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TitleLSD1/KDM1A mutations associated to a newly described form of intellectual disability impair demethylase activity and binding to transcription factors.
Journal, issue, pagesHum. Mol. Genet., Vol. 25, Page 2578-2587, Year 2016
Publish dateApr 6, 2016 (structure data deposition date)
AuthorsPilotto, S. / Speranzini, V. / Marabelli, C. / Rusconi, F. / Toffolo, E. / Grillo, B. / Battaglioli, E. / Mattevi, A.
External linksHum. Mol. Genet. / PubMed:27094131
MethodsX-ray diffraction
Resolution2.6 - 3.31 Å
Structure data

PDB-5l3b:
Human LSD1/CoREST: LSD1 D556G mutation
Method: X-RAY DIFFRACTION / Resolution: 3.3 Å

PDB-5l3c:
Human LSD1/CoREST: LSD1 E379K mutation
Method: X-RAY DIFFRACTION / Resolution: 3.31 Å

PDB-5l3d:
Human LSD1/CoREST: LSD1 Y761H mutation
Method: X-RAY DIFFRACTION / Resolution: 2.6 Å

Chemicals

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

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsOXIDOREDUCTASE/REPRESSOR / OXIDOREDUCTASE-REPRESSOR complex / Histone demethylase / chromatin / flavin / FAD

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