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== '''Activation''' ==
== '''Activation''' ==
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The activation of the leptin receptor is done through the CRH2, IGD and FN III domains.
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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.
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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, but completely devoid of biological activity.
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In the FN III domains, there are two conserved cysteines that are crucial for the activation of the receptor.
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In contrast, the receptor functionality is hardly affected when the CRH1 domain is deleted.
== '''Signaling pathways''' ==
== '''Signaling pathways''' ==
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The leptin receptor has cytokine receptor characteristics. The transduction of the signal by this type of receptor involves the formation of multimeric complexes. This leads to the recruitment of tyrosine kinases, in particular those of the JAK family, which will phosphorylate STAT-like transcription factors at the cytoplasmic tail of the receptor. Recruitment and activation of secondary signalling molecules enable the lept signalling via the MAPK, PI3K, AMPK and mTOR pathways.
== '''Regulation''' ==
== '''Regulation''' ==
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The best known regulation of the leptin receptor is negative regulation by OB-RGRP. The gene encoding the leptin receptor (OB-R) also encodes a second transcript called OB-R gene related protein (OB-RGRP). Stopping the expression of the OB-RGRP gene by interfering RNAs increases the sensitivity of the cells' receptors to leptin. This prevents the development of obesity despite a diet that may be high in fat.

Revision as of 22:10, 12 January 2021

3V6O: Leptin receptor-antibody complex

Leptin receptor

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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
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