Sandbox Reserved 1240

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{{Sandbox_Reserved_Jason_Telford}}<!-- PLEASE ADD YOUR CONTENT BELOW HERE -->
{{Sandbox_Reserved_Jason_Telford}}<!-- PLEASE ADD YOUR CONTENT BELOW HERE -->
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==Structure==
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==<b>Structure</b>==
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<StructureSection load='1qki' size='340' side='right' caption='Caption for this structure' scene=''>
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<StructureSection load='1qki' size='340' side='right' caption='Glucose-6-Phosphate Dehydrogenase at a resolution of 3.0 Å' scene=''>
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Overall, the structure of Glucose-6-Phosphate Dehydrogenase (G6PD) is a tetramer, composed of a dimer of dimers. G6PD also features a structural nicotinamide adenine, which is only present in eukaryotes. G6PD is 515 amino acids long This is a default text for your page ''''''. Click above on '''edit this page''' to modify. Be careful with the &lt; and &gt; signs.
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Overall, the structure of Glucose-6-Phosphate Dehydrogenase (<i>G6PD</i>) is a tetramer, composed of a dimer of dimers. Glucose-6-Phosphate Dehydrogenase also features a structural nicotinamide adenine, which is only present in eukaryotes and is rare biologically. Glucose-6-Phosphate Dehydrogenase is 515 amino acids long.
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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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== <b>Structural highlights </b> ==
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The two dimers are held together in a tetramer by charge-charge interactions. Each dimer has a structural NAD+. This NAD+ may serve to stabilize the dimers.
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</StructureSection>
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== <b>Function</b> ==
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== Function ==
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Glucose-6-Phosphate Dehydrogenase is the rate-limiting enzyme in the pentose phosphate pathway. G6PD converts Glucose-6-Phosphate into 6-phosphoglucono-δ-lactone. Dysfunction of G6PD has multiple down stream effects. The pentose phosphate pathway synthesizes precursors for multiple other biosynthetic pathways. For example, it synthesizes nucleotide precursors for DNA synthesis.
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== <b>Disease </b>==
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== Disease ==
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Glucose-6-Phosphate Dehydrogenase deficiency is associated with many diseases, some of which include Hemolytic Anemia and Favism. Hemolytic Anemia results in erythrocytes being destroyed before their typical life span is over. Hemolytic anemia can lead to many problems, including cardiovascular arrhythmia, cardiomegaly (enlarged heart), and fatigue. Hemolytic anemia can present with different severity, but can be treated with drugs.
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== Relevance ==
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Favism is a disease associated with G6PD deficiency that can cause oxidative stress as a result of consuming fava beans. Favism and G6PD are X-linked diseases that are thus more prevalent in men than women.
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== Structural highlights ==
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== <b>Relevance </b> ==
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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.
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Glucose-6-Phosphate Dehydrogenase plays a key role in maintaining homeostasis. Not only does it catalyze the rate limiting step of the oxidative pentose phosphate pathway, it maintains the shape of red blood cells by protecting against potential deadly reactive oxygen species. Glucose-6-Phosphate dehydrogenase deficiency is the most common enzyme deficiency in humans, affecting over 400 million people worldwide. G6PD deficiency resulted in 4100 deaths worldwide in 2013.
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</StructureSection>
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== <b>References</b> ==
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== References ==
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<references/>
<references/>
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Au, Shannon et al. "Human Glucose-6-Phosphate Dehydrogenase: The Crystal Structure Reveals A Structural NADP+ Molecule And Provides Insights Into Enzyme
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Deficiency". N.p., 2017. Web. 20 Apr. 2017.
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Berg, Jeremy, John Tymoczko, and Lubert Stryer. "Glucose 6-Phosphate Dehydrogenase Plays A Key Role In Protection Against Reactive Oxygen Species".
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Ncbi.nlm.nih.gov. N.p., 2017. Web. 20 Apr. 2017.
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"G6PD Gene - Genecards | G6PD Protein | G6PD Antibody". Genecards.org. N.p., 2017. Web. 20 Apr. 2017.
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"Glucose-6-Phosphate Dehydrogenase". Wikipedia.org. N.p., 2017. Web. 20 Apr. 2017.
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"What Is Hemolytic Anemia? - NHLBI, NIH". Nhlbi.nih.gov. N.p., 2017. Web. 20 Apr. 2017.

Current revision

This Sandbox is Reserved from Jan 17 through June 31, 2017 for use in the course Biochemistry II taught by Jason Telford at the Maryville University, St. Louis, USA. This reservation includes Sandbox Reserved 1225 through Sandbox Reserved 1244.
To get started:
  • Click the edit this page tab at the top. Save the page after each step, then edit it again.
  • Click the 3D button (when editing, above the wikitext box) to insert Jmol.
  • show the Scene authoring tools, create a molecular scene, and save it. Copy the green link into the page.
  • Add a description of your scene. Use the buttons above the wikitext box for bold, italics, links, headlines, etc.

More help: Help:Editing

Contents

Structure

Glucose-6-Phosphate Dehydrogenase at a resolution of 3.0 Å

Drag the structure with the mouse to rotate

Function

Glucose-6-Phosphate Dehydrogenase is the rate-limiting enzyme in the pentose phosphate pathway. G6PD converts Glucose-6-Phosphate into 6-phosphoglucono-δ-lactone. Dysfunction of G6PD has multiple down stream effects. The pentose phosphate pathway synthesizes precursors for multiple other biosynthetic pathways. For example, it synthesizes nucleotide precursors for DNA synthesis.

Disease

Glucose-6-Phosphate Dehydrogenase deficiency is associated with many diseases, some of which include Hemolytic Anemia and Favism. Hemolytic Anemia results in erythrocytes being destroyed before their typical life span is over. Hemolytic anemia can lead to many problems, including cardiovascular arrhythmia, cardiomegaly (enlarged heart), and fatigue. Hemolytic anemia can present with different severity, but can be treated with drugs.

Favism is a disease associated with G6PD deficiency that can cause oxidative stress as a result of consuming fava beans. Favism and G6PD are X-linked diseases that are thus more prevalent in men than women.

Relevance

Glucose-6-Phosphate Dehydrogenase plays a key role in maintaining homeostasis. Not only does it catalyze the rate limiting step of the oxidative pentose phosphate pathway, it maintains the shape of red blood cells by protecting against potential deadly reactive oxygen species. Glucose-6-Phosphate dehydrogenase deficiency is the most common enzyme deficiency in humans, affecting over 400 million people worldwide. G6PD deficiency resulted in 4100 deaths worldwide in 2013.

References

    Au, Shannon et al. "Human Glucose-6-Phosphate Dehydrogenase: The Crystal Structure Reveals A Structural NADP+ Molecule And Provides Insights Into Enzyme 
        Deficiency". N.p., 2017. Web. 20 Apr. 2017.
    Berg, Jeremy, John Tymoczko, and Lubert Stryer. "Glucose 6-Phosphate Dehydrogenase Plays A Key Role In Protection Against Reactive Oxygen Species". 
         Ncbi.nlm.nih.gov. N.p., 2017. Web. 20 Apr. 2017.
    "G6PD Gene - Genecards | G6PD Protein | G6PD Antibody". Genecards.org. N.p., 2017. Web. 20 Apr. 2017.
    "Glucose-6-Phosphate Dehydrogenase". Wikipedia.org. N.p., 2017. Web. 20 Apr. 2017.
    "What Is Hemolytic Anemia? - NHLBI, NIH". Nhlbi.nih.gov. N.p., 2017. Web. 20 Apr. 2017.
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