2hre: Difference between revisions

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==Disease==
==Disease==
Known disease associated with this structure: Protoporphyria, erythropoietic OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=177000 177000]], Protoporphyria, erythropoietic, recessive, with liver failure OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=177000 177000]]
Known disease associated with this structure: Protoporphyria, erythropoietic, autosomal dominant OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=612386 612386]], Protoporphyria, erythropoietic, autosomal recessive OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=612386 612386]]


==About this Structure==
==About this Structure==
2HRE is a [[Single protein]] structure of sequence 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=2HRE OCA].  
2HRE is a 4 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=2HRE OCA].  


==Reference==
==Reference==
Substrate interactions with human ferrochelatase., Medlock A, Swartz L, Dailey TA, Dailey HA, Lanzilotta WN, Proc Natl Acad Sci U S A. 2007 Feb 6;104(6):1789-93. Epub 2007 Jan 29. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/17261801 17261801]
<ref group="xtra">PMID:17261801</ref><references group="xtra"/>
[[Category: Ferrochelatase]]
[[Category: Ferrochelatase]]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Dailey, H A.]]
[[Category: Dailey, H A.]]
[[Category: Dailey, T A.]]
[[Category: Dailey, T A.]]
Line 39: Line 38:
[[Category: Protoporphyrin ix]]
[[Category: Protoporphyrin ix]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 29 09:40:18 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb 18 02:59:47 2009''

Revision as of 00:59, 18 February 2009

File:2hre.png

Template:STRUCTURE 2hre

Structure of human ferrochelatase variant E343K with protoporphyrin IX bound

Template:ABSTRACT PUBMED 17261801

Disease

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

About this Structure

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

Reference

  1. Medlock A, Swartz L, Dailey TA, Dailey HA, Lanzilotta WN. Substrate interactions with human ferrochelatase. Proc Natl Acad Sci U S A. 2007 Feb 6;104(6):1789-93. Epub 2007 Jan 29. PMID:17261801

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