Sandbox Reserved 1606

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(New page: {{Sandbox_Reserved_CH462_Biochemistry_II}}<!-- PLEASE ADD YOUR CONTENT BELOW HERE --> ==Your Heading Here (maybe something like 'Structure')== <StructureSection load='1stp' size='340' side...)
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{{Sandbox_Reserved_CH462_Biochemistry_II}}<!-- PLEASE ADD YOUR CONTENT BELOW HERE -->
{{Sandbox_Reserved_CH462_Biochemistry_II}}<!-- PLEASE ADD YOUR CONTENT BELOW HERE -->
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==Your Heading Here (maybe something like 'Structure')==
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==ABCG2 Multidrug Transporter==
<StructureSection load='1stp' size='340' side='right' caption='Caption for this structure' scene=''>
<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 ''''''. 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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==Introduction==
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The [https://en.wikipedia.org/wiki/ABCG2 ABCG2 multidrug transporter] is part of the ATP-binding cassette (ABC) transporter family. Also know as the breast cancer resistance protein (BCRP), ABCG2 has physiological roles in various tissue cells including the mammary gland and the blood-brain, bloodtestis, and maternal-fetal barriers.<ref name="Taylor"/>
== Function ==
== Function ==
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Transports xenobiotic molecules out of the cell (molecules that shouldn't be there) to protect cellular tissue
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== Disease ==
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== Structural highlights ==
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===ATP Bound and Unbound Conformations===
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== Relevance ==
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[[Image:Example.jpg]]
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== Structural highlights ==
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===Cavities and Lysine Plug===
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==Disease==
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===Cancer===
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ABCG2 contributes to [https://en.wikipedia.org/wiki/Multiple_drug_resistance multidrug resistance] in cancer cells by exporting anti-tumor drugs out of cells which is an obstacle in cancer treatment.<ref name="Taylor"/>
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brief description of the cancer genes listed in the papers (papers talk about how some cancers had more expression of abcg2 genes)
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===ABCG2 as a Target for Inhibition===
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Talk about how and why it would be a good target for the treatment of cancer
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.
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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</StructureSection>
</StructureSection>
== References ==
== References ==
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<ref name="Taylor">PMID:28554189</ref>
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<references/>
<references/>
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==Student Contributors===

Revision as of 19:55, 23 March 2020

This Sandbox is Reserved from Jan 13 through September 1, 2020 for use in the course CH462 Biochemistry II taught by R. Jeremy Johnson at the Butler University, Indianapolis, USA. This reservation includes Sandbox Reserved 1598 through Sandbox Reserved 1627.
To get started:
  • Click the edit this page tab at the top. Save the page after each step, then edit it again.
  • 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

ABCG2 Multidrug Transporter

Caption for this structure

Drag the structure with the mouse to rotate

References

[1]

  1. 1.0 1.1 1.2 Taylor NMI, Manolaridis I, Jackson SM, Kowal J, Stahlberg H, Locher KP. Structure of the human multidrug transporter ABCG2. Nature. 2017 Jun 22;546(7659):504-509. doi: 10.1038/nature22345. Epub 2017 May, 29. PMID:28554189 doi:http://dx.doi.org/10.1038/nature22345

Student Contributors=

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