Ceruloplasmin
From Proteopedia
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CP mutation causes the autosomal recessive disorder - Aceruloplasminemia which results in accumulation of iron in the brain. | CP mutation causes the autosomal recessive disorder - Aceruloplasminemia which results in accumulation of iron in the brain. | ||
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| + | == Structural highlights == | ||
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| + | <scene name='46/467272/Cv/5'>Cu-O-Cu coordination site</scene>. | ||
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</StructureSection> | </StructureSection> | ||
Revision as of 10:57, 18 January 2016
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3D structures of ceruloplasmin
Updated on 18-January-2016
1kcw, 2j5w, 4enz – hCP - human
4ejx – hCP + myeloperoxidase
References
- ↑ Hellman NE, Gitlin JD. Ceruloplasmin metabolism and function. Annu Rev Nutr. 2002;22:439-58. Epub 2002 Apr 4. PMID:12055353 doi:http://dx.doi.org/10.1146/annurev.nutr.22.012502.114457
