2qd1: Difference between revisions

Line 20:

==Disease==

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~~]]

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==

2QD1 is a ~~[[Single protein]]~~ structure of ~~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=2QD1 OCA].

2QD1 is a 4 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=2QD1 OCA].

==Reference==

A pi-helix switch selective for porphyrin deprotonation and product release in human ferrochelatase., Medlock AE, Dailey TA, Ross TA, Dailey HA, Lanzilotta WN, J Mol Biol. 2007 Nov 2;373(4):1006-16. Epub 2007 Aug 23. PMID:~~[http:~~//~~www.ncbi.nlm.nih.gov/pubmed/17884090 17884090]~~

[[Category: Ferrochelatase]]

[[Category: Homo sapiens]]

~~[[Category: Single protein]]~~

[[Category: Dailey, H A.]]

[[Category: Dailey, T A.]]

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[[Category: Protopophyrin ix]]

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on ~~Sun Jul 27 19~~:25:~~01 2008~~''

''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 16:17:28 2009''

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@@ Line 20: / Line 20: @@
 ==Disease==
-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]]
+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==
-QD1 is a [[Single protein]] structure of 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=2QD1 OCA].
+QD1 is a 4 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=2QD1 OCA].
 ==Reference==
-A pi-helix switch selective for porphyrin deprotonation and product release in human ferrochelatase., Medlock AE, Dailey TA, Ross TA, Dailey HA, Lanzilotta WN, J Mol Biol. 2007 Nov 2;373(4):1006-16. Epub 2007 Aug 23. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/17884090 17884090]
+<ref group="xtra">PMID:17884090</ref><references group="xtra"/>
 [[Category: Ferrochelatase]]
 [[Category: Homo sapiens]]
-[[Category: Single protein]]
 [[Category: Dailey, H A.]]
 [[Category: Dailey, T A.]]
@@ Line 40: / Line 39: @@
 [[Category: Protopophyrin ix]]
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 19:25:01 2008''
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 16:17:28 2009''