Aureusidin synthase and Endoplasmic reticulum

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

Difference between Aureusidin synthase and Endoplasmic reticulum

Aureusidin synthase vs. Endoplasmic reticulum

Aureusidin synthase (AmAS1) is an enzyme with systematic name 2',4,4',6'-tetrahydroxychalcone 4'-O-beta-D-glucoside:oxygen oxidoreductase. 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.

Similarities between Aureusidin synthase and Endoplasmic reticulum

Aureusidin synthase and Endoplasmic reticulum have 3 things in common (in Unionpedia): Amino acid, Glycoprotein, Redox.

Amino acid

Amino acids are organic compounds containing amine (-NH2) and carboxyl (-COOH) functional groups, along with a side chain (R group) specific to each amino acid.

Amino acid and Aureusidin synthase · Amino acid and Endoplasmic reticulum · See more »

Glycoprotein

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

Aureusidin synthase and Glycoprotein · Endoplasmic reticulum and Glycoprotein · See more »

Redox

Redox (short for reduction–oxidation reaction) (pronunciation: or) is a chemical reaction in which the oxidation states of atoms are changed.

Aureusidin synthase and Redox · Endoplasmic reticulum and Redox · See more »

The list above answers the following questions

What Aureusidin synthase and Endoplasmic reticulum have in common
What are the similarities between Aureusidin synthase and Endoplasmic reticulum

Aureusidin synthase and Endoplasmic reticulum Comparison

Aureusidin synthase has 41 relations, while Endoplasmic reticulum has 91. As they have in common 3, the Jaccard index is 2.27% = 3 / (41 + 91).

References

This article shows the relationship between Aureusidin synthase and Endoplasmic reticulum. To access each article from which the information was extracted, please visit:

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