8iu2

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Current revision (12:04, 30 October 2024) (edit) (undo)
 
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== Disease ==
== Disease ==
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[https://www.uniprot.org/uniprot/OPSR_HUMAN 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.
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[https://www.uniprot.org/uniprot/OPSR_HUMAN OPSR_HUMAN] X-linked cone dysfunction syndrome with myopia;Blue cone monochromatism;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 ==
== Function ==
[https://www.uniprot.org/uniprot/OPSR_HUMAN OPSR_HUMAN] Visual pigments are the light-absorbing molecules that mediate vision. They consist of an apoprotein, opsin, covalently linked to cis-retinal.
[https://www.uniprot.org/uniprot/OPSR_HUMAN OPSR_HUMAN] Visual pigments are the light-absorbing molecules that mediate vision. They consist of an apoprotein, opsin, covalently linked to cis-retinal.

Current revision

Cryo-EM structure of Long-wave-sensitive opsin 1

PDB ID 8iu2

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