stjames 0.0.115__py3-none-any.whl → 0.0.117__py3-none-any.whl

stjames/atomium_stjames/mmcif.py

@@ -512,7 +512,7 @@ def add_atom_to_polymer(atom: dict[str, Any], aniso: dict[int, Any], model: dict
     try:
         model["polymer"][mol_id]["residues"][res_id]["atoms"][int(atom["id"])] = atom_dict_to_atom_dict(atom, aniso)
     except Exception:
-        name = atom["auth_comp_id"]
+        name = atom.get("auth_comp_id") or atom.get("label_comp_id") or "UNKNOWN"
         try:
             model["polymer"][mol_id]["residues"][res_id] = {
                 "name": name,
@@ -553,7 +553,7 @@ def add_atom_to_non_polymer(atom: dict[str, Any], aniso: dict[int, Any], model:
     try:
         model[mol_type][mol_id]["atoms"][int(atom["id"])] = atom_dict_to_atom_dict(atom, aniso)
     except Exception:
-        name = atom["auth_comp_id"]
+        name = atom.get("auth_comp_id") or atom.get("label_comp_id") or "UNKNOWN"
         model[mol_type][mol_id] = {
             "name": name,
             "full_name": names.get(name).upper() if names.get(name) is not None and names.get(name).lower() != "water" else None,  # type: ignore [union-attr]

stjames/workflows/__init__.py

@@ -21,6 +21,7 @@ from .multistage_opt import *
 from .nmr import *
 from .pka import *
 from .pose_analysis_md import *
+from .protein_binder_design import *
 from .protein_cofolding import *
 from .redox_potential import *
 from .scan import *
@@ -51,6 +52,7 @@ WORKFLOW_NAME = Literal[
     "pka",
     "pose_analysis_md",
     "protein_cofolding",
+    "protein_binder_design",
     "redox_potential",
     "scan",
     "solubility",
@@ -80,6 +82,7 @@ WORKFLOW_MAPPING: dict[WORKFLOW_NAME, Workflow] = {
     "pka": pKaWorkflow,  # type: ignore [dict-item]
     "pose_analysis_md": PoseAnalysisMolecularDynamicsWorkflow,  # type: ignore [dict-item]
     "protein_cofolding": ProteinCofoldingWorkflow,  # type: ignore [dict-item]
+    "protein_binder_design": ProteinBinderDesignWorkflow,  # type: ignore [dict-item]
     "redox_potential": RedoxPotentialWorkflow,  # type: ignore [dict-item]
     "scan": ScanWorkflow,  # type: ignore [dict-item]
     "solubility": SolubilityWorkflow,  # type: ignore [dict-item]

stjames/workflows/conformer_search.py

@@ -9,9 +9,10 @@ from ..base import LowercaseStrEnum
 from ..constraint import Constraint
 from ..method import Method, XTBMethod
 from ..mode import Mode
+from ..molecule import Molecule
 from ..types import UUID, FloatPerAtom, round_float_per_atom
 from .multistage_opt import MultiStageOptMixin
-from .workflow import MoleculeWorkflow
+from .workflow import MoleculeWorkflow, SMILESWorkflow
 
 _sentinel = object()
 
@@ -377,12 +378,16 @@ class ConformerSearchMixin(ConformerGenMixin, MultiStageOptMixin):
         return self
 
 
-class ConformerSearchWorkflow(ConformerSearchMixin, MoleculeWorkflow):
+class ConformerSearchWorkflow(ConformerSearchMixin, SMILESWorkflow, MoleculeWorkflow):
     """
     ConformerSearch Workflow.
 
