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3fj6
From Proteopedia
(Difference between revisions)
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| + | [[Image:3fj6.jpg|left|200px]] | ||
| - | The | + | <!-- |
| + | The line below this paragraph, containing "STRUCTURE_3fj6", creates the "Structure Box" on the page. | ||
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| + | {{STRUCTURE_3fj6| PDB=3fj6 | SCENE= }} | ||
| - | + | ===Human dihydroorotate dehydrogenase in complex with a leflunomide derivative inhibitor 2=== | |
| - | Description: Human dihydroorotate dehydrogenase complexed with a leflunomide derivative | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
| + | The line below this paragraph, {{ABSTRACT_PUBMED_19351152}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 19351152 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_19351152}} | ||
| + | |||
| + | ==About this Structure== | ||
| + | 3FJ6 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=3FJ6 OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:19351152</ref><references group="xtra"/> | ||
| + | [[Category: Dihydroorotate oxidase]] | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Heikkila, T.]] | ||
| + | [[Category: Alpha-beta barrel tim barrel]] | ||
| + | [[Category: Fad]] | ||
| + | [[Category: Flavoprotein]] | ||
| + | [[Category: Membrane]] | ||
| + | [[Category: Mitochondrion]] | ||
| + | [[Category: Mitochondrion inner membrane]] | ||
| + | [[Category: Oxidoreductase]] | ||
| + | [[Category: Polymorphism]] | ||
| + | [[Category: Pyrimidine biosynthesis]] | ||
| + | [[Category: Transit peptide]] | ||
| + | |||
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jun 10 18:02:20 2009'' | ||
Revision as of 15:02, 10 June 2009
Human dihydroorotate dehydrogenase in complex with a leflunomide derivative inhibitor 2
Template:ABSTRACT PUBMED 19351152
About this Structure
3FJ6 is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Davies M, Heikkila T, McConkey GA, Fishwick CW, Parsons MR, Johnson AP. Structure-based design, synthesis, and characterization of inhibitors of human and Plasmodium falciparum dihydroorotate dehydrogenases. J Med Chem. 2009 May 14;52(9):2683-93. PMID:19351152 doi:10.1021/jm800963t
Page seeded by OCA on Wed Jun 10 18:02:20 2009
