General Information of MET (ID: META00548)
Name GlcCer(d18:1/18:0)
Synonyms   Click to Show/Hide Synonyms of This Metabolite
1-O-b-D-Glucopyranosyl-ceramide; 1-O-beta-delta-Glucopyranosyl-ceramide; C18 GlcCer; Ganglioside GL1a; Gaucher cerebroside', GLC-beta1->1'cer, 'GlcCeramide; GlcCer(D18:1/18:0); Glucocerebroside; Glucosylceramide; N-(Octadecanoyl)-1-beta-glucosyl-sphing-4-enine; beta-D-Glucosyl-(11)-N-octadecanoylsphing-4-enine; beta-D-Glucosyl-N-stearoylsphingosine
Source Endogenous;Food
Structure Type   Glycosphingolipids  (Click to Show/Hide the Complete Structure Type Hierarchy)
Lipids and lipid-like molecules
Sphingolipids
Glycosphingolipids
PubChem CID
11958364
HMDB ID
HMDB0004972
Formula
C42H81NO8
Structure
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3D MOL is unavailable 2D MOL
  Click to Show/Hide the Molecular/Functional Data (External Links/Property/Function) of This Metabolite
KEGG ID
C01190
ChEBI ID
84719
FooDB ID
FDB023559
ChemSpider ID
10132611
METLIN ID
7225
Physicochemical Properties Molecular Weight 728.1 Topological Polar Surface Area 149
XlogP 12.4 Complexity 814
Heavy Atom Count 51 Rotatable Bond Count 35
Hydrogen Bond Donor Count 6 Hydrogen Bond Acceptor Count 8
Function
GlcCer(d18:1/18:0) is a glycosphingolipid (ceramide and oligosaccharide)or oligoglycosylceramide with one or more sialic acids (i.e. n-acetylneuraminic acid) linked on the sugar chain. It is a component the cell plasma membrane which modulates cell signal transduction events. Gangliosides have been found to be highly important in immunology. Ganglioside GL1a carries a net-negative charge at pH 7.0 and is acidic. Gangliosides can amount to 6% of the weight of lipids from brain, but they are found at low levels in all animal tissues.Cerebrosides are glycosphingolipids. There are four types of glycosphingolipids, the cerebrosides, sulfatides, globosides and gangliosides. Cerebrosides have a single sugar group linked to ceramide. The most common are galactocerebrosides (containing galactose), the least common are glucocerebrosides (containing glucose). Galactocerebrosides are found predominantly in neuronal cell membranes. In contrast glucocerebrosides are not normally found in membranes. Instead, they are typically intermediates in the synthesis or degradation of more complex glycosphingolipids. Galactocerebrosides are synthesized from ceramide and UDP-galactose. Excess lysosomal accumulation of glucocerebrosides is found in Gaucher disease.
Regulatory Network
Full List of Protein(s) Regulating This Metabolite
      Bone morphogenic antagonist (BMA)
            DAN domain family member 5 (DAND5) Click to Show/Hide the Full List of Regulating Pair(s):   1 Pair(s)
               Detailed Information Protein   Info click to show the details of this protein
               Regulating Pair Experim Info click to show the details of experiment for validating this pair [1]
                      Introduced Variation Knockdown (siRNA) of DAND5
                      Induced Change GlcCer(d18:1/18:0) concentration: decrease
                      Summary Introduced Variation         Induced Change 
                      Disease Status Healthy individual
                      Details It is reported that knockdown of DAND5 leads to the decrease of glcCer(d18:1/18:0) levels compared with control group.
References
1 Golgi alkaline ceramidase regulates cell proliferation and survival by controlling levels of sphingosine and S1P. FASEB J. 2006 Sep;20(11):1813-25.

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