Nutmeg and SPICE: Models and Data for Biomolecular Machine Learning
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Abstract (arXiv)
We describe version 2 of the SPICE dataset, a collection of quantum chemistry calculations for training machine learning potentials. It expands on the original dataset by adding much more sampling of chemical space and more data on non-covalent interactions. We train a set of potential energy functions called Nutmeg on it. They are based on the TensorNet architecture. They use a novel mechanism to improve performance on charged and polar molecules, injecting precomputed partial charges into the model to provide a reference for the large scale charge distribution. Evaluation of the new models shows they do an excellent job of reproducing energy differences between conformations, even on highly charged molecules or ones that are significantly larger than the molecules in the training set. They also produce stable molecular dynamics trajectories, and are fast enough to be useful for routine simulation of small molecules.
Key facts. Cited by 7 papers in the map (data through 14 Oct 2026). Builds on 5 of its 39 references that are in the map. First posted on arXiv 18 Jun 2024.
Builds on
5 of 39 references.
References · 5
- 2022MACE: Higher Order Equivariant Message Passing Neural Networks for Fast and Accurate Force Fieldscited by 474
- 2022Learning Local Equivariant Representations for Large-Scale Atomistic Dynamicscited by 256
- 2021SpookyNet: Learning Force Fields with Electronic Degrees of Freedom and Nonlocal Effectscited by 104
- 2022SPICE, A Dataset of Drug-like Molecules and Peptides for Training Machine Learning Potentialscited by 82
- 2023TensorNet: Cartesian Tensor Representations for Efficient Learning of Molecular Potentialscited by 54
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Citing papers per year: 2024: 1; 2025: 4; 2026: 2.
7 papers.
- 2025Learning Smooth and Expressive Interatomic Potentials for Physical Property Predictioncited by 84
- 2025High-performance training and inference for deep equivariant interatomic potentialscited by 17
- 2024On the design space between molecular mechanics and machine learning force fieldscited by 4
- 2025Training Dynamics of Learning 3D-Rotational Equivariancecited by 1
- 2026Faster Molecular Dynamics with Neural Network Potentials via Distilled Multiple Time-Stepping and Non-Conservative Forcescited by 1
- 2025Performance of universal machine-learned potentials with explicit long-range interactions in biomolecular simulationscited by 0
- 2026Transferable Implicit Solvent Machine Learning Potential for Drugs and Proteins Approaching Ab Initio Accuracycited by 0
- 2026Transferable Implicit Solvent Machine Learning Potential for Drugs and Proteins Approaching Ab Initio Accuracy12 Jul 2026
- 2026Faster Molecular Dynamics with Neural Network Potentials via Distilled Multiple Time-Stepping and Non-Conservative Forces16 Feb 2026
- 2025Training Dynamics of Learning 3D-Rotational Equivariance2 Dec 2025
- 2025Performance of universal machine-learned potentials with explicit long-range interactions in biomolecular simulations14 Aug 2025
- 2025High-performance training and inference for deep equivariant interatomic potentials22 Apr 2025
- 2025Learning Smooth and Expressive Interatomic Potentials for Physical Property Prediction17 Feb 2025
- 2024On the design space between molecular mechanics and machine learning force fields3 Sep 2024