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2qd1

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Revision as of 16:25, 27 July 2008 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 OMIM:[177000], Protoporphyria, erythropoietic, recessive, with liver failure OMIM:[177000]

About this Structure

2QD1 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 19:25:01 2008

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