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CHEBI ONTOLOGY - ANNOTATIONS

The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at http://www.ebi.ac.uk/chebi/. The data is made available under the Creative Commons License (CC BY 3.0, http://creativecommons.org/licenses/by/3.0/). For more information see: Degtyarenko et al. (2008) ChEBI: a database and ontology for chemical entities of biological interest. Nucleic Acids Res. 36, D344–D350.

Term:ketoaldonic acid derivative
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Accession:CHEBI:63394 term browser browse the term
Definition:A monosaccharide derivative that is formally obtained from a ketoaldonic acid.
Synonyms:related_synonym: ketoaldonic acid derivatives


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CMP-N-acetyl-beta-neuraminic acid term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cmas cytidine monophosphate N-acetylneuraminic acid synthetase affects abundance ISO CMAS protein affects the abundance of Cytidine Monophosphate N-Acetylneuraminic Acid CTD PMID:27380425 NCBI chr 4:176,994,129...177,012,445
Ensembl chr 4:176,994,129...177,012,444
JBrowse link
N-acetylneuraminic acid term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cmas cytidine monophosphate N-acetylneuraminic acid synthetase affects abundance ISO CMAS protein affects the abundance of N-Acetylneuraminic Acid; CMAS protein affects the abundance of N-Acetylneuraminic Acid analog CTD PMID:27380425 NCBI chr 4:176,994,129...177,012,445
Ensembl chr 4:176,994,129...177,012,444
JBrowse link
G Gne glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase increases chemical synthesis EXP GNE protein results in increased chemical synthesis of N-Acetylneuraminic Acid CTD PMID:9305888 NCBI chr 5:59,511,738...59,553,421
Ensembl chr 5:59,512,872...59,553,416
JBrowse link
G Nans N-acetylneuraminate synthase increases chemical synthesis ISO NANS results in increased chemical synthesis of N-Acetylneuraminic Acid CTD PMID:27213289 NCBI chr 5:62,109,352...62,126,492
Ensembl chr 5:62,109,328...62,126,494
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 19810
    role 19758
      chemical role 19283
        donor 18416
          Bronsted acid 18283
            oxoacid 18235
              carbon oxoacid 18119
                carboxylic acid 18108
                  carbohydrate acid 759
                    ketoaldonic acid 628
                      ketoaldonic acid derivative 3
                        2-amino-2,3,7-trideoxy-D-lyxo-hept-6-ulosonic acid 0
                        3-dehydro-L-gulonic acid 6-phosphate 0
                        5-acetamido-3,5-dideoxy-L-arabino-hept-2-ulopyranosonic acid 0
                        N,N-diacetyllegionaminic acid 0
                        ascorbic acid derivative + 0
                        legionaminic acid + 0
                        neuraminic acids + 3
                        pseudaminic acid + 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 19810
    subatomic particle 19808
      composite particle 19808
        hadron 19808
          baryon 19808
            nucleon 19808
              atomic nucleus 19808
                atom 19808
                  main group element atom 19696
                    p-block element atom 19696
                      carbon group element atom 19599
                        carbon atom 19588
                          organic molecular entity 19588
                            organic group 18527
                              organic divalent group 18520
                                organodiyl group 18520
                                  carbonyl group 18427
                                    carbonyl compound 18427
                                      carboxylic acid 18108
                                        carbohydrate acid 759
                                          ketoaldonic acid 628
                                            ketoaldonic acid derivative 3
                                              2-amino-2,3,7-trideoxy-D-lyxo-hept-6-ulosonic acid 0
                                              3-dehydro-L-gulonic acid 6-phosphate 0
                                              5-acetamido-3,5-dideoxy-L-arabino-hept-2-ulopyranosonic acid 0
                                              N,N-diacetyllegionaminic acid 0
                                              ascorbic acid derivative + 0
                                              legionaminic acid + 0
                                              neuraminic acids + 3
                                              pseudaminic acid + 0
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