Hello,
In my understanding of NMR, the loops and terminii that adopt very
different conformations in the structure ensemble rather reflect the
fact that for those residues, the number of constraints is lower, thus
the number of structures that fulfil the constraints is larger.... A
dynamics study of the protein will be much more informative.
Cécile
Le 26/05/2021 à 17:29, S. Mohanty a écrit :
Hi Harry,
The superpose/overlay of all the structures in PyMol should inform you
the rigid part of the protein as well as the flexible part. The rigid
part would have very low backbone RMSD or overlay tightly and the
flexible part (loops, N-term and C-term etc.) would not superpose
tightly. If you check literature, the dynamics of the protein may have
been studied through NMR relaxation.
Smita
On Wednesday, May 26, 2021, 10:05:05 AM CDT, Harry Powell - CCP4BB
<0000193323b1e616-dmarc-requ...@jiscmail.ac.uk> wrote:
Hi
Given that there are plenty of people on this BB who are structural
biologists rather than “just” crystallographers, I thought someone
here might be able to help.
If I have a structure in the PDB (e.g. 2kv5) that is an ensemble of
structures that fit the NOEs, is there a tool available that will give
me some idea about the bits of the structure that do not vary much
(“rigid”) and the bits that are all over the place (“flexible”)?
Would superpose or gesamt be a good tool for this? Ideally I’d like
something that could add a figure to the B columns in a PDB file so I
could see something in QTMG (or PyMol if forced…) or do other useful
things with the information.
Harry
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