Accelerating drug target inhibitor discovery with a deep generative foundation model.
Chenthamarakshan V. et al, (2023), Science advances, 9
Reduced neutralization of SARS-CoV-2 B.1.617 by vaccine and convalescent serum
Liu C. et al, (2021), Cell, 184, 4220 - 4236.e13
Evidence of escape of SARS-CoV-2 variant B.1.351 from natural and vaccine-induced sera
Zhou D. et al, (2021), Cell, 184, 2348 - 2361.e6
Reduced neutralization of SARS-CoV-2 B.1.1.7 variant by convalescent and vaccine sera
Supasa P. et al, (2021), Cell, 184, 2201 - 2211.e7
The antigenic anatomy of SARS-CoV-2 receptor binding domain
Dejnirattisai W. et al, (2021), Cell, 184, 2183 - 2200.e22
Glutathione facilitates enterovirus assembly by binding at a druggable pocket.
Duyvesteyn HME. et al, (2020), Communications biology, 3
Glutathione facilitates enterovirus assembly by binding at a druggable pocket.
Duyvesteyn HME. et al, (2020), Communications biology, 3
Phage G Structure at 6.1 Å Resolution, Condensed DNA, and Host Identity Revision to a Lysinibacillus
González B. et al, (2020), Journal of Molecular Biology
A structural basis for antibody-mediated neutralization of Nipah virus reveals a site of vulnerability at the fusion glycoprotein apex.
Avanzato VA. et al, (2019), Proceedings of the National Academy of Sciences of the United States of America, 116, 25057 - 25067
Assembly of complex viruses exemplified by a halophilic euryarchaeal virus
De Colibus L. et al, (2019), Nature Communications, 10
The structure of a prokaryotic viral envelope protein expands the landscape of membrane fusion proteins
El Omari K. et al, (2019), Nature Communications, 10
Author Correction: Pathogen-derived HLA-E bound epitopes reveal broad primary anchor pocket tolerability and conformationally malleable peptide binding
Walters LC. et al, (2018), Nature Communications, 9
Pathogen-derived HLA-E bound epitopes reveal broad primary anchor pocket tolerability and conformationally malleable peptide binding
Walters LC. et al, (2018), Nature Communications, 9
Near-atomic structure of Japanese encephalitis virus reveals critical determinants of virulence and stability
Wang X. et al, (2017), Nature Communications, 8
High-speed fixed-target serial virus crystallography
Roedig P. et al, (2017), Nature Methods, 14, 805 - 810
Potent neutralization of hepatitis A virus reveals a receptor mimic mechanism and the receptor recognition site
Wang X. et al, (2017), Proceedings of the National Academy of Sciences, 114, 770 - 775
Structure of human Aichi virus and implications for receptor binding
Zhu L. et al, (2016), Nature Microbiology, 1
The crystal structure of human dopamine β-hydroxylase at 2.9 Å resolution
Vendelboe TV. et al, (2016), Science Advances, 2
A RANKL mutant used as an inter-species vaccine for efficient immunotherapy of osteoporosis
Liu C. et al, (2015), Scientific Reports, 5