User:Brittany Stankavich/Sandbox 2

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(New page: ==Glucocorticoid Receptor== <StructureSection load='1stp' size='340' side='right' caption='Caption for this structure' scene=''> This is a default text for your page '''Brittany Stankavich...)
Current revision (13:57, 31 January 2017) (edit) (undo)
 
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==Glucocorticoid Receptor==
 
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<StructureSection load='1stp' size='340' side='right' caption='Caption for this structure' scene=''>
 
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This is a default text for your page '''Brittany Stankavich/Sandbox 2'''. Click above on '''edit this page''' to modify. Be careful with the &lt; and &gt; signs.
 
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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.
 
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== Function ==
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<StructureSection load='5emq' size='340' side='right' caption='The DNA-binding domain of the human glucocorticoid receptor acting as a homodimer' scene='73/732470/Gr-dbd/1'>
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Human glucocorticoid receptor (GR) is a protein encoded by the gene NR3C1 (Nuclear Receptor Subfamily 3, Group C, Member 1). GR functions as both a transcription factor binding glucocorticoid response elements to activate transcription of genes as well as a regulator of other transcription factors.
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== Glucose Homeostasis ==
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Glucocorticoids (GC) are involved extensively in the regulation of physiological glucose levels.
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=== Gluconeogenesis ===
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Gluconeogenesis occurs mainly in the liver to generate glucose from non-carbohydrate substrates such as lactate, glycerol, and gluconeogenic amino acids such as alanine<ref name="Homeo">DOI:10.1007/978-1-4939-2895-8_5</ref>. [[insert pathway]]
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GC increase the activity of gluconeogenesis in hepatic cells predominantly by activating the transcription of genes encoding gluconeogenic enzymes such as pyruvate carboxylase (PC), cytosolic phosphoenolpyruvate carboxykinase (PCK1), fructose-1,6-bisphosphatase 1 (FBP1), phosphofructokinase 2/fructose bisphosphatase 2 complex (PFKFB1), glucose-6-phosphatase catalytic subunit (G6PC), and glucose-6-phosophate (G6P) transporter<ref name= "Homeo"/>. GC coordinate with an intracellular glucocorticoid receptor (GR) to initiate signal transduction. Prior to the GC/GR binding however, GR is complexed with a chaperone Hsp90 in the cytoplasm. Upon binding of the GC to the GR, the Hsp90 chaperone dissociates from the GR and the resulting GR/GC complex enters the nucleus<ref name= "Homeo"/>. The GR is then recruited to specific genomic sequences called glucocorticoid response elements (GRE) <ref name= "Homeo"/>.
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== Disease ==
== Disease ==
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== Structural highlights ==
== Structural highlights ==
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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.
 
</StructureSection>
</StructureSection>
== References ==
== References ==
<references/>
<references/>

Current revision

The DNA-binding domain of the human glucocorticoid receptor acting as a homodimer

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References

  1. 1.0 1.1 1.2 1.3 Kuo T, McQueen A, Chen TC, Wang JC. Regulation of Glucose Homeostasis by Glucocorticoids. Adv Exp Med Biol. 2015;872:99-126. doi: 10.1007/978-1-4939-2895-8_5. PMID:26215992 doi:http://dx.doi.org/10.1007/978-1-4939-2895-8_5

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Brittany Stankavich

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