Open Access Article
This Open Access Article is licensed under a Creative Commons Attribution 3.0 Unported Licence
Correction: Synthetic ramoplanin analogues are accessible by effective incorporation of arylglycines in solid-phase peptide synthesis
Edward
Marschall
abc,
Rachel W.
Cass
abc,
Komal M.
Prasad
abc,
James D.
Swarbrick
d,
Alasdair I.
McKay
e,
Jennifer A. E.
Payne
abc,
Max J.
Cryle
*abc and
Julien
Tailhades
*abc
aDepartment of Biochemistry and Molecular Biology, The Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia. E-mail: max.cryle@monash.edu; julien.tailhades@monash.edu
bEMBL Australia, Monash University, Clayton, VIC 3800, Australia
cARC Centre of Excellence for Innovations in Peptide and Protein Science, Clayton, VIC 3800, Australia
dDepartment of Microbiology, Monash University, Clayton, VIC 3800, Australia
eDepartment of Chemistry, Monash University, Clayton, VIC 3800, Australia
First published on 4th January 2024
Abstract
Correction for ‘Synthetic ramoplanin analogues are accessible by effective incorporation of arylglycines in solid-phase peptide synthesis’ by Edward Marschall et al., Chem. Sci., 2024, 15, 195–203, https://doi.org/10.1039/D3SC01944F.
The authors regret that the number of distance restraints used to obtain the final structure ensemble was incorrectly stated on the sixth page of the manuscript. The corrected sentence should read: “The final structure ensemble was calculated in CYANA67 and is based on 330 assigned NOEs (Table S3 and Fig. S6†) which included 104 long-range NOEs and had good precision (backbone RMSD = 0.17 Å, heavy atom RMSD = 0.49 Å) and residual restraint violations.”
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
| This journal is © The Royal Society of Chemistry 2024 |