I am wondering what is the overall experience with N-linked glycosylation contribution to the ab initio model - i.e. how much will be the glycan visible in the shape of the envelope. I am assuming that when the N-linked glycosylation is more or less flexible it wont be "visible" in the shape of the envelope, similarly to electron densities in high-resolution structures. But when the glycan is stabilized and rigid than it will be more significantly pronounced in the ab initio envelope.
Are these correct assumptions?
Calculation of SAXS and SANS profiles (CRYSOL, CRYSON), superposition of models (SUPCOMB, DAMAVER, DAMCLUST), database DARA
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