Zheng Ruan

Zheng Ruan

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Zheng Ruan

Department of Structural Biology, Van Andel Institute, Grand Rapids, USA

Research Focus & Metrics

Academic Career Length

16Years (2011-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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3 June 2020 in Nature
Verified
Journal Article
Closed access
PDF file
ZRZheng Ruan
Zheng Ruan
IOIan J. Orozco
Ian J. Orozco
JDJuan Du
Juan Du
WLWei Lü
Wei Lü

1 August 2016 in Molecular Cell
Verified
Journal Article
Closed access
JSJonathan A. Stefely
Jonathan A. Stefely
FLFloriana Licitra
Floriana Licitra
LLLeila Laredj
Leila Laredj
ARAndrew G. Reidenbach
Andrew G. Reidenbach
ZKZachary A. Kemmerer
Zachary A. Kemmerer
DPDavid J. Pagliarini
David J. Pagliarini

9 May 2013 in Nucleic Acids Research
Verified
Journal Article
Open access
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TSTimothy I Shaw
Timothy I Shaw
ZRZheng Ruan
Zheng Ruan
TGTravis C. Glenn
Travis C. Glenn
LLLiang Liu
Liang Liu
The coalescent methods for species tree reconstruction are increasingly popular because they can accommodate coalescence and multilocus data sets. Herein, we present STRAW, a web server that offers workflows for reconstruction of phylogenies of species using three species tree methods—MP-EST, STAR and NJst. The input data are a collection of rooted gene trees (for STAR and MP-EST methods) or unrooted gene trees (for NJst). The output includes the estimated species tree, modified Robinson-Foulds distances between gene trees and the estimated species tree and visualization of trees to compare gene trees with the estimated species tree. The web sever is available at http://bioinformatics.publichealth.uga.edu/SpeciesTreeAnalysis/.

4 November 2020 in Nature
Verified
Journal Article
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ZRZheng Ruan
Zheng Ruan
JOJames Osei-Owusu
James Osei-Owusu
JDJuan Du
Juan Du
ZQZhaozhu Qiu
Zhaozhu Qiu
WLWei Lü
Wei Lü

24 June 2021 in Nature Structural & Molecular Biology
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Journal Article
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ZRZheng Ruan
Zheng Ruan
Emery HaleyEmery Haley
Emery Haley
IOIan J. Orozco
Ian J. Orozco
MSMark Sabat
Mark Sabat
RMRichard Myers
Richard Myers
WLWei Lü
Wei Lü

13 August 2018 in Proceedings of the National Academy of Sciences
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Journal Article
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ZRZheng Ruan
Zheng Ruan
NKNatarajan Kannan
Natarajan Kannan
Significance: The α C– β 4 loop is a conserved structural motif present in all eukaryotic protein kinases. This study focuses on epidermal growth factor receptor (EGFR), a receptor tyrosine kinase that harbors many recurrent insertion mutations in the α C– β 4 loop. We show that EGFR activity and drug sensitivity are strongly dependent on the nature, size, and location of mutations in the loop and that even subtle variations in the loop have a dramatic effect on kinase dynamics and free-energy landscape. These findings inform ongoing drug-discovery efforts on EGFR kinases and provide a structural framework for investigating the role of the understudied α C– β 4 loop in kinase regulation, dynamics, and evolution.