Dear CCP4s
I am trying to solve a structure for which I have two datasets: One comes from
a selenomethionine derivatized crystal at 3 A resolution and the second comes
from a native one that gave 2.6A. I have obtained workable experimental phases
by SAD using SOLVE/RESOLVE. With this I have b
Dear AllI would like to know whether oxidation of Se entails any problem for
SAD or MAD experiments and/ or how to resolve it. Cannot use DTT or reducing
agents in my protein (extracellular and disulphide bonds are
important).ThanksDr. R.DepetrisWeill Cornell Medical College
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Hello All:
I would like to know if anyone has or knows how to gte this Ecoli strain which
proved to be good for periplasmic protein expression. Ecoli K12 SB 536.
If not, which other strain is good for that?
Thannks Much
Dr. R. Depetris
Weill Cornell Medical College
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Dear All
I am working with a viral protein that contains an ectodomain, a TM segment and
a cytoplasmic region. I was wondering if there is a general strategy that
allows the addition of the transmembrane segment to the ectodomain without
compromising solubility and secretion.
Thanks
Dr. R. D