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Structure paper

TitleNovel human D-amino acid oxidase inhibitors stabilize an active-site lid-open conformation.
Journal, issue, pagesBiosci. Rep., Vol. 34, Year 2014
Publish dateMay 20, 2014 (structure data deposition date)
AuthorsTerry-Lorenzo, R.T. / Chun, L.E. / Brown, S.P. / Heffernan, M.L. / Fang, Q.K. / Orsini, M.A. / Pollegioni, L. / Hardy, L.W. / Spear, K.L. / Large, T.H.
External linksBiosci. Rep. / PubMed:25001371
MethodsX-ray diffraction
Resolution2.4 - 2.85 Å
Structure data

PDB-4qfc:
Co-crystal structure of compound 3 (4-hydroxy-6-[2-(7-hydroxy-2-oxo-4-phenyl-2h-chromen-6-yl)ethyl]pyridazin-3(2h)-one) and FAD bound to human DAAO at 2.4A
Method: X-RAY DIFFRACTION / Resolution: 2.4 Å

PDB-4qfd:
Co-crystal structure of compound 2 (3-(7-hydroxy-2-oxo-4-phenyl-2H-chromen-6-yl)propanoic acid) and FAD bound to human DAAO at 2.85A
Method: X-RAY DIFFRACTION / Resolution: 2.85 Å

Chemicals

ChemComp-FAD:
FLAVIN-ADENINE DINUCLEOTIDE / FAD*YM

ChemComp-31T:
4-hydroxy-6-[2-(7-hydroxy-2-oxo-4-phenyl-2H-chromen-6-yl)ethyl]pyridazin-3(2H)-one

ChemComp-K:
Unknown entry

ChemComp-HOH:
WATER

ChemComp-NA:
Unknown entry

ChemComp-31R:
3-(7-hydroxy-2-oxo-4-phenyl-2H-chromen-6-yl)propanoic acid

Source
  • homo sapiens (human)
Keywordsoxidoreductase/oxidoreductase inhibitor / OXIDASE / OXIDOREDUCTASE / DAAO / D-AMINO ACID OXIDASE / FAD dependent / NMDAR / schizophrenia / D-serine competitive / oxidoreductase-oxidoreductase inhibitor complex / NMDA receptor

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