User:Karsten Theis/AI tutorial: Difference between revisions

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moveto 0.0 { -97 855 -510 89.56} 300.0 0.0 0.0 {38.343720000000005 74.45217999999998 85.45410000000003} 34.78371098010064 {0 0 0} 0 0 0 3.0 0.0 0.0;
moveto 0.0 { -97 855 -510 89.56} 300.0 0.0 0.0 {38.343720000000005 74.45217999999998 85.45410000000003} 34.78371098010064 {0 0 0} 0 0 0 3.0 0.0 0.0;
</nowiki>
</nowiki>
<scene name='79/799553/Etransfer/2'>Electron transfer</scene>
<nowiki>
load "=1JRO" filter "biomolecule 2"                                  # The structure contains 2 dimers, we are loading the second dimer
restrict none
define ~focal FES:E, FAD:E, MTE:F                                    # Ligands involved in electron transfer (in chain E, F, not G, H)
select ~focal; wireframe 0.36; Spacefill 25%                          # ball-and-stick
select (sulfur and MTE:F) or FES:E.FE2; bondOrder single
select 3001:E.S2 or 3002:E.FE1; label "Fe2S2"; color label [xffa500]; # label electron carriers
select FAD:E.O2; label "FAD"                                          # label electron donor
select ~focal; set labelOffset 4 4;                                  # offset for all labels
center visible; zoom 400; spin on                                    # there is no good single view, so spin
set measurementUnits Angstroms                                        # units for the measurements below
measure ([FAD]3005:E.C7M) ([FES]3002:E.S1)                            # shortest path for electrons
measure ([FES]3002:E.FE2) ([FES]3001:E.S2)
measure ([FES]3001:E.FE1) ([MTE]3003:F.C2)
</nowiki>


<scene name='78/786673/Nagal_galsa_superposition/1'>Superposition</scene>
<scene name='78/786673/Nagal_galsa_superposition/1'>Superposition</scene>