Search research articles
Contact Us
Filters
Showing results (11-20 of 29) with videos related to
Page
of 3
Sort By:
Journal of Structural Biology: X
|
August 4, 2020
<i>In crystallo</i>-screening for discovery of human norovirus 3C-like protease inhibitors
Jingxu Guo, Alice Douangamath, Weixiao Song, et al.
RSC Chemical Biology
|
August 17, 2022
Discovery of novel druggable pockets on polyomavirus VP1 through crystallographic fragment-based screening to develop capsid assembly inhibitors
Evgenii M Osipov, Ali H Munawar, Steven Beelen, et al.
Molecular Cell
|
November 28, 2002
Topography for independent binding of alpha-helical and PPII-helical ligands to a peroxisomal SH3 domain
Alice Douangamath, Fabian V Filipp, André T J Klein, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications
|
November 30, 2012
Structure of ribose 5-phosphate isomerase from the probiotic bacterium Lactobacillus salivarius UCC118
Carina M C Lobley, Pierre Aller, Alice Douangamath, et al.
Nature Communications
|
August 12, 2021
Structure, mechanism and crystallographic fragment screening of the SARS-CoV-2 NSP13 helicase
Joseph A Newman, Alice Douangamath, Setayesh Yadzani, et al.
Elife
|
March 7, 2023
Room-temperature crystallography reveals altered binding of small-molecule fragments to PTP1B
Tamar Skaist Mehlman, Justin T Biel, Syeda Maryam Azeem, et al.
Journal of Visualized Experiments : Jove
|
June 14, 2021
Achieving Efficient Fragment Screening at XChem Facility at Diamond Light Source
Alice Douangamath, Ailsa Powell, Daren Fearon, et al.
Journal of Medicinal Chemistry
|
March 5, 2004
Crystal structures of Staphylococcusaureus methionine aminopeptidase complexed with keto heterocycle and aminoketone inhibitors reveal the formation of a tetrahedral intermediate
Alice Douangamath, Glenn E Dale, Allan D'Arcy, et al.
Cell Chemical Biology
|
June 26, 2021
An automatic pipeline for the design of irreversible derivatives identifies a potent SARS-CoV-2 M<sup>pro</sup> inhibitor
Daniel Zaidman, Paul Gehrtz, Mihajlo Filep, et al.
European Journal of Medicinal Chemistry
|
October 26, 2024
Rational fragment-based design of compounds targeting the PWWP domain of the HRP family
Thibault Vantieghem, Nayyar A Aslam, Evgenii M Osipov, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
Journal of Structural Biology: X
|
August 4, 2020
<i>In crystallo</i>-screening for discovery of human norovirus 3C-like protease inhibitors
Jingxu Guo, Alice Douangamath, Weixiao Song, et al.
RSC Chemical Biology
|
August 17, 2022
Discovery of novel druggable pockets on polyomavirus VP1 through crystallographic fragment-based screening to develop capsid assembly inhibitors
Evgenii M Osipov, Ali H Munawar, Steven Beelen, et al.
Molecular Cell
|
November 28, 2002
Topography for independent binding of alpha-helical and PPII-helical ligands to a peroxisomal SH3 domain
Alice Douangamath, Fabian V Filipp, André T J Klein, et al.
Acta Crystallographica. Section F, Structural Biology and Crystallization Communications
|
November 30, 2012
Structure of ribose 5-phosphate isomerase from the probiotic bacterium Lactobacillus salivarius UCC118
Carina M C Lobley, Pierre Aller, Alice Douangamath, et al.
Nature Communications
|
August 12, 2021
Structure, mechanism and crystallographic fragment screening of the SARS-CoV-2 NSP13 helicase
Joseph A Newman, Alice Douangamath, Setayesh Yadzani, et al.
Elife
|
March 7, 2023
Room-temperature crystallography reveals altered binding of small-molecule fragments to PTP1B
Tamar Skaist Mehlman, Justin T Biel, Syeda Maryam Azeem, et al.
Journal of Visualized Experiments : Jove
|
June 14, 2021
Achieving Efficient Fragment Screening at XChem Facility at Diamond Light Source
Alice Douangamath, Ailsa Powell, Daren Fearon, et al.
Journal of Medicinal Chemistry
|
March 5, 2004
Crystal structures of Staphylococcusaureus methionine aminopeptidase complexed with keto heterocycle and aminoketone inhibitors reveal the formation of a tetrahedral intermediate
Alice Douangamath, Glenn E Dale, Allan D'Arcy, et al.
Cell Chemical Biology
|
June 26, 2021
An automatic pipeline for the design of irreversible derivatives identifies a potent SARS-CoV-2 M<sup>pro</sup> inhibitor
Daniel Zaidman, Paul Gehrtz, Mihajlo Filep, et al.
European Journal of Medicinal Chemistry
|
October 26, 2024
Rational fragment-based design of compounds targeting the PWWP domain of the HRP family
Thibault Vantieghem, Nayyar A Aslam, Evgenii M Osipov, et al.
Page
of 3