An example of using MBP as a crystallization tag:
Ke A, Wolberger C. Insights into binding cooperativity of
MATa1/MATalpha2 from the crystal structure of a MATa1
homeodomain-maltose binding protein chimera.
Protein Sci. 2003 Feb;12(2):306-12
Ho
You might find this review useful:
X-ray Crystallography and NMR: Complementary Views of
Structure and Dynamics, Nature Structural Biology 4, 862-865 (1997).
The pre-publication manuscript is available on my website,
publication section.
Axel Brunger
On Nov 14, 2008, at 3:13 PM, Boaz Shaanan
Thanks Boaz,
They are protein crystals confirmed by spectra.
Deliang
- Original Message -
From: Boaz Shaanan
To: deliang
Sent: Friday, November 14, 2008 3:21 PM
Subject: Re: [ccp4bb] off-topic: soft crystals?
Hi,
You might like to check the content of those crystals b
oops, I forgot to give the reference:
Science (1992), vol. 257, p. 961
Boaz
- Original Message -
From: Young-Tae Lee <[EMAIL PROTECTED]>
Date: Friday, November 14, 2008 23:57
Subject: Re: [ccp4bb] X-Ray versus NMR Structure
To: CCP4BB@JISCMAIL.AC.UK
> Here are some of my thoughts
Hi,
I don't know what you mean by a systematic comparison between NMR and X-ray
structures, but in this paper from 1992 (maybe it's not good enough because
it's more than 10 years old - according to a recent paper in Science, articles
older than 10 years are referred to much less frequently th
Here are some of my thoughts and I was also seeking good references
pointing out systematic comparison of X-ray and NMR approaches.
Both X-ray and NMR structures are models calculated from experimental
data. Therefore coordinates from both structures have uncertainty and
are inevitably some
Hi Deliang,
I have an experience with soft crystals:
I used to work with a protein which crystallized fine and diffracted
fine. However, after opening the crystallization well few times,
crystals turned soft and they stopped diffracting. If I remember
correctly, letting crystals sit for a long ti
Hi there,
Do you ever have experience with the diffraction quality of soft crystals? I
just harvested some. They are 30K membrane protein, growing 10 months, size
~0.6mm*0.2mm*0.02mm, but as soft as a hair, no sharp surfaces.
We don't have synchrotron time in a few months and no experience with
How about this one:
Can't
Refine
Your
Structure
To
Acceptable
Likelihood
Typical error bars on crystallographic data are ~5% (R_sym), but with
very few exceptions the models in the PDB do not fit their corresponding
observations to better than ~40% error (R_cryst for intensities).
Gerard? W
> I've noticed that
> several papers describe NMR structures as "atomic resolution
> structures" and I'm just wondering what people think of this.
I think that "atomic resolution" is one of those terms which mean
different things to different people. There are clearly two groups
among crystal
Here's another paper you might want to have a look at:
Carson et al. His-tag impact on structure. Acta Crystallogr D Biol
Crystallogr (2007) vol. 63 (Pt 3) pp. 295-301
and here's the Structural Genomics paper (or one of them, I believe
there was another one which I originally thought of):
Li
Also check out the following reviews:
Protein Sci. 2003 July; 12(7): 13131322.
Crystal structures of fusion proteins with large-affinity tags
Douglas R. Smyth, Marek K. Mrozkiewicz, William J. McGrath, Pawel Listwan, and
Bostjan Kobe1
Gene Volume 281, Issues 1-2, 27 December 2001, Pages 1-9
Hi David:
I haven't read all my email yet so apologize if this has already been
mentioned, but Fred Allain and Gabriele Varani did something along
these lines specifically for nucleic acids (RNA):
F.H.T. Allain and G. Varani. How Accurately and Precisely can RNA
Structure be determined by
Regarding 64-bit linux, Phil Evans has set up a couple of boxes here at
MRC-LMB running 64-bit CentOS. These boxes run a 32-bit firefox and the
default gcj (gnu compiler for java) that comes with CentOS.
As for the protocol errors you are getting on windows I have never come
across them but a prel
I think we should slowly arrive in the 21st century and realize that
methods are complementary to each other.
I've never done NMR by myself only some xray stuff and attempts to
merge EM data with xray almost 10 years ago to arrive at ab initio
phases.
Sure one can argue what information can y
Actually on further thought I see that the problems associated with
restraining residual Biso's are even more serious, and even my
suggestion of ensuring that there's a flexible linker would not get
around it. Suppose you have a domain with an associated TLS group
connected to a flexible linker wh
Dear Tassos, Bernhard and David,
If I may push this humourous response (obviously tainted with
crystallographic bias) a little further, I would say that my favourite
mnemonic for the acronym "NMR" is
N eeds
M or
Google chrome works perfect for this
regards
spyros
O/H Nicholas Keep ??:
I have questions about baubles in general. I find that using firefox
(3.0.4 windows) baubles logs do not open directly from ccp4i or imosflm
and I get an error "i is not a registered protocol" (or c) which I think
is
I have questions about baubles in general. I find that using firefox
(3.0.4 windows) baubles logs do not open directly from ccp4i or imosflm
and I get an error "i is not a registered protocol" (or c) which I think
is the drive the file is on. However if I open the file in via "open
file "then it
Hi Pavel
I think Ethan made my point very nicely, so I don't really have much to
add, except maybe a concrete example will help. Let's keep it as simple
and ideal as possible: I hope you'll agree that any proposed method has
to at least work perfectly in the ideal case before you try to apply i
But there is a more fundamental difference. Crystallography determines the
positions (more or less accurate) whereas NMR measures distances between
certain atoms. NMR is local, 1-dimensinal information that -with enough data-
can be used to generate a three dimensional model compatible with it,
although I agree with the statement below, I would say that X-ray
crystallography also only generates a molecular model (not "a
structure"). Rather than a structure, X-ray crystallography generates
an electron density map. The quality of the model based in it depends
on the quality of this
Since I don't like attachments, I will first iterate the title of the
attached publication:
"Traditional Biomolecular Structure Determination by NMR Spectroscopy
Allows for Major Errors "
It immediately reminded me of an older one (ehm .. one author in
common!), addressed at that time mos
*PhD Position: Structural biology of protein-protein interactions in the
muscle Z-disk*
We are seeking a highly motivated PhD student to work on structural
characterization of important protein complexes centered on major
players of the Z-disk of striated muscle: alpha-actinin and filamin.
Bi
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