3gvw | pdb_00003gvw

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File:3gvw.jpg

Template:STRUCTURE 3gvw

Single-chain UROD F217Y (YF) mutation

Template:ABSTRACT PUBMED 19362562

Disease

Known disease associated with this structure: Porphyria cutanea tarda OMIM:[176100], Porphyria, hepatoerythropoietic OMIM:[176100]

About this Structure

3GVW is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Phillips JD, Warby CA, Whitby FG, Kushner JP, Hill CP. Substrate shuttling between active sites of uroporphyrinogen decarboxylase is not required to generate coproporphyrinogen. J Mol Biol. 2009 Jun 5;389(2):306-14. Epub 2009 Apr 10. PMID:19362562 doi:10.1016/j.jmb.2009.04.013

Page seeded by OCA on Wed Dec 23 09:52:25 2009

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OCA

[1] Phillips JD, Warby CA, Whitby FG, Kushner JP, Hill CP. Substrate shuttling between active sites of uroporphyrinogen decarboxylase is not required to generate coproporphyrinogen. J Mol Biol. 2009 Jun 5;389(2):306-14. Epub 2009 Apr 10. PMID:19362562 doi:10.1016/j.jmb.2009.04.013

3gvw | pdb_00003gvw

Contents

Single-chain UROD F217Y (YF) mutation

Disease

About this Structure

Reference

Proteopedia Page Contributors and Editors (what is this?)

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