Sandbox Reserved 312
From Proteopedia
(Difference between revisions)
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{{STRUCTURE_2fbv| PDB=2fbv | SCENE= }} | {{STRUCTURE_2fbv| PDB=2fbv | SCENE= }} | ||
+ | Werner (WRN) protein protects human from cancer; as well as, premature aging. 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. | ||
=Function= | =Function= | ||
=Structure= | =Structure= | ||
- | <scene name='Sandbox_Reserved_312/Ligand/2'>Ligand</scene> | + | Magnesium <scene name='Sandbox_Reserved_312/Ligand/2'>Ligand</scene> |
===Crystallization=== | ===Crystallization=== |
Revision as of 06:02, 3 March 2011
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:
More help: Help:Editing |
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2fbv, resolution 2.40Å () | |||||||||
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Ligands: | |||||||||
Gene: | WRN, RECQ3, RECQL2 (Homo sapiens) | ||||||||
Related: | 2fbt, 2fbx, 2fby, 2fc0 | ||||||||
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Resources: | FirstGlance, OCA, RCSB, PDBsum | ||||||||
Coordinates: | save as pdb, mmCIF, xml |
Werner (WRN) protein protects human from cancer; as well as, premature aging. 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.
Contents |
Function
Structure
Magnesium