GPCR classes
The human GPCRome divides into structural classes that share a common seven-transmembrane fold but differ in their extracellular architecture and ligand-recognition strategy.
Class A · Rhodopsin
The largest class by far — aminergic, peptide, lipid, nucleotide and chemokine receptors, plus the opsins. Most approved GPCR drugs act here.
Browse Rhodopsin →Class B1 · Secretin
Secretin-family receptors for large peptide hormones such as GLP-1, glucagon, and PTH. Major metabolic and endocrine targets.
Browse Secretin →Class B2 · Adhesion
Adhesion GPCRs with large extracellular domains and self-cleaving GAIN domains. Roles in development and immunity; largely under-explored.
Browse Adhesion →Class C · Glutamate
Dimeric receptors with large Venus-flytrap ligand domains — metabotropic glutamate, GABA-B, calcium-sensing, and taste-1 receptors.
Browse Glutamate →Class F · Frizzled
Frizzled and Smoothened receptors transducing Wnt and Hedgehog signalling. Central to development and oncology.
Browse Frizzled →Class T2 · Taste 2
Bitter taste receptors, expressed in the tongue and, surprisingly, throughout the body.
Browse Taste 2 →Class O1 · Odorant (class I)
Human class I odorant receptors (the OR51/52/56 families) — the ancestral “fish-like” clade humans share with aquatic vertebrates. A small group, but all human genes.
Browse Odorant (class I) →Class O2 · Odorant (class II)
Human class II (“tetrapod”) odorant receptors — the single largest gene family in the human genome.
Browse Odorant (class II) →