3hcr: Difference between revisions
From Proteopedia
Jump to navigationJump to search
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
{{Seed}} | |||
[[Image:3hcr.jpg|left|200px]] | |||
The | <!-- | ||
The line below this paragraph, containing "STRUCTURE_3hcr", creates the "Structure Box" on the page. | |||
You may change the PDB parameter (which sets the PDB file loaded into the applet) | |||
or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | |||
or leave the SCENE parameter empty for the default display. | |||
--> | |||
{{STRUCTURE_3hcr| PDB=3hcr | SCENE= }} | |||
===Human Ferrochelatase with deuteroporphyrin and Ni 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 | |||
(as it appears on PubMed at http://www.pubmed.gov), where 19703464 is the PubMed ID number. | |||
--> | |||
{{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== | |||
3HCR 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=3HCR 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 22:26:18 2009'' | |||
Revision as of 20:26, 11 November 2009
Human Ferrochelatase with deuteroporphyrin and Ni 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
3HCR 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 22:26:18 2009