defined in LINKR record. The same applies when
I want to refine just A502-A504 alpha1,6 glycosidic bond without refine
A503.
I am just wondering what is the state of the art for branch chain handling
in coot or another interactive refinement program.
best regards,
Heping Zheng
> On 22/11/11 00
I remembered that people had crystallize a series of
streptavidin-2-iminobiotin structures at a low pH. If it might help, check
the following PDBIDs:
2RTD
2RTE
2RTI
2RTK
2RTL
> Hi everyone
>
> I have a protein that is extraordinarily stable at PH=3.0 or even 2.0.
>
> I want to crystallize it in
Ronnie --
The list that I have in a home database contains 89 instances of a CXC in
53 files when C-C forms a disulfide bond. The records returned are ordered
by the name of "X" residue from CXC motif for convenience.
There is indeed PRO in one case (2zxt), but it is not the major
observation in
If you want to use absorption spectroscopy, it depends on whether or not the
heavy atom under investigation have significant absorption at the X-ray
wavelength you have at home lab. If that is the case, you should be able to see
the absorption and tell whether or not the heavy atom has been inco
