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Cataloging natural sialic acids and other nonulosonic acids (NulOs), and their representation using the Symbol Nomenclature for Glycans

  • SNFG Discussion Group
  • University of California at San Diego
  • N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
  • National Institutes of Health
  • University of California at Davis
  • Biognos AB
  • Justus Liebig University Giessen
  • National Research Council of Canada
  • University of Georgia
  • Johns Hopkins University
  • Utrecht University
  • Imperial College London
  • Technical University of Denmark
  • Stanford University
  • Swiss Institute of Bioinformatics
  • Research Center of Medical Glycoscience
  • Sanford-Burnham-Prebys Research Institute
  • The Noguchi Institute
  • Scripps Research Institute
  • University of California at Santa Barbara
  • Bijvoet Center
  • Soka University
  • Swiss Federal Institute of Technology Zurich
  • Griffith University Queensland
  • Kyoto University
  • RIKEN
  • Georgetown University
  • Macquarie University
  • Albert Einstein College of Medicine
  • National Institute for Bioprocessing Research & Training
  • Max Planck Institute of Colloids and Interfaces
  • George Washington University
  • Harvard University
  • NextMove Software Limited
  • French National Centre for Scientific Research
  • Washington University St. Louis
  • The University of Osaka

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

Nonulosonic acids or non-2-ulosonic acids (NulOs) are an ancient family of 2-ketoaldonic acids (α-ketoaldonic acids) with a 9-carbon backbone. In nature, these monosaccharides occur either in a 3-deoxy form (referred to as “sialic acids”) or in a 3,9-dideoxy “sialic-acid-like” form. The former sialic acids are most common in the deuterostome lineage, including vertebrates, and mimicked by some of their pathogens. The latter sialic-acid-like molecules are found in bacteria and archaea. NulOs are often prominently positioned at the outermost tips of cell surface glycans, and have many key roles in evolution, biology and disease. The diversity of stereochemistry and structural modifications among the NulOs contributes to more than 90 sialic acid forms and 50 sialic-acid-like variants described thus far in nature. This paper reports the curation of these diverse naturally occurring NulOs at the NCBI sialic acid page (https://www.ncbi.nlm.nih.gov/glycans/sialic.html) as part of the NCBI-Glycans initiative. This includes external links to relevant Carbohydrate Structure Databases. As the amino and hydroxyl groups of these monosaccharides are extensively derivatized by various substituents in nature, the Symbol Nomenclature For Glycans (SNFG) rules have been expanded to represent this natural diversity. These developments help illustrate the natural diversity of sialic acids and related NulOs, and enable their systematic representation in publications and online resources.

Original languageEnglish
Pages (from-to)99-103
Number of pages5
JournalGlycobiology
Volume33
Issue number2
DOIs
StatePublished - Feb 1 2023

Keywords

  • NulO
  • glycans
  • nonulosonic acid
  • sialic acid
  • symbol nomenclature

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