Evidence map›Paper›PMID 32227201›Full record

ArticleBioinformatics (Oxford, England)2020

FUpred: detecting protein domains through deep-learning-based contact map prediction.

Wei Zheng, Xiaogen Zhou, Qiqige Wuyun, Robin Pearce, Yang Li, Yang Zhang

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

34 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  9. Semi-supervised segmentation of RNA 3D structures using density-based clustering.Computational and structural biotechnology journal · 2025
    Article
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  12. Recent Progress of Protein Tertiary Structure Prediction.Molecules (Basel, Switzerland) · 2024
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Wei ZhengDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI 48109.
Xiaogen ZhouDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI 48109.
Qiqige WuyunComputer Science and Engineering Department, Michigan State University, East Lansing, MI 48824, USA.
Robin PearceDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI 48109.
Yang LiDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI 48109.
Yang ZhangDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI 48109.

Funding

Structure-based functional annotation of microbial genomesR01AI134678 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Lydia Petra Freddolino, SCOTT J. HULTGREN · 2018 to 2026
$6.5M
I-TASSER based atomic-level protein structure predictionR01GM083107 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHANG, YANG · 2008 to 2019
$3.5M
Template-based docking refinement approach to protein-protein structure modelingR01GM116960 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHANG, YANG · 2016 to 2019
$1.4M
Advanced approaches to protein structure predictionR35GM136422 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHANG, YANG · 2020 to 2021
$946k
NIAID NIH HHS R01 AI134678NIGMS NIH HHS R01 GM083107NIGMS NIH HHS R01 GM116960NIGMS NIH HHS R35 GM136422
6 · The paper itself

Abstract

motivationProtein domains are subunits that can fold and function independently. Correct domain boundary assignment is thus a critical step toward accurate protein structure and function analyses. There is, however, no efficient algorithm available for accurate domain prediction from sequence. The problem is particularly challenging for proteins with discontinuous domains, which consist of domain segments that are separated along the sequence.

resultsWe developed a new algorithm, FUpred, which predicts protein domain boundaries utilizing contact maps created by deep residual neural networks coupled with coevolutionary precision matrices. The core idea of the algorithm is to retrieve domain boundary locations by maximizing the number of intra-domain contacts, while minimizing the number of inter-domain contacts from the contact maps. FUpred was tested on a large-scale dataset consisting of 2549 proteins and generated correct single- and multi-domain classifications with a Matthew's correlation coefficient of 0.799, which was 19.1% (or 5.3%) higher than the best machine learning (or threading)-based method. For proteins with discontinuous domains, the domain boundary detection and normalized domain overlapping scores of FUpred were 0.788 and 0.521, respectively, which were 17.3% and 23.8% higher than the best control method. The results demonstrate a new avenue to accurately detect domain composition from sequence alone, especially for discontinuous, multi-domain proteins. AVAILABILITY AND IMPLEMENTATION: https://zhanglab.ccmb.med.umich.edu/FUpred. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Deep LearningAlgorithmsComputational BiologyNeural Networks, ComputerProtein DomainsSoftware

Identifiers

PMID32227201
PMCPMC7320627

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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.