Jmol/Depth from surface

Atoms Colored By Surfacedistance

Here is a cross-section (slab) of acetylcholinesterase (2ace) with . The commands are simply

restrict not solvent # hides water
spacefill only
select ach # acetylcholine substrate model
color black
select protein
color surfacedistance

In Proteopedia's Molecular Scene Authoring Tools (SAT), you can enter these commands in the slot below the molecule. There will be a delay (about 20 sec on my computer) while JSmol calculates the surfacedistance for each atom. However, once the scene is saved as a green link, the colors are saved and displayed without re-calculation when the green link is clicked.

Color Schemes

The default color scheme^[1] for surfacedistance is red-white-blue, "rwb" in Jmol command language. You can apply other color schemes, such as the ("roygb").

color property surfacedistance "roygb"

Reporting Surfacedistance

These commands will be much faster, especially for larger molecules, if done in the standalone Jmol Java application. The Jmol command^[2] to report the maximum surfacedistance for any atom in a model is

print {*}.surfacedistance.max # Reports 10.25 for 2ace.

The asterisk "⁎" means "all atoms". The atom expression must be enclosed in curly brackets "{...}". Anything after "#" is a comment, which is not part of the command to Jmol.

Three enzymes that are roughly spherical with 527-575 amino acids each are 2ace, 1CRL, and 1o86. Their maximum surfacedepth values are 10.25, 9.58, and 7.94 Å respectively. A script that you can download (right click, save link as) reports the average surfacedepth values for each amino acid, secondary structures, and common chemical elements. Average values were normalized to a maximum depth of 10.0 Å, and averaged. For this small sample of 3 enzymes:

• The sidechain of Trp was deepest (2.5).
• In order of increasing depth: the sidechains nitrogens and oxygens of charged amino acids (Asp, Glu, Lys, Arg) 0.8 < the sidechain O,N of Asn, Gln 1.1 < the entire sidechains of Val, Leu, Ile 1.4 < the entire sidechains of Phe, Tyr, Trp 2.3 Å.
• Lys and Glu (0.3, 0.5) are shallower than Asp and Arg (~1).
• In order of increasing depth: atoms in coil 1.3 < helices 1.6 < β strands 2.4 Å.

Tunnel Isosurface Colored By Surfacedistance

Selecting By Surfacedistance