Sandbox Reserved 1648: Difference between revisions

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The activation of the leptin receptor <ref name="ref3"/> is done through the '''CRH2, IGD and FN III''' domains <ref> The Leptin Receptor Complex: Heavier Than Expected? : https://www.frontiersin.org/articles/10.3389/fendo.2017.00030/full </ref>.  
The activation of the leptin receptor <ref name="ref3"/> is done through the '''CRH2, IGD and FN III''' domains <ref> The Leptin Receptor Complex: Heavier Than Expected? : https://www.frontiersin.org/articles/10.3389/fendo.2017.00030/full </ref>.  


The '''CRH2''' domain is the main leptin binding site on the receptor. This domain is required for the activation of the receptor. It is composed of a region of four consecutive hydrophobic residues. In particular, <scene name='86/868181/Leu_13/1'>Leu13</scene> and '''Leu86''' of leptin interact with '''<scene name='86/868181/Leu_504/1'>Leu504</scene>''' (pink in viewer) in CRH2 forming a bond via hydrophobic interactions<ref>Mapping of the interface between leptin and the leptin receptor CRH2 domain : https://jcs.biologists.org/content/118/11/2519 </ref>.
The '''CRH2''' domain is the main leptin binding site on the receptor. This domain is required for the activation of the receptor. It is composed of a region of four consecutive hydrophobic residues. In particular, <scene name='86/868181/Leu_13/1'>Leu13</scene> and '''Leu86''' of leptin interact with '''<scene name='86/868181/Leu_504/1'>Leu504</scene>''' (pink in viewer) in CRH2 forming a bond via hydrophobic interactions<ref>Mapping of the interface between leptin and the leptin receptor CRH2 domain : https://jcs.biologists.org/content/118/11/2519 </ref>. In contrast, the receptor functionality is hardly affected when the CRH1 domain is deleted.


The '''IGD''' domain has no affinity for leptin but is nevertheless '''required''' for receptor activation. In the absence of this domain, the result is a receptor with a wild-type affinity for leptin. However, the receptor is completely devoid of biological activity.
The '''IGD''' domain has no affinity for leptin but is nevertheless '''required''' for receptor activation. In the absence of this domain, the result is a receptor with a wild-type affinity for leptin. However, the receptor is completely devoid of biological activity.
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In the '''FN III''' domains, there are two conserved '''cysteines''' ('''Cys-672 and Cys-751''' <ref>Leptin receptor activation depends on critical cysteine residues in its fibronectin type III subdomains : https://www.jbc.org/article/S0021-9258(20)61429-6/fulltext </ref>) that are crucial for the activation of the receptor.  
In the '''FN III''' domains, there are two conserved '''cysteines''' ('''Cys-672 and Cys-751''' <ref>Leptin receptor activation depends on critical cysteine residues in its fibronectin type III subdomains : https://www.jbc.org/article/S0021-9258(20)61429-6/fulltext </ref>) that are crucial for the activation of the receptor.  


In contrast, the receptor functionality is hardly affected when the CRH1 domain is deleted.
Moreover, in order to form an '''activated 2:4 leptin:ObR complex''', the leptin clusters '''two pre-formed ObR dimers'''.  
 


== '''Signaling pathways''' ==
== '''Signaling pathways''' ==

Revision as of 18:28, 24 January 2021

3V6O: Leptin receptor-antibody complex

Leptin receptor

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References