Hi Yasser, These are scientific issues that would probably be better answered by literature searching and reading some relevant papers, but here are my opinions: (1) Why use B-factor when SASA already directly describes the solvent- accessibility of atoms in the structure? They are two different things. Yes, you would often expect them to be correlated, but I don't see any reason to complicate your decision by considering B- factor. There are factors such as crystal packing that would cause deviations from the expected correlation. Personally, I would just use coloring by areaSAS or areaSES values (as mentioned in the earlier mail) in Chimera to decide on some cutoff, and then stick with it, or use the GetArea server to calculate % exposed and use that instead. (2) I'm not aware of any commonly used B-factor cutoff, and it seems like the value would depend on what you were going to do after applying the cutoff. I'm not even sure if the values from one structure can be compared to the values from another without some kind of normalization. Other people may have different opinions, or more knowledge in this area, however! Elaine ----- Elaine C. Meng, Ph.D. UCSF Computer Graphics Lab (Chimera team) and Babbitt Lab Department of Pharmaceutical Chemistry University of California, San Francisco On Apr 7, 2010, at 8:24 AM, Yasser Almeida Hernández wrote:
Thanks for your answer... About this i have an idea resumed in two question: In principle an solvent-exposed residue must have in average high value of b-factor, so will be very flexible.
1 - Can i say that those residues that have and average b-factor up to a cutoff value AND an areaSAS (or % of that area) superior than a other cutoff value, will be exposed to the solvent???
2 - There is a cutoff value of b-factor for the residues flexibility?
Best regards