3hcp
From Proteopedia
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| + | {{STRUCTURE_3hcp| PDB=3hcp | SCENE= }} | ||
| - | + | ===Human ferrochelatase with Mn and deuteroporphyrin bound=== | |
| - | Description: Human ferrochelatase with Mn and deuteroporphyrin bound | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
| + | The line below this paragraph, {{ABSTRACT_PUBMED_19703464}}, adds the Publication Abstract to the page | ||
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| + | {{ABSTRACT_PUBMED_19703464}} | ||
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| + | ==Disease== | ||
| + | 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== | ||
| + | 3HCP is a 2 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=3HCP OCA]. | ||
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| + | ==Reference== | ||
| + | <ref group="xtra">PMID:19703464</ref><references group="xtra"/> | ||
| + | [[Category: Ferrochelatase]] | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Dailey, H A.]] | ||
| + | [[Category: Lanzilotta, W N.]] | ||
| + | [[Category: Medlock, A E.]] | ||
| + | [[Category: 2fe-2]] | ||
| + | [[Category: Disease mutation]] | ||
| + | [[Category: Ferrochelatase]] | ||
| + | [[Category: Heme biosynthesis]] | ||
| + | [[Category: Iron]] | ||
| + | [[Category: Iron-sulfur]] | ||
| + | [[Category: Lyase]] | ||
| + | [[Category: Membrane]] | ||
| + | [[Category: Metal selectivity]] | ||
| + | [[Category: Metal-binding]] | ||
| + | [[Category: Mitochondrion]] | ||
| + | [[Category: Mitochondrion inner membrane]] | ||
| + | [[Category: Polymorphism]] | ||
| + | [[Category: Porphyrin biosynthesis]] | ||
| + | [[Category: Transit peptide]] | ||
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| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Nov 11 22:26:04 2009'' | ||
Revision as of 20:26, 11 November 2009
Contents |
Human ferrochelatase with Mn and deuteroporphyrin bound
Template:ABSTRACT PUBMED 19703464
Disease
Known disease associated with this structure: Protoporphyria, erythropoietic, autosomal dominant OMIM:[612386], Protoporphyria, erythropoietic, autosomal recessive OMIM:[612386]
About this Structure
3HCP is a 2 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Medlock AE, Carter M, Dailey TA, Dailey HA, Lanzilotta WN. Product release rather than chelation determines metal specificity for ferrochelatase. J Mol Biol. 2009 Oct 23;393(2):308-19. Epub 2009 Aug 22. PMID:19703464 doi:10.1016/j.jmb.2009.08.042
Page seeded by OCA on Wed Nov 11 22:26:04 2009
Categories: Ferrochelatase | Homo sapiens | Dailey, H A. | Lanzilotta, W N. | Medlock, A E. | 2fe-2 | Disease mutation | Heme biosynthesis | Iron | Iron-sulfur | Lyase | Membrane | Metal selectivity | Metal-binding | Mitochondrion | Mitochondrion inner membrane | Polymorphism | Porphyrin biosynthesis | Transit peptide
