2q6z
From Proteopedia
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[[Image:2q6z.png|left|200px]] | [[Image:2q6z.png|left|200px]] | ||
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{{STRUCTURE_2q6z| PDB=2q6z | SCENE= }} | {{STRUCTURE_2q6z| PDB=2q6z | SCENE= }} | ||
===Uroporphyrinogen Decarboxylase G168R single mutant apo-enzyme=== | ===Uroporphyrinogen Decarboxylase G168R single mutant apo-enzyme=== | ||
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{{ABSTRACT_PUBMED_17240319}} | {{ABSTRACT_PUBMED_17240319}} | ||
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| - | ==Disease== | ||
| - | Known disease associated with this structure: Porphyria cutanea tarda OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176100 176100]], Porphyria, hepatoerythropoietic OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176100 176100]] | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[2q6z]] is a 1 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=2Q6Z OCA]. | |
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:017240319</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Uroporphyrinogen decarboxylase]] | [[Category: Uroporphyrinogen decarboxylase]] | ||
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[[Category: Stadtmueller, B M.]] | [[Category: Stadtmueller, B M.]] | ||
[[Category: Whitby, F G.]] | [[Category: Whitby, F G.]] | ||
| + | [[Category: Lyase]] | ||
[[Category: Uroporphyrinogen decarboxylase enzyme urod g168r coproporphyrinogen]] | [[Category: Uroporphyrinogen decarboxylase enzyme urod g168r coproporphyrinogen]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 04:17:20 2009'' | ||
Revision as of 17:54, 7 January 2013
Uroporphyrinogen Decarboxylase G168R single mutant apo-enzyme
Template:ABSTRACT PUBMED 17240319
About this Structure
2q6z is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Phillips JD, Whitby FG, Stadtmueller BM, Edwards CQ, Hill CP, Kushner JP. Two novel uroporphyrinogen decarboxylase (URO-D) mutations causing hepatoerythropoietic porphyria (HEP). Transl Res. 2007 Feb;149(2):85-91. PMID:17240319 doi:10.1016/j.trsl.2006.08.006
