hello amber users,
I tried to load a double stranded tRNA sequence having a minor RNA base INOSINE ( the sequence had been taken from pdb 1XNQ) in xleap. I used leaprc.rna.ff02 force field to start xleap, but unfortunately xleap could not recognise the INOSINE residue. I even loaded the all_modrna.ff08.lib, hoping that the situation will improve, INOSINE still remained unrecognised by xleap.
When I tried loading another double stranded RNA sequence having all standard residues ( G and C), I could easily generate the prmtop and inpcrd files.
Am I choosing a wrong force field for the INOSINE containing sequence?
Kindly help me out.
with regards, thanking in advance.
Gunajyoti
Neh university
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Received on Thu Sep 17 2009 - 01:30:02 PDT
