniprot, affinity_col="IC50 (nM)"):
    """
    Structure-activity relationship analysis for a target.
    Retrieves all compounds with affinity data and ranks by potency.
    """
    target_data = query_target_affinity(df, target_uniprot, [affinity_col])

    if target_data.empty:
        return target_data

    # Add pIC50 (negative log of IC50 in molar)
    if affinity_col in target_data.columns:
        target_data = target_data[target_data[affinity_col].notna()].copy()
        target_data["pAffinity"] = -((target_data[affinity_col] * 1e-9).apply(
            lambda x: __import__('math').log10(x)
        ))
        target_data = target_data.sort_values("pAffinity", ascending=False)

    return target_data

# Most potent compounds against EGFR (P00533)
# sar = sar_analysis(df, "P00533", "IC50 (nM)")
# print(sar.head(20))

6. Polypharmacology Profile

def polypharmacology_profile(df, ligand_smiles_or_name, affinity_cutoff_nM=1000):
    """
    Find all targets a compound binds to.
    Uses PubChem CID or SMILES for matching.
    """
    # Search by ligand SMILES (exact match)
    mask = df["Ligand SMILES"] == ligand_smiles_or_name

    ligand_data = df[mask].copy()

    # Filter by affinity
    aff_cols = ["Ki (nM)", "IC50 (nM)", "Kd (nM)"]
    has_aff = pd.Series(False, index=ligand_data.index)
    for col in aff_cols:
        if col in ligand_data.columns:
            has_aff |= ligand_data[col] <= affinity_cutoff_nM

    result = ligand_data[has_aff][
        ["Target Name", "UniProt (SwissProt) Primary ID of Target Chain"] + aff_cols
    ].dropna(how='all')

    return result.sort_values("Ki (nM)")

Query Workflows

Workflow 1: Find Best Inhibitors for a Target

import pandas as pd

def find_best_inhibitors(uniprot_id, affinity_type="IC50 (nM)", top_n=20):
    """Find the most potent inhibitors for a target in BindingDB."""
    df = load_bindingdb("BindingDB_All.tsv")  # Load once and reuse
    result = query_target_affinity(df, uniprot_id, [affinity_type])

    if result.empty:
        print(f"No data found for {uniprot_id}")
        return result

    result = result.sort_values(affinity_type).head(top_n)
    print(f"Top {top_n} inhibitors for {uniprot_id} by {affinity_type}:")
    for _, row in result.iterrows():
        print(f"  {row['PubChem CID']}: {row[affinity_type]:.1f} nM | SMILES: {row['Ligand SMILES'][:40]}...")
    return result

Workflow 2: Selectivity Profiling

  1. Get all affinity data for your compound across all targets
  2. Compare affinity ratios between on-target and off-targets
  3. Identify selectivity cliffs (structural changes that improve selectivity)
  4. Cross-reference with ChEMBL for additional selectivity data

Workflow 3: Machine Learning Dataset Preparation

def prepare_ml_dataset(df, uniprot_ids, affinity_col="IC50 (nM)",
                        max_affinity_nM=100000, min_count=50):
    """Prepare BindingDB data for ML model training."""
    records = []
    for uid in uniprot_ids:
        target_df = query_target_affinity(df, uid, [affinity_col], max_affinity_nM)
        if len(target_df) >= min_count:
            target_df = target_df.copy()
            target_df["target"] = uid
            records.append(target_df)

    if not records:
        return pd.DataFrame()

    combined = pd.concat(records)
    # Add pAffinity (normalized)
    combined["pAffinity"] = -((combined[affinity_col] * 1e-9).apply(
        lambda x: __import__('math').log10(max(x, 1e-12))
    ))
    return combined[["Ligand SMILES", "target", "pAffinity", affinity_col]].dropna()

Key Data Fields

FieldDescription
Ligand SMILES2D structure of the compound
Ligand InChI KeyUnique chemical identifier
Ki (nM)Inhibition constant (equilibrium, functional)
Kd (nM)Dissociation constant (thermodynamic, binding)
IC50 (nM)Half-maximal inhibitory concentration
EC50 (nM)Half-maximal effective concentration
kon (M-1-s-1)Association rate constant
koff (s-1)Dissociation rate constant
UniProt (SwissProt) Primary IDTarget UniProt accession
Target NameProtein name
PDB ID(s) for Ligand-Target ComplexCrystal structures
PubChem CIDPubChem compound ID
ChEMBL ID of LigandChEMBL compound ID

Affinity Interpretation

AffinityClassificationDrug-likeness
< 1 nMSub-nanomolarVery potent (picomolar range)
1–10 nMNanomolarPotent, typical for approved drugs
10–100 nMModerateCommon lead compounds
100–1000 nMWeakFragment/starting point
> 1000 nMVery weakGenerally below drug-relevance threshold

Best Practices

  • Use Ki for direct binding: Ki reflects true binding affinity independent of enzymatic mechanism
  • IC50 context-dependency: IC50 values depend on substrate concentration (Cheng-Prusoff equation)
  • Normalize units: BindingDB reports in nM; verify units when comparing across studies
  • Filter by target organism: Use Target Source Organism to ensure human protein data
  • Handle missing values: Not all compounds have all measurement types
  • Cross-reference with ChEMBL: ChEMBL has more curated activity data for medicinal chemistry

Additional Resources

平台分布

Codex

32%
按下载量换算46

Claude

29.28%
按下载量换算42

Cursor

19%
按下载量换算27

Gemini CLI

9.98%
按下载量换算14

安全审计

Gen Agent Trust Hub

通过

Socket

通过

Snyk

可疑

权限和风险

需要联网

该 Skill 可能需要联网访问来源站点、仓库或外部 API;具体网络访问范围需要结合源码和 README 复核。

安装前确认

本站仅展示第三方公开信息,不托管安装包,不提供自动安装或运行环境。安装前应自行审查源码、依赖和命令行为。来源安全扫描存在提醒或未通过项,安装前请自行复核。目前只有一个公开来源,建议同时核对源仓库。

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