biosensors reveals distinct conformational signatures of β-arrestin1 and 2 when bound to active PTH1R (P-R Here, we show differences between conformational changes that are induced by P-R* or R* receptor states

Commun Biol 2020 , 3 (1), 786. https://doi.org/10.1038/s42003-020-01518-8 . (3) Monk, P. .; Madala, P.; Fairlie, D. P.

P., Macdonald, C. B., Mehrota, E., Grimes, P. R., ... & Manglik, A. (2024).

Hunter P. Persechino M, Hedderich JB, Kolb P, Hilger D. Changeux J-P, Christopoulos A. González-Maeso J, Weisstaub NV, Zhou M, Chan P, Ivic L, Ang R, et al. Rößler P, Mayer D, Tsai CJ, Veprintsev DB, Schertler GFX, Gossert AD.

FLNA absence reduced the basal number of hetero-dimers (-36.8 ± 6.3% reduction of PLA events in M2, P both A7 and M2 (+20.0 ± 11.8% and +44.1 ± 16.3% increase of PLA events in A7 and M2, respectively, P

B., Panova, O., Hilger, D., Casiraghi, M., He, F., Maul, L., Gmeiner, P., Kobilka, B. K., Hildebrand, P. W., & Skiniotis, G. (2023).

The fission yeast Schizosaccharomyces pombe has two mating types, Plus (P) and Minus (M). Here, we investigated the stringency of the two GPCRs, Mam2 and Map3, for their respective pheromones, P-factor

affinities from previous studies.[13] Besides traditional dopaminergic ligands, the affinities of the P- Therapeutics   2016 , 165 , 164–177. https://doi.org/10.1016/j.pharmthera.2016.06.007 . (2)         Sokoloff, P. P. U.; Lüdeke, S.; Koch, P.; Rinken, A.; Keller, M. T.; Schwille, P.; Jungmann, R.

. -11.6 placebo, p<0.0001) at Week 5 (Cohen’s d effect size of 0.61).

Embo j, 2012. 31(6): p. 1364-78. 2. Xiao, P., et al., Tethered peptide activation mechanism of the adhesion GPCRs ADGRG2 and ADGRG4. Nature, 2022. 604(7907): p. 628-630. 7.

Associated with Huntington Disease "Highly Statistically Significant Reduction in Chorea Movements (p

.; Allongue, P.; Chazalviel, J.-N.; Gouget-Laemmel, A.

As GTP stabilizes and migrates towards the P loop, it causes the TCAT motif to shift, a key movement

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contributor article Canonical chemokine receptors as scavenging “decoys” Shivani Sachdev, Brendan Creemer, Thomas

bioinformatics tools offer the potential to explore larger portions of the β-arrestin interactome (Crépieux, P. with overlapping sites may experience mutually exclusive binding due to steric hindrance (Crépieux, P.

coupling between extracellular and transmembrane domains modulates holo-adhesion GPCR function Szymon P

Thomas Südhof, but did not start working on them right away.

receptors, data mapper, structure similarity search and models of physiological ligand complexes Luis P

-P., Macdonald, C. B., Mehrotra, E., Patrick Rockefeller Grimes, Zahm, A. M., Trinidad, D.

challenge in the Dahl SS rat GPCRs in Neuroscience Neurokinin-2 receptor negatively modulates substance P

and TM7 on the other hand, form possible dimerization interfaces (Ploier, B. et al. 2016; Dijkman, P.

They also showed higher protein levels of phospho-glycogen synthase kinase-3β (p-GSK3β), as well as total

Toxicol. 52, 179–197. https://doi.org/10. 1146/annurev.pharmtox.010909.105800 Tsao, P.

, 572–579. https://doi.org/10.1124/jpet.110.173005 Casella, I., Ambrosio, C., Grò, M.C., Molinari, P.

towards previously established chemical space, limiting their ability to identify truly novel chemotypes”(Thomas

Aylin Hanyaloglu, Caroline Gorvin, and Alejandra Tomas.

Alejandra Tomas, et al. for their research on Engineered mini-G proteins block the internalization of

ß-arrestin functional specificity at C-X-C chemokine receptor 5 (CXCR5) Panjamaporn Sangwung , Alejandra Tomas

Structural explanation of the receptor binding mechanism of a highly potent antagonist analog Isaikina, P.