2prm

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[[Image:2prm.png|left|200px]]
[[Image:2prm.png|left|200px]]
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{{STRUCTURE_2prm| PDB=2prm | SCENE= }}
{{STRUCTURE_2prm| PDB=2prm | SCENE= }}
===The structures of apo- and inhibitor bound human dihydroorotate dehydrogenase reveal conformational flexibility within the inhibitor binding site===
===The structures of apo- and inhibitor bound human dihydroorotate dehydrogenase reveal conformational flexibility within the inhibitor binding site===
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{{ABSTRACT_PUBMED_18672895}}
{{ABSTRACT_PUBMED_18672895}}
==About this Structure==
==About this Structure==
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2PRM 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=2PRM OCA].
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[[2prm]] 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=2PRM OCA].
==Reference==
==Reference==
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<ref group="xtra">PMID:18672895</ref><references group="xtra"/>
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<ref group="xtra">PMID:018672895</ref><references group="xtra"/>
[[Category: Dihydroorotate dehydrogenase]]
[[Category: Dihydroorotate dehydrogenase]]
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Oxidoreductase]]
[[Category: Oxidoreductase]]
[[Category: Protein inhibitor complex]]
[[Category: Protein inhibitor complex]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 19:41:41 2009''
 

Revision as of 15:20, 7 January 2013

Template:STRUCTURE 2prm

The structures of apo- and inhibitor bound human dihydroorotate dehydrogenase reveal conformational flexibility within the inhibitor binding site

Template:ABSTRACT PUBMED 18672895

About this Structure

2prm is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

  • Walse B, Dufe VT, Svensson B, Fritzson I, Dahlberg L, Khairoullina A, Wellmar U, Al-Karadaghi S. The structures of human dihydroorotate dehydrogenase with and without inhibitor reveal conformational flexibility in the inhibitor and substrate binding sites. Biochemistry. 2008 Aug 26;47(34):8929-36. Epub 2008 Aug 2. PMID:18672895 doi:10.1021/bi8003318

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