2qd1: Difference between revisions

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|PDB= 2qd1 |SIZE=350|CAPTION= <scene name='initialview01'>2qd1</scene>, resolution 2.20&Aring;
|PDB= 2qd1 |SIZE=350|CAPTION= <scene name='initialview01'>2qd1</scene>, resolution 2.20&Aring;
|SITE=  
|SITE=  
|LIGAND= <scene name='pdbligand=FES:FE2/S2+(INORGANIC)+CLUSTER'>FES</scene>, <scene name='pdbligand=PP9:PROTOPORPHYRIN+IX'>PP9</scene>, <scene name='pdbligand=CHD:CHOLIC+ACID'>CHD</scene> and <scene name='pdbligand=IMD:IMIDAZOLE'>IMD</scene>
|LIGAND= <scene name='pdbligand=CHD:CHOLIC+ACID'>CHD</scene>, <scene name='pdbligand=FES:FE2/S2+(INORGANIC)+CLUSTER'>FES</scene>, <scene name='pdbligand=IMD:IMIDAZOLE'>IMD</scene>, <scene name='pdbligand=PP9:PROTOPORPHYRIN+IX'>PP9</scene>
|ACTIVITY= [http://en.wikipedia.org/wiki/Ferrochelatase Ferrochelatase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.99.1.1 4.99.1.1]  
|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Ferrochelatase Ferrochelatase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.99.1.1 4.99.1.1] </span>
|GENE= FECH ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|GENE= FECH ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
|DOMAIN=
|RELATEDENTRY=[[2qd3|2QD3]], [[2qd4|2QD4]], [[2qd5|2QD5]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2qd1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2qd1 OCA], [http://www.ebi.ac.uk/pdbsum/2qd1 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2qd1 RCSB]</span>
}}
}}


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==Disease==
==Disease==
Known diseases 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 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]]


==About this Structure==
==About this Structure==
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[[Category: Medlock, A E.]]
[[Category: Medlock, A E.]]
[[Category: Ross, T A.]]
[[Category: Ross, T A.]]
[[Category: CHD]]
[[Category: FES]]
[[Category: IMD]]
[[Category: PP9]]
[[Category: ferrochelatase]]
[[Category: ferrochelatase]]
[[Category: heme biosynthesis]]
[[Category: heme biosynthesis]]
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[[Category: protopophyrin ix]]
[[Category: protopophyrin ix]]


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