+    This workflow supports both SMILES and 3D molecular input. Some conformer generation settings
+    support both methods; others (like CREST) require 3D information. Only one should be supplied.
+
     Inherited:
     :param initial_molecule: Molecule of interest
+    :param initial_smiles: SMILES of the molecule of interest
     :param conf_gen_mode: Mode for calculations
     :param conf_gen_settings: settings for conformer generation
     :param mso_mode: Mode for MultiStageOptSettings
@@ -401,6 +406,21 @@ class ConformerSearchWorkflow(ConformerSearchMixin, MoleculeWorkflow):
     :param energies: energies of the molecules
     """
 
+    initial_smiles: str = ""
+    initial_molecule: Molecule | None = None  # type: ignore [assignment]
+
     # Results
     conformer_uuids: list[list[UUID | None]] = Field(default_factory=list)
     energies: Annotated[FloatPerAtom, AfterValidator(round_float_per_atom(6))] = Field(default_factory=list)
+
+    @model_validator(mode="after")
+    def validate_mol_input(self) -> Self:
+        """Ensure that only one of initial_molecule or initial_smiles is set."""
+
+        if not (bool(self.initial_smiles) ^ bool(self.initial_molecule)):
+            raise ValueError("Can only set one of initial_molecule and initial_smiles")
+
+        if isinstance(self.conf_gen_settings, iMTDSettings) and (self.initial_molecule is None):
+            raise ValueError("iMTDSettings requires `initial_molecule` to be set")
+
+        return self

stjames/workflows/docking.py

@@ -1,6 +1,6 @@
 """Docking workflow."""
 
-from typing import Annotated, Self, TypeAlias
+from typing import Annotated, Literal, Self, TypeAlias
 
 from pydantic import AfterValidator, ConfigDict, field_validator, model_validator
 
@@ -46,12 +46,23 @@ class VinaSettings(DockingSettings):
     """
     Controls how AutoDock Vina is run.
 
+    :param executable: which Vina implementation is run.
+    :param scoring_function: which scoring function is employed.
     :param exhaustiveness: how many times Vina attempts to find a pose.
         8 is typical, 32 is considered relatively careful.
     """
 
+    executable: Literal["qvina2", "vina"] = "vina"
+    scoring_function: Literal["vinardo", "vina"] = "vinardo"
     exhaustiveness: int = 8
 
+    @model_validator(mode="after")
+    def check_executable_scoring_function(self) -> Self:
+        """Check if the combination of exectuable and scoring function is supported."""
+        if (self.executable == "qvina2") and (self.scoring_function == "vinardo"):
+            raise ValueError("qvina2 does not implement the vinardo scoring function!")
+        return self
+
 
 class DockingWorkflow(MoleculeWorkflow):
     """

stjames/workflows/pose_analysis_md.py

@@ -76,8 +76,8 @@ class PoseAnalysisMolecularDynamicsWorkflow(SMILESWorkflow):
     protein_uuid: UUID | None = None
     ligand_residue_name: str = "LIG"
 
-    num_trajectories: PositiveInt = 4
-    equilibration_time_ns: Annotated[PositiveFloat, AfterValidator(round_float(3))] = 5
+    num_trajectories: PositiveInt = 1
+    equilibration_time_ns: Annotated[PositiveFloat, AfterValidator(round_float(3))] = 1
     simulation_time_ns: Annotated[PositiveFloat, AfterValidator(round_float(3))] = 10
 
