8iu2

Structural highlights

Disease

OPSR_HUMAN Blue cone monochromatism;X-linked cone dysfunction syndrome with myopia;NON RARE IN EUROPE: Partial color blindness, protan type;Cone rod dystrophy. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry.

Function

OPSR_HUMAN Visual pigments are the light-absorbing molecules that mediate vision. They consist of an apoprotein, opsin, covalently linked to cis-retinal.