--- On Mon, 24/1/11, Eleanor Dodson wrote:
From: Eleanor Dodson
Subject: Re: [ccp4bb] Merging statistics and systematic absences
To: CCP4BB@JISCMAIL.AC.UK
Date: Monday, 24 Jan
Dear All,
Electron density picture is attached here.
or
https://docs.google.com/leaf?id=0B89uj7DSbtUWNDRmMzZhNTAtMzlkMC00MDllLTgxYmItNDI0NzUwMjdlNTli&hl=en
I am working on a structure at 1.45 Ang resolution. I have noticed a density
that looks like water. However, it is surrounded by by six ot
Hi Everyone,
I have to crystallize one protein which contains a zinc fingure motifs, I am
facing a problem in crystallization. I already used 388 buffers . Can anyone
suggest me some books or papers freely available online on Buffers required for
crystallization.
Thanks
Use ALINE sequence editor. if you multiple sequence alignment file from
clustalW, you can open in ALINE software and generate publication quality of
image.
http://crystal.bcs.uwa.edu.au/px/charlie/software/aline/
--- On Thu, 18/8/11, Yuri wrote:
From: Yuri
Subject: [ccp4bb] Sequence Alignm
hi,
i have install CCP4 in /home/chandan/ccp4/ccp4-6.1.1. its open perfectly in
this directory by using ccp4i command.
but when i create a new user account in linux, then
ccp4i was not working in new user account.
please suggest me how i can
Dear Christine,
Your fist question is regarding range of energy in high affinity. In Autodock
Vina high affinity energy varies from -9 to -11 Kcal/mol. In my opinion -4.5
to -3.0 Kcal/mol is moderate affinity for ligand.
Second question is how to save individual orientation of Vina output in
