lociPARSE: A Locality-aware Invariant Point Attention Model for Scoring RNA 3D Structures

A scoring function that can reliably assess the accuracy of a 3D RNA structural model in the absence of experimental structure is not only important for model evaluation and selection but also useful for scoring-guided conformational sampling. However, high-fidelity RNA scoring has proven to be difficult using conventional knowledge-based statistical potentials and currently available machine learning-based approaches. Here, we present lociPARSE, a locality-aware invariant point attention architecture for scoring RNA 3D structures. Unlike existing machine learning methods that estimate superposition-based root-mean-square deviation (RMSD), lociPARSE estimates Local Distance Difference Test (lDDT) scores capturing the accuracy of each nucleotide and its surrounding local atomic environment in a superposition-free manner, before aggregating information to predict global structural accuracy. Tested on multiple datasets including CASP15, lociPARSE significantly outperforms existing statistical potentials (rsRNASP, cgRNASP, DFIRE-RNA, and RASP) and machine learning methods (ARES and RNA3DCNN) across complementary assessment metrics. lociPARSE is freely available at https://github.com/Bhattacharya-Lab/lociPARSE.

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Publication Details

Journal
Journal of Chemical Information and Modeling
Published
2024-11-11
DOI
https://doi.org/10.1021/acs.jcim.4c01621
Citations
9
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
2.10

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article

lociPARSE: A Locality-aware Invariant Point Attention Model for Scoring RNA 3D Structures

Debswapna Bhattacharya, Sumit Tarafder
9 citations
Journal of Chemical Information and Modeling
RNA and protein synthesis mechanisms
2.10
article

lociPARSE: A Locality-aware Invariant Point Attention Model for Scoring RNA 3D Structures

Debswapna Bhattacharya, Sumit Tarafder
article en
9 citations

Abstract

A scoring function that can reliably assess the accuracy of a 3D RNA structural model in the absence of experimental structure is not only important for model evaluation and selection but also useful for scoring-guided conformational sampling. However, high-fidelity RNA scoring has proven to be difficult using conventional knowledge-based statistical potentials and currently available machine learning-based approaches. Here, we present lociPARSE, a locality-aware invariant point attention architecture for scoring RNA 3D structures. Unlike existing machine learning methods that estimate superposition-based root-mean-square deviation (RMSD), lociPARSE estimates Local Distance Difference Test (lDDT) scores capturing the accuracy of each nucleotide and its surrounding local atomic environment in a superposition-free manner, before aggregating information to predict global structural accuracy. Tested on multiple datasets including CASP15, lociPARSE significantly outperforms existing statistical potentials (rsRNASP, cgRNASP, DFIRE-RNA, and RASP) and machine learning methods (ARES and RNA3DCNN) across complementary assessment metrics. lociPARSE is freely available at https://github.com/Bhattacharya-Lab/lociPARSE.

Journal of Chemical Information and ModelingVol. 64(22)
Virginia Tech (US)
National Institute of General Medical Sciences, Division of Biological Infrastructure
Openalex Percentile: Top 12%
RNA and protein synthesis mechanisms
2.10
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