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1jpi

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{{Seed}}
 
[[Image:1jpi.png|left|200px]]
[[Image:1jpi.png|left|200px]]
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{{STRUCTURE_1jpi| PDB=1jpi | SCENE= }}
{{STRUCTURE_1jpi| PDB=1jpi | SCENE= }}
===Phe232Leu mutant of human UROD, human uroporphyrinogen III decarboxylase===
===Phe232Leu mutant of human UROD, human uroporphyrinogen III decarboxylase===
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{{ABSTRACT_PUBMED_11719352}}
{{ABSTRACT_PUBMED_11719352}}
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==Disease==
 
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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==
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1JPI is a 1 chain 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=1JPI OCA].
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[[1jpi]] 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=1JPI OCA].
==Reference==
==Reference==
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<ref group="xtra">PMID:11719352</ref><references group="xtra"/>
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<ref group="xtra">PMID:011719352</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Uroporphyrinogen decarboxylase]]
[[Category: Uroporphyrinogen decarboxylase]]
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[[Category: Whitby, F G.]]
[[Category: Whitby, F G.]]
[[Category: Heme biosynthesis]]
[[Category: Heme biosynthesis]]
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[[Category: Lyase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 17:49:53 2009''
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Revision as of 11:23, 5 December 2012

Template:STRUCTURE 1jpi

Phe232Leu mutant of human UROD, human uroporphyrinogen III decarboxylase

Template:ABSTRACT PUBMED 11719352

About this Structure

1jpi is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • Phillips JD, Parker TL, Schubert HL, Whitby FG, Hill CP, Kushner JP. Functional consequences of naturally occurring mutations in human uroporphyrinogen decarboxylase. Blood. 2001 Dec 1;98(12):3179-85. PMID:11719352

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