Great work from post-doctoral fellow @joanzone.bsky.social:
New preprint on identifying active structures of protein kinases -- capable of binding ATP, Mg ions & especially substrates -- +modeling all 437 human catalytic protein kinase domains in their active conformation.
doi.org/10.64898/202...
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And once again many thanks to my friend and colleague @hakimi.bsky.social for discovering the Toxoplasma protein GRA24 - it has a very tight binding KIM motif that we used to stabilise the MEK-ERK complex!
www.cell.com/structure/fu...
Molecular basis of mitogen-activated protein kinase ERK2 activation by its upstream kinase MEK1 www.biorxiv.org/content/10.64898/2026.01.19.700303v1 #cryoEM
Molecular basis of mitogen-activated protein kinase ERK2 activation by its upstream kinase MEK1 https://www.biorxiv.org/content/10.64898/2026.01.19.700303v1
Molecular basis of mitogen-activated protein kinase ERK2 activation by its upstream kinase MEK1 https://www.biorxiv.org/content/10.64898/2026.01.19.700303v1
Wonderful support from Pauline Juyoux and Guy Schoehn IBS Grenoble on the amazing new CM02 microscope, @gervasiolab.bsky.social for wonderful MD studies!
β
MEK1 binds ERK2 at multiple sites remote from the activation loop
β
Molecular details of phosphorylation of the ERK2 activation loop tyrosine
β
MEK1 can bind ERK2 in the absence of nucleotide - suggesting a processive mechanism
β
ERK2 binding destabilises the regulatory A-helix of MEK1
Then HR-HAIR from @olibclarke.bsky.social really improved our reconstructions www.biorxiv.org/content/10.1...
HexAufoil grids from Chris Russo's group @mrclmb.bsky.social gave amazing results for this 86 kDa complex!
New Preprint alert! Excited to share our latest work on the #MAPKinases from stellar PhD student Jill von Velsen. First structures of the MAP2K MEK1 activating its substrate MAPK between 2.9 and 3.6A - amazing resolutions for such a small and mobile complex! www.biorxiv.org/content/10.6...
I'm looking forward to speaking at this course (and finally seeing my PhD-labmate @mattbowler.bsky.social's institute in Grenoble)!
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#EMBOMacromolecular will highlight the strategic use of cutting-edge protein structure prediction methods, and recent advances in in situ structural biology. Apply by 18 Feb to join us at EMBL Grenoble! π§¬
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Very pleased to be on the organizing committee of the EMBO course Structural Characterization of Macromolecular Complexes in 2026! We have a fantastic line up of speakers and tutors, please share widely!
πapply here: www.embl.org/about/info/c...
Are you working on challenging projects in structural biology?
#EMBOMacromolecular will highlight the strategic use of cutting-edge protein structure prediction methods, and recent advances in in situ structural biology. Apply by 18 Feb to join us at EMBL Grenoble! π§¬
s.embl.org/mmo26-01-bl
Another amazing drug repurposing study from Silvia Diaz Martin Alexandre Bougdour Christopher Swale and @hakimi.bsky.social Very pleased to have supported the structural work on our favorite protein family - the kinases!
Nature Com. now live! π Silviaβs amazing PhD supervised by Alex βthe Greatestβ & Christopherβs big-bang contribution. Huge thanks to our stellar team & collaborators. We went fishing in the FDA pond and hooked LY2090314 π£ Blocks GSK3 π―in #Toxoplasma & #Crypto
www.nature.com/articles/s41...
For sure, Macronβs troubles are partly of his own making. But there is something immensely sad about a pro-European leader and standard-bearer for the democratic centre ending up with such a political mess
These results are truly impressive! But I do worry that #cryoEM is moving into a phase where progress is made by optimizing parameter settings for black box programs. The devil is often in the details, and I am not sure how this could be implemented in #relion, as stated, without more info.
Zeus had his Hydra βοΈ, now Toxoplasma has its own.
Meet Hydra: not a monster, but a brand-new protein domain.
It multimerizes like crazy & rewrites the chromatin landscape 𧬠in Toxoplasma.
Our team and colleagues from @embl.org #Grenoble just dropped the preprint π
www.biorxiv.org/content/10.1...
We believe that maintaining MAP kinase signaling when ATP levels have been depleted, for example under hypoxic conditions, that occur under a number of cell stresses, such as cancer and atherosclerosis, would be an advantage.
Using radiolabeled nucleotides @PaulineJYX was able to demonstrate clearly that the beta-phosphate is transferred to p38. She then also showed that the other MAP2Ks also show this property, but that RIP2K does not.
While preparing the MKK6-p38 complex for structural studies (science.org/doi/10.1126/scβ¦) we noticed that p38 was activated by MKK6 in the presence of ADP as well as ATP
In our new paper @asbmb.bsky.social JBC we detail our surprising discovery that the MAP2Ks can use ADP to phosphorylate their substrate MAPKs β driven by @paulineJYX @ErikaPellegri13 and @jvonvelsen
t.co/spLZbaz5Wk
Thrilled to share my first paper, now out in
@natmicrobiol.nature.com! Huge thanks to my amazing supervisor @hakimi.bsky.social and everyone who contributed to this work!
www.nature.com/articles/s41...
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We are very happy. The Editors of Journal of Applied Crystallography have chosen figures from our article (journals.iucr.org/j/issues/202...) to feature as the cover image for the February 2025 issue. THANKS
RIP Sine. She hired me as beamline scientist on ID14 @esrfsynchrotron 17 years ago and was a great director putting automation to the fore ultimately leading to @ID30_MASSIF1