3hx2
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 3hx2 is ON HOLD Authors: Hurley, T.D., Vidal, R. Description: Crystal structure of human ferritin Phe167SerfsX26 mutant. This file is a part 1/3 of...) |
|||
| Line 1: | Line 1: | ||
| - | + | {{Seed}} | |
| + | [[Image:3hx2.jpg|left|200px]] | ||
| - | The | + | <!-- |
| + | The line below this paragraph, containing "STRUCTURE_3hx2", creates the "Structure Box" on the page. | ||
| + | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
| + | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | ||
| + | or leave the SCENE parameter empty for the default display. | ||
| + | --> | ||
| + | {{STRUCTURE_3hx2| PDB=3hx2 | SCENE= }} | ||
| - | + | ===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=== | |
| - | Description: 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 struc | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | ==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== | ||
| + | 3HX2 is a 48 chains structure of 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]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:18755684</ref><references group="xtra"/> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Hurley, T D.]] | ||
| + | [[Category: Vidal, R.]] | ||
| + | [[Category: Disorder]] | ||
| + | [[Category: Iron]] | ||
| + | [[Category: Iron storage]] | ||
| + | [[Category: Iron storage protein]] | ||
| + | [[Category: Metal-binding]] | ||
| + | |||
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug 19 13:40:27 2009'' | ||
Revision as of 10:40, 19 August 2009
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
Disease
Known disease associated with this structure: Basal ganglia disease, adult-onset OMIM:[134790], Hyperferritinemia-cataract syndrome OMIM:[134790]
About this Structure
3HX2 is a 48 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- 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
Page seeded by OCA on Wed Aug 19 13:40:27 2009
