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Structural and Molecular Insights into GPCR Function Endogenous l- to d-amino acid residue isomerization

Zhang, and L. Ma. 2008.

Binding of Stalk-derived Peptide Agonists GPCR Binders, Drugs, and more In silico exploration of 4(α-l-rhamnosyloxy

HDAC3 inhibition to activate autophagy in head kidney macrophages from turbot (Scophthalmus maximus L.

 Marion Lanier ,   Brian K Shoichet ,  Esther Martinborough ,  Jonathan F Fay ,  Can Cao ,   Bryan L

L., & Fowler, D. M. (2011).

Sakmar, Debbie L. Hay, Lukas Grätz, and more. Check out some of the latest GPCR discoveries below!

Endogenous l- to d-amino acid residue isomerization modulates selectivity between distinct neuropeptide

and dopamine D2 receptor is required for selective potentiation of dopamine D2 receptor function by L-

Katharina Grotsch, Bryan L Roth, Valery V Fokin  et al. for their research on Virtual Screening of a

L., & Garcia, K. C. (2015). Structural biology.

L., Stepniewski, T.

Signalling 4 (RGS4) negatively modulates nociceptin/orphanin FQ opioid receptor signalling: Implication for l-Dopa-induced

In the skin, OR51E2 was shown to play a role in human melanocyte homeostasis (Gelis L. et. al 2016) and

was performed highlighted a new hydrophobic conserved motif composed of phenylalanine (F)/leucine (L)

L.