All tools utilized within MolClaw skills connect via the MCP protocol. This skill is the unified guide for connecting to the deployed MCP server before invoking tools.
原文语言:英语
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SkillsMP 已收集 InternScience/MolClaw 中的 63 个 Skill。打开任一 Skill 可查看来源和详情。
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All tools utilized within MolClaw skills connect via the MCP protocol. This skill is the unified guide for connecting to the deployed MCP server before invoking tools.
原文语言:英语
Formats extracted execution patterns into standard MolClaw skill documents. Accepts structured input from the Skill Crystallization Meta-Workflow (L2-12) and outputs a properly formatted L1 or L2 skill document conforming to MolClaw conventions. This skill…
原文语言:英语
Predict the ADMET (absorption, distribution, metabolism, excretion, and toxicity) properties of the input molecules.
原文语言:英语
Predict binding affinity between target protein sequence and small molecule SMILES using Boltz-2.
原文语言:英语
Retrieve SMILES strings by compound name using PubChem with an NCI resolver fallback.
原文语言:英语
Generate new molecules de novo.
原文语言:英语
End-to-end docking-score ranking using EquiScore for candidate molecules against a target protein.
原文语言:英语
Repair and clean PDB or mmCIF structures with PDBFixer, returning a repaired PDB path and topology counts.
原文语言:英语
Run GoCa coarse-grained protein MD pipeline and collect key simulation artifacts from a unified run directory.
原文语言:英语
Run HDOCKlite docking for protein complexes and return run directories with ranked models.
原文语言:英语
**PRIMARY tool for all single-structure interaction analysis.** MCP-exposed protein–ligand / peptide / protein–protein interaction analysis and Schrödinger-style multi-dimensional visualization. Pure Python/NumPy engine covering 9 interaction types with 2D…
原文语言:英语
Generate new molecules sampling from the input two warhead fragments.
原文语言:英语
Calculate both Tanimoto similarities and the count of shared structural fragments between a target molecule and a list of candidate molecules via Morgan fingerprints.
原文语言:英语
Generate new molecules sampling from the input molecule.
原文语言:英语
Runs OpenAWSEM simulations and extracts representative trajectory frames for downstream ensemble analysis.
原文语言:英语
Repair a protein PDB or mmCIF structure with PDBFixer and write a repaired PDB.
原文语言:英语
Generate new peptide molecules sampling from the input peptide sequence.
原文语言:英语
Execution-ready protein-ligand MM/GB(PB)SA workflow with explicit MCP handoffs and optional analysis.
原文语言:英语
Run OpenMM protein MD and extract evenly spaced trajectory frames for downstream structural analysis.
原文语言:英语
Execution-ready protein-protein MM/GB(PB)SA workflow with MCP-exposed tool names, strict file validation, and failure guards.
原文语言:英语
Search the target protein sequence information from the input gene name or uniprot id.
原文语言:英语
Retrieve and download a protein structure file (.pdb or .cif) using a gene name, UniProt ID, or PDB ID.
原文语言:英语
Perform molecular docking using QuickVina2-GPU between target protein structure and small molecules.
原文语言:英语
Generate new molecules sampling from the input scaffold.
原文语言:英语
Run BioEmu sequence sampling and extract ensemble structures for downstream conformation analysis.
原文语言:英语
Render a molecule from a SMILES string or a server-side molecular structure file with the MolClaw MCP tool `visualize_molecule`.
原文语言:英语
Render a server-side PDB protein structure as a PNG with the MolClaw MCP tool `visualize_protein`.
原文语言:英语
Predict protein structures with Chai-1 from sequence or FASTA input and return model scoring summaries.
原文语言:英语
Chroma toolkit skill covering chroma_monomer for single-chain generation, chroma_complex for multi-chain assembly generation, and chroma_symmetry for symmetry-constrained protein design.
原文语言:英语
[CURRENTLY UNAVAILABLE] DiffDock protein-ligand docking. This tool is not deployed on the current MCP server. Use molclaw-quickvina-docking or molclaw-karmadock-tool as alternatives.
原文语言:英语
Calculate disease reversal scores for the provided molecules relative to a specific disease.
原文语言:英语
High-level large-scale virtual screening workflow (10+ ligands) combining property filtering, QuickVina docking, EquiScore rescoring, and consensus ranking for target prioritization.
原文语言:英语
Compute the drug-likeness metrics (QED score and Number of violations of Lipinski's Rule of Five) of the input candidate molecules (SMILES format).
原文语言:英语
Unified EquiScore skill for pocket extraction, pocket scoring, and end-to-end docking-to-score pipeline execution.
原文语言:英语
Use ESMFold model to predict 3D structure of the input protein sequence.
原文语言:英语
Design linear or cyclic peptide binders from receptor FASTA sequences using EvoBind2 with structured result outputs.
原文语言:英语
Extract protein sequence of each chain from the protein structure file (pdb format).
原文语言:英语
Implement data transmission between the local computer and the MCP Server using Base64 encoding
原文语言:英语
FoldX protein stability and mutation analysis tool. Supports 8 modes: structure repair (RepairPDB), stability calculation (Stability), mutation ΔΔG (BuildModel), complex interface energy (AnalyseComplex), alanine scanning (AlaScan), position scanning…
原文语言:英语
Use fpocket to detect binding pockets and output their detailed properties for the input protein. This offers a more concise approach to pocket identification.
原文语言:英语