Sandbox Reserved 1372
From Proteopedia
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<StructureSection load='1f88' size='340' side='right' caption='Crystal Structure of Bovine Rhodopsin' scene=''> | <StructureSection load='1f88' size='340' side='right' caption='Crystal Structure of Bovine Rhodopsin' scene=''> | ||
- | <scene name='77/777692/ | + | The protein Bovine Rhodopsin is a photoreceptor that aids in the sensory perception of light stimulus in environments with low light intensity. They are found in the eyes of many organisms, specifically in the tightly packed disks that compose the outer segment of the retina's photoreceptive rod cells. It features a seven-transmembrane helix core and is a G protein-coupled receptor embedded in the lipid bilayer of cell membranes that undergoes a structural change following photoactivation. The <scene name='77/777692/Mercury/1'>mercury</scene> and <scene name='77/777692/Zinc/1'>zinc</scene> ions that are attached to the <scene name='77/777692/Folded_polypeptide/1'>folded polypeptide</scene> aid in this structural change. |
- | This is a default text for your page ''''''. Click above on '''edit this page''' to modify. Be careful with the < and > signs. | ||
- | 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. | ||
== Disease == | == Disease == | ||
+ | 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. | ||
+ | |||
- | == Relevance == | ||
== Structural highlights == | == Structural highlights == | ||
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== References == | == References == | ||
<references/> | <references/> | ||
+ | https://en.wikipedia.org/wiki/Rhodopsin | ||
+ | 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
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References
https://en.wikipedia.org/wiki/Rhodopsin https://www.britannica.com/science/rhodopsin