     temperature: Annotated[PositiveFloat, AfterValidator(round_float(3))] = 300

stjames/workflows/protein_binder_design.py

@@ -0,0 +1,303 @@
+"""Protein-binder-design workflow."""
+
+from enum import Enum
+from typing import Annotated, TypeAlias
+
+from pydantic import AfterValidator
+
+from ..base import Base, LowercaseStrEnum, round_optional_float
+from ..types import UUID
+from .workflow import Workflow
+
+ProteinUUID: TypeAlias = UUID
+
+
+class BoltzGenSecondaryStructure(Base):
+    """
+    Represents the secondary structure assignments for a protein.
+
+    :param id: Optional identifier for this secondary structure annotation.
+    :param sheet: String encoding the residue indices comprising β-sheet structures
+                  (e.g., "1,3..11" for residues 1, and 3 through 11).
+    :param helix: String encoding residue indices comprising helices.
+    :param loop: String encoding residue indices comprising loop or coil regions.
+    """
+
+    id: str | None = None
+    sheet: str | None = None
+    helix: str | None = None
+    loop: str | None = None
+
+
+class BoltzGenProteinEntity(Base):
+    """
+    Represents a protein entity, either a designed or natural sequence.
+
+    :param id: Unique identifier for the protein.
+    :param sequence: Protein sequence, may contain amino acids and numbers for designed regions.
+    :param secondary_structure: Optional assigned secondary structure.
+    :param cyclic: Whether the protein is cyclic (True/False). Optional.
+    """
+
+    id: str
+    sequence: str  # can include amino acids as well as numbers for designed regions
+    secondary_structure: BoltzGenSecondaryStructure | None = None
+    # binding_types: BindingType | None = None - we may want to add this later but not used in examples.
+    cyclic: bool | None = None
+
+
+class BoltzGenLigandEntity(Base):
+    """
+    Represents a ligand entity (non-protein), such as a small molecule.
+
+    :param id: Unique identifier for the ligand.
+    :param smiles: SMILES string representation of the ligand.
+    """
+
+    id: str
+    smiles: str
+    # binding_types: str | None = None - we may want to add this later but not used in examples.
+
+
+class BoltzGenRegionSelection(Base):
+    """
+    Defines a region of a protein chain by specifying its chain identifier and (optionally) residue indices.
+
+    :param chain_id: Identifier for the protein chain (e.g., 'A', 'B', etc.).
+    :param residue_indices: Residues to select, specified as a string in the format "5..7,13" or "5..15,50..".
+    """
+
+    chain_id: str | None = None
+    residue_indices: str | None = None
+
+
+class BoltzGenProximityRegionSelection(BoltzGenRegionSelection):
+    """
+    Defines a region of a protein chain based on spatial proximity to a selection of residues.
+
+    Inherits:
+        BoltzGenRegionSelection
+
+    :param radius: Radius in angstroms (Å) used to select all residues within proximity to the specified region.
+    """
+
+    radius: int | None = None
+
+
+class BoltzGenBindingType(Base):
+    """
+    Represents the binding interface specification for a given protein chain.
+
+    :param chain_id: Identifier for the protein chain (e.g., 'A', 'B', etc.).
+    :param binding: Residue indices or regions that are required to participate in binding
+        (e.g., "5..7,13" or "all" for the whole chain).
+    :param not_binding: Residue indices or regions that should explicitly not participate in binding
+        (e.g., "5..7,13" or "all" for excluding the entire chain).
+    """
+
+    chain_id: str | None = None
+    binding: str | None = None
+    not_binding: str | None = None
+
+
+class BoltzGenSecondaryStructureOptions(str, Enum):
+    UNSPECIFIED = "UNSPECIFIED"
+    LOOP = "LOOP"
+    HELIX = "HELIX"
+    SHEET = "SHEET"
+
+
+class BoltzGenDesignInsertion(Base):
+    """
+    Represents an insertion site for protein design in a specific chain.
+
+    :param chain_id: Identifier of the chain where the insertion occurs.
+    :param residue_index: Position in the chain after which the insertion is to be made.
