XPD Helicase (3CRV)
From Proteopedia
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</StructureSection> | </StructureSection> | ||
== References == | == References == | ||
- | Fan, | + | Fan, L., Fuss, J. O., Cheng, Q. J., Arvai, A. S., Hammel, M., Roberts, V. A., Cooper, P. K., and Tainer, J. A. (2008) XPD helicase structures and activities: Insights into the cancer and aging phenotypes from XPD mutations. |
Revision as of 16:30, 10 April 2016
Contents |
XPD Helicase
|
Function
Disease
Xeroderma Pigmentosum(XP)
Cockayne Syndrome combined with XP (XP/CS)
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
Fan, L., Fuss, J. O., Cheng, Q. J., Arvai, A. S., Hammel, M., Roberts, V. A., Cooper, P. K., and Tainer, J. A. (2008) XPD helicase structures and activities: Insights into the cancer and aging phenotypes from XPD mutations.
Proteopedia Page Contributors and Editors (what is this?)
Matt Kohler, Bashir Noor, Chih Hao Huang, Michal Harel, Mark Heslin, Shane Devlin