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Structure paper

TitleDevelopment and crystallographic evaluation of histone H3 peptide with N-terminal serine substitution as a potent inhibitor of lysine-specific demethylase 1.
Journal, issue, pagesBioorg. Med. Chem., Vol. 25, Page 2617-2624, Year 2017
Publish dateNov 14, 2016 (structure data deposition date)
AuthorsAmano, Y. / Kikuchi, M. / Sato, S. / Yokoyama, S. / Umehara, T. / Umezawa, N. / Higuchi, T.
External linksBioorg. Med. Chem. / PubMed:28336409
MethodsX-ray diffraction
Resolution2.53 - 2.69 Å
Structure data

PDB-5h6q:
Crystal structure of LSD1-CoREST in complex with peptide 11
Method: X-RAY DIFFRACTION / Resolution: 2.53 Å

PDB-5h6r:
Crystal structure of LSD1-CoREST in complex with peptide 13
Method: X-RAY DIFFRACTION / Resolution: 2.6 Å

PDB-5x60:
Crystal structure of LSD1-CoREST in complex with peptide 9
Method: X-RAY DIFFRACTION / Resolution: 2.69 Å

Chemicals

ChemComp-GOL:
GLYCEROL

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

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsOXIDOREDUCTASE/TRANSCRIPTION/INHIBITOR / DEMETHYLASE / AMINE OXIDASE / CHROMATIN / HISTONE / FAD / COREPRESSOR / OXIDOREDUCTASE-TRANSCRIPTION-INHIBITOR complex / OXIDOREDUCTASE/TRANSCRIPTION / OXIDOREDUCTASE-TRANSCRIPTION complex

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