All-Atom Simulations Uncover Structural and Dynamical Properties of STING Proteins in the Membrane System
Author:
Affiliation:
1. Boston University, Boston, Massachusetts02215, United States
2. Lawrence Berkeley National Laboratory, Berkeley, California94720, United States
3. Department of Chemistry, Fort Hays State University, Hays, Kansas67601, United States
Funder
Workforce Development for Teachers and Scientists
National Institutes of Health
National Institute of General Medical Sciences
Lawrence Berkeley National Laboratory
Sustainable Horizons Institute
Publisher
American Chemical Society (ACS)
Subject
Library and Information Sciences,Computer Science Applications,General Chemical Engineering,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jcim.2c00595
Reference50 articles.
1. Modular Architecture of the STING C-Terminal Tail Allows Interferon and NF-κB Signaling Adaptation
2. Structural basis of STING binding with and phosphorylation by TBK1
3. The triggers of the cGAS-STING pathway and the connection with inflammatory and autoimmune diseases
4. Cryo-EM structures of STING reveal its mechanism of activation by cyclic GMP–AMP
5. Cyclic di-GMP Sensing via the Innate Immune Signaling Protein STING
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