You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
By default, the crosslinking restraints, for all crosslinked residue pairs (r1, r2), will add contributions from all copies of that residue. I.e., for two copies of a molecule (c1 and c2), four contributions are added to the restraint: [c1r1-c1r2], [c1r1-c2r2], [c2r1-c1r2], [c2r1-c2r2]. The restraint is evaluated on the residue pair with the smallest distance.
Certain crosslinks, however, can be unambiguously assigned as intermolecular. Specifically, those crosslinked peptides that have overlapping sequence must come from different macromolecules. It would be nice to be able to flag these type of crosslinks and remove the intra-molecular contributions. This is especially important because, since the two crosslinked residues are likely very close in sequence, they are likely to be satisfied by the intra-molecular contribution.
I think the best way to do this would be:
Utilize the link_type_key and create a conditional in the restraint code that looks for link_type_key=="Interlink" or link_type_key=="Intralink" and creates the appropriate contributions. A link_type_key=="Ambiguouslink" could be used for crosslinks without this information. These keys may have to be manually added to the crosslinking datafile or manually identified in the XLDB. The XLDB code could also automatically detect these overlapping peptides.
The text was updated successfully, but these errors were encountered:
It is a good idea, it never happened to me, and it must be included!
Riccardo Pellarin, PhD
===================
Institut Pasteur
CNRS UMR 3528
25, rue du Docteur Roux
75724 Paris Cedex 15, France
[email protected]
+33 (0)1 44 38 93 63
On Wed, Oct 24, 2018 at 7:22 PM Daniel Saltzberg ***@***.***> wrote:
By default, the crosslinking restraints, for all crosslinked residue pairs
(r1, r2), will add contributions from all copies of that residue. I.e., for
two copies of a molecule (c1 and c2), four contributions are added to the
restraint: [c1r1-c1r2], [c1r1-c2r2], [c2r1-c1r2], [c2r1-c2r2]. The
restraint is evaluated on the residue pair with the smallest distance.
Certain crosslinks, however, can be unambiguously assigned as
intermolecular. Specifically, those crosslinked peptides that have
overlapping sequence must come from different macromolecules. It would be
nice to be able to flag these type of crosslinks and remove the
intra-molecular contributions. This is especially important because, since
the two crosslinked residues are likely very close in sequence, they are
likely to be satisfied by the intra-molecular contribution.
I think the best way to do this would be:
Utilize the link_type_key and create a conditional in the restraint code
that looks for link_type_key=="Interlink" or link_type_key=="Intralink"
and creates the appropriate contributions. A
link_type_key=="Ambiguouslink" could be used for crosslinks without this
information. These keys may have to be manually added to the crosslinking
datafile or manually identified in the XLDB. The XLDB code could also
automatically detect these overlapping peptides.
—
You are receiving this because you are subscribed to this thread.
Reply to this email directly, view it on GitHub
<#245>, or mute the thread
<https://github.com/notifications/unsubscribe-auth/ACXOkKXrBO1jD9pqcZxCAgQ2gnNib0ftks5uoKHwgaJpZM4X4axB>
.
By default, the crosslinking restraints, for all crosslinked residue pairs (r1, r2), will add contributions from all copies of that residue. I.e., for two copies of a molecule (c1 and c2), four contributions are added to the restraint: [c1r1-c1r2], [c1r1-c2r2], [c2r1-c1r2], [c2r1-c2r2]. The restraint is evaluated on the residue pair with the smallest distance.
Certain crosslinks, however, can be unambiguously assigned as intermolecular. Specifically, those crosslinked peptides that have overlapping sequence must come from different macromolecules. It would be nice to be able to flag these type of crosslinks and remove the intra-molecular contributions. This is especially important because, since the two crosslinked residues are likely very close in sequence, they are likely to be satisfied by the intra-molecular contribution.
I think the best way to do this would be:
Utilize the
link_type_key
and create a conditional in the restraint code that looks forlink_type_key=="Interlink"
orlink_type_key=="Intralink"
and creates the appropriate contributions. Alink_type_key=="Ambiguouslink"
could be used for crosslinks without this information. These keys may have to be manually added to the crosslinking datafile or manually identified in the XLDB. The XLDB code could also automatically detect these overlapping peptides.The text was updated successfully, but these errors were encountered: