2qd3
From Proteopedia
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{{STRUCTURE_2qd3|  PDB=2qd3  |  SCENE=  }}   | {{STRUCTURE_2qd3|  PDB=2qd3  |  SCENE=  }}   | ||
| - | + | ===Wild type human ferrochelatase crystallized with ammonium sulfate===  | |
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==Disease==  | ==Disease==  | ||
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[[Category: Lyase]]  | [[Category: Lyase]]  | ||
[[Category: Protoporphyrin ix]]  | [[Category: Protoporphyrin ix]]  | ||
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| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 18:21:48 2008''  | ||
Revision as of 15:21, 27 July 2008
Contents | 
Wild type human ferrochelatase crystallized with ammonium sulfate
Template:ABSTRACT PUBMED 17884090
Disease
Known disease associated with this structure: Protoporphyria, erythropoietic OMIM:[177000], Protoporphyria, erythropoietic, recessive, with liver failure OMIM:[177000]
About this Structure
2QD3 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
A pi-helix switch selective for porphyrin deprotonation and product release in human ferrochelatase., Medlock AE, Dailey TA, Ross TA, Dailey HA, Lanzilotta WN, J Mol Biol. 2007 Nov 2;373(4):1006-16. Epub 2007 Aug 23. PMID:17884090
Page seeded by OCA on Sun Jul 27 18:21:48 2008