+    :param number_of_residues: Number of residues to insert at the specified site (can be a string pattern).
+    :param secondary_structure: Desired secondary structure type for the inserted residues
+        ("UNSPECIFIED", "LOOP", "HELIX", or "SHEET"). Optional.
+    """
+
+    chain_id: str
+    residue_index: int
+    number_of_residues: str
+    secondary_structure: BoltzGenSecondaryStructureOptions | None = None
+
+
+class BoltzGenFileEntity(Base):
+    """
+    Represents a protein structure input and its associated region selection and design specifications
+    for the BoltzGen binder design workflow.
+
+    :param uuid: Unique identifier for the protein structure.
+    :param include: List of regions to include in the design or analysis context.
+    :param exclude: List of regions to explicitly exclude from consideration (e.g., for ignoring noisy/irrelevant regions).
+    :param include_proximity: List of regions defined by spatial proximity (e.g., residues within a given radius).
+    :param binding_types: List of binding type constraints or permitted interface regions.
+    :param design: List of regions that are being subject to design (mutable, allowed to change).
+    :param secondary_structure: List of desired or annotated secondary structure definitions for selected regions.
+    :param design_insertions: List of new regions to be inserted with specified properties (e.g., insertion sites, structure preferences).
+    """
+
+    uuid: ProteinUUID
+    include: list[BoltzGenRegionSelection] = []
+    exclude: list[BoltzGenRegionSelection] = []
+    # fuse: None  - we may want to add this later but not used in examples.
+    include_proximity: list[BoltzGenProximityRegionSelection] = []
+    binding_types: list[BoltzGenBindingType] = []
+    # structure_groups: None - we may want to add this later but not used in examples.
+    design: list[BoltzGenRegionSelection] = []
+    secondary_structure: list[BoltzGenSecondaryStructure] = []
+    design_insertions: list[BoltzGenDesignInsertion] = []
+
+
+class BoltzGenAtomSpecification(Base):
+    """
+    Atom specification for a protein chain, used for applying constraints or referencing atoms.
+
+    :param chain_id: Identifier for the protein chain (e.g., "A", "B").
+    :param index: Residue index the atom belongs to (integer, 1-based).
+    :param atom_name: Name of the atom (e.g., "CA", "N", "O", etc.).
+    """
+
+    chain_id: str
+    index: int
+    atom_name: str
+
+
+class BoltzGenConstraint(Base):
+    """
+    Describes a covalent or spatial constraint between two specified atoms in the context of protein design.
+
+    :param atom1: First atom in the constraint.
+    :param atom2: Second atom in the constraint.
+    """
+
+    atom1: BoltzGenAtomSpecification
+    atom2: BoltzGenAtomSpecification
+
+
+class BoltzGenInput(Base):
+    """
+    Represents the primary input schema for the boltzgen application.
+
+    :param protein_entities: Protein chains that are designed or targeted for binding.
+    :param ligand_entities: Small molecules or other non-protein ligands relevant to the design.
+    :param file_entities: 3d protein structures and input settings related to them.
+    :param constraints: Covalent bond constraints
+    """
+
+    protein_entities: list[BoltzGenProteinEntity] = []
+    ligand_entities: list[BoltzGenLigandEntity] = []
+    file_entities: list[BoltzGenFileEntity] = []
+    constraints: list[BoltzGenConstraint] = []
+
+
+class BoltzGenScores(Base):
+    """
+    Compact, interpretable metrics for a designed binder.
+    ↑ higher is better, ↓ lower is better
+
+    :param quality_score: aggregate model quality (↑)
+    :param num_filters_passed: number of QC/heuristic filters passed (↑)
+    :param iptm: inter-chain pTM confidence, 0–1 (↑)
+    :param design_ptm: design pTM confidence, 0–1 (↑)
+    :param min_interaction_pae: minimum interface PAE in Å (↓)
+    :param bb_rmsd: backbone RMSD in Å (↓)
+    :param delta_sasa_refolded: ΔSASA of interface after refolding, Ų (↑ typically indicates better burial)
+    :param plip_hbonds_refolded: count of hydrogen bonds at the interface (↑)
