In vitro selection of macrocyclic peptide inhibitors containing cyclic γ2,4-amino acids targeting the SARS-CoV-2 main protease
γ-Amino acids can play important roles in the biological activities of natural products; however, ribosomal incorporation of γ-amino acids into peptides is challenging. Here we report how a selection campaign employing a non-canonical peptide library containing cyclic γ2,4-amino acids (cγAAs) result...
Egile Nagusiak: | Miura, T, Malla, TR, Owen, D, Tumber, A, Brewitz, L, McDonough, M, Salah, E, Terasaka, N, Katoh, T, Lukacik, P, Strain-Damerell, C, Mikolajek, H, Walsh, M, Kawamura, A, Schofield, C, Suga, H |
---|---|
Formatua: | Journal article |
Hizkuntza: | English |
Argitaratua: |
Springer Nature
2023
|
Antzeko izenburuak
-
Penicillin derivatives inhibit the SARS-CoV-2 main protease by reaction with its nucleophilic cysteine
nork: Malla, TR, et al.
Argitaratua: (2022) -
Studies on the selectivity of the SARS-CoV-2 papain-like protease reveal the importance of the P2' proline of the viral polyprotein
nork: Chan, HTH, et al.
Argitaratua: (2023) -
Mass spectrometric assays reveal discrepancies in inhibition profiles for the SARS-CoV-2 papain-like protease
nork: Brewitz, L, et al.
Argitaratua: (2022) -
Mass spectrometric assays monitoring the deubiquitinase activity of the SARS-CoV-2 papain-like protease inform on the basis of substrate selectivity and have utility for substrate identification
nork: Brewitz, L, et al.
Argitaratua: (2023) -
Mass spectrometry reveals potential of β-lactams as SARS-CoV-2 Mpro inhibitors.
nork: Malla, TR, et al.
Argitaratua: (2021)