CCP4BB@JISCMAIL.AC.UK
Sent: Tue, Apr 16, 2013 7:39 pm
Subject: [ccp4bb] Difficult data
Hello,
I am having a few issues with a data set I have been working on recently,
and was hoping to get some ideas on how to deal with it, if anyone is in
the mood.
I have been working with a very small
advice would be: go back to
the lab and try to get another crystal form.
Herman
From: CCP4 bulletin board [mailto:CCP4BB@JISCMAIL.AC.UK] On Behalf Of Stephen
Campbell
Sent: Wednesday, April 17, 2013 5:53 AM
To: CCP4BB@JISCMAIL.AC.UK
Subject: Re: [ccp4bb] Difficult
, 2013 7:39 pm
Subject: [ccp4bb] Difficult data
Hello,
I am having a few issues with a data set I have been working on recently, and
was hoping to get some ideas on how to deal with it, if anyone is in the mood.
I have been working with a very small bacterocin (about 3 kDa) and set up some
Hello,
I am having a few issues with a data set I have been working on recently,
and was hoping to get some ideas on how to deal with it, if anyone is in
the mood.
I have been working with a very small bacterocin (about 3 kDa) and set up
some crystal trays in hope of getting some high
Maybe you crystallized something else? Did you look up that unit cell in the
PDB?
I am having a few issues with a data set I have been working on recently, and
was hoping to get some ideas on how to deal with it, if anyone is in the mood.
.
Yes- this has happened to us so often recently that I've taken to checking every
new crystal form against the nearest cell server before starting heavy atom
search.
That would account for the poor reproducibility.
Yeast glutamate-cysteine ligase (e.g. 3LVV) crystallizes with nearly identical
Hi Everybody,
Thanks so much for all the help! I suppose I should give more info.
Marco, the data is twinned - I forgot about that in my initial posting. I
can't remember the stats, but it is not a perfect twin. I thought that
Phaser accounted for twinning, and I haven't got a solution good
