It looks like as if your PDB is corrupt. For example there atoms B
that should not be present inamino acids.
Garib
On 9 Jul 2007, at 19:55, JINJIN ZHANG wrote:
Hello all,
I'm working on a protein-DNA complex. My protein is a trimer and
the crystal has 3 trimers in an AU. I used a pdb
You might also want to loook into using parathone for freezing... Or
collection at 260K indeed!
Flip
-Original Message-
From: CCP4 bulletin board [mailto:[EMAIL PROTECTED] On Behalf Of
mesters
Sent: Tuesday, July 10, 2007 11:01
To: CCP4BB@JISCMAIL.AC.UK
Subject: Re: [ccp4bb] Help with
Jeroen brings up a good point. Back in the old days, around 5 B. C.
(Before Cryo), we would use a chilled air generator to blow a stream
of cold air along the capillary axis to keep the crystals just above
their freezing point--it made a huge difference in crystal lifetime.
I recall a
I have a Shelx HKLF4 formated reflection file that I would like to
convert to a mtz file. The primary reason is to transfer the freeR
set. I found a couple of convoluted ways of converting the
reflection data, but no real way of getting the freeR set to transfer.
Any suggestions?
Cheers
This notification is posted on behalf of Prof Wim Hol. Interested parties
should reply to him at:
[EMAIL PROTECTED]
or at the address below.
Postdoctoral Fellow Structural Biology of the RNA editing editosome
JOB DESCRIPTION:
The project aims at understanding the
You can use f2mtz with the format identifier to convert the file:
8 snip- script start --
#/bin/bash
f2mtz hklin yourshelxfile.hkl hklout yourmtzfile.mtz eof
cellyou cell dimensions
symm your space group
format '(3F4.0,2F8.2,F4.0)'
ctypout H H H J Q R
LABOUT H K L
