lematic values(> 1.0) exist on middle parts but not
on N-/C- terminal residues.
Have you ever experienced this problem? How did you solve this problem?
Welcome any comments.
Best,
Hyunchul Kim
iven chain ID(e.g. 'A' or ' ')
>
> How can I obtain full chain structures without ligand structure by other
> methods than clicking one by one at any website.
>
> Thanks in advance.
>
> Best,
> Hyunchul Kim
>
> --
> Dr
w can I obtain full chain structures without ligand structure by other
methods than clicking one by one at any website.
Thanks in advance.
Best,
Hyunchul Kim
Hello Miguel,
Thank you for your reply.
It's related to the total SASA of a protein structure but not that of
per residue. However, it still give me a hint. :)
Best,
Hyunchul Kim
On Tue, 2007-07-24 at 08:12 +0200, Miguel Ortiz-LombardÃa wrote:
> Hello Hyunchul Kim,
>
> I fo
I am interested in the SASA per residue.
On Tue, 2007-07-24 at 14:43 +0900, Hyunchul Kim wrote:
> Hi all,
>
> Resolution doesn't matter when solvent accessible surface area(SASA) is
> calculated?
>
> If resolution is poor, I think that the SASA is not likely to be
>
Any comments are welcome :)
Thank you in advance.
Best,
Hyunchul Kim
Dear all,
I understood what they mean.
ASA -> Solvent accessible surface area
BSA -> Buried area among Solvent accessible surface area when it make
interaction
Sorry for self-questioning and -answering.
Best,
Hyunchul Kim
Forwarded Message
> From: Hyunchul Ki
has 0.00 square angstrom for both ASA and
BSA. How can this happen? I believe that ASA should be bigger than 0.00,
for instance, 100 angstrom square.
Best,
Hyunchul Kim
Ph.D candidate
Bioinformatics program
Keio University, Japan
accessible area by AREAIMOL but that
doesn't contain information for ratio or standard accessible area.
Any comment are welcome.
Thank you in advance,
Best,
Hyunchul Kim
