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User:Harrison L. Smith/Sandbox1
From Proteopedia
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The insulin receptor is a dimer of heterodimers made of two alpha subunits and two beta subunits <ref name=”Tatulian”>PMID:26322622</ref>. The <scene name='83/832953/Alpha_chain/1'>Alpha chain</scene> is on the extracellular side of the membrane and is critical for binding insulin. There are <scene name='83/832953/Four_binding_site_locations/1'>four binding site locations</scene> that have the potential to interact with insulin on the extracellular side of the membrane, but it is generally more common for only one or two insulin molecules to bind to the receptor due to the occurrence of negative affinity at the binding site. The <scene name='83/832953/Beta_chains/1'>Beta chains</scene> are transmembrane subunits that contain a <scene name='83/832934/Tyrosine_kinase_region/1'>Tyrosine Kinase Region</scene>. Beta chains experience a conformation change that brings them from a V shape to a T shape upon activation or binding of an insulin molecule. When the two subunits are brought near to eachother in the activated T form, each Tyrosine Kinase region autophosphorylates its counterpart at particular Tyrosines. | The insulin receptor is a dimer of heterodimers made of two alpha subunits and two beta subunits <ref name=”Tatulian”>PMID:26322622</ref>. The <scene name='83/832953/Alpha_chain/1'>Alpha chain</scene> is on the extracellular side of the membrane and is critical for binding insulin. There are <scene name='83/832953/Four_binding_site_locations/1'>four binding site locations</scene> that have the potential to interact with insulin on the extracellular side of the membrane, but it is generally more common for only one or two insulin molecules to bind to the receptor due to the occurrence of negative affinity at the binding site. The <scene name='83/832953/Beta_chains/1'>Beta chains</scene> are transmembrane subunits that contain a <scene name='83/832934/Tyrosine_kinase_region/1'>Tyrosine Kinase Region</scene>. Beta chains experience a conformation change that brings them from a V shape to a T shape upon activation or binding of an insulin molecule. When the two subunits are brought near to eachother in the activated T form, each Tyrosine Kinase region autophosphorylates its counterpart at particular Tyrosines. | ||
| - | == Function == | + | == Function & Structure== |
[[Image:Insulin inverted v.png|250px|right|thumb|Figure 1. An image of the inactive Insulin Receptor Alpha subunit in the inverted V conformation. This image shows only a protomer of the inactive alpha subunit because the entire inactive alpha subunit dimer has been unable to be photographed because the transition state has yet to be determined.]] | [[Image:Insulin inverted v.png|250px|right|thumb|Figure 1. An image of the inactive Insulin Receptor Alpha subunit in the inverted V conformation. This image shows only a protomer of the inactive alpha subunit because the entire inactive alpha subunit dimer has been unable to be photographed because the transition state has yet to be determined.]] | ||
Revision as of 21:25, 29 March 2020
Homo sapiens Insulin Receptor Ectodomain
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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
- ↑ Tatulian SA. Structural Dynamics of Insulin Receptor and Transmembrane Signaling. Biochemistry. 2015 Sep 15;54(36):5523-32. doi: 10.1021/acs.biochem.5b00805. Epub , 2015 Sep 3. PMID:26322622 doi:http://dx.doi.org/10.1021/acs.biochem.5b00805
- ↑ Weis F, Menting JG, Margetts MB, Chan SJ, Xu Y, Tennagels N, Wohlfart P, Langer T, Muller CW, Dreyer MK, Lawrence MC. The signalling conformation of the insulin receptor ectodomain. Nat Commun. 2018 Oct 24;9(1):4420. doi: 10.1038/s41467-018-06826-6. PMID:30356040 doi:http://dx.doi.org/10.1038/s41467-018-06826-6
- ↑ Uchikawa E, Choi E, Shang G, Yu H, Bai XC. Activation mechanism of the insulin receptor revealed by cryo-EM structure of the fully liganded receptor-ligand complex. Elife. 2019 Aug 22;8. pii: 48630. doi: 10.7554/eLife.48630. PMID:31436533 doi:http://dx.doi.org/10.7554/eLife.48630
- ↑ Wilcox G. Insulin and insulin resistance. Clin Biochem Rev. 2005 May;26(2):19-39. PMID:16278749
- ↑ 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
