Dear all,
I am now working on a very low resolution phase determination (around 4.5A
with hg anomalous signal around 5.5 A). I can find the Hg sites and get the
phase, but the density map is not so good.
Two components of my protein complex (about 1/3) has a homologue model
which is also can not
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Dear Faisal,
none of the secondary structure prediction programs are perfect
(although dssp is pretty good). This means you should always check the
predictions yourself, at least at the boundaries of helices and
beta-strands and then fine-tune the gra
Thanx to all
Your suggestions really worked and solved my problem.
regards
Faisal
On Fri, Sep 27, 2013 at 2:08 AM, Parthasarathy Sampathkumar <
spart...@gmail.com> wrote:
> Hi Faisal,
>
> you could run dssp2pdb by James Stroud (
> http://www.jamesstroud.com/software/dssp2pdb/ ) to convert ds
Hi Faisal,
you could run dssp2pdb by James Stroud (
http://www.jamesstroud.com/software/dssp2pdb/ ) to convert dssp output into
PDB readable format as part of the header. When you open resultant PDB in
PyMOL, secondary structure as defined by dssp would be displayed.
OR
one could also define sec
Dear Faisal,
I usually assign in PYMOL the secondary structure generally obeying DSSP
output.
You have to use the alter command. eg:
alter myprotein and resi 103:106, ss='H'
Bytheway, pymol swaps inside and outside color on left handed helices,
wich you might also have.
Hope this helps,
Ma
Dear all
Sorry for the off topic question.
My protein has few G310 helices. It is clearly visible through STRIDE or
DSSP, but when i open the structure in PYMOL it didnt show it. Other
visualization graphics like CHIMERA and VMD are able to pick few of them
but not all the G310 helices..For manu
Rasmol has always done this. Just use slab …
best wishes
Pete
On 5 Sep 2013, at 21:30, Arthur Glasfeld wrote:
> I am hoping to create some images of protein cross-sections where the atoms
> are depicted as spheres, and the spheres that are "cut" by the slab are shown
> as solids with the s