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User:Ivan E. Wang/Sandbox 1

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'''Retinal Pigment Epithelium 65 (Retinoid Isomerohydrolase) complex with (''R''/''S'')-emixustat and palmitate'''
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[[Media:RPE65_with_emixustat.mp4|PLACEHOLDER] width="576" height="324"]
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[[/Media:RPE65_with_emixustat.mp4]]
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<StructureSection load='4rsc' size='340' side='right' caption='Emixustat bound in the active site of RPE65' scene=''>
 
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Retinal pigment epithelium 65 (RPE65) also known as retinoid isomerohydrolase is a 65 kDa enzyme located within the human retinal pigment epithelium cells responsible for the chemical conversion of ''all-trans''-retinyl ester to ''11-cis''-retinol in the visual cycle.
 
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</StructureSection>
 
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(PLACEHOLDER This is a default text for your page '''Ivan E. Wang/Sandbox 1'''. 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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[[Media:RPE65_with_emixustat.mp4|PLACEHOLDER]]
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== Structural Features of RPE65 ==
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(PLACEHOLDER)
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== Enzymatic Catalyzed Reaction ==
 
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[[Image:Visual Cycle.jpg|thumb|left|alt=Figure 2: Human Visual Cycle| Figure 2: The canonical Visual Cycle in Humans <ref>DOI 10.1016/j.bbadis.2018.04.014</ref>]]
 
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[[Media:RPE65_with_emixustat.mp4]]
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= Protein-Ligand Interaction =
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== Endogenous Ligand ==
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(PLACEHOLDER)
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== Exogenous Ligand ==
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<StructureSection load='4ryy' size='340' side='right' caption='(''R'')-emixustat bound in the active site of RPE65' scene=''>
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=== (''R'')-Emixustat (ACU-4429) ===
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(''R'')-emixustat (ACU-4429) is an investigational small molecule inhibitor of RPE65 first invented by a British-American chemist, Ian L. Scott. Formulated as an hydrochloride salt, (''R'')-emixustat hydrochloride is taken by mouth and functions as a visual cycle modulator (VCM) to reduce toxic retinal byproducts such as A2E.
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In 2008, Acucela Inc. partnered with Otsuka Pharmaceutical Company for the continued development of (''R'')-emixustat as a potential inhibitor of RPE65. Currently (''R'')-emixustat is in Phase III clinical trials in the United States for the potential treatment of Stargard's disease, a juvenile form of atrophic (dry) age dependent macular degeneration (AMD). Additionally, (''R'')-emixustat is investigated as potential therapy for diabetic retinopathy and diabetic macular edema.
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</StructureSection>
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<StructureSection load='4ryz' size='340' side='right' caption='(''S'')-emixustat bound in the active site of RPE65' scene=''>
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=== (''S'')-Emixustat ===
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</StructureSection>
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== ''R/S'' Enantiomers Differences ==
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= Disease Implications =
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= Medical Relevance =
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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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= References =
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<references/>
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Current revision

[[Media:RPE65_with_emixustat.mp4|PLACEHOLDER] width="576" height="324"] /Media:RPE65_with_emixustat.mp4


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Media:RPE65_with_emixustat.mp4

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Ivan E. Wang

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