Welcome to the Predict a Secondary Structure Common to Two Sequences Web Server

The Predict a Secondary Structure Common to Two Sequences server takes two sequences, determines common secondary structures, and calculates base pairing probabilities. Two component programs are run, Dynalign and PARTS. Additionally, it creates two alignment files of the sequences. The structure predictions and the alignments can be constrained using constraint files. Note also that the server assumes the sequences are RNA.

If you plan to leave this page while waiting for calculations to complete, please make sure you have entered a valid email address below. Leaving this page without entering a valid email address will render results inaccessible.

If you need specific help using the Predict a Secondary Structure Common to Two Sequences server, please click here.

:
RNAstructure tools have been updated to version which includes several improvements.
Please contact us with any questions or issues regarding this update.

Select Sequence 1 Input:

- OR -
Enter your sequence title and content below (replaces upload if present).
Please enter nucleotides only, no headers or comments in content.
Valid nucleotides are A, C, G, T, U, and X (unknown nucleotide). Lower case nucleotides are forced single stranded in calculation.




Select Sequence 2:

- OR -
Enter your sequence title and content below (replaces upload if present).
Please enter nucleotides only, no headers or comments in content.
Valid nucleotides are A, C, G, T, U, and X (unknown nucleotide). Lower case nucleotides are forced single stranded in calculation.




Select Dynalign Options:

If a default value is left blank, the value is treated as if it was not changed at all.




Select PARTS Options:


If a default value is left blank, the value is treated as if it was not changed at all.

Specify the minimum and maximum probabilities to show on the dot plot.
If a specified probability is out of range, it is ignored.



Designate Address to Email Results: