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2fg8
From Proteopedia
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{{STRUCTURE_2fg8| PDB=2fg8 | SCENE= }} | {{STRUCTURE_2fg8| PDB=2fg8 | SCENE= }} | ||
| - | + | ===Structure of Human Ferritin L Chain=== | |
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| - | + | The line below this paragraph, {{ABSTRACT_PUBMED_16790936}}, adds the Publication Abstract to the page | |
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==Disease== | ==Disease== | ||
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[[Category: Wang, Z M.]] | [[Category: Wang, Z M.]] | ||
[[Category: Ferritin light chain perdeuterated]] | [[Category: Ferritin light chain perdeuterated]] | ||
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Revision as of 22:11, 28 July 2008
Contents |
Structure of Human Ferritin L Chain
Template:ABSTRACT PUBMED 16790936
Disease
Known disease associated with this structure: Basal ganglia disease, adult-onset OMIM:[134790], Hyperferritinemia-cataract syndrome OMIM:[134790]
About this Structure
2FG8 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Structure of human ferritin L chain., Wang Z, Li C, Ellenburg M, Soistman E, Ruble J, Wright B, Ho JX, Carter DC, Acta Crystallogr D Biol Crystallogr. 2006 Jul;62(Pt 7):800-6. Epub 2006, Jun 20. PMID:16790936
Page seeded by OCA on Tue Jul 29 01:11:24 2008
