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Congenital disorder of glycosylation and Glycosylation

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between Congenital disorder of glycosylation and Glycosylation

Congenital disorder of glycosylation vs. Glycosylation

A congenital disorder of glycosylation (previously called carbohydrate-deficient glycoprotein syndrome) is one of several rare inborn errors of metabolism in which glycosylation of a variety of tissue proteins and/or lipids is deficient or defective. Glycosylation (see also chemical glycosylation) is the reaction in which a carbohydrate, i.e. a glycosyl donor, is attached to a hydroxyl or other functional group of another molecule (a glycosyl acceptor).

Similarities between Congenital disorder of glycosylation and Glycosylation

Congenital disorder of glycosylation and Glycosylation have 16 things in common (in Unionpedia): Asparagine, Carbohydrate, Cytoplasm, Endoplasmic reticulum, Fucose, Fucosylation, Glycoprotein, Glycosyltransferase, Golgi apparatus, Lectin, Lipid, Mannose, N-Acetylglucosamine, N-linked glycosylation, Oligosaccharide, Protein.

Asparagine

Asparagine (symbol Asn or N), is an α-amino acid that is used in the biosynthesis of proteins.

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Carbohydrate

A carbohydrate is a biomolecule consisting of carbon (C), hydrogen (H) and oxygen (O) atoms, usually with a hydrogen–oxygen atom ratio of 2:1 (as in water); in other words, with the empirical formula (where m may be different from n).

Carbohydrate and Congenital disorder of glycosylation · Carbohydrate and Glycosylation · See more »

Cytoplasm

In cell biology, the cytoplasm is the material within a living cell, excluding the cell nucleus.

Congenital disorder of glycosylation and Cytoplasm · Cytoplasm and Glycosylation · See more »

Endoplasmic reticulum

The endoplasmic reticulum (ER) is a type of organelle found in eukaryotic cells that forms an interconnected network of flattened, membrane-enclosed sacs or tube-like structures known as cisternae.

Congenital disorder of glycosylation and Endoplasmic reticulum · Endoplasmic reticulum and Glycosylation · See more »

Fucose

Fucose is a hexose deoxy sugar with the chemical formula C6H12O5.

Congenital disorder of glycosylation and Fucose · Fucose and Glycosylation · See more »

Fucosylation

Fucosylation is the process of adding fucose sugar units to a molecule.

Congenital disorder of glycosylation and Fucosylation · Fucosylation and Glycosylation · See more »

Glycoprotein

Glycoproteins are proteins that contain oligosaccharide chains (glycans) covalently attached to amino acid side-chains.

Congenital disorder of glycosylation and Glycoprotein · Glycoprotein and Glycosylation · See more »

Glycosyltransferase

Glycosyltransferases (GTFs, Gtfs) are enzymes (EC 2.4) that establish natural glycosidic linkages.

Congenital disorder of glycosylation and Glycosyltransferase · Glycosylation and Glycosyltransferase · See more »

Golgi apparatus

The Golgi apparatus, also known as the Golgi complex, Golgi body, or simply the Golgi, is an organelle found in most eukaryotic cells.

Congenital disorder of glycosylation and Golgi apparatus · Glycosylation and Golgi apparatus · See more »

Lectin

Lectins are carbohydrate-binding proteins, macromolecules that are highly specific for sugar moieties of other molecules.

Congenital disorder of glycosylation and Lectin · Glycosylation and Lectin · See more »

Lipid

In biology and biochemistry, a lipid is a biomolecule that is soluble in nonpolar solvents.

Congenital disorder of glycosylation and Lipid · Glycosylation and Lipid · See more »

Mannose

Mannose, packaged as the nutritional supplement "d-mannose", is a sugar monomer of the aldohexose series of carbohydrates.

Congenital disorder of glycosylation and Mannose · Glycosylation and Mannose · See more »

N-Acetylglucosamine

N-Acetylglucosamine (N-acetyl-D-glucosamine, or GlcNAc, or NAG) is a monosaccharide and a derivative of glucose.

Congenital disorder of glycosylation and N-Acetylglucosamine · Glycosylation and N-Acetylglucosamine · See more »

N-linked glycosylation

N-linked glycosylation, is the attachment of the sugar molecule oligosaccharide known as glycan to a nitrogen atom (the amide nitrogen of an asparagine (Asn) residue of a protein), in a process called N-glycosylation, studied in biochemistry.

Congenital disorder of glycosylation and N-linked glycosylation · Glycosylation and N-linked glycosylation · See more »

Oligosaccharide

An oligosaccharide (from the Greek ὀλίγος olígos, "a few", and σάκχαρ sácchar, "sugar") is a saccharide polymer containing a small number (typically three to ten) of monosaccharides (simple sugars).

Congenital disorder of glycosylation and Oligosaccharide · Glycosylation and Oligosaccharide · See more »

Protein

Proteins are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues.

Congenital disorder of glycosylation and Protein · Glycosylation and Protein · See more »

The list above answers the following questions

Congenital disorder of glycosylation and Glycosylation Comparison

Congenital disorder of glycosylation has 153 relations, while Glycosylation has 75. As they have in common 16, the Jaccard index is 7.02% = 16 / (153 + 75).

References

This article shows the relationship between Congenital disorder of glycosylation and Glycosylation. To access each article from which the information was extracted, please visit:

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