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2wv8
From Proteopedia
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| - | + | [[Image:2wv8.png|left|200px]] | |
| - | [[Image:2wv8. | + | |
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{{STRUCTURE_2wv8| PDB=2wv8 | SCENE= }} | {{STRUCTURE_2wv8| PDB=2wv8 | SCENE= }} | ||
| - | === | + | ===Complex of human dihydroorotate dehydrogenase with the inhibitor 221290=== |
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| + | The line below this paragraph, {{ABSTRACT_PUBMED_20183850}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 20183850 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_20183850}} | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[2wv8]] 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=2WV8 OCA]. | |
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| + | ==Reference== | ||
| + | <ref group="xtra">PMID:020183850</ref><references group="xtra"/> | ||
[[Category: Dihydroorotate dehydrogenase]] | [[Category: Dihydroorotate dehydrogenase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
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[[Category: Transit peptide]] | [[Category: Transit peptide]] | ||
[[Category: Transmembrane]] | [[Category: Transmembrane]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug 25 08:50:31 2010'' | ||
Revision as of 08:00, 25 April 2012
Complex of human dihydroorotate dehydrogenase with the inhibitor 221290
Template:ABSTRACT PUBMED 20183850
About this Structure
2wv8 is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Fritzson I, Svensson B, Al-Karadaghi S, Walse B, Wellmar U, Nilsson UJ, da Graca Thrige D, Jonsson S. Inhibition of human DHODH by 4-hydroxycoumarins, fenamic acids, and N-(alkylcarbonyl)anthranilic acids identified by structure-guided fragment selection. ChemMedChem. 2010 Apr 6;5(4):608-17. PMID:20183850 doi:10.1002/cmdc.200900454
Categories: Dihydroorotate dehydrogenase | Homo sapiens | Al-Karadaghi, S. | Dahlberg, L. | Fritzson, I. | Svensson, B. | Walse, B. | Wellmar, U. | Enzyme inhibition | Flavoprotein | Inflamation | Mitochondrion inner membrane | Oxidoreductase | Pyrimidine biosynthesis | Structure-based drug design | Transit peptide | Transmembrane
