3sfk: Difference between revisions

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'''Unreleased structure'''
[[Image:3sfk.jpg|left|200px]]


The entry 3sfk is ON HOLD until Paper Publication
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{{STRUCTURE_3sfk|  PDB=3sfk  |  SCENE=  }}


Authors: Deng, X., Phillips, M.
===Crystal structure of Plasmodium falciparum dihydroorotate dehydrogenase bound with Inhibitor DSM267===


Description: Crystal structure of Plasmodium falciparum dihydroorotate dehydrogenase bound with Inhibitor DSM267
 
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{{ABSTRACT_PUBMED_21696174}}
 
==About this Structure==
[[3sfk]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Plasmodium_falciparum_3d7 Plasmodium falciparum 3d7]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3SFK OCA].
 
==Reference==
<ref group="xtra">PMID:021696174</ref><references group="xtra"/>
[[Category: Dihydroorotate dehydrogenase]]
[[Category: Plasmodium falciparum 3d7]]
[[Category: Deng, X.]]
[[Category: Phillips, M.]]
[[Category: Alpha beta barrel oxidoreductase]]
[[Category: Alpha beta fold]]
[[Category: Flavoprotein]]
[[Category: Fmn]]
[[Category: Inhibitor dsm267]]
[[Category: Mitochondrion inner membrane]]
[[Category: Oxidoreductase-oxidoreductase inhibitor complex]]
[[Category: Plasmodium falciparum membrane mitochondrion]]
[[Category: Pyrimidine biosynthesis]]

Revision as of 18:43, 6 July 2011

File:3sfk.jpg

Template:STRUCTURE 3sfk

Crystal structure of Plasmodium falciparum dihydroorotate dehydrogenase bound with Inhibitor DSM267

Template:ABSTRACT PUBMED 21696174

About this Structure

3sfk is a 1 chain structure with sequence from Plasmodium falciparum 3d7. Full crystallographic information is available from OCA.

Reference

  1. Coteron JM, Marco M, Esquivias J, Deng X, White KL, White J, Koltun M, El Mazouni F, Kokkonda S, Katneni K, Bhamidipati R, Shackleford D, Barturen I, Ferrer S, Jimenez-Diaz MB, Gamo FJ, Goldsmith EJ, Charman B, Bathurst I, Floyd D, Matthews D, Burrows JN, Rathod PK, Charman SA, Phillips MA. Structure-guided lead optimization of triazolopyrimidine-ring substituents identifies potent Plasmodium falciparum dihydroorotate dehydrogenase inhibitors with clinical candidate potential. J Med Chem. 2011 Jun 22. PMID:21696174 doi:10.1021/jm200592f

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