2qd5
From Proteopedia
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{{STRUCTURE_2qd5| PDB=2qd5 | SCENE= }} | {{STRUCTURE_2qd5| PDB=2qd5 | SCENE= }} | ||
===Structure of wild type human ferrochelatase in complex with a lead-porphyrin compound=== | ===Structure of wild type human ferrochelatase in complex with a lead-porphyrin compound=== | ||
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{{ABSTRACT_PUBMED_17884090}} | {{ABSTRACT_PUBMED_17884090}} | ||
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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== | ==About this Structure== | ||
| - | + | [[2qd5]] is a 2 chain structure with 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=2QD5 OCA]. | |
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:017884090</ref><references group="xtra"/> |
[[Category: Ferrochelatase]] | [[Category: Ferrochelatase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
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[[Category: Lyase]] | [[Category: Lyase]] | ||
[[Category: Protoporphyrin ix]] | [[Category: Protoporphyrin ix]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Feb 18 00:05:48 2009'' | ||
Revision as of 20:58, 7 January 2013
Structure of wild type human ferrochelatase in complex with a lead-porphyrin compound
Template:ABSTRACT PUBMED 17884090
About this Structure
2qd5 is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Medlock AE, Dailey TA, Ross TA, Dailey HA, Lanzilotta WN. A pi-helix switch selective for porphyrin deprotonation and product release in human ferrochelatase. J Mol Biol. 2007 Nov 2;373(4):1006-16. Epub 2007 Aug 23. PMID:17884090 doi:10.1016/j.jmb.2007.08.040
