3hx2: Difference between revisions

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{{Seed}}
[[Image:3hx2.png|left|200px]]
[[Image:3hx2.png|left|200px]]


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{{ABSTRACT_PUBMED_19923220}}
{{ABSTRACT_PUBMED_19923220}}


==Disease==
==About this Structure==
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]]
[[3hx2]] is a 48 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=3HX2 OCA].


==About this Structure==
==See Also==
3HX2 is a 48 chains structure with sequences 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=3HX2 OCA].
*[[Ferritin]]


==Reference==
==Reference==
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[[Category: Iron storage protein]]
[[Category: Iron storage protein]]
[[Category: Metal-binding]]
[[Category: Metal-binding]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb  3 09:05:45 2010''

Revision as of 23:43, 14 March 2011

File:3hx2.png

Template:STRUCTURE 3hx2

Crystal structure of human ferritin Phe167SerfsX26 mutant. This file is a part 1/3 of the split entry and contains the copies 1 and 2 of the total six copies of the biological unit that are present in the crystallographic asymmetric unit. The entire structure contains six copies of the biological unit in the crystallographic asymmetric unit and is described in remark 400

Template:ABSTRACT PUBMED 19923220

About this Structure

3hx2 is a 48 chain structure of Ferritin with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  1. Baraibar MA, Muhoberac BB, Garringer HJ, Hurley TD, Vidal R. Unraveling of the E-helices and disruption of 4-fold pores are associated with iron mishandling in a mutant ferritin causing neurodegeneration. J Biol Chem. 2010 Jan 15;285(3):1950-6. Epub 2009 Nov 18. PMID:19923220 doi:10.1074/jbc.M109.042986
  2. Baraibar MA, Barbeito AG, Muhoberac BB, Vidal R. Iron-mediated aggregation and a localized structural change characterize ferritin from a mutant light chain polypeptide that causes neurodegeneration. J Biol Chem. 2008 Nov 14;283(46):31679-89. Epub 2008 Aug 28. PMID:18755684 doi:10.1074/jbc.M805532200

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