Laboratory: Zhang Initiative Research Unit,
Advanced Science Institute, RIKEN, Japan.
(Unit Leader: Dr. Kam Zhang)
Job title and Job description: Postdoctoral Researchers
Job description:
We are seeking a highly motivated and experienced computational
structural biologist to join the Zhang Ini
In my hands GFP fusions can produce colorless crystals (but still have GFP!)
depending on the condition. Sometimes the crystals gradually become
colorless with time - bleaching or perhaps some chemical effect - no idea.
I've not tested the colorless crystals with UV to see if they still glow.
Arte
Yes. There are two ways:
1) replace $CBIN/refmac5 with refmac5.6
2) on ccp4i click "System administration", select "configure interface" and jus
below
"Give full path name for CCP4 programs to overcome name conflicts" click "Add a
program"
There will appear two fields. On the right field type r
@R.Brown
I'm using DENZO
I'm trying POINTLESS but I don't understand "unmerged data" -what's that? is it
the spot images which are used for "peak search" during data processing?
Both SFCHECK & phenix.xtriage showed the information about pst & twinning.
However I've tried a thorough process of rein
Is it possible to use refmac 5.6 with the ccp4i Refmac5 task?
Can I just copy the 5.6 binary over the 5.5 binary distributed with CCP4?
It looks like the new refmac has a number of new keywords which wouldn't be
accessible doing this, but would it otherwise be compatible? If so, where
does the di
Dear experts,
Thank you very much for your input. Here are my answers for your questions:
>To me, the first 3 pictures suggest that there is a faint greenish tinge in
the little shapes (hopefully >crystalline) there. I guess the idea of the
Topaz chip is that you can take it as is to the x-ray be
Postdoctoral candidates: Postdoctoral Position in Membrane Transport
The Pinkett laboratory at Northwestern University is seeking a highly
motivated individual for a postdoctoral fellow position in the field of
protein structural biology. The individual will join a research team
studying the str
Not with membrane proteins, however we use our Mosquito with 20 nl seeding
standard.
Strip 1 Protein, Strip 2 Seed stock solution
We first copy the plate by either picking up protein, then reservoir and
dispensing together 200-400 nl or we multidispense protein and add the
reservoir later (larg
What GFP did you use, your pH is 4.6 or something around there according to
your picture. If the pH is true GFP will be colorless. You certainly have some
more GFP lying around (without your protein fused to it), just titrate it and
see what pH dependency you have.
Jürgen
-
Jürgen Bosch
Johns
Dear Everyone,
As an MX representative of the Diamond User Committee we are writing
to remind you that the deadline is fast approaching for Expressions of
Interest in Diamond’s Phase III Beamline proposals, three of which are
aimed at MX. The three relevant beamlines and their representatives
are
Hi Tri,
To me, the first 3 pictures suggest that there is a faint greenish tinge in the
little shapes (hopefully crystalline) there. I guess the idea of the Topaz chip
is that you can take it as is to the x-ray beam or am I wrong?
Cheers,
Boaz
- Original Message -
F
That seems the right procedure.
I presume the two crystals have similar cell, etc?
What is the Riso plot from scaleit look like - if it is 55% + then there
is no isomorphism, but if it is < 30% then the map should be reasonable.
which phase did you use for the map calculation?
Eleanor
intekh
Dear CCP4 community,
I wonder if anybody has experience about the color of GFP crystals. Is there
any chance that the GFP crystal will become colorless? We are working on one
membrane protein fused with GFP. Since we got some crystals which didn't
show any color (Condition 01), I am not sure if I
Hi Intekhab Alam,
an Fobs-Fobs' map usually works only if the two crystals are
isomorphous, which means that there are neither large cell constant
changes nor any other larger structural changes (like overall rotations,
domain movements, other rearrangements) than the bound compound (ligand,
Hi Folks
I have a query regarding the difference map between the two structures
ligand bound data (2.5A) and native (2.8A).
I tried to calculate the fourier difference map between two data sets ligand
bound- native.
The protocol in CCP4 that i used is as:
1.merge the mtz file of native nad ligand b
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