Weight | 105.093 g/mol |
---|---|
Formula | C3H7NO3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 3 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
L-serine (25821-52-7, 56-45-1)
Serine · L Serine
Score:
#545 in Biochemistry
,
#1657 in Biology
,
#1956 in Chemistry
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- DNA Double-stranded Breaks Induce Histone H2AX Phosphorylation on Serine 139 (Journal of Biological Chemistry, 1998)
- Serine Phosphorylation of Death Agonist BAD in Response to Survival Factor Results in Binding to 14-3-3 Not BCL-XL (Cell, 1996)
- Regulation of Neuronal Survival by the Serine-Threonine Protein Kinase Akt (Science, 1997)
- Cyclic AMP stimulates somatostatin gene transcription by phosphorylation of CREB at serine 133 (Cell, 1989)
- NF-B activation by tumour necrosis factor requires the Akt serinethreonine kinase (Nature, 1999)
- Mammalian Ras interacts directly with the serine/threonine kinase raf (Cell, 1993)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Serine
- L Serine
-
SMILESC(C(C(=O)O)N)O
-
InChIKeyMTCFGRXMJLQNBG-UHFFFAOYSA-N
- Pubchem - L-serine
- Wikipedia - L-Serine
Serine (abbreviated as Ser or S) encoded by the codons UCU, UCC, UCA, UCG, AGU and AGC 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), a carboxyl group (which is in the deprotonated COO form in physiological conditions), and a side chain consisting of a hydroxymethyl group (see hydroxyl), classifying it as a polar amino acid. It can be synthesized in the human body under normal physiological circumstances, making it a nonessential amino acid.
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