Glutamate-1-semialdehyde: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
CSV import
 
Line 41: Line 41:
[[Category:Organic compounds]]
[[Category:Organic compounds]]
[[Category:Tetrapyrrole biosynthesis]]
[[Category:Tetrapyrrole biosynthesis]]
<gallery>
File:Glutamate-1-semialdehyde.svg|Glutamate-1-semialdehyde
</gallery>

Latest revision as of 05:21, 3 March 2025


Overview of Glutamate-1-semialdehyde


Chemical Compound
Identifiers
CAS Number
PubChem CID
ChemSpider ID
UNII
ChEBI
ChEMBL
Properties
Chemical Formula
Molar Mass
Appearance
Density
Melting Point
Boiling Point
Hazards
GHS Pictograms [[File:|50px]]
GHS Signal Word
GHS Hazard Statements
NFPA 704 [[File:|50px]]
References

Glutamate-1-semialdehyde is an important intermediate in the biosynthesis of porphyrins and chlorophyll. It is a derivative of glutamic acid and plays a crucial role in the C5 pathway of tetrapyrrole synthesis.

Biosynthesis[edit]

Glutamate-1-semialdehyde is synthesized from glutamyl-tRNA by the enzyme glutamyl-tRNA reductase. This reaction is a key step in the conversion of glutamate to 5-aminolevulinic acid (ALA), which is the first common precursor in the biosynthesis of all tetrapyrroles, including heme, chlorophyll, and vitamin B12.

Function[edit]

In the C5 pathway, glutamate-1-semialdehyde is converted to 5-aminolevulinic acid by the enzyme glutamate-1-semialdehyde aminotransferase. This conversion is essential for the production of porphyrin rings, which are the building blocks of many important biological molecules.

Clinical Significance[edit]

Disruptions in the biosynthesis of glutamate-1-semialdehyde can lead to disorders in heme production, such as porphyria. Understanding the role of glutamate-1-semialdehyde in these pathways can help in the development of treatments for such conditions.

See also[edit]

References[edit]

<references />