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Ron O. Dror

Stanford University · US
Area of research
Molecular Biology · Cellular and Molecular Neuroscience
Research interest
Research interests include Receptor Mechanisms and Signaling, Protein Structure and Dynamics, Neuropeptides and Animal Physiology, and Computational Drug Discovery Methods.
h-index
93
citations
48,899
works
363
NIH funding
primary concept
Chemistry
email

Recent publications

RNA-Puzzles Round V: blind predictions of 23 RNA structures
Nature Methods 2024cited by 59position: middledoi
GPR161 structure uncovers the redundant role of sterol-regulated ciliary cAMP signaling in the Hedgehog pathway
Nature Structural & Molecular Biology 2024cited by 35position: middledoi
A positively tuned voltage indicator for extended electrical recordings in the brain
Nature Methods 2023cited by 83position: middledoi
Structural basis for ion selectivity in potassium-selective channelrhodopsins
Cell 2023cited by 52position: middledoi
Signaling snapshots of a serotonin receptor activated by the prototypical psychedelic LSD
Neuron 2022cited by 151position: middledoi
Structural basis for channel conduction in the pump-like channelrhodopsin ChRmine
Cell 2022cited by 146position: middledoi
Autoantibody mimicry of hormone action at the thyrotropin receptor
Nature 2022cited by 57position: middledoi
Atypical structural snapshots of human cytomegalovirus GPCR interactions with host G proteins
Science Advances 2022cited by 41position: middledoi
Simple biochemical features underlie transcriptional activation domain diversity and dynamic, fuzzy binding to Mediator
eLife 2021cited by 188position: middledoi
Structure and mechanism of the SGLT family of glucose transporters
Nature 2021cited by 142position: middledoi
Selective G protein signaling driven by substance P–neurokinin receptor dynamics
Nature Chemical Biology 2021cited by 93position: middledoi
Leveraging nonstructural data to predict structures and affinities of protein–ligand complexes
Proceedings of the National Academy of Sciences 2021cited by 38position: lastdoi
A positively Tuned Voltage Indicator Reveals Electrical Correlates of Calcium Activity in the Brain
bioRxiv (Cold Spring Harbor Laboratory) 2021cited by 14position: middledoi
Structure of hepcidin-bound ferroportin reveals iron homeostatic mechanisms
Nature 2020cited by 333position: middledoi
Angiotensin and biased analogs induce structurally distinct active conformations within a GPCR
Science 2020cited by 246position: middledoi
Molecular mechanism of biased signaling in a prototypical G protein–coupled receptor
Science 2020cited by 240position: lastdoi
Structure of a Signaling Cannabinoid Receptor 1-G Protein Complex
Cell 2019cited by 445position: middledoi
Angiotensin Analogs with Divergent Bias Stabilize Distinct Receptor Conformations
Cell 2019cited by 290position: middledoi
Smoothened stimulation by membrane sterols drives Hedgehog pathway activity
Nature 2019cited by 207position: middledoi
Molecular Dynamics Simulation for All
Neuron 2018cited by 2,954position: lastdoi
Structure of the µ-opioid receptor–Gi protein complex
Nature 2018cited by 684position: middledoi
Catalytic activation of β-arrestin by GPCRs
Nature 2018cited by 222position: middledoi
Structural insights into binding specificity, efficacy and bias of a β2AR partial agonist
Nature Chemical Biology 2018cited by 201position: middledoi
Crystal structure of the natural anion-conducting channelrhodopsin GtACR1
Nature 2018cited by 123position: middledoi
Structural mechanisms of selectivity and gating in anion channelrhodopsins
Nature 2018cited by 93position: middledoi
G<sub>i</sub>- and G<sub>s</sub>-coupled GPCRs show different modes of G-protein binding
Proceedings of the National Academy of Sciences 2018cited by 76position: middledoi
Crystal Structure of an LSD-Bound Human Serotonin Receptor
Cell 2017cited by 461position: middledoi
Identification of Phosphorylation Codes for Arrestin Recruitment by G Protein-Coupled Receptors
Cell 2017cited by 451position: middledoi
D<sub>4</sub>dopamine receptor high-resolution structures enable the discovery of selective agonists
Science 2017cited by 247position: middledoi
Mechanism of intracellular allosteric β2AR antagonist revealed by X-ray crystal structure
Nature 2017cited by 205position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Brian K. Kobilka · Stanford University12 papers (2012–2022)Naomi R. Latorraca · University of California, Berkeley10 papers (2017–2020)Aashish Manglik · Chan Zuckerberg Initiative (United States)9 papers (2013–2024)Carl‐Mikael Suomivuori · Technical University of Munich7 papers (2020–2024)William I. Weis · Stanford University6 papers (2012–2019)David E. Shaw · D. E. Shaw Research5 papers (2012–2018) · 5 papers (2015–2017)Daniel Hilger · Ludwig-Maximilians-Universität München5 papers (2015–2019) · 5 papers (2015–2022)Georgios Skiniotis · Stanford Medicine5 papers (2018–2022)Robert J. Lefkowitz · Howard Hughes Medical Institute4 papers (2017–2020)Joseph M. Paggi · Massachusetts Institute of Technology4 papers (2018–2021)Bryan L. Roth · University of North Carolina at Chapel Hill4 papers (2017–2022)Wayne L. Hubbell · Doheny Eye Institute4 papers (2015–2019)Scott A. Hollingsworth · NovaBay Pharmaceuticals (United States)4 papers (2018–2021)Ouliana Panova · Stanford University3 papers (2021–2022)Andrew C. Kruse · Harvard University3 papers (2016–2020)Daniel H. Arlow · University of California, Berkeley3 papers (2012–2015)Dean P. Staus · Duke University3 papers (2019–2020)Michael J. Robertson · Indiana University Health3 papers (2019–2022)