Sandbox Reserved 1232
From Proteopedia
(Difference between revisions)
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| - | <Structure load='' size='350' frame='true' align='right' caption='Insert caption here' scene='Insert optional scene name here' />{{Sandbox_Reserved_Jason_Telford}}<!-- PLEASE ADD YOUR CONTENT BELOW HERE --> | ||
==Structure== | ==Structure== | ||
| - | + | MAJOR PRION PROTEIN (5L6R:A) | |
| + | It is believed | ||
| + | The image shown is the average structure produced by NMR constraints. | ||
== Function == | == Function == | ||
| - | The | + | The normal function of the prion protein functions as a transport protein in Homo Sapiens. |
| + | In it's mutated state the prion protein functions in the development of amyloid disease (misfiled proteins that stick together forming fibrils). | ||
== Disease == | == Disease == | ||
| - | The disease associated with a mutated Prion protein is Spongiform Ecephalopathies. | + | The disease associated with a mutated Prion protein is Spongiform Ecephalopathies. |
== Relevance == | == Relevance == | ||
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</StructureSection> | </StructureSection> | ||
== References == | == References == | ||
| - | <references/> | ||
Revision as of 19:40, 29 March 2017
Contents |
Structure
MAJOR PRION PROTEIN (5L6R:A) It is believed The image shown is the average structure produced by NMR constraints.
Function
The normal function of the prion protein functions as a transport protein in Homo Sapiens. In it's mutated state the prion protein functions in the development of amyloid disease (misfiled proteins that stick together forming fibrils).
Disease
The disease associated with a mutated Prion protein is Spongiform Ecephalopathies.
Relevance
Structural highlights
This is a sample scene created with SAT to by Group, and another to make of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.
</StructureSection>
