[Biopython] Understanding pdb biopython

[Sanjeev Sariya]

Hi Joao,Thank you for response.If all residues aren't resolved in crystal, then extracting sequence from pdb, wouldn't be a good call.
 I will be working a lot [~100s or 1000s] in near future. Is there any way, I can find break in my pdb file?

- Another doubt, I've, while printing the chain.ids in script. Many times, I get  chain " ", that is a space. In script sent, code looks like:
        st=PDBParser(QUIET=True).get_structure('X',i)
        ko=st.get_chains()
        for i in ko:
            print i.id 
Why space name is present? 

Thanks.

     On Saturday, October 25, 2014 12:32 AM, João Rodrigues <anaryin at gmail.com> wrote:
   

 Hi there,
The numbering in your PDB file is not continuous and it matches to regions in the structure that are missing residues. Open your PDB structure in Pymol and you'll see. Alternatively, print the C-N distances (peptide bond) for consecutive residues and you'll also notice when they are larger than ~3Å it corresponds to your break. 

As for your discrepancy between the sequences in the FASTA file and the PDB, that's just because not all residues are resolved in the crystal structure.
Cheers,
João
2014-10-24 13:10 GMT-05:00 Sanjeev Sariya <s.sariya_work at ymail.com>:

Hi All,I'm having a hard time using and understanding biopython pdb../read_pdb_file.py 3OE6.pdb
I'm attaching python script, pdb file, fasta file and output with mail.I'have following doubts:- When I print the sequence I get in broken pieces. Why?- Also the sequence printed doesn't match with the fasta file (attached).- Am I doing making a silly mistake?
I am running script as:
python read_pdb_file.py 3OE6.pdb 
Kindly help and guide.


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