Local Geometry Recovers but Cooperative Structure Does Not: Residue-Resolved Limits of All-Atom Reconstruction from...

Intrinsically disordered proteins (IDPs) drive diverse cellular processes through broad conformational ensembles, but experimental characterization of these ensembles is sparse and high-quality training data is scarce, holding back artificial intelligence (AI) approaches to ensemble prediction. Single-bead coarse-grained (CG) force fields such as CALVADOS, parametrized directly against experimental observables, currently provide a more reliable route to disordered ensembles than direct AI prediction. CG sampling lacks atomistic resolution and must be paired with backmapping; the atomistic information recoverable from this two-step process is shaped jointly by the CG representation and the backmapping algorithm, and the interplay between these contributions is not well characterized. We benchmarked CODLAD, a recently published latent-diffusion backmapping pipeline, on 23 Protein Ensemble Database (PED) systems using a dual-input design: the same architecture receives either PED-reference Cα coordinates or independently sampled CALVADOS Cα trajectories. This design separates paired reconstruction error, measurable for PED+CODLAD, from unpaired CG-input-associated ensemble deviations, measurable for CG+CODLAD at the distribution level. Reconstruction from PED conformers achieved 0.56 ± 0.08 Å backbone root-mean-square deviation and preserved local geometry. Reconstruction from CALVADOS-sampled Cα trajectories preserved the Cα framework and bond geometry, while ensemble-level deviations relative to PED were localized to proline backbone geometry and cooperative secondary structure, both consistent with information not carried by an unconstrained single-bead representation. The benchmark quantifies which atomistic properties can be recovered after projecting a CG ensemble into all-atom space and identifies improved CG geometric encoding and sequence-conditioned AI priors as the directions for further progress.