3kxu
From Proteopedia
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[[Image:3kxu.png|left|200px]] | [[Image:3kxu.png|left|200px]] | ||
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{{ABSTRACT_PUBMED_20159981}} | {{ABSTRACT_PUBMED_20159981}} | ||
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- | ==Disease== | ||
- | 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== | ||
- | + | [[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== | ||
+ | *[[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
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