Sandbox Reserved 1166

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== Structure ==
== Structure ==
=== Class B structural components ===
=== Class B structural components ===
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As opposed to class A glucagon receptors which have a proline kink, in all secretin-like class B glucagon receptors there is a Glycine at position 393 in Helix VII which allows for a helical bend. This Glycine and therefore this <scene name='72/721537/Gly_393_helical_bend/1'>helical bend</scene> is fully conserved in all secretin-like class B receptors and is an important part of the FQGxxVxxYCF motif.
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As opposed to class A glucagon receptors which have a proline kink, in all secretin-like class B glucagon receptors there is a Glycine at position 393 in Helix VII which allows for a <scene name='72/721537/Gly_393_helical_bend/1'>helical bend</scene>. This Glycine and therefore this helical bend is fully conserved in all secretin-like class B receptors and is an important part of the FQGxxVxxYCF motif.
Another important structural component found in all secretin-like class B receptors are the two conserved salt bridges found between Arg 346 and Glu 406 and Arg 173 and Glu 406. Since there is no conservation of these residues in class A receptors these salt bridges are likely an important feature of secretin-like class B receptors.
Another important structural component found in all secretin-like class B receptors are the two conserved salt bridges found between Arg 346 and Glu 406 and Arg 173 and Glu 406. Since there is no conservation of these residues in class A receptors these salt bridges are likely an important feature of secretin-like class B receptors.

Revision as of 13:20, 22 March 2016

This Sandbox is Reserved from Jan 11 through August 12, 2016 for use in the course CH462 Central Metabolism taught by R. Jeremy Johnson at the Butler University, Indianapolis, USA. This reservation includes Sandbox Reserved 1160 through Sandbox Reserved 1184.
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class B Human Glucagon Receptor

class B human glucagon receptor

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