- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
In: Proteins: Structure, Function, and Bioinformatics 91.11 (2023). DOI:10.1002/prot.26543
In: Proteins: Structure, Function, and Bioinformatics 91 : 11 John Wiley & Sons, Inc., 2023-07-05 - S. 1496-1509
- Ereignis
-
Veröffentlichung
- (wo)
-
Erlangen
- (wer)
-
Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
- (wann)
-
2023
- Urheber
-
Chen, Xiyu
Leyendecker, Sigrid
van den Bedem, Henry
- DOI
-
10.1002/prot.26543
- URN
-
urn:nbn:de:101:1-2024030104074297837961
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:56 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Chen, Xiyu
- Leyendecker, Sigrid
- van den Bedem, Henry
- Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
Entstanden
- 2023
Ähnliche Objekte (12)
The H163A mutation unravels an oxidized conformation of the SARS-CoV-2 main protease
Allostery in homodimeric SARS-CoV-2 main protease
α-Ketoamide Inhibitors of SARS-CoV-2 Main Protease
Statine-based peptidomimetic compounds as inhibitors for SARS-CoV-2 main protease (SARS-CoV‑2 Mpro)
SARS‐CoV‐2 Papain‐Like Protease: Structure, Function and Inhibition
Inhibitor induced conformational changes in SARS-COV-2 papain-like protease
Crystal structure of SARS-CoV-2 main protease in complex with protease inhibitor PF-07321332
Analysis of the efficacy of HIV protease inhibitors against SARS-CoV-2′s main protease
Structure-activity relationships of benzamides and isoindolines designed as SARS-CoV protease inhibitors effective against SARS-CoV-2
Structure‐Activity Relationships of Benzamides and Isoindolines Designed as SARS‐CoV Protease Inhibitors Effective against SARS‐CoV‐2
Oridonin Inhibits SARS‐CoV‐2 by Targeting Its 3C‐Like Protease
Oridonin Inhibits SARS‐CoV‐2 by Targeting Its 3C‐Like Protease
The H163A mutation unravels an oxidized conformation of the SARS-CoV-2 main protease
Allostery in homodimeric SARS-CoV-2 main protease
α-Ketoamide Inhibitors of SARS-CoV-2 Main Protease
Statine-based peptidomimetic compounds as inhibitors for SARS-CoV-2 main protease (SARS-CoV‑2 Mpro)
SARS‐CoV‐2 Papain‐Like Protease: Structure, Function and Inhibition
Inhibitor induced conformational changes in SARS-COV-2 papain-like protease
Crystal structure of SARS-CoV-2 main protease in complex with protease inhibitor PF-07321332
Analysis of the efficacy of HIV protease inhibitors against SARS-CoV-2′s main protease
Structure-activity relationships of benzamides and isoindolines designed as SARS-CoV protease inhibitors effective against SARS-CoV-2
Structure‐Activity Relationships of Benzamides and Isoindolines Designed as SARS‐CoV Protease Inhibitors Effective against SARS‐CoV‐2
Oridonin Inhibits SARS‐CoV‐2 by Targeting Its 3C‐Like Protease
Oridonin Inhibits SARS‐CoV‐2 by Targeting Its 3C‐Like Protease
The H163A mutation unravels an oxidized conformation of the SARS-CoV-2 main protease
Allostery in homodimeric SARS-CoV-2 main protease
α-Ketoamide Inhibitors of SARS-CoV-2 Main Protease
Statine-based peptidomimetic compounds as inhibitors for SARS-CoV-2 main protease (SARS-CoV‑2 Mpro)
SARS‐CoV‐2 Papain‐Like Protease: Structure, Function and Inhibition
Inhibitor induced conformational changes in SARS-COV-2 papain-like protease
Crystal structure of SARS-CoV-2 main protease in complex with protease inhibitor PF-07321332
Analysis of the efficacy of HIV protease inhibitors against SARS-CoV-2′s main protease
Structure-activity relationships of benzamides and isoindolines designed as SARS-CoV protease inhibitors effective against SARS-CoV-2
Structure‐Activity Relationships of Benzamides and Isoindolines Designed as SARS‐CoV Protease Inhibitors Effective against SARS‐CoV‐2
Oridonin Inhibits SARS‐CoV‐2 by Targeting Its 3C‐Like Protease