Atom Label Key

Naming Convention for α-amino acids


Atom Label

Description


CMain chain Carbon of amide/acid
CAMain chain α carbon
NMain chain nitrogen of amide/amine
OMain chain Oxygen of amide/acid
HMain chain hydrogen of amide
HAMain chain hydrogen of on the α carbon
CBβ Carbon, first carbon of the sidechain
HB?Hydrogen on the β Carbon. '?' is a number 1,2 or 3
OGOxygen on the β Carbon.
CG?γ Carbon. - the '?' if present is a number 1 or 2

The results are shown. The H from the -OH group on C6 is now on the amino acid side chain. The phosphate group has been transferred to the alcohol carbon of glucose and ADP is the other product.

Lysine


Name3 Letter1 Letter
Lysine LYS K

Unprotonated (base form - neutral)
lysine
Protonated (acid form - positively charged)
dominant in water
lys3d


Drawn as if part of protein to emphasize the sidechain properties The "Sidechain Polarity" button draws an an envelope around the sidechain that is colored by charge according to the scale above.

pKR in H2O= 9 Free amino acid Mass = 146 g/M
Probability of being found in a:
α-Helix β-Sheet β-Turn
75% 50% 60%
Special Attributes

This amino acid sidechain ends with a primary amine which is generally protonated and ionized (positively) at physiological pH.

The charge means that it is usually on the surface of a water soluble protein where it is exposed to water

In the demonstration below the lysine is at the beginning of an α-helix and interestingly the terminal amine group in this particular case does not appear to be sticking out into water - but rather looks to be buried in the protein... such is the way


In the demonstration below you may "left click and drag" to rotate the molecule "SHIFT left click and drag (up or down)" to make smaller or bigger
Click on the white squares in succession to turn or/off identifying features. Some text describing the issues is in the lower right text box



Atom Label Description

Click an atom to diplay it's identity here


Messages about the currently highlighted features

Jmol: an open-source Java viewer for chemical structures in 3D. http://www.jmol.org/