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Structure paper

TitleThe structures of human dihydroorotate dehydrogenase with and without inhibitor reveal conformational flexibility in the inhibitor and substrate binding sites
Journal, issue, pagesBiochemistry, Vol. 47, Page 8929-8936, Year 2008
Publish dateMay 4, 2007 (structure data deposition date)
AuthorsWalse, B. / Dufe, V.T. / Svensson, B. / Fritzson, I. / Dahlberg, L. / Khairoullina, A. / Wellmar, U. / Al-Karadaghi, S.
External linksBiochemistry / PubMed:18672895
MethodsX-ray diffraction
Resolution2.1 - 3 Å
Structure data

PDB-2prh:
The structures of apo- and inhibitor bound human dihydroorotate dehydrogenase reveal conformational flexibility within the inhibitor binding site
Method: X-RAY DIFFRACTION / Resolution: 2.4 Å

PDB-2prl:
The structures of apo- and inhibitor bound human dihydroorotate dehydrogenase reveal conformational flexibility within the inhibitor binding site
Method: X-RAY DIFFRACTION / Resolution: 2.1 Å

PDB-2prm:
The structures of apo- and inhibitor bound human dihydroorotate dehydrogenase reveal conformational flexibility within the inhibitor binding site
Method: X-RAY DIFFRACTION / Resolution: 3 Å

Chemicals

ChemComp-FMN:
FLAVIN MONONUCLEOTIDE

ChemComp-ORO:
OROTIC ACID

ChemComp-238:
6-CHLORO-2-(2'-FLUOROBIPHENYL-4-YL)-3-METHYLQUINOLINE-4-CARBOXYLIC ACID

ChemComp-DDQ:
DECYLAMINE-N,N-DIMETHYL-N-OXIDE

ChemComp-HOH:
WATER

ChemComp-SO4:
SULFATE ION

ChemComp-ACT:
ACETATE ION

ChemComp-R2C:
5-METHOXY-2-[(4-PHENOXYPHENYL)AMINO]BENZOIC ACID

Source
  • homo sapiens (human)
KeywordsOXIDOREDUCTASE / protein inhibitor complex

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