Sandbox Reserved 1372

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You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.
 
== Function ==
== Function ==
Rhodopsin is composed of both a protein molecule known as scotopsin and a cofactor known as retinal. When light hits the retinal, this sparks a series of conformational changes in the opsin embedded in the cell membrane of rods, signaling a signal transduction pathway leading to a conformational change in the opsin. This eventually sends a cGMP to process the incoming light, which close voltage gated cation channels and hypopolarizes the retinal cells. This whole process is known as visual phototransduction.
Rhodopsin is composed of both a protein molecule known as scotopsin and a cofactor known as retinal. When light hits the retinal, this sparks a series of conformational changes in the opsin embedded in the cell membrane of rods, signaling a signal transduction pathway leading to a conformational change in the opsin. This eventually sends a cGMP to process the incoming light, which close voltage gated cation channels and hypopolarizes the retinal cells. This whole process is known as visual phototransduction.
== Disease ==
== Disease ==
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The presence of rhodopsin is heavily dependent on the presence of Vitamin A in one's body, so a Vitamin A deficiency can cause an opoprotein being present instead of rhodopsin which causes night vision loss. Also there is a disease known as Lebers Congenital Amaurosis which is a rare inherited eye disease that causes photoreceptor cells to not develop properly causing early blindness and reduced function of rhodopsin.
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The presence of rhodopsin is heavily dependent on the presence of Vitamin A in one's body, so a Vitamin A deficiency can cause a lack of rhodopsin which causes night vision loss. Also there is a disease known as Lebers Congenital Amaurosis which is a rare inherited eye disease that causes photoreceptor cells to not develop properly causing early blindness and reduced function of rhodopsin. A mutation in the rhodopsin can also can cause retinitis pigmentosa, which leads to photoreceptor apoptosis causing decreased vision in low light settings, as well as loss of peripheral vision.
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== Relevance ==
 
== Structural highlights ==
== Structural highlights ==
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== References ==
== References ==
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https://en.wikipedia.org/wiki/Rhodopsin
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https://www.britannica.com/science/rhodopsin

Current revision

This Sandbox is Reserved from January through July 31, 2018 for use in the course HLSC322: Principles of Genetics and Genomics taught by Genevieve Houston-Ludlam at the University of Maryland, College Park, USA. This reservation includes Sandbox Reserved 1311 through Sandbox Reserved 1430.
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Bovine Rhodopsin

Crystal Structure of Bovine Rhodopsin

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References

https://en.wikipedia.org/wiki/Rhodopsin https://www.britannica.com/science/rhodopsin

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