Translations:Flavin adenine dinucleotide/6/en: Difference between revisions

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Message definition (Flavin adenine dinucleotide)
Flavin adenine dinucleotide consists of two portions: the [[adenine]] [[nucleotide]] ([[adenosine monophosphate]]) and the [[flavin mononucleotide]] (FMN) bridged together through their [[phosphate]] groups. Adenine is bound to a cyclic [[ribose]] at the [[Nucleic acid nomenclature|1']] carbon, while phosphate is bound to the ribose at the [[Nucleic acid nomenclature|5']] carbon to form the adenine nucledotide. [[Riboflavin]] is formed by a carbon-nitrogen (C-N) bond between the [[Flavin group|isoalloxazine]] and the [[ribitol]]. The phosphate group is then bound to the terminal ribose carbon, forming a FMN. Because the bond between the isoalloxazine and the ribitol is not considered to be a [[glycosidic bond]], the flavin mononucleotide is not truly a nucleotide. This makes the dinucleotide name misleading; however, the flavin mononucleotide group is still very close to a nucleotide in its structure and chemical properties. [[File:FAD to FADH2 reduction.svg|422px|thumb|left|Reaction of FAD to form FADH<sub>2</sub>]] [[File:Flavin Adenine Dinucleotide Spectrum.png|thumb|Approximate absorption spectrum for FAD]]

Flavin adenine dinucleotide consists of two portions: the adenine nucleotide (adenosine monophosphate) and the flavin mononucleotide (FMN) bridged together through their phosphate groups. Adenine is bound to a cyclic ribose at the 1' carbon, while phosphate is bound to the ribose at the 5' carbon to form the adenine nucledotide. Riboflavin is formed by a carbon-nitrogen (C-N) bond between the isoalloxazine and the ribitol. The phosphate group is then bound to the terminal ribose carbon, forming a FMN. Because the bond between the isoalloxazine and the ribitol is not considered to be a glycosidic bond, the flavin mononucleotide is not truly a nucleotide. This makes the dinucleotide name misleading; however, the flavin mononucleotide group is still very close to a nucleotide in its structure and chemical properties.

Reaction of FAD to form FADH2
Approximate absorption spectrum for FAD