Dear all,

I am fitting a 25 Å negative stain EM map of a protein in complex with its FAb. 
I have restraints on the protein region the FAb recognises (from ELISAs on 
truncated versions of the protein) but I do not have the sequence of the FAb.

I have a model for the protein and I picked a FAb from the PDB to be a 
representative FAb model which I believe is good enough to fit a 25 Å negative 
stain EM map. By "good enough" I mean: this model would answer the question: " 
Can I fit this map with the protein and a FAb model and would the relative 
FAb:protein arrangement satisfy the known restraints on the FAb epitope?"

A PDB search with "unknown sequence" returns 17 entries:
1IVI,1TNV,1HR3,1QTJ,4CAT,2PGK,1PYK,1KGA,4GL8,1HKG,2YHX,1GRH,3LDH,4I79,1SNB,6IJ1,3CKM

What is your experience with depositing into the PDB structures of proteins of 
unknown sequence?

And as a user, would you accept an entry with a FAb as poly-Ala or Calphas only 
and poly-UNK?

Thank you for any feedback you'll be able to let me have,

with best wishes,

Pietro










Pietro Roversi

Lecturer (Teaching and Research) https://le.ac.uk/natural-sciences/

LISCB Wellcome Trust ISSF Fellow

<https://bit.ly/2I4Wm5Z>https://le.ac.uk/liscb/research-groups/pietro-roversi


Leicester Institute of Structural and Chemical Biology
Department of Molecular and Cell Biology, University of Leicester
Henry Wellcome Building
Lancaster Road, Leicester, LE1 7HB
England, United Kingdom

Skype: roversipietro
Mobile phone  +44 (0) 7927952047
Tel. +44 (0)116 2297237



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