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2qd1

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Revision as of 14:17, 16 February 2009 by OCA (Talk | contribs)
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Image:2qd1.png

Template:STRUCTURE 2qd1

Contents

2.2 Angstrom Structure of the human ferrochelatase variant E343K with substrate bound

Template:ABSTRACT PUBMED 17884090

Disease

Known disease associated with this structure: Protoporphyria, erythropoietic, autosomal dominant OMIM:[612386], Protoporphyria, erythropoietic, autosomal recessive OMIM:[612386]

About this Structure

2QD1 is a 4 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • Medlock AE, Dailey TA, Ross TA, Dailey HA, Lanzilotta WN. A pi-helix switch selective for porphyrin deprotonation and product release in human ferrochelatase. J Mol Biol. 2007 Nov 2;373(4):1006-16. Epub 2007 Aug 23. PMID:17884090 doi:10.1016/j.jmb.2007.08.040

Page seeded by OCA on Mon Feb 16 16:17:28 2009

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