Evidence map›Paper›PMID 37973874›Full record

ArticleNature communications2023

ProRefiner: an entropy-based refining strategy for inverse protein folding with global graph attention.

Xinyi Zhou, Guangyong Chen, Junjie Ye, Ercheng Wang, Jun Zhang, Cong Mao, Zhanwei Li, Jianye Hao, Xingxu Huang, Jin Tang and 1 more

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 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
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  5. Review
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  8. Review
  9. Computational tools for plant genomics and breeding.Science China. Life sciences · 2024
    Review
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  12. Article
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

11 authors.

Xinyi ZhouDepartment of Computer Science and Engineering, The Chinese University of Hong Kong, Central Ave, Hong Kong, China.ORCID 0000-0002-1574-4913
Guangyong ChenZhejiang Lab, Kechuang Avenue, Hangzhou, China. gychen@zhejianglab.com.ORCID 0000-0002-5892-8608
Junjie YeNoah's Ark Lab, Huawei, Shenzhen, China.
Ercheng WangZhejiang Lab, Kechuang Avenue, Hangzhou, China.
Jun ZhangState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.ORCID 0000-0002-7630-8162
Cong MaoState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Zhanwei LiZhejiang Lab, Kechuang Avenue, Hangzhou, China.
Jianye HaoNoah's Ark Lab, Huawei, Shenzhen, China.
Xingxu HuangZhejiang Lab, Kechuang Avenue, Hangzhou, China.
Jin TangZhejiang Lab, Kechuang Avenue, Hangzhou, China.
Pheng Ann HengDepartment of Computer Science and Engineering, The Chinese University of Hong Kong, Central Ave, Hong Kong, China.

Funding

National Natural Science Foundation of China (National Science Foundation of China) 22007082National Natural Science Foundation of China (National Science Foundation of China) 62006219National Natural Science Foundation of China (National Science Foundation of China) 62376254Natural Science Foundation of Guangdong Province (Guangdong Natural Science Foundation) 2022A1515011579Natural Science Foundation of Zhejiang Province (Zhejiang Provincial Natural Science Foundation) LQ21B030013
6 · The paper itself

Abstract

Inverse Protein Folding (IPF) is an important task of protein design, which aims to design sequences compatible with a given backbone structure. Despite the prosperous development of algorithms for this task, existing methods tend to rely on noisy predicted residues located in the local neighborhood when generating sequences. To address this limitation, we propose an entropy-based residue selection method to remove noise in the input residue context. Additionally, we introduce ProRefiner, a memory-efficient global graph attention model to fully utilize the denoised context. Our proposed method achieves state-of-the-art performance on multiple sequence design benchmarks in different design settings. Furthermore, we demonstrate the applicability of ProRefiner in redesigning Transposon-associated transposase B, where six out of the 20 variants we propose exhibit improved gene editing activity.

Indexed as

AlgorithmsProteinsEntropyProtein FoldingProteins

Identifiers

PMID37973874
PMCPMC10654420

What OpenQuestion holds

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Registered trials

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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.