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Long-wave-sensitive opsin 1 (human protein name often used for the red cone pigment; gene symbol OPN1LW) (OPN1LW (also LWS opsin; in non-human species often abbreviated LWS))

Target
OPN1LW (also LWS opsin; in non-human species often abbreviated LWS)
Molecular classification
G protein-coupled receptor (GPCR), rhodopsin-like class A, Visual pigment (cone photopsin), Seven-transmembrane receptor binding retinal (11-cis retinal chromophore)
01

Overview

Long-wavelength-sensitive opsins are cone visual pigments belonging to the rhodopsin-like GPCR family that bind 11-cis retinal via a protonated Schiff base to Lys296; light absorption triggers retinal isomerization, conformational changes, and G-protein activation to initiate phototransduction. They form one of four vertebrate cone opsin classes and typically exhibit peak spectral sensitivities in the long-wavelength range (~525–565 nm for vitamin A1-based pigments), with spectral tuning influenced by specific amino acid positions (notably 180, 197, 277, 285, 308) and a unique anion (chloride) sensitivity mediated by His197 that can shift λmax to longer wavelengths. In humans, the canonical gene/protein is OPN1LW (Long-wave-sensitive opsin 1), commonly referred to as the red cone opsin. LWS opsins show evolutionary diversification across vertebrates, with paralog expansions and substitutions affecting spectral sensitivity and adaptive coloration/vision, as documented in teleosts where LWS gene duplicates can subfunctionalize and shift expression through development.

Other names
Long-wave-sensitive opsin 1 (human)LWS opsin; LWS (class)Red-sensitive opsin; red cone opsin; photopsin I (context-dependent common names)Gene symbol: OPN1LW (human); lws (generic locus in many vertebrates)
02

Mechanism of action

Not applicable/none established. Opsin activation physiologically occurs via photon absorption causing 11-cis retinal → all-trans retinal isomerization, leading to GPCR activation (meta II) and G-protein signaling

03

Biological functions

Phototransduction in cone photoreceptors (light absorption → retinal photoisomerization → G protein activation)Color vision with peak spectral sensitivity in the long-wavelength range (approx. 525–565 nm depending on species/opsin variant and chromophore)Spectral tuning via amino acid substitutions at key residues (e.g., 180, 197, 277, 285, 308) and chloride binding at His197 that shifts λmax to longer wavelengths in many LWS pigmentsCoupling to heterotrimeric G proteins after activation (metarhodopsin-like intermediates), triggering downstream signaling
04

Disease associations

Other: Natural variation and selection at the LWS opsin locus associated with adaptive differences in color perception among fish populations/species; changes at nonsynonymous sites can shift spectral sensitivity and are targets of selectionOther: In humans, variants in OPN1LW underlie red–green color vision deficiencies (inferred from the protein/gene identity; UniProt entry describes red cone opsin). Note: specific clinical variants are cataloged for OPN1LW, though not detailed in the provided sources; this point is standard knowledge for OPN1LW but not explicitly cited in the search results
05

Safety considerations

Not applicable as a therapeutic target; no notable on-target pharmacologic safety profile reported
06

Interacting drugs

None established for therapeutic use. LWS opsins are not known to have approved pharmacologic ligands used clinically
07

Biomarkers

None established for patient selection or efficacy monitoring in therapy. Variation at the LWS/OPN1LW locus can serve as a genetic marker for spectral sensitivity differences in research contexts (evolutionary/ecological genetics)

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