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Sandbox Reserved 312

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Revision as of 06:23, 3 March 2011 by Theolina Dimitrow (Talk | contribs)
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This Sandbox is Reserved from January 10, 2010, through April 10, 2011 for use in BCMB 307-Proteins course taught by Andrea Gorrell at the University of Northern British Columbia, Prince George, BC, Canada.
To get started:
  • Click the edit this page tab at the top. Save the page after each step, then edit it again.
  • Click the 3D button (when editing, above the wikitext box) to insert Jmol.
  • show the Scene authoring tools, create a molecular scene, and save it. Copy the green link into the page.
  • Add a description of your scene. Use the buttons above the wikitext box for bold, italics, links, headlines, etc.

More help: Help:Editing


PDB ID 2fbv

Drag the structure with the mouse to rotate
2fbv, resolution 2.40Å ()
Ligands:
Gene: WRN, RECQ3, RECQL2 (Homo sapiens)
Related: 2fbt, 2fbx, 2fby, 2fc0
Resources: FirstGlance, OCA, RCSB, PDBsum
Coordinates: save as pdb, mmCIF, xml


Werner (WRN) protein is one of the five human RecQDNA helicases, which unwinds DNA strands. WRN has a functional exonuclease domain .WRN protein protects human from cancer; as well as, premature aging.


Contents

Function

Structure

WRN is a enzyme with both magnesium and ATP-dependent DNA-helicase activity with a 3'->5' exonuclease activity towards double-stranded DNA. Magnesium

Crystallization

Active Site

Substrate-Binding Site

Clinical significance

When the gene coding for WRN is mutated a autosomal recessive disorder causing rapid aging(osteoporosis, atherosclerosis and cancer). This is known as Werner syndrome which appears at puberty.

Reference

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