XPD Helicase (3CRV)

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== '''XPD Helicase''' ==
== '''XPD Helicase''' ==
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<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 '''3crv/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 ==
== Function ==
== Disease ==
== Disease ==

Revision as of 15:55, 10 April 2016

Contents

XPD Helicase

Function

Disease

Xeroderma Pigmentosum(XP), Cockayne Syndrome combined with XP (XP/CS) and Trichothiodystrophy(TTD)

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>

References

Proteopedia Page Contributors and Editors (what is this?)

Matt Kohler, Bashir Noor, Chih Hao Huang, Michal Harel, Mark Heslin, Shane Devlin

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