Hello Paul,

thank you for the kind reply.

Btw. wouldn't AI-assisted coding help you? Americans are already pretty
near this milestone - you get like the most of it written and than just go
through it and make it perfect... I think it is like with the progressive
Italians making their marble sculptures using 400 000 USD robots - they
make 99 %, but the final human touch makes them perfect...

OK, I may drop a line to Sjors. May be I will add, besides stressing how
important is the cross-eye stereo, some other suggestions, like a hot key
for moving by 10 residues (thanks for space forward and shift+space
backward, that is awesome) (ctrl+space 10 forward and ctrl+shift+space 10
backward?).

Michal
---
Michal Navrátil, PhD


čt 22. 1. 2026 v 18:39 odesílatel Paul Emsley <[email protected]>
napsal:

> Hello Michal,
>
> On 21/01/2026 01:58, Michal Navratil wrote:
>
> > Dear Prof. Emsley,
> >
> Max Perutz once came to York to give a presentation to the PhD students
> where he was introduced as "Professor Perutz" - he gently corrected the
> host saying "I work at the LMB, I am not a professor - but my son is!"
> The audience chuckled. (Likewise I am not a professor either.)
>
> >
> > thank you for estimating how much of your precious time would be needed.
> >
> > I really appreciated the cross-eye stereo feature, because I could
> > refine my structures just everywhere using my notebook. And in our
> > lab, I was not bound to the few computers with 3D goggles , which were
> > btw. crappy and constantly failing.
>
> Likewise ours. Pre-covid I routinely saw people using stereo. Post-covid
> I have seen no-one.
>
> >
> > On the other hand, there were some other, perhaps more important
> > issues in Coot. For example, grabbing a certain part of peptide chains
> > for the quick fitting feature (into el. dens. map) in a large protein
> > was pretty laborious and slow, and at least I often grabbed some
> > completely different parts of the protein.
> If your molten zone is more than about 200 residues that can be an issue
> on older hardware, but still, it sounds disappointing. For large
> regions, using the GM restraints is a good idea, I have a YouTube video
> on it I think, and I did one for SBGrid several years ago now (and
> things have become smoother and faster since then).
> >
> > Also, selecting multiple amino acids on a large protein was quite
> > difficult - one had to constantly scroll back and forth in a small
> > single line window... That was quite unpractical.
>
> Sound painful. Typically, one extracts (copies) a working fragment
> (using Copy Fragment), does the modelling operations on that, the slots
> that fragment back into the main molecule using Replace Fragment.
>
> Or you can make the residue selection using Python, for example
>
> coot.refine_residues_py(0, [["A", r, ""] for r in range(10,21)])
>
> >
> > I wish someone had the patience to teach me programming things like
> > this...
>
> Funny you should mention that. I have been working on a way to have
> Claude communicate with Coot (i.e. "program" Coot using prose). I am
> enthusiastic about it and will write it up soon - in a blog article at
> least.
>
>
> >  I wish there wasn't so much sheer disregard like this for
> > scientists... I wish I could fund you for the one extra week of your
> > work, or write a letter to the King Charles III about how such work is
> > worth funding...
>
> Made me laugh. A letter to the king probably won't do much good.
> However, if you or anyone else would like to send a letter of support
> for my work to my boss (who doesn't see the value of Coot and/or my work
> in the way that I do (he isn't a crystallographer)) that would be more
> valuable.
>
> His name is Sjors Scheres, scheres@(same-place-as-me)
>
> Regards,
>
> Paul.
>
>
>
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