+    :param plip_saltbridge_refolded: count of salt bridges at the interface (↑)
+    :param liability_score: composite liabilities score (↓)
+    :param liability_high_severity_violations: count of high-severity liabilities (↓)
+    :param liability_num_violations: total liability count (↓)
+    :param helix: fraction helical content, 0–1
+    :param sheet: fraction β-sheet content, 0–1
+    :param loop: fraction loop/coil content, 0–1
+    :param design_largest_hydrophobic_patch_refolded: largest hydrophobic patch area after refolding, Ų
+    :param design_hydrophobicity: overall design hydrophobicity score (unitless)
+    :param num_tokens: sequence length / token count
+    """
+
+    quality_score: Annotated[float | None, AfterValidator(round_optional_float(3))] = None
+    num_filters_passed: int | None = None
+
+    iptm: Annotated[float | None, AfterValidator(round_optional_float(3))] = None
+    design_ptm: Annotated[float | None, AfterValidator(round_optional_float(3))] = None
+    min_design_to_target_pae: Annotated[float | None, AfterValidator(round_optional_float(3))] = None
+    design_to_target_iptm: Annotated[float | None, AfterValidator(round_optional_float(3))] = None
+    min_interaction_pae: Annotated[float | None, AfterValidator(round_optional_float(3))] = None
+
+    bb_rmsd: Annotated[float | None, AfterValidator(round_optional_float(3))] = None
+    delta_sasa_refolded: Annotated[float | None, AfterValidator(round_optional_float(3))] = None
+
+    plip_hbonds_refolded: int | None = None
+    plip_saltbridge_refolded: int | None = None
+
+    liability_score: Annotated[float | None, AfterValidator(round_optional_float(3))] = None
+    liability_high_severity_violations: int | None = None
+    liability_num_violations: int | None = None
+
+    helix: Annotated[float | None, AfterValidator(round_optional_float(3))] = None
+    sheet: Annotated[float | None, AfterValidator(round_optional_float(3))] = None
+    loop: Annotated[float | None, AfterValidator(round_optional_float(3))] = None
+    design_largest_hydrophobic_patch_refolded: Annotated[float | None, AfterValidator(round_optional_float(3))] = None
+    design_hydrophobicity: Annotated[float | None, AfterValidator(round_optional_float(3))] = None
+    num_tokens: int | None = None
+
+
+class ProteinBinderDesignResult(Base):
+    """
+    The output; a designed binder.
+
+    :param sequence: the sequence
+    :param bound_structure: the PDB of the structure bound to the target
+    :param scores: the scores for the generated structure
+    """
+
+    binder_sequence: str | None = None
+    bound_structure: ProteinUUID | None = None
+    scores: BoltzGenScores | None = None
+
+
+class BoltzGenProtocol(LowercaseStrEnum):
+    """
+    The predefined protocol used for generation + filtering.
+    """
+
+    PROTEIN_ANYTHING = "protein-anything"
+    PEPTIDE_ANYTHING = "peptide-anything"
+    PROTEIN_SMALL_MOLECULE = "protein-small_molecule"
+    NANOBODY_ANYTHING = "nanobody-anything"
+
+
+class BoltzGenSettings(Base):
+    """
+    The settings for running BoltzGen.
+
+    :param num_designs: how many designs to generate
+    :param protocol: which protocol to use
+    :param binding_residue: a dict mapping the chain ID to which residues should bind.
+        the string follows the BoltzGen format of specifying ranges of residue indices (refer to their documentation).
+        examples include "5..7,13" or "5..15,50..".
+    """
+
+    protocol: BoltzGenProtocol = BoltzGenProtocol.PROTEIN_ANYTHING
+    num_designs: int = 100
+    budget: int = 20
+
+
+class ProteinBinderDesignWorkflow(Workflow):
+    """
+    A workflow for generating proteins or peptides that bind to something.
+
+
+    New:
+    :param binder_design_input: the input to the protein binder design workflow
+    :param binder_design_settings: the settings for the protein generation method employed
+    :param generated_binders: the output structures
+    """
+
+    binder_design_input: BoltzGenInput = BoltzGenInput()
+    binder_design_settings: BoltzGenSettings = BoltzGenSettings()
+
+    generated_binders: list[ProteinBinderDesignResult] = []

stjames/workflows/protein_cofolding.py

@@ -1,4 +1,4 @@
-"""Protein cofolding Workflow."""
+"""Protein cofolding workflow."""
 
 from typing import Annotated, Literal, TypeAlias
 
@@ -26,6 +26,7 @@ class Token(BaseModel):
     input_type: Literal["ligand", "protein"]
     input_index: int
     token_index: int
+    atom_name: str | None = None
 
 
 class ContactConstraint(BaseModel):

{stjames-0.0.115.dist-info → stjames-0.0.117.dist-info}/METADATA

@@ -1,6 +1,6 @@
 Metadata-Version: 2.4
 Name: stjames
-Version: 0.0.115
+Version: 0.0.117
 Summary: standardized JSON atom/molecule encoding scheme
 Author-email: Corin Wagen <corin@rowansci.com>
 Project-URL: Homepage, https://github.com/rowansci/stjames

{stjames-0.0.115.dist-info → stjames-0.0.117.dist-info}/RECORD

@@ -25,7 +25,7 @@ stjames/thermochem_settings.py,sha256=ZTLz31v8Ltutde5Nfm0vH5YahWjcfFWfr_R856Kffx
 stjames/types.py,sha256=PGEZeqGnomgWUSHcMuUftzvZt7l4VwaQ1Pi-7vEkibg,4773
 stjames/atomium_stjames/__init__.py,sha256=gZkzC7i9D_fmWUTN55gtygITo3-qvJUda5CXLR0jyCQ,306
 stjames/atomium_stjames/data.py,sha256=-hzwBpTHq5JetsOVyopUJswKnKAkMtJ_XkONxjXVupU,5675
-stjames/atomium_stjames/mmcif.py,sha256=em1fNt6577OaUjL7Pctru7aJp3ceZ9kEnj5w6BRWdVs,27090
+stjames/atomium_stjames/mmcif.py,sha256=n6cFdODKzRA6r4_Cp4dgtmAJrIlj-YBotCFT4skzuTI,27182
 stjames/atomium_stjames/pdb.py,sha256=hoEV1xmbkYkXW8A6YX5uspvSRvGlhzM1o_BiikQ6DiU,23734
 stjames/atomium_stjames/utilities.py,sha256=-YtM7sRMvMk0wWrC3svWUWH4CGI0NtY77nXsg9tjHfc,4964
 stjames/data/__init__.py,sha256=O59Ksp7AIqwOELCWymfCx7YeBzwNOGCMlGQi7tNLqiE,24
@@ -37,14 +37,14 @@ stjames/data/read_nist_isotopes.py,sha256=y10FNjW43QpC45qib7VHsIghEwT7GG5rsNwHdc
 stjames/data/symbol_element.json,sha256=vl_buFusTqBd-muYQtMLtTDLy2OtBI6KkBeqkaWRQrg,1186
 stjames/optimization/__init__.py,sha256=47DEQpj8HBSa-_TImW-5JCeuQeRkm5NMpJWZG3hSuFU,0
 stjames/optimization/freezing_string_method.py,sha256=eEQBqbYHgJH9gVRLDIFtGuPcsHHMLAAt1hF3jtq70lo,2285
-stjames/workflows/__init__.py,sha256=I-s6f6uz7PXpeKsvQlL04wswId2mW2u7thk309TC7ng,3165
+stjames/workflows/__init__.py,sha256=RoqcRk27PTu9UfHFQQtu5quiBipsx4NGvDPst5S1EOc,3317
 stjames/workflows/admet.py,sha256=qFUpCFiLW-3gzuEjCMNBJ6DEG_vquJcPAsN4SVZRfdE,1289
 stjames/workflows/basic_calculation.py,sha256=sAgHBcNHE72ZbZPB9vyZShALRC4zOVw6It6cpJlbX2A,911
 stjames/workflows/bde.py,sha256=g_In-caftXiimrhfdptHjpfrYQUs3vF58qYmRnaTN8g,10825
 stjames/workflows/conformer.py,sha256=18aO6ngMBeGAmQkBdLGCCHr398RIYr1v2hD2IT1u4cc,3005
-stjames/workflows/conformer_search.py,sha256=sQayHL5aGY8WssQOGW4lPh1aXLfcPJewG9WUiC8il6A,14744
+stjames/workflows/conformer_search.py,sha256=1kBUT0yCcTPTCtxg1tlTKHRRXkfNYNqzla_89lDEL9k,15696
 stjames/workflows/descriptors.py,sha256=T4tc7xdtBdxESGO86KR323jPQ2pgwxBqgV0khA6MEgQ,584
-stjames/workflows/docking.py,sha256=sJFSGyIve-q55UEir2rV9Pk7L09_pPuSy2K00JLvA68,4138
+stjames/workflows/docking.py,sha256=t30kqeFXQ0yrlqvN6Jdwt0SdfnJLDsfK-7yFi0gwNbY,4753
 stjames/workflows/double_ended_ts_search.py,sha256=ovJgEVFc6c3mijCE3TKAY70YvqNmAZ5Y4XgV4-tIxBI,3127
 stjames/workflows/electronic_properties.py,sha256=GT3-NC7w-dbcOJ-3AzJ7LgzH6frTbiH2Iyb9BCa-SvY,4112
 stjames/workflows/fukui.py,sha256=095GDGSSEc5PDD1aoKM8J7icgR5tfwS5Bs9XxFQHge4,2387
@@ -56,8 +56,9 @@ stjames/workflows/molecular_dynamics.py,sha256=HqWNxxPSAphfI0DdbTERFkq8UeBjEvhnA
 stjames/workflows/multistage_opt.py,sha256=UN-4WLsT2WEjO5KqDPrcCkb708Co-ZScHx3g2bto768,16597
 stjames/workflows/nmr.py,sha256=1QEF4SB6dWIr-jzLEZ7V972UnRUOTufOJSHwIGyV3dM,2681
 stjames/workflows/pka.py,sha256=i-jzl2lN0yRWc0tgrWSBCplITEByfRyEQrlUhjnzcBc,4580
-stjames/workflows/pose_analysis_md.py,sha256=KLxSSuM60UpVawDI2xTvsMXoLHFIlA2CtVbpD0uePF4,4803
-stjames/workflows/protein_cofolding.py,sha256=cN0WUh8trrWwzNvoU75hB-VectIer-g5sMKgibQJcfE,4293
+stjames/workflows/pose_analysis_md.py,sha256=dpWVKC-8fPdw6ExIXk9xbeVBDUMUYQECpixb-oFa23I,4803
+stjames/workflows/protein_binder_design.py,sha256=KnPKQJTMrSO5xfw64Bh7T0wHck1NtysVwkVgHs1cGws,12013
+stjames/workflows/protein_cofolding.py,sha256=w7Sg_ttU4bcJb7wlVcI_AAsLM9WVAJcU5ucbNb5Iyzw,4326
 stjames/workflows/redox_potential.py,sha256=7S18t9Y3eynSnA3lZbRlvLfdbgeBopdiigLzt1zxg5c,3871
 stjames/workflows/scan.py,sha256=DXQBpa2t2PowAtOwmdgpxaSLq--fEShljzAGSb8Nf5U,2993
 stjames/workflows/solubility.py,sha256=lfCVvJjqEaddLUpK6WBxjB7u12Sci-K95A5_qIMkIRM,3028
@@ -65,8 +66,8 @@ stjames/workflows/spin_states.py,sha256=0degmE-frovgoXweshZyjfjqL7nkbaFoO9YoJhvQ
 stjames/workflows/strain.py,sha256=paYxDDQTB1eYP_c2kLVz1-QX7Vpw0LLb3ujnFin_SOM,1834
 stjames/workflows/tautomer.py,sha256=7eYKziGPg8Km6lfowTzSkgJfJ4SHUPrAmnTf8Bi-SB0,1164
 stjames/workflows/workflow.py,sha256=OE05pt2ZOd8TzTOlBngXCVg9wv_553ZR60VNRPlq0f8,1953
-stjames-0.0.115.dist-info/licenses/LICENSE,sha256=i05z7xEhyrg6f8j0lR3XYjShnF-MJGFQ-DnpsZ8yiVI,1084
-stjames-0.0.115.dist-info/METADATA,sha256=SXjEZ5InRPFPo1QtWBhil1BqW-YIjY9b-xH8pt1F-3Y,1725
-stjames-0.0.115.dist-info/WHEEL,sha256=_zCd3N1l69ArxyTb8rzEoP9TpbYXkqRFSNOD5OuxnTs,91
-stjames-0.0.115.dist-info/top_level.txt,sha256=FYCwxl6quhYOAgG-mnPQcCK8vsVM7B8rIUrO-WrQ_PI,8
-stjames-0.0.115.dist-info/RECORD,,
+stjames-0.0.117.dist-info/licenses/LICENSE,sha256=i05z7xEhyrg6f8j0lR3XYjShnF-MJGFQ-DnpsZ8yiVI,1084
+stjames-0.0.117.dist-info/METADATA,sha256=LH_VdqC55gK6JJ0beT4uW6xifSRAfMJLQoIh3VpMAHg,1725
+stjames-0.0.117.dist-info/WHEEL,sha256=_zCd3N1l69ArxyTb8rzEoP9TpbYXkqRFSNOD5OuxnTs,91
+stjames-0.0.117.dist-info/top_level.txt,sha256=FYCwxl6quhYOAgG-mnPQcCK8vsVM7B8rIUrO-WrQ_PI,8
+stjames-0.0.117.dist-info/RECORD,,