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'''Hydroxylysine''' is an [[amino acid]], C<sub>6</sub>H<sub>14</sub>N<sub>2</sub>O<sub>3</sub>. It is most widely known as a component of [[collagen]]. A standard amino acid with the R' group consisting of an amino terminated butyl hydrocarbon chain, with a hydroxyl group on the carbon atom before the amino group. See also [[lysine]] which lacks the hydroxyl group of hydrolysine.
{| align="right" border="1" cellspacing="0" cellpadding="3" style="margin: 0 0 0 0.5em; background: #FFFFFF; border-collapse: collapse; border-color: #C0C090;"
! {{chembox header}}| '''{{PAGENAME}}'''
|-
| [[Common name]]
| hydroxylysine
|-
| [[IUPAC nomenclature|Systematic name]]
| 2,6-diamino-5-<br>hydroxyhexanoic acid
|-
| [[Chemical formula]]
| C<sub>6</sub>H<sub>14</sub>N<sub>2</sub>O<sub>3</sub>
|}
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'''Hydroxylysine''' is an [[amino acid]], C<sub>6</sub>H<sub>14</sub>N<sub>2</sub>O<sub>3</sub>. It is most widely known as a component of [[collagen]]. A standard amino acid with the R' group consisting of an amino terminated butyl hydrocarbon chain, with a hydroxyl group on the carbon atom before the amino group. See also [[lysine]] which lacks the hydroxyl group of hydrolysine.


Structure is: [[Amine|NH2]] - [[Hydrocarbon|CH2]] - [[Alcohol|CHOH]] - [[Hydrocarbon|CH2]] - [[Hydrocarbon|CH2]] - [[Amino acid|C2H4NO2]]
Structure is: [[Amine|NH2]] - [[Hydrocarbon|CH2]] - [[Alcohol|CHOH]] - [[Hydrocarbon|CH2]] - [[Hydrocarbon|CH2]] - [[Amino acid|C2H4NO2]]

Revision as of 04:48, 17 October 2005

Hydroxylysine
Common name hydroxylysine
Systematic name 2,6-diamino-5-
hydroxyhexanoic acid
Chemical formula C6H14N2O3

Hydroxylysine is an amino acid, C6H14N2O3. It is most widely known as a component of collagen. A standard amino acid with the R' group consisting of an amino terminated butyl hydrocarbon chain, with a hydroxyl group on the carbon atom before the amino group. See also lysine which lacks the hydroxyl group of hydrolysine.

Structure is: NH2 - CH2 - CHOH - CH2 - CH2 - C2H4NO2

Number of hydrogens vary due to carboxyl/amino groups and the acidity or alkilinity of their sorroundings.

See http://herkules.oulu.fi/isbn9514267990/html/x319.html for more in depth information about the biological context of this amino acid.