Weight | 182.651 g/mol |
---|---|
Formula | C6H15ClN2O2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 3 |
Aromatic Rings | 0 |
Rotatable Bonds | 5 |
L-Lysine hydrochloride
Lysine · Lysine Hydrochloride · L Lysine
6150-68-1, 10098-89-2, 657-27-2
Score:
#478 in Biochemistry
,
#1522 in Biology
,
#1783 in Chemistry
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- PERIODATE-LYSINE-PARAFORMALDEHYDE FIXATIVE A NEW FIXATIVE FOR IMMUNOELECTRON MICROSCOPY (Journal of Histochemistry and Cytochemistry, 1974)
- Lysine acetylation targets protein complexes and co-regulates major cellular functions. (Science, 2009)
- Role of Histone H3 Lysine 27 Methylation in Polycomb-Group Silencing (Science, 2002)
- Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins (Nature, 2001)
- Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain (Nature, 2001)
- Regulation of Heterochromatic Silencing and Histone H3 Lysine-9 Methylation by RNAi (Science, 2002)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Lysine
- Lysine Hydrochloride
- L Lysine
- Lysine Acetate
- L-Lysine
- Enisyl
-
SMILESC(CCN)CC(C(=O)O)N.Cl
-
InChIKeyBVHLGVCQOALMSV-UHFFFAOYSA-N
- Pubchem - L-Lysine hydrochloride
- Wikipedia - lysine hydrochloride
Lysine (abbreviated as Lys or K), encoded by the codons AAA and AAG, is an -amino acid that is used in the biosynthesis of proteins. It contains an -amino group (which is in the protonated NH3+ form under biological conditions), an -carboxylic acid group (which is in the deprotonated COO form under biological conditions), and a side chain lysyl ((CH2)4NH2), classifying it as a charged (at physiological pH), aliphatic amino acid. It is essential in humans, meaning the body cannot synthesize it and thus it must be obtained from the diet.
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