Correction: Roson-Calero et al. Cyclic Peptide MV6, an Aminoglycoside Efficacy Enhancer Against Acinetobacter baumannii. Antibiotics 2024, 13, 1147
Natalia Roson-Calero, Jimmy Lucas, María A. Gomis-Font, Roger de Pedro-Jové, Antonio Oliver, Clara Ballesté-Delpierre, Jordi Vila

Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsAntibiotic Resistance in Bacteria · Antimicrobial Peptides and Activities
1. Error in Figure
In the original publication [1], there was a mistake in Figure 1 as published. The molecule represented in Figure 1 is inaccurate, as the order of the amino acids is reversed, and the amine group of D-Pro(NH_2_) must be eliminated. The corrected Figure 1 appears below.
2. Text Correction
There was an error in the original publication [1]. The sequence of MV6 specified in the Section “2.1. MV6 Structure” is incorrect. It includes an additional amino group in the first D-Proline composing the peptide. Additionally, the correct pattern of MV6 is Arg-D-Pro-Trp, not Trp-D-Pro-Arg.
A correction has been made to Section 2. Results, “2.1. MV6 Structure”, first paragraph:
The MV6 cyclic peptide was selected for further study against A. baumannii from a synthetic library of 28 cyclic peptides following a small-scale “shot in the dark” approach in which each peptide was tested in combination with various antibiotics and bacterial species. Its structure consists of six amino acids, two arginine residues (Arg), two D-proline residues (D-Pro), and two tryptophan residues (Trp), arranged in a cyclic configuration. The final structure is &Arg-D-Pro-Trp-Arg-D-Pro-Trp& (Figure 1).
The authors state that the scientific conclusions are unaffected. This correction was approved by the Academic Editor. The original publication has also been updated.
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