Do you want to read a STRIDE (or DSSP) output or do you want to implement the method in MDAnalysis?

In anyway we'll need a secondary structure topology attribute. What should be its value for the atoms that are not part of a protein? numpy.nan?

DSSP (new) is open source http://swift.cmbi.ru.nl/gv/dssp/ ; a while back I looked into wrapping but that was too complicated. A cython reimplementation that uses a Universe would be useful.

Ok I've started this. I've got a conda build recipe for STRIDE here which should allow conda install stride to get the binary in place. I've then got a pystride python package, which runs the binary and returns the output. Then within MDA we can have a layer (probably MDAnalysis.analysis.stride) which takes mda objects (AtomGroup and Universe) and goes to and from the pystride package.

I'm a little hesitant to put the stride stuff into core/ because it relies on an external binary, which can be a little flaky.

It for sure should not go in core as it calls an external program. Also, now that I think about it, we do not have support for time dependent topologies, so we cannot store the secondary structure in a topology attribute. I uses Martini too much, I forgot secondary structures could change over time...

@jbarnoud I was actually thinking today we could do time dependent TopologyAttrs by having a mechanism similar to what @mnmelo used for UpdatingAtomGroup which lazily refreshes contents if the current ts.frame is different.

You could consider the secondary structure an auxiliary that is indexed with residue index.

Then you just have to write an AuxParser for the STRIDE or DSSP output.

If you want to do selections then instead of using time-dependent topologies, add something to the selection language to select on Aux data, similar to prop z > 3.

I removed "STRIDE" from the issue title because of licensing concerns MDAnalysis/stride#2. A secondary structure detection would be great (especially if we could do it natively without piping into external tools).

It would be great if we had "pydssp" ... see MDAnalysis/dssp#1