Sandbox Reserved 1646: Difference between revisions

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=== Ligand binding ===
=== Ligand binding ===


The overall pocket in GnRH1R is defined by the N terminus, TM2, TM3, TM5, TM6, and TM7, forming a highly hydrophobic <scene name='86/868179/Gnrh1_colored/5'>binding site</scene> with a few polar residues (D98, N102, K121, and N305)
The overall pocket in GnRH1R is defined by the N terminus, TM2, TM3, TM5, TM6, and TM7, forming a highly <scene name='86/868179/Binding_site/3'>hydrophobic binding site</scene> with a few polar residues (D98, N102, K121, and N305)
The orthosteric binding pocket of GnRH1R is solvent-accessible, appears relatively shallow and plasticity is indicated with respect to different ligands. Structural analysis provides the possibility to design orally deliverable small molecules with activity towards the receptor.
The orthosteric binding pocket of GnRH1R is solvent-accessible, appears relatively shallow and plasticity is indicated with respect to different ligands. Structural analysis provides the possibility to design orally deliverable small molecules with activity towards the receptor.
A detailed interaction network for elagolix has been described<ref>DOI: 10.1038/s41467-020-19109-w</ref> in which the N-terminus, residue Y283 and a polar <scene name='86/868179/Interacton-elox/2'>interaction network</scene> formed by residues D98 and K121 are of particular importance for ligand recognition.
A detailed interaction network for elagolix has been described<ref>DOI: 10.1038/s41467-020-19109-w</ref> in which the N-terminus, residue Y283 and a polar <scene name='86/868179/Interacton-elox/2'>interaction network</scene> formed by residues D98 and K121 are of particular importance for ligand recognition.