A large amount of hypotheticals can be found in Plasmodium :-)
Jürgen
-
Jürgen Bosch
Johns Hopkins Bloomberg School of Public Health
Department of Biochemistry & Molecular Biology
Johns Hopkins Malaria Research Institute
615 North Wolfe Street, W8708
Baltimore, MD 21205
Phone: +1-410-614-4742
Lab:
David is absolutely right. There is no design, Jacob, we just
instinctively look for it everywhere because seeking purpose instead of
understanding mechanism conveys advantage to our species. Your
rationale is flawed - just because it is imaginable (with caveats) does
not mean that it must exist
Dear All,
My new Mac is affected by a bizarre software bug (or a feature), which has
been reported on this board earlier. In fact, it has been more than a year
since this problem was first reported, but it has not been resolved yet as
far as I can tell. Namely, it is not possible to add the ARP/wA
Dear CCP4bb,
I am posting an advert for a postdoctoral position at Celgene, San Diego
on behalf of a friend. Please apply for this position via the Celgene
website at www.celgene.com :-
*A postdoctoral fellow is sought in structural biology at Celgene, San
Diego.*
Celgene is a multinational
Hi Jacob and Mike,
An additional thought exercise would be to consider if your
exogenously added protein is itself heritable. Essentially trying
Mike's idea 1, but instead of expecting the protein to get into the
genome and in that way have it's "information" stored, look to see if
the protein it
Hi Jacob,
A couple more things to think about:
1.) How to get a Nobel Prize: Try an experiment if you have the means.
Transform/transfect your favorite cell type with exogenous protein sequences.
Sequence and see if they ever appear in the genome. Go after it...
2.) I realize that the idea of
I would like to have the following Post Doc Research Fellow opportunity
posted please.
Thanks very much,
Chandra
*Chandra Farnsworth*
*Staffing Consultant*
Genentech, Inc.
Research and Early Development
650-225-7110
--
Dear Daniel,
probably the first and easiest thing you could check is whether the freezing
conditions are suboptimal, by a room temperature measurement.
If that fails, you can add another purification step to your complex (certainly
worth a try), and/ or a restricted proteolysis, which might chop
On Wed, Sep 08, 2010 at 08:21:33PM +0200, Nikos Pinotsis wrote:
> quite straightforward with
> moleman2
> and the command stat
... after the command 'xyz align', but the 'stats'-command tells you about it.
Tim
>
> On Wed, September 8, 2010 19:37, Brett, Thomas wrote:
> > Hi all:
> > Is there prog
Hello Rongjin Guan,
when I enter 'dimer ncs' at www.ixquick.com, there are quite a few hits, some of
which could be of interest for you. Why do you think this could be a
crystallization artefact?
Tim
On Wed, Sep 08, 2010 at 12:50:43PM -0400, Rongjin Guan wrote:
> Dear All,
>
> I have a structur
Hi Cyrstallographers
I made the crystal of triple complex and the M.W is about 500 kDa.
However, the diffraction is about 8 A.
At first, the crystal form was needle. the needle form was changed by
addtive screening.
the crystal condition is under 1 M ammonium formate with Hepes (pH 7.5).
Cr
quite straightforward with
moleman2
and the command stat
On Wed, September 8, 2010 19:37, Brett, Thomas wrote:
> Hi all:
> Is there program or utility out there that will give maximum protein
> dimensions (length and width) from the pdb file? I'm sure there is, just
> curious what people use.
> Th
Hi all:
Is there program or utility out there that will give maximum protein dimensions
(length and width) from the pdb file? I'm sure there is, just curious what
people use.
Thanks,
-Tom
I don't think this is uncommon at all. For
example, we published a structure where 10 chains did not bind
ligand at all, and 2 chains did in the ASU (see PDB 3E3I). We have
also recently solved a structure where two active sites in the ASU
are in different states
Dear All,
I have a structure with two complexes in the asymmetric unit, and the
interactions
on the interface are not the same in the two complexes. Briefly, there are two
additional
hydrogen bonds in one complex, but not in the other. This coule be due to
crystallization
artefact, but may have
On 09/07/10 22:10, Jacob Keller wrote:
In terms of "usefulness," I was actually thinking about cells learning how
to make new proteins from other cells,
Which they do already by exchanging genes
or perhaps an immune system could use
the info to make the right choice of starting materials.
Th
On Sep 8, 2010, at 6:31 AM, Jerry McCully wrote:
> Dear All:
>
> In my case, a 15KD protein without disufide bonds was expressed as
> inclusion bodies in E.coli but can be refolded as monomers with a very low
> solubility.
>
> Adding glycerol did not help so far.
>
> To incre
Expression of Interest
The Section of Genetics, Cell Biology and Development, Department of
Biology, University of Patras, Greece, is seeking potential postdoctoral
partners of any nationality for a joint grant application to fund 2-3
years research projects
Expression of Interest
The Section of Genetics, Cell Biology and Development, Department of
Biology, University of Patras, Greece, is seeking potential postdoctoral
partners of any nationality for a joint grant application to fund 2-3
years
research projects
19 matches
Mail list logo
