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3kxu

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[[Image:3kxu.png|left|200px]]
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{{ABSTRACT_PUBMED_20159981}}
{{ABSTRACT_PUBMED_20159981}}
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==Disease==
 
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Known disease associated with this structure: Basal ganglia disease, adult-onset OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134790 134790]], Hyperferritinemia-cataract syndrome OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134790 134790]]
 
==About this Structure==
==About this Structure==
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3KXU is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3KXU OCA].
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[[3kxu]] is a 1 chain structure of [[Ferritin]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3KXU OCA].
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==See Also==
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*[[Ferritin]]
==Reference==
==Reference==
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[[Category: Iron storage protein]]
[[Category: Iron storage protein]]
[[Category: Metal binding protein]]
[[Category: Metal binding protein]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu May 20 08:59:59 2010''
 

Revision as of 01:53, 27 December 2010

Template:STRUCTURE 3kxu

Contents

Crystal structure of human ferritin FTL498InsTC pathogenic mutant

Template:ABSTRACT PUBMED 20159981

About this Structure

3kxu is a 1 chain structure of Ferritin with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  • Luscieti S, Santambrogio P, Langlois d'Estaintot B, Granier T, Cozzi A, Poli M, Gallois B, Finazzi D, Cattaneo A, Levi S, Arosio P. Mutant ferritin L-chains that cause neurodegeneration act in a dominant-negative manner to reduce ferritin iron incorporation. J Biol Chem. 2010 Apr 16;285(16):11948-57. Epub 2010 Feb 16. PMID:20159981 doi:10.1074/jbc.M109.096404

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