Weight | 132.119 g/mol |
---|---|
Formula | C4H8N2O3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 3 |
Aromatic Rings | 0 |
Rotatable Bonds | 3 |
L-asparagine (70-47-3)
Asparagine
Score:
#602 in Biochemistry
,
#1748 in Biology
,
#2066 in Chemistry
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- Assembly of asparagine-linked oligosaccharides. (Annual Review of Biochemistry, 1985)
- Asparagine Hydroxylation of the HIF Transactivation Domain: A Hypoxic Switch (Science, 2002)
- Synthesis and Processing of Asparagine-Linked Oligosaccharides (Annual Review of Biochemistry, 1981)
- Asparagine and Glutamine: Using Hydrogen Atom Contacts in the Choice of Side-chain Amide Orientation (Journal of Molecular Biology, 1999)
- Deglycosylation of asparagine-linked glycans by peptide: N- glycosidase F (Biochemistry, 1985)
- Hypoxia inducible factor (HIF) asparagine hydroxylase is identical to factor inhibiting HIF (FIH) and is related to the cupin structural family (Journal of Biological Chemistry, 2002)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Asparagine
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SMILESC(C(C(=O)O)N)C(=O)N
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InChIKeyDCXYFEDJOCDNAF-UHFFFAOYSA-N
- Pubchem - L-asparagine
- Wikipedia - L-asparagine
Asparagine (abbreviated as Asn or N), encoded by the codons AAU and AAC, is an -amino acid that is used in the biosynthesis of proteins. It contains an -amino group (which is in the protonated NH+ 3 form under biological conditions), an -carboxylic acid group (which is in the deprotonated COO form under biological conditions), and a side chain carboxamide, classifying it as a polar (at physiological pH), aliphatic amino acid. It is non-essential in humans, meaning the body can synthesize it.
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