Evidence map›Paper›PMID 36828844›Full record

ArticleNature communications2023

Evaluating native-like structures of RNA-protein complexes through the deep learning method.

Chengwei Zeng, Yiren Jian, Soroush Vosoughi, Chen Zeng, Yunjie Zhao

Abstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Chengwei Zeng *Institute of Biophysics and Department of Physics, Central China Normal University, Wuhan, 430079, China.
Yiren Jian *Department of Computer Science, Dartmouth College, Hanover, NH, 03755, USA.
Soroush VosoughiDepartment of Computer Science, Dartmouth College, Hanover, NH, 03755, USA.
Chen ZengDepartment of Physics, The George Washington University, Washington, DC, 20052, USA.ORCID 0000-0001-7778-6388
Yunjie ZhaoInstitute of Biophysics and Department of Physics, Central China Normal University, Wuhan, 430079, China. yjzhaowh@mail.ccnu.edu.cn.ORCID 0000-0002-5256-9456

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA-protein complexes underlie numerous cellular processes, including basic translation and gene regulation. The high-resolution structure determination of the RNA-protein complexes is essential for elucidating their functions. Therefore, computational methods capable of identifying the native-like RNA-protein structures are needed. To address this challenge, we thus develop DRPScore, a deep-learning-based approach for identifying native-like RNA-protein structures. DRPScore is tested on representative sets of RNA-protein complexes with various degrees of binding-induced conformation change ranging from fully rigid docking (bound-bound) to fully flexible docking (unbound-unbound). Out of the top 20 predictions, DRPScore selects native-like structures with a success rate of 91.67% on the testing set of bound RNA-protein complexes and 56.14% on the unbound complexes. DRPScore consistently outperforms existing methods with a roughly 10.53-15.79% improvement, even for the most difficult unbound cases. Furthermore, DRPScore significantly improves the accuracy of the native interface interaction predictions. DRPScore should be broadly useful for modeling and designing RNA-protein complexes.

Indexed as

Deep LearningAlgorithmsModels, MolecularMolecular Docking SimulationProtein BindingProtein ConformationProteinsRNAProteinsRNA

Identifiers

PMID36828844
PMCPMC9958188

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.