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#structuralbiology

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New Presidential executive order on proteins:

All amino acids now to be right w̶i̶n̶g̶ handed.

Leftist amino acids to be outlawed.

(Also, Z-DNA is deemed to be Communist, and is prohibited.)

Trans- and cis- peptide bonds to be banned.

Non-binary amino acid Glycine to be banned.

Proline is not a real amino acid and will be banned immediately.

Phenylalanine looks and sounds a bit like Fentanyl, banned immediately.

@strucbio #StructuralBiology #PDB

This study investigates the surprising limitations of AlphaFold 2 (AF2) in predicting protein structures—specifically its tendency to confidently predict β-solenoid folds for repeat proteins, even when the structures are unrealistic or unstable.

🔗 AlphaFold 2, but not AlphaFold 3, predicts confident but unrealistic β-solenoid structures for repeat proteins. DOI: doi.org/10.1016/j.csbj.2025.01

📚 CSBJ: csbj.org/

Our new preprint on the impact of protein phosphorylation on structures is now out!

Protein phosphorylation is a key regulator of cellular processes.It's ubiquitous, yet the function and relevance of most phosphosites is unknown. Understanding phosphosite function requires elucidating the structural mechanisms through which it acts. (1)

biorxiv.org/content/10.1101/20

@bioinformatics @strucbio #bioinformatics #protein #StructuralBiology

bioRxiv · Global comparative structural analysis of responses to protein phosphorylationPost-translational modifications (PTMs), particularly protein phosphorylation, are key regulators of cellular processes, impacting numerous aspects of protein activity. Despite widespread phosphorylation of eukaryotic proteomes, the function of most phosphosites remains unknown. Elucidating the structural mechanisms underlying phosphorylation is crucial for understanding its regulatory roles. Here, we conducted a comparative structural analysis of phosphorylated and non-phosphorylated proteins taken from the Protein Data Bank (PDB). Our study systematically evaluates how phosphorylation affects backbone conformation, protein dynamics, and mechanical strain. We found that phosphorylation commonly induces small, stabilizing conformational changes through conformational selection and frequently modulates local residue fluctuations, influencing overall protein motion. Notably, a small but significant subset of phosphosites shows mechanical coupling with functional sites, aligning with the domino model of allosteric signal transduction. This work provides a foundation for studying phosphorylation and other PTMs in their structural context, which will guide the rational design of synthetic phosphosites and enable the engineering of PTM-driven regulatory circuits in synthetic biology. ### Competing Interest Statement The authors have declared no competing interest.

Juan Mateos-Garcia of Google DeepMind wants equitable use of their tools like AlphaFold. They solved protein structure prediction in 2020 and this is helpful for drug discovery, but researchers in LMIC have barriers to adoption.

Used OpenAlex & PDB to study 20.6K papers citing AlphaFold. LMIC researchers are underrepresented, but study of diseases affecting LMICs is overrepresented - esp. work on natural products.

#Introduction #Introduktion

I've spent a lot of my life doing #StructuralBiology and playing #Music #ClassicalMusic.

I like to #read #books, mostly #fantasy but also #clifi and #scifi.
A fan of both #StarTrek and #StarWars, each has its merits. (Yes TNG is the best, but only because I grew up with it).

Currently I'm interested in #biosustainability #sustainability, #enzymology and #ProteinEngineering. I think those technologies are important for our future together.

Danish 🇩🇰