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Structure paper

TitleBinding site for activator MDL-801 on SIRT6.
Journal, issue, pagesNat. Chem. Biol., Vol. 17, Page 519-521, Year 2021
Publish dateJan 21, 2020 (structure data deposition date)
AuthorsYou, W. / Steegborn, C.
External linksNat. Chem. Biol. / PubMed:33649599
MethodsX-ray diffraction
Resolution1.75 - 2.13 Å
Structure data

PDB-6xuy:
Human Sirt6 13-308 in complex with ADP-ribose
Method: X-RAY DIFFRACTION / Resolution: 2.13 Å

PDB-6xv1:
Human Sirt6 13-308 in complex with ADP-ribose and the activator MDL-801
Method: X-RAY DIFFRACTION / Resolution: 1.95 Å

PDB-6xv6:
Human Sirt6 3-318 in complex with ADP-ribose
Method: X-RAY DIFFRACTION / Resolution: 1.75 Å

PDB-6xvg:
Human Sirt6 3-318 in complex with ADP-ribose and the activator MDL-801
Method: X-RAY DIFFRACTION / Resolution: 2.1 Å

Chemicals

ChemComp-AR6:
[(2R,3S,4R,5R)-5-(6-AMINOPURIN-9-YL)-3,4-DIHYDROXY-OXOLAN-2-YL]METHYL

ChemComp-ZN:
Unknown entry

ChemComp-PGE:
TRIETHYLENE GLYCOL

ChemComp-SO4:
SULFATE ION

ChemComp-HOH:
WATER

ChemComp-8L9:
5-[[3,5-bis(chloranyl)phenyl]sulfonylamino]-2-[(5-bromanyl-4-fluoranyl-2-methyl-phenyl)sulfamoyl]benzoic acid

ChemComp-NCA:
NICOTINAMIDE / medication*YM

ChemComp-GOL:
GLYCEROL

Source
  • homo sapiens (human)
KeywordsHYDROLASE / Deacylase / Activator / Allosteric / Isoform-selective

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