We apologize for Proteopedia being slow to respond. For the past two years, a new implementation of Proteopedia has been being built. Soon, it will replace this 18-year old system. All existing content will be moved to the new system at a date that will be announced here.

User:Harrison L. Smith/Sandbox1

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 3: Line 3:
This is a default text for your page '''Harrison L. Smith/Sandbox1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
This is a default text for your page '''Harrison L. Smith/Sandbox1'''. 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.
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.
 +
 +
==Introduction==
 +
The insulin receptor is a vital proponent of cellular function. It plays a key role in a variety of cellular pathways including glucose homeostasis, regulation of lipid, protein, and carbohydrate metabolism, gene expression, and even modulation of brain neurotransmitter levels. '''This page focuses specifically on the insulin receptor's role in glucose homeostasis'''.
 +
 +
==Structural Highlights==
 +
[[Image: 2.18_T_2.png|400px|right|thumb|Figure 1. The Coolest Image of this Protein!]]
 +
<scene name='83/837254/Zoom_in_on_alphasubunit/1'>Zoom in on Alpha Subunit</scene>
== Function ==
== Function ==
 +
The insulin receptor's function in regards to glucose homeostasis is to begin the signaling pathway that will eventually move glucose transporters to the cell surface which will allow glucose to passively defuse into the cell. The glucose receptor is inactive in the absence of insulin. When insulin does bind to the receptor, it undergoes a conformation change, activating it. Once activated, the intracellular Beta subunits autophosphorylate, and downstream signaling begins by the phosphorylation of the Insulin Receptor Substrate (IRS).
===Conformation Change===
===Conformation Change===
 +
The insulin receptor has two conformations, an active and inactive state. The inactive form predominates in low-levels of circulating insulin, whereas the active conformation is seen when insulin binds to any of the 4 receptor sites. The inactive conformation resembles an inverted V, and the active conformation resembles a T. Upon the binding of insulin to any of the four binding sites, the conformation change will begin, causing the Beta subunit's tyrosine kinase domains to move close together, allowing them to autophosphorylate. This autophosphorylation is what activates the insulin receptor and allows it to participate in further downstream signaling pathways.
 +
-
== Disease ==
 
-
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3678701/ Life Habits Related to Type 2 Diabetes]
 
== Relevance ==
== Relevance ==
-
<ref name="Ransey"> PMID:28504306</ref>.
+
As mentioned in the Introduction, the insulin receptor is relevant to numerous biological functions of the body. In a healthy, normal-functioning human, each cell has many insulin receptors that reacts to insulin when blood glucose levels rise. Without properly functioning insulin receptors, medical intervention is necessary for survival.
 +
=== Disease ===
 +
One of the most common diseases involving the insulin receptor is diabetes mellitus. There are two types of diabetes- which are referred to as type 1 and type 2 diabetes. Type 1 diabetes is classified as "insulin dependent" and is characterized by an inability for the body to produce insulin. This is most often the result of damage or insufficiency in the Islets of Langerhans in the pancreas. Type 2 diabetes is classified as "insulin independent" and is the result of the body producing insufficient amounts of insulin, or not responding to the insulin. This often occurs because of high blood-glucose levels. Both types of diabetes are often treated with insulin injections, and diet and lifestyle changes.
 +
 
 +
[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1010832/ Treatment of Diabetes with Insulin]
<ref name="Wilcox"> PMID:16278749</ref>.
<ref name="Wilcox"> PMID:16278749</ref>.
 +
<ref name= "Riddle"> PMID: 6351440</ref>.
 +
-
== Structural highlights ==
 
-
[[Image: 2.18_T_2.png|400px|right|thumb|Figure 1. The Coolest Image of this Protein!]]
 
-
<scene name='83/837254/Zoom_in_on_alphasubunit/1'>Zoom in on Alpha Subunit</scene>
 
This is a sample scene created with SAT to <scene name="/12/3456/Sample/1">color</scene> by Group, and another to make <scene name="/12/3456/Sample/2">a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.
This is a sample scene created with SAT to <scene name="/12/3456/Sample/1">color</scene> by Group, and another to make <scene name="/12/3456/Sample/2">a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

Revision as of 21:33, 23 March 2020

Homo sapiens Insulin Receptor Ectodomain

Insulin Receptor Ectodomain 6SOF

Drag the structure with the mouse to rotate

References

  1. 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
  2. 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
  3. Wilcox G. Insulin and insulin resistance. Clin Biochem Rev. 2005 May;26(2):19-39. PMID:16278749
  4. Riddle MC. Treatment of diabetes with insulin. From art to science. West J Med. 1983 Jun;138(6):838-46. PMID:6351440

Student Contributors

  • Harrison Smith
  • Alyssa Ritter

Proteopedia Page Contributors and Editors (what is this?)

Harrison L. Smith

Personal tools