9qp4
From Proteopedia
Jump to navigationJump to search
Pre-active dark-state structure of human short-wave-sensitive opsin (OPN1SW)
| ||||||||||||
Structural highlights
DiseaseOPSB_HUMAN Tritanopia. The disease is caused by variants affecting the gene represented in this entry. FunctionC562_ECOLX Electron-transport protein of unknown function.OPSB_HUMAN Visual pigments are the light-absorbing molecules that mediate vision. They consist of an apoprotein, opsin, covalently linked to cis-retinal (Probable). Required for the maintenance of cone outer segment organization in the ventral retina, but not essential for the maintenance of functioning cone photoreceptors (By similarity). Involved in ensuring correct abundance and localization of retinal membrane proteins (By similarity). May increase spectral sensitivity in dim light (By similarity).[UniProtKB:P51491][1] References
| ||||||||||||||||||||
This page was last modified 04:47, 24 June 2026.