3hcp: Difference between revisions
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{{Seed}} | |||
[[Image:3hcp.jpg|left|200px]] | |||
The | <!-- | ||
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{{STRUCTURE_3hcp| PDB=3hcp | SCENE= }} | |||
===Human ferrochelatase with Mn and deuteroporphyrin bound=== | |||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | <!-- | ||
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(as it appears on PubMed at http://www.pubmed.gov), where 19703464 is the PubMed ID number. | |||
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{{ABSTRACT_PUBMED_19703464}} | |||
==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]. | |||
==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]] | |||
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Nov 11 22:26:04 2009'' | |||
