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[51], the Authors would like to correct in order to accurately present the data. It was written: \u201cThe binding pose of 3\u03b1-Gal2 in complex with M86 was not informative physiologically, as it did not permit it to be extended by the third sugar residue. The +1 Gal was deep in the binding pocket and its OH4 pointed towards the polypeptide chain, while it should point towards a cleft inside which the +2 GlcNAc would be localized. In case of the human antibody complex, there was no obvious +2 GlcNAc binding site. The authors suggest that this residue projects outwards and does not make a significant contribution to binding, similarly to \u03b1-Gal-binding lectins. Porcine iGb3 glycolipids, which contain glucose in the +2 site, do not affect anti-\u03b1-Gal immune response [52, 53]. This suggests that the +2 residue identity is important for affinity of some anti-\u03b1-Gal antibodies. Thus, only experimental structures of anti-\u03b1-Gal antibodies complexed with a Gal\u03b1-1,3-Gal\u00df-1,4-GlcNAc trisaccharide can resolve the significance of the +2 residue in binding.\u201d It should be written as \u201cThese structures show that in both cases, 3\u03b1-Gal2 sits deep inside the binding pocket, and the \u20131 Gal must be the terminal residue. The OH1 hydroxyl of the +1 Gal residue points away from the polypeptide and towards the solvent, permitting extension of the disaccharide by +2 and downstream molecules. No obvious +2 GlcNAc binding site can be found in either complexes: the authors suggest that this residue projects outwards and does not make a significant contribution to binding, similarly to \u03b1-Gal-binding lectins. However, porcine iGb3 glycolipids, which contain glucose in the +2 site, do not affect anti-\u03b1-Gal immune response [52, 53]. This suggests that the +2 residue identity is important for affinity of some anti-\u03b1-Gal antibodies. Experimental structures of anti-\u03b1-Gal antibodies complexed with a Gal\u03b1-1,3-Gal\u00df-1,4-GlcNAc trisaccharide can ultimately resolve the significance of the +2 residue in binding.\u201d","order":8,"name":"change_details","label":"Change Details","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"3 July 2026","order":9,"name":"change_date","label":"Change Date","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"Correction","order":10,"name":"change_type","label":"Change Type","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"A Correction to this paper has been published:","order":11,"name":"change_details","label":"Change Details","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"https:\/\/doi.org\/10.1007\/s10719-026-10224-2","URL":"https:\/\/doi.org\/10.1007\/s10719-026-10224-2","order":12,"name":"change_details","label":"Change Details","group":{"name":"ArticleHistory","label":"Article History"}},{"order":1,"name":"Ethics","group":{"name":"EthicsHeading","label":"Declarations"}},{"value":"The authors declare no competing interests.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Competing interests"}},{"value":"This article does not contain any studies with human participants or animals performed by any of the authors.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethical approval"}},{"value":"The authors declare no competing interests.","order":4,"name":"Ethics","group":{"name":"EthicsHeading","label":"Conflict of interest"}},{"value":"Not applicable","order":5,"name":"Ethics","group":{"name":"EthicsHeading","label":"Clinical trial number"}}],"article-number":"19"}}