Sandbox Reserved 1372
From Proteopedia
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== 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 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. | ||
== Relevance == | == Relevance == |
Revision as of 03:40, 27 February 2018
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
- ↑ Hanson, R. M., Prilusky, J., Renjian, Z., Nakane, T. and Sussman, J. L. (2013), JSmol and the Next-Generation Web-Based Representation of 3D Molecular Structure as Applied to Proteopedia. Isr. J. Chem., 53:207-216. doi:http://dx.doi.org/10.1002/ijch.201300024
- ↑ Herraez A. Biomolecules in the computer: Jmol to the rescue. Biochem Mol Biol Educ. 2006 Jul;34(4):255-61. doi: 10.1002/bmb.2006.494034042644. PMID:21638687 doi:10.1002/bmb.2006.494034042644