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<StructureSection load='4FXO' size='340' side='right' caption='Caspase-6' scene=''>
<StructureSection load='4FXO' size='340' side='right' caption='Caspase-6' scene=''>
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Caspase-6 is an endopeptidase[https://en.wikipedia.org/wiki/Endopeptidase] involved in apoptosis. In terms of its catalytic function, it is a part of the cysteine-aspartate family [https://en.wikipedia.org/wiki/Caspase]. Before Caspase-6 is a functional and active dimer, the enzyme exists as a <scene name='75/752344/Caspase-6_zymogen/1'>procaspase</scene>, also known as zymogen [https://en.wikipedia.org/wiki/Zymogen]. Zymogen activation is largely conserved across the caspase family, however, Caspase-6 is unique in that it becomes active through self-cleavage rather than cleavage by a separate enzyme. The unprocessed enzyme exists as a dimer and contains a <scene name='75/752344/Caspase-6_small_subunit/1'>small</scene> consisting of two helices and <scene name='75/752344/Caspase-6_large_real/1'>large</scene> subunit consisting of three helices, a <scene name='75/752344/Caspase-6_pro-domain/1'>pro-domain</scene>, as well as an intersubunit linker. All helices of both subunits surround a beta sheet sheet core. In order to take its active form, the intersubunit linker is bound to the active site of Caspase-6, where it is then cleaved.
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Caspase-6 is an endopeptidase[https://en.wikipedia.org/wiki/Endopeptidase] involved in apoptosis. In terms of its catalytic function, it is a part of the cysteine-aspartate family [https://en.wikipedia.org/wiki/Caspase]. Before Caspase-6 becomes functional and active, the enzyme exists as a <scene name='75/752344/Caspase-6_zymogen/1'>procaspase</scene>, also known as a zymogen [https://en.wikipedia.org/wiki/Zymogen]. In solution, two zymogens are associated together, forming a homodimer. Zymogen activation, the process by which Caspase-6 becomes active, is largely conserved across the caspase family, however, Caspase-6 is unique in that it becomes active through self-cleavage rather than cleavage by a separate enzyme. Each zymogen of the unprocessed enzyme contains a <scene name='75/752344/Caspase-6_small_subunit/1'>small</scene> consisting of two helices and <scene name='75/752344/Caspase-6_large_real/1'>large</scene> subunit consisting of three helices, a <scene name='75/752344/Caspase-6_pro-domain/1'>pro-domain</scene>, as well as an intersubunit linker. The helices surround a beta sheet core. In order to become active, the intersubunit linker is bound to the active site of Caspase-6, where it is then cleaved. After cleavage, the four processed subunits, two originating from each zymogen, remain closely associated together through intermolecular forces, forming a dimer of dimers.
[[Image:Caspase-6 protein.jpg|100 px|left|thumb|Caspase-6 Protein]]
[[Image:Caspase-6 protein.jpg|100 px|left|thumb|Caspase-6 Protein]]

Revision as of 22:46, 17 April 2017

Caspase-6 in Homo sapiens

Caspase-6

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Loganne Wertz

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